SLMS - People

UCL School of Life and Medical Sciences

Prof Sanjay Sisodiya

Personal Profile

Name:	Sanjay Sisodiya	Email:	s.sisodiya@ucl.ac.uk
Title:	Prof	Tel:	020 3448 8612
Department:	Clinical & Experimental Epilepsy	Fax:	020 3448 8615
Position:	Professor of Neurology	Address:	Queen Square, , London, WC1N 3BG
Research Domain:	Genetics (Frontier Disciplines), Neuroscience	Web Page:	Personal Web Page

Profile

Research Description

Genetic causes of epilepsy, treatment responses and outcomes Drug resistance Population genetics and pharmacogenomics Neuropathology Genetic neuroimaging

Research Activities

Antiepileptic drug action and interaction

Epilepsy - developmental malformations, pathology, drug resistance, population genetics

Neurology

Education Description

Teaching to undergraduates and postgraduates, including lecturing on MSc Courses at UCL.

UCL Collaborators

Prof Philip Patsalos; Prof Simon Shorvon; Prof Matthias Koepp; Prof David Hunt; Prof Tony Moore; Prof John Duncan; Prof Emrah Duzel; Dr Maria Thom; Prof Ley Sander

External Collaborators

Publications

2013

Goc J, Liu J, Sisodiya S, Thom M (2013). A study of gliogenesis in the vicinity of depth electrode tracts.
Bandopadhyay R, Liu J, Sisodiya SM, Thom M (2013). A comparative study of the dentate gyrus in hippocampal sclerosis in epilepsy and dementia.
Brooke-Ball H, Tachrount M, Sisodiya S, Thom M (2013). Mild malformations of cortical development (type II) in temporal lobe epilepsy.
Clayton LM, Stern WM, Newman WD, Sander JW, Acheson J, Sisodiya SM (2013). Evolution of visual field loss over ten years in individuals taking vigabatrin.. Epilepsy Res, , - . doi:10.1016/j.eplepsyres.2013.02.014
Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF, Genetics Commission of the International League Against Epilepsy (2013). SCN1A testing for epilepsy: Application in clinical practice.. Epilepsia, 54(5), 946 - 952. doi:10.1111/epi.12168
Shepherd C, Liu J, Goc J, Martinian L, Jacques TS, Sisodiya SM, Thom M (2013). A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II.. Epilepsia, 54(5), 898 - 908. doi:10.1111/epi.12143
Coppola A, Chinthapalli K, Hammond P, Sander JW, Sisodiya SM (2013). Pediatric diagnosis not made until adulthood: A case of Wolf-Hirschhorn syndrome. Gene, 512(2), 532 - 535.

2012

Thom M, Liagkouras I, Martinian L, Liu J, Catarino CB, Sisodiya SM (2012). Variability of sclerosis along the longitudinal hippocampal axis in epilepsy: A post mortem study. Epilepsy Research, 102(1-2), 45 - 59.
Martinian L, Catarino CB, Thompson P, Sisodiya SM, Thom M (2012). Calbindin D28K expression in relation to granule cell dispersion, mossy fibre sprouting and memory impairment in hippocampal sclerosis: a surgical and post mortem series.. Epilepsy Res, 98(1), 14 - 24. doi:10.1016/j.eplepsyres.2011.08.011
Novy J, Catarino CB, Chinthapalli K, Smith SM, Clayton-Smith J, Hennekam RCM, Hammond P, Sisodiya SM (2012). Another cause of vaccine encephalopathy: A case of Angelman syndrome. European Journal of Medical Genetics, 55(5), 338 - 341.
Chaudhary UJ, Centeno M, Carmichael DW, Vollmar C, Rodionov R, Bonelli S, Stretton J, Pressler R, Eriksson SH, Sisodiya S, Friston K, Duncan JS, Lemieux L, Koepp M (2012). Imaging the interaction: Epileptic discharges, working memory, and behavior.. Hum Brain Mapp, , - . doi:10.1002/hbm.22115
Gaitatzis A, Sisodiya SM, Sander JW (2012). The somatic comorbidity of epilepsy: a weighty but often unrecognized burden.. Epilepsia, 53(8), 1282 - 1293. doi:10.1111/j.1528-1167.2012.03528.x
Galizia EC, Palmer R, Waters JJ, Koepp MJ, Hennekam RCM, Sisodiya SM (2012). The idic(15) syndrome: Expanding the phenotype. American Journal of Medical Genetics, Part A, 158 A(6), 1505 - 1508.
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann O, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga J-J, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, Van Eijk K, Van Erp TGM, Van Tol M-J, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, De Almeida MAA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HHH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Hernández MCV, Van Den Heuvel M, Van Der Wee NJ, Van Haren NEM, Veltman JA, Völzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack CR, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW, Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, Decarli C, Seshadri S, Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, De Zubicaray GI, Deary IJ, Donohoe G, De Geus EJC, Espeseth T, Fernéndez G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, Mcdonald C, Mcintosh AM, Mcmahon FJ, Mcmahon KL, Meyer-Lindenberg A, Morris DW, Müller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Sämann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44(5), 552 - 561.
Thom M, Liagkouras I, Martinian L, Liu J, Catarino CB, Sisodiya SM (2012). Variability of sclerosis along the longitudinal hippocampal axis in epilepsy: A post mortem study. Epilepsy Research, , - .
Caruana Galizia E, Palmer R, Waters JJ, Koepp MJ, Hennekam RCM, Sisodiya SM (2012). The idic(15) Syndrome: expanding the phenotype. American Journal of Medical Genetics Part A, , - .
Liu JY, Kasperavičiūtė D, Martinian L, Thom M, Sisodiya SM (2012). Neuropathology of 16p13.11 deletion in epilepsy.. PLoS One, 7(4), e34813 - . doi:10.1371/journal.pone.0034813
Clayton LM, Devile M, Punte T, de Haan GJ, Sander JW, Acheson JF, Sisodiya SM (2012). Patterns of peripapillary retinal nerve fiber layer thinning in vigabatrin-exposed individuals.. Ophthalmology, 119(10), 2152 - 2160. doi:10.1016/j.ophtha.2012.05.009
Novy J, Bell G, Sisodiya SM, Sander JW (2012). SOMATIC CO-MORBIDITIES ARE A MAJOR ISSUE IN PEOPLE WITH EPILEPSY.
Belluzzo M, Novy J, Bell G, Koepp M, Sisodiya SM, Sander JW (2012). LATE-LIFE REMISSION IN INTRACTABLE EPILEPSY: "BURNT OUT EPILEPSY'' OR NATURAL HISTORY?.
Chinthapalli K, Bartolini E, Novy J, Suttie M, Marini C, Falchi M, Fox Z, Clayton L, Sander JW, Guerrini R, Depondt C, Hennekam R, Hammond P, Sisodiya SM (2012). DENSE SURFACE MODELS OF FACE SHAPE ASSIST IN PREDICTING PATHOGENIC COPY NUMBER VARIANTS.
Thom M, Liu J, Sander JW, Sisodiya SM (2012). AUDIT OF LOCAL NEUROPATHOLOGY PRACTICE IN SUDEP AUTOPSIES.
Clayton LM, Devile M, Punte T, De Haan G-J, Sander JW, Acheson JF, Sisodiya SM (2012). Patterns of peripapillary retinal nerve fiber layer thinning in vigabatrin-exposed individuals. Ophthalmology, 119(10), 2152 - 2160.
Coppola A, Chinthapalli K, Hammond P, Sander JW, Sisodiya SM (2012). Pediatric diagnosis not made until adulthood: A case of Wolf-Hirschhorn syndrome. Gene, , - .
Chinthapalli K, Bartolini E, Novy J, Suttie M, Marini C, Falchi M, Fox Z, Clayton LM, Sander JW, Guerrini R, Depondt C, Hennekam R, Hammond P, Sisodiya SM (2012). Atypical face shape and genomic structural variants in epilepsy.. Brain, 135(Pt 10), 3101 - 3114. doi:10.1093/brain/aws232
Novy J, Catarino CB, Chinthapalli K, Smith SM, Clayton-Smith J, Hennekam RCM, Hammond P, Sisodiya SM (2012). Another cause of vaccine encephalopathy: A case of Angelman syndrome. European Journal of Medical Genetics, 55(5), 338 - 341.
Aronica E, Sisodiya SM, Gorter JA (2012). Cerebral expression of drug transporters in epilepsy. Advanced Drug Delivery Reviews, 64(10), 919 - 929.
Gaitatzis A, Sisodiya SM, Sander JW (2012). The somatic comorbidity of epilepsy: A weighty but often unrecognized burden. Epilepsia, 53(8), 1282 - 1293.
Feast A, Martinian L, Liu J, Catarino CB, Thom M, Sisodiya SM (2012). Investigation of hypoxia-inducible factor-1α in hippocampal sclerosis: a postmortem study.. Epilepsia, 53(8), 1349 - 1359. doi:10.1111/j.1528-1167.2012.03591.x
Liu JY, Thom M, Catarino CB, Martinian L, Figarella-Branger D, Bartolomei F, Koepp M, Sisodiya SM (2012). Neuropathology of the blood-brain barrier and pharmaco-resistance in human epilepsy.. Brain, 135(Pt 10), 3115 - 3133. doi:10.1093/brain/aws147
Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E, European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium , Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium , European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium , Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein DB (2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.. Nat Genet, 44(9), 1030 - 1034. doi:10.1038/ng.2358
Heinzen EL, Depondt C, Cavalleri GL, Ruzzo EK, Walley NM, Need AC, Ge D, He M, Cirulli ET, Zhao Q, Cronin KD, Gumbs CE, Campbell CR, Hong LK, Maia JM, Shianna KV, McCormack M, Radtke RA, O'Conner GD, Mikati MA, Gallentine WB, Husain AM, Sinha SR, Chinthapalli K, Puranam RS, McNamara JO, Ottman R, Sisodiya SM, Delanty N, Goldstein DB (2012). Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.. Am J Hum Genet, 91(2), 293 - 302. doi:10.1016/j.ajhg.2012.06.016
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Valdés Hernández MC, Van den Heuvel M, van der Wee NJ, Van Haren NE, Veltman JA, Völzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack CR, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW, Alzheimer's Disease Neuroimaging Initiative , EPIGEN Consortium , IMAGEN Consortium , Saguenay Youth Study Group , Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, DeCarli C, Seshadri S, Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium , Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, de Zubicaray GI, Deary IJ, Donohoe G, de Geus EJ, Espeseth T, Fernández G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meyer-Lindenberg A, Morris DW, Müller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Sämann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM, Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium (2012). Identification of common variants associated with human hippocampal and intracranial volumes.. Nat Genet, 44(5), 552 - 561. doi:10.1038/ng.2250
Martinian L, Catarino CB, Thompson P, Sisodiya SM, Thom M (2012). Calbindin D28K expression in relation to granule cell dispersion, mossy fibre sprouting and memory impairment in hippocampal sclerosis: A surgical and post mortem series. Epilepsy Research, 98(1), 14 - 24.
McCormack M, Urban TJ, Shianna KV, Walley N, Pandolfo M, Depondt C, Chaila E, O'Conner GD, Kasperavičiūtė D, Radtke RA, Heinzen EL, Sisodiya SM, Delanty N, Cavalleri GL (2012). Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.. Pharmacogenomics, 13(4), 399 - 405. doi:10.2217/pgs.11.165
Novy J, Catarino CB, Chinthapalli K, Smith SM, Clayton-Smith J, Hennekam RC, Hammond P, Sisodiya SM (2012). Another cause of vaccine encephalopathy: a case of Angelman syndrome.. Eur J Med Genet, 55(5), 338 - 341. doi:10.1016/j.ejmg.2012.01.008
Galizia EC, Srikantha M, Palmer R, Waters JJ, Lench N, Ogilvie CM, Kasperavičiūtė D, Nashef L, Sisodiya SM (2012). Array comparative genomic hybridization: results from an adult population with drug-resistant epilepsy and co-morbidities.. Eur J Med Genet, 55(5), 342 - 348. doi:10.1016/j.ejmg.2011.12.011
Webb TR, Matarin M, Gardner JC, Kelberman D, Hassan H, Ang W, Michaelides M, Ruddle JB, Pennell CE, Yazar S, Khor CC, Aung T, Yogarajah M, Robson AG, Holder GE, Cheetham ME, Traboulsi EI, Moore AT, Sowden JC, Sisodiya SM, Mackey DA, Tuft SJ, Hardcastle AJ (2012). X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.. Am J Hum Genet, 90(2), 247 - 259. doi:10.1016/j.ajhg.2011.12.019
Lockwood-Estrin G, Thom M, Focke NK, Symms MR, Martinian L, Sisodiya SM, Duncan JS, Eriksson SH (2012). Correlating 3T MRI and histopathology in patients undergoing epilepsy surgery.. J Neurosci Methods, 205(1), 182 - 189. doi:10.1016/j.jneumeth.2011.12.014
Aronica E, Sisodiya SM, Gorter JA (2012). Cerebral expression of drug transporters in epilepsy.. Adv Drug Deliv Rev, 64(10), 919 - 929. doi:10.1016/j.addr.2011.11.008
Lescai F, Bonfiglio S, Bacchelli C, Chanudet E, Waters A, Sisodiya SM, Kasperavičiute D, Williams J, Harold D, Hardy J, Kleta R, Cirak S, Williams R, Achermann JC, Anderson J, Kelsell D, Vulliamy T, Houlden H, Wood N, Sheerin U, Tonini GP, Mackay D, Hussain K, Sowden J, Kinsler V, Osinska J, Brooks T, Hubank M, Beales P, Stupka E (2012). Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes. PLoS ONE, 7(12), - .

2011

Sisodiya S (2011). Array CGH in adults with epilepsy.
Eriksson SH (2011). Epilepsy and sleep. In Rugg-Gunn FJ, Sander JW, Smalls JE (Ed.), Epilepsy 2011: from science to society. A practical guide to epilepsy (pp. 193 - 202). : Meritus Communications.
Arrigoni FI, Matarin M, Thompson PJ, Michaelides M, McClements ME, Redmond E, Clarke L, Ellins E, Mohamed S, Pavord I, Klein N, Hunt DM, Moore AT, Halcox J, Sisodiya SM (2011). Erratum: Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy (European Journal of Human Genetics (2011) 19 (131-137) DOI:10.1038/ejhg.2010.147). European Journal of Human Genetics, 19(9), 1018 - 1018.
Sisodiya S (2011). Epilepsy: the new order-classifying focal cortical dysplasias.. Nat Rev Neurol, 7(3), 129 - 130. doi:10.1038/nrneurol.2011.15
Chinthapalli VK, Bartolini E, Novy J, Suttie M, Hennekam R, Marini C, Depondt C, Guerrini R, Hammond P, Sisodiya S (2011). THE USE OF STEREOPHOTOGRAMMETRY TO DETECT COPY NUMBER VARIATION IN PEOPLE WITH EPILEPSY.
Feast A, Thom M, Sisodiya S, Martinian L (2011). The role of hypoxia-inducible factor-1 alpha in unilateral cases of hippocampal sclerosis using human postmortem tissue. Is it neuroprotective?.
Kasperavičiute D, Catarino CB, Chinthapalli K, Clayton LMS, Thom M, Martinian L, Cohen H, Adalat S, Bockenhauer D, Pope SA, Lench N, Koltzenburg M, Duncan JS, Hammond P, Hennekam RCM, Land JM, Sisodiya SM (2011). Uncovering genomic causes of co-morbidity in epilepsy: Gene-driven phenotypic characterization of rare microdeletions. PLoS ONE, 6(8), - .
Reuber M, Jamnadas-Khoda J, Broadhurst M, Grunewald R, Howell S, Koepp M, Sisodiya S, Walker M (2011). Psychogenic nonepileptic seizure manifestations reported by patients and witnesses.. Epilepsia, 52(11), 2028 - 2035. doi:10.1111/j.1528-1167.2011.03162.x
Thom M, Narkiewicz M, Martinian L, Phadke R, Thompson P, Koepp M, Caboclo L, Claudia C, Sanjay S (2011). NEUROFIBRILLARY TANGLE PATHOLOGY AND BRAAK STAGING IN CHRONIC EPILEPSY: A POSTMORTEM STUDY.
Clayton LM, Acheson J, Sisodiya SM (2011). Reply.. Ann Neurol, 70(4), 672 - 673. doi:10.1002/ana.22594
Payne NE, Cross JH, Sander JW, Sisodiya SM (2011). The ketogenic and related diets in adolescents and adults--a review.. Epilepsia, 52(11), 1941 - 1948. doi:10.1111/j.1528-1167.2011.03287.x
Clayton LM, Sander JW, Acheson J, Sisodiya SM (2011). THE EVOLUTION OF VISUAL FIELD LOSS IN INDIVIDUALS WHO CONTINUE VIGABATRIN THERAPY OVER A 10-YEAR PERIOD.
Thom M, Toma A, An S, Martinian L, Hadjivassiliou G, Ratilal B, Dean A, McEvoy A, Sisodiya SM, Brandner S (2011). One hundred and one dysembryoplastic neuroepithelial tumors: an adult epilepsy series with immunohistochemical, molecular genetic, and clinical correlations and a review of the literature.. J Neuropathol Exp Neurol, 70(10), 859 - 878. doi:10.1097/NEN.0b013e3182302475
Thom M, Liu JY, Thompson P, Phadke R, Narkiewicz M, Martinian L, Marsdon D, Koepp M, Caboclo L, Catarino CB, Sisodiya SM (2011). Neurofibrillary tangle pathology and Braak staging in chronic epilepsy in relation to traumatic brain injury and hippocampal sclerosis: a post-mortem study.. Brain, 134(Pt 10), 2969 - 2981. doi:10.1093/brain/awr209
Kasperavičiūtė D, Catarino CB, Chinthapalli K, Clayton LM, Thom M, Martinian L, Cohen H, Adalat S, Bockenhauer D, Pope SA, Lench N, Koltzenburg M, Duncan JS, Hammond P, Hennekam RC, Land JM, Sisodiya SM (2011). Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions.. PLoS One, 6(8), e23182 - . doi:10.1371/journal.pone.0023182
Arrigoni FI, Matarin M, Thompson PJ, Michaelides M, McClements ME, Redmond E, Clarke L, Ellins E, Mohamed S, Pavord I, Klein N, Hunt DM, Moore AT, Halcox J, Sisodiya SM (2011). Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy.. Eur J Hum Genet, 19(9), 1018 - . doi:10.1038/ejhg.2011.73
Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM (2011). Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.. Brain, 134(Pt 10), 2982 - 3010. doi:10.1093/brain/awr129
Centeno M, Feldmann M, Harrison NA, Rugg-Gunn FJ, Chaudhary U, Falcon C, Lemieux L, Thom M, Smith SJ, Sisodiya SM (2011). Epilepsy causing pupillary hippus: an unusual semiology.. Epilepsia, 52(8), e93 - e96. doi:10.1111/j.1528-1167.2011.03137.x
Catarino CB, Kasperavičiūtė D, Thom M, Cavalleri GL, Martinian L, Heinzen EL, Dorn T, Grunwald T, Chaila E, Depondt C, Krämer G, Delanty N, Goldstein DB, Sisodiya SM (2011). Genomic microdeletions associated with epilepsy: not a contraindication to resective surgery.. Epilepsia, 52(8), 1388 - 1392. doi:10.1111/j.1528-1167.2011.03087.x
Guerrini R, Striano P, Catarino C, Sisodiya SM (2011). Neuroimaging and neuropathology of Dravet syndrome.. Epilepsia, 52 Suppl 2, 30 - 34. doi:10.1111/j.1528-1167.2011.02998.x
McCormack M, Alfirevic A, Bourgeois S, Farrell JJ, Kasperavičiūtė D, Carrington M, Sills GJ, Marson T, Jia X, de Bakker PI, Chinthapalli K, Molokhia M, Johnson MR, O'Connor GD, Chaila E, Alhusaini S, Shianna KV, Radtke RA, Heinzen EL, Walley N, Pandolfo M, Pichler W, Park BK, Depondt C, Sisodiya SM, Goldstein DB, Deloukas P, Delanty N, Cavalleri GL, Pirmohamed M (2011). HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.. N Engl J Med, 364(12), 1134 - 1143. doi:10.1056/NEJMoa1013297
Liu JYW, Catarino CB, Liagkouras I, Labrum R, Davis M, Woodward C, Cross JH, Jacques TS, Koepp M, Martinian L, Thom M, Sisodiya SM (2011). Neuropathology of Dravet syndrome.
Thom M, An S, Martinian L, Sisodiya SM, Dean A, McEvoy A, Brandner S, Toma A (2011). 101 DNTs: histological subtypes, molecular genetics and clinical correlations in an adult epilepsy series.
Clayton LM, Dévilé M, Punte T, Kallis C, de Haan GJ, Sander JW, Acheson J, Sisodiya SM (2011). Retinal nerve fiber layer thickness in vigabatrin-exposed patients.. Ann Neurol, 69(5), 845 - 854. doi:10.1002/ana.22266
Sisodiya SM, Mefford HC (2011). Genetic contribution to common epilepsies.. Curr Opin Neurol, 24(2), 140 - 145. doi:10.1097/WCO.0b013e328344062f
Novy J, Patsalos PN, Sander JW, Sisodiya SM (2011). Lacosamide neurotoxicity associated with concomitant use of sodium channel-blocking antiepileptic drugs: a pharmacodynamic interaction?. Epilepsy Behav, 20(1), 20 - 23. doi:10.1016/j.yebeh.2010.10.002
Arrigoni FI, Matarin M, Thompson PJ, Michaelides M, McClements ME, Redmond E, Clarke L, Ellins E, Mohamed S, Pavord I, Klein N, Hunt DM, Moore AT, Halcox J, Sisodiya SM (2011). Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy.. Eur J Hum Genet, 19(2), 131 - 137. doi:10.1038/ejhg.2010.147
Becker F, Zimprich F, Sisodiya S, Lerche H (2011). Pharmacogenetics: New options in the treatment of epilepsy? | Pharmakogenetik: Neue Wege in der Epilepsietherapie?. Zeitschrift fur Epileptologie, 24(2), 123 - 127.

2010

Sisodiya S (2010). Epilepsy genetics what is common, what is rare?.
Kensche M, Sander JW, Sisodiya SM (2010). Significant hypotension following buccal midazolam administration.. BMJ Case Rep, 2010, - . doi:10.1136/bcr.09.2010.3371
Avbersek A, Sisodiya S (2010). Does the primary literature provide support for clinical signs used to distinguish psychogenic nonepileptic seizures from epileptic seizures?. J Neurol Neurosurg Psychiatry, 81(7), 719 - 725. doi:10.1136/jnnp.2009.197996
Feldmann M, Asselin MC, Wang SN, McMahon A, Walker M, Anton J, Hinz R, Sisodiya S, Duncan J, Koepp M (2010). Tariquidar inhibition of P-glycoprotein activity in patients with temporal lobe epilepsy measured with PET and (R)-[C-11]Verapamil. doi:10.1016/j.neuroimage.2010.04.122
Orlova KA, Tsai V, Baybis M, Heuer GG, Sisodiya S, Thom M, Strauss K, Aronica E, Storm PB, Crino PB (2010). Early progenitor cell marker expression distinguishes type II from type I focal cortical dysplasias.. J Neuropathol Exp Neurol, 69(8), 850 - 863. doi:10.1097/NEN.0b013e3181eac1f5
Narkiewicz M, Martinian L, Phadke R, Catarino CJFBS, Sisodiya SM, Thom M (2010). Braak staging in an epilepsy post mortem series.
Clayton LM, Duncan JS, Sisodiya SM, Acheson JF (2010). Delayed, rapid visual field loss in a patient after ten years of vigabatrin therapy.. Eye (Lond), 24(1), 185 - 186. doi:10.1038/eye.2009.64
Kasperaviciūte D, Catarino CB, Heinzen EL, Depondt C, Cavalleri GL, Caboclo LO, Tate SK, Jamnadas-Khoda J, Chinthapalli K, Clayton LM, Shianna KV, Radtke RA, Mikati MA, Gallentine WB, Husain AM, Alhusaini S, Leppert D, Middleton LT, Gibson RA, Johnson MR, Matthews PM, Hosford D, Heuser K, Amos L, Ortega M, Zumsteg D, Wieser HG, Steinhoff BJ, Krämer G, Hansen J, Dorn T, Kantanen AM, Gjerstad L, Peuralinna T, Hernandez DG, Eriksson KJ, Kälviäinen RK, Doherty CP, Wood NW, Pandolfo M, Duncan JS, Sander JW, Delanty N, Goldstein DB, Sisodiya SM (2010). Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.. Brain, 133(Pt 7), 2136 - 2147. doi:10.1093/brain/awq130
Liu JY, Martinian L, Thom M, Sisodiya SM (2010). Immunolabeling recovery in archival, post-mortem, human brain tissue using modified antigen retrieval and the catalyzed signal amplification system.. J Neurosci Methods, 190(1), 49 - 56. doi:10.1016/j.jneumeth.2010.04.020
Hadjivassiliou G, Martinian L, Squier W, Blumcke I, Aronica E, Sisodiya SM, Thom M (2010). The application of cortical layer markers in the evaluation of cortical dysplasias in epilepsy.. Acta Neuropathol, 120(4), 517 - 528. doi:10.1007/s00401-010-0686-x
Heinzen EL, Radtke RA, Urban TJ, Cavalleri GL, Depondt C, Need AC, Walley NM, Nicoletti P, Ge D, Catarino CB, Duncan JS, Kasperaviciūte D, Tate SK, Caboclo LO, Sander JW, Clayton L, Linney KN, Shianna KV, Gumbs CE, Smith J, Cronin KD, Maia JM, Doherty CP, Pandolfo M, Leppert D, Middleton LT, Gibson RA, Johnson MR, Matthews PM, Hosford D, Kälviäinen R, Eriksson K, Kantanen AM, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Wieser HG, Zumsteg D, Ortega M, Wood NW, Huxley-Jones J, Mikati M, Gallentine WB, Husain AM, Buckley PG, Stallings RL, Podgoreanu MV, Delanty N, Sisodiya SM, Goldstein DB (2010). Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.. Am J Hum Genet, 86(5), 707 - 718. doi:10.1016/j.ajhg.2010.03.018
Chaudhry AS, Urban TJ, Lamba JK, Birnbaum AK, Remmel RP, Subramanian M, Strom S, You JH, Kasperaviciute D, Catarino CB, Radtke RA, Sisodiya SM, Goldstein DB, Schuetz EG (2010). CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance dose.. J Pharmacol Exp Ther, 332(2), 599 - 611. doi:10.1124/jpet.109.161026
Thom M, Liagkouras I, Elliot KJ, Martinian L, Harkness W, McEvoy A, Caboclo LO, Sisodiya SM (2010). Reliability of patterns of hippocampal sclerosis as predictors of postsurgical outcome.. Epilepsia, 51(9), 1801 - 1808. doi:10.1111/j.1528-1167.2010.02681.x

2009

Sisodiya S (2009). THE TRANSPORTER SIDE: MULTIPLE-DRUG TRANSPORTERS AND THEIR GENETIC VARIABILITY IN RELATION TO DRUG RESPONSE IN EPILEPSY. EPILEPSIA, 50, 16 - 16.
Martinian L, Boer K, Middeldorp J, Hol EM, Sisodiya SM, Squier W, Aronica E, Thom M (2009). Expression patterns of glial fibrillary acidic protein (GFAP)-delta in epilepsy-associated lesional pathologies. Neuropathology and Applied Neurobiology, 35(4), 394 - 405. doi:10.1111/j.1365-2990.2008.00996.x
Tsai V, Orlova KA, Baybis M, Heuer GG, Sisodiya S, Thom M, Strauss KA, Aronica E, Storm PB, Crino PB (2009). STEM CELL PROTEIN EXPRESSION AND MTOR PATHWAY ACTIVATION DISTINGUISHES TYPE I FROM TYPE II FOCAL CORTICAL DYSPLASIAS.
Feldmann M, Sisodiya S, Asselin MC, Duncan JS, Koepp MJ (2009). EFFECT OF P-GP INHIBITION IN DRUG-RESISTANT TLE USING A SINGLE-DOSE OF TARIQUIDAR.
Catarino C, Caboclo L, Koepp M, Yogarajah M, Martinian L, Thom M, Sisodiya S (2009). THE NEUROPATHOLOGY OF CHRONIC EPILEPSY: WHOLE BRAIN STUDIES IN A LARGE POSTMORTEM COHORT.
Williams E, Yogarajah M, Burdett J, Duncan J, Sisodiya S, Koepp M, Fong J (2009). HIPPOCAMPAL CHANGES AND DISSOCIATIVE SEIZURES.
Tsai V, Orlova KA, Baybis M, Heuer GG, Sisodiya S, Thom M, Strauss KA, Aronica E, Storm PB, Crino PB (2009). STEM CELL PROTEIN EXPRESSION AND MTOR PATHWAY ACTIVATION DISTINGUISHES TYPE I FROM TYPE II FOCAL CORTICAL DYSPLASIAS.
Feldmann M, Sisodiya S, Asselin MC, Duncan JS, Koepp MJ (2009). EFFECT OF P-GP INHIBITION IN DRUG-RESISTANT TLE USING A SINGLE-DOSE OF TARIQUIDAR.
Farrell F, McCauley L, Smith S, Feldman M, Centeno M, Harriso N, Sisodiya S (2009). EPILEPSY CAUSING PUPILLARY HIPPUS.
Koepp MJ, Sisodiya S, Langer O, Ryvlin P (2009). IMAGING DRUG-RESISTANCE.
Sisodiya SM (2009). The genetic basis of multi-drug resistance.
Catarino CB, Liu JY, Liagkouras I, Birch R, Zuberi SM, Koepp MJ, Martinian L, Thom M, Sisodiya SM (2009). DRAVET SYNDROME: CLINICAL, GENETIC, AND NEUROPATHOLOGICAL CHARACTERIZATION IN A SERIES OF PATIENTS.
Clayton LM, Duncan J, Sisodiya SM, Acheson J (2009). OPTICAL COHERENCE TOMOGRAPHY IN PATIENTS TAKING VIGABATRIN: EXPLORING A STRUCTURE-FUNCTION RELATIONSHIP.
Stagg CJ, Lang B, Hest JG, Cavey A, Johansen-Berg H, Coles A, Hart Y, Sisodiya SM, Wroe S, Duncan JS, Vincent A, Palace J (2009). SERUM AUTOANTIBODIES TO GLUTAMIC ACID DECARBOXYLASE ARE ASSOCIATED WITH REDUCED CORTICAL GABA LEVELS IN PATIENTS WITH EPILEPSY.
Srikandarajah N, Martinian L, Sisodiya SM, Squier W, Blumcke I, Aronica E, Thom M (2009). Doublecortin expression in FCD type I and II in epilepsy.
Hadjivassiliou G, Martinian L, Sisodiya SM, Squier W, Blumcke I, Aronica E, Thom M (2009). Cortical layer markers in the evaluation of cortical dysplasias in epilepsy.
Blanc FI, Martinian L, Sisodiya SM, Thom M (2009). Post-mortem investigation of widespread cortical and white matter changes in hippocampal sclerosis.
Cavalleri GL, Weale ME, Kalviainen R, Berkovic SF, O'Brien TJ, Delanty N, Sisodiya SM, Goldstein D (2009). GENETIC MAPPING IN SPORADIC EPILEPSY.
Powell HWR, Yogarajah M, Duncan J, Smith S, Sisodiya SM (2009). LONG-TERM EEG MONITORING IN EPILEPSY: IS IT WORTH THE EFFORT?.
Petrovski S, Scheffer IE, Sisodiya SM, O'Brien TJ, Berkovic SF, EPIGEN Consortium (2009). Lack of replication of association between scn1a SNP and febrile seizures.. Neurology, 73(22), 1928 - 1930. doi:10.1212/WNL.0b013e3181c3fd6f
Thom M, Martinian L, Catarino C, Yogarajah M, Koepp MJ, Caboclo L, Sisodiya SM (2009). Bilateral reorganization of the dentate gyrus in hippocampal sclerosis: a postmortem study.. Neurology, 73(13), 1033 - 1040. doi:10.1212/WNL.0b013e3181b99a07
Sisodiya SM, Fauser S, Cross JH, Thom M (2009). Focal cortical dysplasia type II: biological features and clinical perspectives.. Lancet Neurol, 8(9), 830 - 843. doi:10.1016/S1474-4422(09)70201-7
Srikandarajah N, Martinian L, Sisodiya SM, Squier W, Blumcke I, Aronica E, Thom M (2009). Doublecortin expression in focal cortical dysplasia in epilepsy.. Epilepsia, 50(12), 2619 - 2628. doi:10.1111/j.1528-1167.2009.02194.x
Martinian L, Boer K, Middeldorp J, Hol EM, Sisodiya SM, Squier W, Aronica E, Thom M (2009). Expression patterns of glial fibrillary acidic protein (GFAP)-delta in epilepsy-associated lesional pathologies.. Neuropathol Appl Neurobiol, 35(4), 394 - 405. doi:10.1111/j.1365-2990.2009.00996.x
Eriksson SH, Thom M, Symms MR, Focke NK, Martinian L, Sisodiya SM, Duncan JS (2009). Cortical neuronal loss and hippocampal sclerosis are not detected by voxel-based morphometry in individual epilepsy surgery patients. Human Brain Mapping, 30(10), 3351 - 3360. doi:10.1002/hbm.20757
Sisodiya SM, Marini C (2009). Genetics of antiepileptic drug resistance. Current Opinion in Neurology, 22(2), 150 - 156. doi:10.1097/WCO.0b013e32832923ec
Walker MC, Sisodiya S (2009). Epilepsy and sleep. In Sander JW, Rugg-Gunn FJ, Smalls JE (Ed.), Epilepsy 2009: from benchside to bedside. A practical guide to epilepsy. Lecture notes from the Twelfth Epilepsy Teaching Weekend, 18-20 September 2009, St. Anne's College, Oxford (pp. 181 - 186). : International League Against Epilepsy (UK Chapter) and National Society for Epilepsy.
Yogarajah M, Powell HWR, Heaney D, Smith SJM, Duncan JS, Sisodiya SM (2009). Long-term monitoring in refractory epilepsy: the Gowers Unit experience. Journal of Neurology, Neurosurgery and Psychiatry, 80(3), 305 - 310. doi:10.1136/jnnp.2008.144634
Eriksson SH, Free SL, Thom M, Symms MR, Martinian L, Duncan JS, Sisodiya SM (2009). Quantitative grey matter histological measures do not correlate with grey matter probability values from in vivo MRI in the temporal lobe. Journal of Neuroscience Methods, 181(1), 111 - 118. doi:10.1016/j.jneumeth.2009.05.001
Sisodiya SM, Manford M (2009). Frontal lobe epilepsy. In Sander JW, Rugg-Gunn FJ, Smalls JE (Ed.), Epilepsy 2009: from benchside to bedside. A practical guide to epilepsy. Lecture notes from the Twelfth Epilepsy Teaching Weekend, 18-20 September 2009, St. Anne's College, Oxford (pp. 151 - 154). : International League Against Epilepsy (UK Chapter) and National Society for Epilepsy.
Thom M, Eriksson S, Martinian L, Caboclo LO, McEvoy AW, Duncan JS, Sisodiya SM (2009). Temporal lobe sclerosis associated with hippocampal sclerosis in temporal lobe epilepsy: neuropathological features. Journal of Neuropathology and Experimental Neurology, 68(8), 928 - 938. doi:10.1097/NEN.0b013e3181b05d67
Fauser S, Sisodiya SM, Martinian L, Thom M, Gumbinger C, Huppertz HJ, Hader C, Strobl K, Steinhoff BJ, Prinz M, Zentner J, Schulze-Bonhage A (2009). Multi-focal occurrence of cortical dysplasia in epilepsy patients. Brain, 132(8), 2079 - 2090. doi:10.1093/brain/awp145
Charlesworth G, Soryal I, Smith S, Sisodiya SM (2009). Acute, localised paroxysmal pain as the initial manifestation of focal seizures: A case report and a brief review of the literature. Pain, 141(3), 300 - 305. doi:10.1016/j.pain.2008.11.005
Lynch JM, Tate SK, Kinirons P, Weale ME, Cavalleri GL, Depondt C, Murphy K, O'Rourke D, Doherty CP, Shianna KV, Wood NW, Sander JW, Delanty N, Goldstein DB, Sisodiya SM (2009). No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy. Epilepsy Research, 83(1), 44 - 51. doi:10.1016/j.eplepsyres.2008.09.003
Kasperaviciute D, Sisodiya SM (2009). Epilepsy pharmacogenetics. Pharmacogenomics, 10(5), 817 - 836. doi:10.2217/pgs.09.34
Sisodiyo SM, Fauser S, Cross JH, Thom M (2009). Focal cortical dysplasia type II: biological features and clinical perspectives. The Lancet Neurology, 8(9), 830 - 843.

2008

Martinian L, Thom M, Sisodiya S (2008). Expression of GFAP-delta in common causes of lesion-related refractory epilepsy.
Thom M, Eriksson SH, Martinian L, Symms MR, McEvoy A, Sisodiya SM, Duncan JS (2008). Volumetric MRI and neuropathological correlations in temporal lobe specimens in patients with hippocampal sclerosis.
Catarino CB, Sisodiya SM (2008). Monogenic focal epilepsies. In Panayiotopoulos CP, Bembadis SR, Sisodiya SM (Ed.), The Educational Kit on Epilepsies: Vol.5 – Focal epilepsy: seizures, syndromes and management (pp. 220 - 229). : Medicinae.
Catarino CB, Sisodiya SM (2008). Genetic and hereditary aspects of epilepsies related to women. In Panayiotopoulos CP, Crawford P, Thompson T (Ed.), The Educational Kit on Epilepsies: Vol.4 – The epilepsies in girls and women (pp. 42 - 48). : Medicinae.
Sisodiya SM, Beck H, Loscher W, Vezzani A (2008). Mechanisms of drug resistance. In Engel J, Pedley TA (Ed.), Epilepsy: a comprehensive textbook (pp. 1279 - 1289). : Wolters Kluwer, Lippincott Williams & Wilkins.
Thom M, Martinian L, Caboclo LO, McEvoy AW, Sisodiya SM (2008). Balloon cells associated with granule cell dispersion in the dentate gyrus in hippocampal sclerosis. Acta Neuropathologica, 115(6), 697 - 700. doi:10.1007/s00401-008-0341-y
O'Dushlaine CT, Dolan C, Weale ME, Stanton A, Croke DT, Kalviainen R, Eriksson K, Kantanen AM, Gibson RA, Hosford D, Sisodiya SM, Gill M, Corvin AP, Morris DW, Delanty N, Cavalleri GL (2008). An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases. European Journal of Human Genetics, 16(2), 176 - 183. doi:10.1038/sj.ejhg.5201938
Thom M, Sisodiya S (2008). Pathology of neocortical epilepsy. In Luders HO (Ed.), Textbook of epilepsy surgery (pp. 1338 - 1348). : informa healthcare.
Walley N, Sisodiya SM, Goldstein DB (2008). Pharmacogenetics and pharmacogenomics. In Engel J, Pedley TA (Ed.), Epilepsy: a comprehensive textbook (pp. 1497 - 1505). : Wolters Kluwer, Lippincott Williams & Wilkins.
Thom M, Sisodiya S, Najm I (2008). Neuropathology of epilepsy. In Love S, Louis DN, Ellison DW (Ed.), Greenfield's neuropathology (pp. 833 - 887). : Hodder Arnold.
Eriksson SH, Thom M, Bartlett PA, Symms MR, McEvoy AW, Sisodiya SM, Duncan JS (2008). PROPELLER MRI visualizes detailed pathology of hippocampal sclerosis. Epilepsia, 49(1), 33 - 39. doi:10.1111/j.1528-1167.2007.01277.x
Sisodiya S (2008). Brain structure, function, and genetics revealed by studies of the eye and face. Current Opinion in Neurology, 21(4), 404 - 409.

2007

Sisodiya S, Thom M, Kroetz D, Kelly L (2007). Response to Janigro et al. [4]. Epilepsia, 48(6), 1219 - 1220.
Jensen S, Free S, Martinian L, Yogarajah M, Sen A, Thom M, Sisodiya S (2007). Quantitation of p-glycoprotein in the human brain microvascular unit: Possible focal impairment of a blood-brain barrier agent in epilepsy.
Henderson RA, Williamson K, Cumming S, Clarke MP, Lynch SA, Hanson IM, FitzPatrick DR, Sisodiya S, van Heyningen V (2007). Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia. EUR J HUM GENET, 15(8), 898 - 901. doi:10.1038/sj.ejhg.5201826
Singh R, Tate SK, Jensen S, Sander JW, Wood NW, Goldstein DB, Sisodiya SM (2007). The genetics of antiepileptic drug response in focal epilepsy: A large candidate gene study.
Sen A, Scott C, Sisodiya SM, St-Peter C (2007). Stertorous breathing is a reliable and easily identifiable sign that aids in differentiating epileptic from dissociative convulsions.
Singh R, Tate SK, Cavalleri G, Weale M, Wood NW, Goldstein DB, Sisodiya SM (2007). Predisposition to secondary generalised tonic-clonic seizures and genetic variation in ion-channel, GABA and glutamate pathway genes.
Singh R, Need AC, Thompson P, Sander J, Goldstein D, Sisodiya SM (2007). Common genetic variation in glutamate receptors is not a major contributor to topiramate-induced cognitive impairment.
Sen A, Thom M, Martinian L, Chandler K, Walker MC, Nikolic M, Sisodiya SM (2007). Deregulation of cyclin dependent kinase 5 in human hippocampal sclerosis.
Thom M, Martinian L, Sisodiya SM (2007). Hippocampal sclerosis and mossy fibre sprouting: a post-mortem study.
Nguyen VHV, Kaiboriboon K, Alldredge BK, Barbaro NM, Bollen AW, Sisodiya SM, Kroetz DL (2007). Brain expression of mitoxantrone resistance protein (MXR) and other ATP-binding cassette (ABC) transporters in patients with medically refractory temporal lobe epilepsy.
Eriksson SH, Thom M, Bartlett PA, Symms MR, McEvoy AW, Sisodiya SM, Duncan JS (2007). Propeller MRI visualises detailed pathology of hippocampal sclerosis.
McKenzie M, Liolitsa D, Akinshina N, Campanella M, Sisodiya S, Hargreaves I, Nirmalananthan N, Sweeney MG, Abou-Sleiman PM, Wood NW, Hanna MG, Duchen MR (2007). Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption. Journal of Biological Chemistry, 282(51), 36845 - 36852. doi:10.1074/jbc.M704158200
Soranzo N, Kelly L, Martinian L, Burley MW, Thom M, Sali A, Kroetz DL, Goldstein DB, Sisodiya SM (2007). Lack of support for a role for RLIP76 (RALBP1) in response to treatment or predisposition to epilepsy. Epilepsia, 48(4), 674 - 683. doi:10.1111/j.1528-1167.2007.00926.x
Henderson RA, Williamson K, Cumming S, Clarke MP, Lynch SA, Hanson IM, Fitzpatrick DR, Sisodiya S, van Heyningen V (2007). Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia. European Journal of Human Genetics, 15(8), 898 - 901. doi:10.1038/sj.ejhg.5201826
Sisodiya SM, Goldstein DB (2007). Drug resistance in epilepsy: more twists in the tale. Epilepsia, 48(12), 2369 - 2370. doi:10.1111/j.1528-1167.2007.01260_1.x
Sen A, Thom M, Martinian L, Yogarajah M, Nikolic M, Sisodiya SM (2007). Increased immunoreactivity of cdk5 activators in hippocampal sclerosis. NeuroReport, 18(5), 511 - 516. doi:10.1097/WNR.0b013e3280586879
Ratilal B, McEvoy A, Sisodiya S, Thom M, Toma A (2007). Diffuse cerebral gangliocytoma in an adult with late-onset refractory epilepsy. Neuropathology and Applied Neurobiology, 33(6), 706 - 709. doi:10.1111/j.1365-2990.2007.00861.x
Cavalleri GL, Walley NM, Soranzo N, Mulley J, Doherty CP, Kapoor A, Depondt C, Lynch JM, Scheffer IE, Heils A, Gehrmann A, Kinirons P, Gandhi S, Satishchandra P, Wood NW, Anand A, Sander T, Berkovic SF, Delanty N, Goldstein DB, Sisodiya SM (2007). A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy. Epilepsia, 48(4), 706 - 712. doi:10.1111/j.1528-1167.2007.00977.x
Goldstein DB, Need AC, Singh R, Sisodiya SM (2007). Potential genetic causes of heterogeneity of treatment effects. The American Journal of Medicine, 120(4(Suppl 1)), S21 - S25. doi:10.1016/j.amjmed.2007.02.004
Sisodiya S, Cross JH, Blumcke I, Chadwick D, Craig J, Crino PB, Debenham P, Delanty N, Elmslie F, Gardiner M, Golden J, Goldstein D, Greenberg DA, Guerrini R, Hanna M, Harris J, Harrison P, Johnson MR, Kirov G, Kullmann DM, Makoff A, Marini C, Nabbout R, Nashef L, Noebels JL, Ottman R, Pirmohamed M, Pitkanen A, Scheffer I, Shorvon S, Sills G, Wood N, Zuberi S (2007). Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disorders, 9(2), 194 - 236. doi:10.1684/epd.2007.0107
Sisodiya SM (2007). Choice of agent in treatment of epilepsy. In Rothwell PM (Ed.), The Lancet: treating individuals: from randomised trials to personalised medicine (pp. 297 - 305). : Elsevier.
Sen A, Thom M, Martinian L, Harding B, Cross JH, Nikolic M, Sisodiya SM (2007). Pathological tau tangles localize to focal cortical dysplasia in older patients. Epilepsia, 48(8), 1447 - 1454. doi:10.1111/j.1528-1167.2007.01107.x
Sen A, Thom M, Nikolic M, Sisodiya SM (2007). The potential role of cyclin-dependent kinase 5 in focal cortical dysplasia. Developmental Neuroscience, 30(1-3), 96 - 104. doi:10.1159/000109855
Heinzen EL, Yoon W, Tate SK, Sen A, Wood NW, Sisodiya SM, Goldstein DB (2007). Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug responsive splice variants of SCN1A. The American Journal of Human Genetics, 80(5), 876 - 883. doi:10.1086/516650
Sisodiya SM, Thompson PJ, Need A, Harris SE, Weale ME, Wilkie SE, Michaelides M, Free SL, Walley N, Gumbs C, Gerrelli D, Ruddle P, Whalley LJ, Starr JM, Hunt DM, Goldstein DB, Deary IJ, Moore AT (2007). Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation. Journal of medical genetics, 44(6), 373 - 380. doi:10.1136/jmg.2006.047407
Walker MC, Sisodiya S (2007). Epilepsy and sleep. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2007: from cell to community. A practical guide to epilepsy. Lecture notes from the Eleventh Epilepsy Teaching Weekend, 28-30 September 2007, St. Anne's College, Oxford (pp. 159 - 164). : Meritus Communications.
Eriksson SH, Free SL, Thom M, Martinian L, Symms MR, Salmenpera TM, McEvoy AW, Harkness W, Duncan JS, Sisodiya SM (2007). Correlation of quantitative MRI and neuropathology in epilepsy surgical resection specimens-T2 correlates with neuronal tissue in gray matter. NeuroImage, 37(1), 48 - 55. doi:10.1016/j.neuroimage.2007.04.051
Sisodiya S (2007). Etiology and management of refractory epilepsies. Nature Clinical Practice Neurology, 3(6), 320 - 330. doi:10.1038/ncpneuro0521
Sen A, Scott C, Sisodiya SM (2007). Stertorous breathing is a reliably identified sign that helps in the differentiation of epileptic from psychogenic non-epileptic convulsions: an audit. Epilepsy Research, 77(1), 62 - 64. doi:10.1016/j.eplepsyres.2007.07.009
Bamiou DE, Free SL, Sisodiya SM, Chong WK, Musiek F, Williamson KA, van Heyningen V, Moore AT, Gadian D, Luxon LM (2007). Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations. Archives of Pediatrics and Adolescent Medicine, 161(5), 463 - 469. doi:10.1001/archpedi.161.5.463
Thom M, Martiman L, Sen A, Squier W, Harding BN, Cross JH, Harkness W, McEvoy A, Sisodiya SM (2007). An investigation of the expression of G(1)-Phase cell cycle proteins in focal cortical dysplasia type IIB. Journal of Neuropathology and Experimental Neurology, 66(11), 1045 - 1055.
Tate SK, Sisodiya SM (2007). Multidrug resistance in epilepsy: a pharmacogenomic update. Expert Opinion on Pharmacotherapy, 8(10), 1441 - 1449. doi:10.1517/14656566.8.10.1441
Sen A, Martinian L, Nikolic M, Walker MC, Thom M, Sisodiya SM (2007). Increased NKCC1 expression in refractory human epilepsy. Epilepsy Research, 74(2-3), 220 - 227. doi:10.1016/j.eplepsyres.2007.01.004
Bamiou DE, Sisodiya S, Musiek FE, Luxon LM (2007). The role of the interhemispheric pathway in hearing. Brain Research Reviews, 56(1), 170 - 182. doi:10.1016/j.brainresrev.2007.07.003
Lynch JM, Sisodiya SM (2007). Genetics of epilepsy. In Schapira AHV (Ed.), Neurology and clinical neuroscience (pp. 681 - 689). : Mosby/Elsevier.
Cavalleri GL, Weale ME, Shianna KV, Singh R, Lynch JM, Grinton B, Szoeke C, Murphy K, Kinirons P, O'Rourke D, Ge D, Depondt C, Claeys KG, Pandolfo M, Gumbs C, Walley N, McNamara J, Mulley JC, Linney KN, Sheffield LJ, Radtke RA, Tate SK, Chissoe SL, Gibson RA, Hosford D, Stanton A, Graves TD, Hanna MG, Eriksson K, Kantanen AM, Kalviainen R, O'Brien TJ, Sander JW, Duncan JS, Scheffer IE, Berkovic SF, Wood NW, Doherty CP, Delanty N, Sisodiya SM, Goldstein DB (2007). Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. The Lancet Neurology, 6(11), 970 - 980. doi:10.1016/S1474-4422(07)70247-8
Bamiou DE, Campbell NG, Musiek FE, Taylor R, Chong WK, Moore A, van Heyningen V, Free S, Sisodiya S, Luxon LM (2007). Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation. International Journal of Audiology, 46(4), 196 - 202. doi:10.1080/14992020601175952
Heinzen EL, Yoon W, Weale ME, Sen A, Wood NW, Burke JR, Welsh-Bohmer KA, Hulette CM, Sisodiya SM, Goldstein DB (2007). Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's disease. Genome Biology, 8(3), R32 - . doi:10.1186/gb-2007-8-3-r32

2006

Tate SK, Singh R, Hung CC, Tai JJ, Depondt C, Cavalleri GL, Sisodiya SM, Goldstein DB, Liou HH (2006). A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance dose. Pharmacogenetics and Genomics, 16(10), 721 - 726.
Lynch JM, Tate SK, Sander J, Wood NW, Goldstein DB, Sisodiya SM (2006). A novel method to characterise the phenotype of levetiracetam response for genetic association studies.
Idrees F, Bloch-Zupan A, Free SL, Vaideanu D, Thompson PJ, Ashley PF, Brice G, Rutland P, Bitner-Glindzicz M, Khaw PT, Fraser S, Sisodiya SM, Sowden JC (2006). A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B(2), 184 - 191.
Duncan JS, Sander JW, Sisodiya SM, Walker MC (2006). Adult epilepsy. The Lancet, 367(9516), 1087 - 1100.
Sisodiya SM (2006). Genetics of drug resistance. CNS Spectrums, 11(2 (Suppl.2)), 35 - 40.
Sisodiya SM, Ragge NK, Cavalleri GL, Hever A, Lorenz B, Schneider A, Williamson KA, Stevens JM, Free SL, Thompson PJ, van Heyningen V, Fitzpatrick DR (2006). Role of SOX2 mutations in human hippocampal malformations and epilepsy. Epilepsia, 47(3), 534 - 542.
Sisodiya SM, Bates SE (2006). Treatment of drug resistance in epilepsy: one step at a time. The Lancet Neurology, 5(5), 380 - 381. doi:10.1016/S1474-4422(06)70422-7
Sisodiya SM, Martinian L, Scheffer GL, van der Valk P, Scheper RJ, Harding BN, Thom M (2006). Vascular colocalization of P-glycoprotein, multidrug-resistance associated protein 1, breast cancer resistance protein and major vault protein in human epileptogenic pathologies. Neuropathology and Applied Neurobiology, 32(1), 51 - 63.
Sen A, Thom M, Martinian L, Jacobs T, Nikolic M, Sisodiya SM (2006). Deregulation of cdk5 in hippocampal sclerosis. Journal of Neuropathology and Experimental Neurology, 65(1), 55 - 65.
Kinirons P, Cavalleri GL, Singh R, Shahwan A, Acheson JF, Wood NW, Goldstein DB, Sisodiya SM, Doherty CP, Delanty N (2006). A pharmacogenetic exploration of vigabatrin-induced visual field constriction. Epilepsy Research, 70(2-3), 144 - 152.
Eriksson SH, Free SL, Thom M, Martinian L, Sisodiya SM (2006). Methodological aspects of 3D and automated 2D analyses of white matter neuronal density in temporal lobe epilepsy. Neuropathology and Applied Neurobiology, 32(3), 260 - 270.
Eriksson SH, Free SL, Thom M, Martinian L, Sisodiya SM (2006). Erratum: Methodological aspects of 3D and automated 2D analyses of white matter neuronal density in temporal lobe epilepsy (Neuropathology and Applied Neurobiology (2006) 32, (260-267)). Neuropathology and Applied Neurobiology, 32(4), 460 - 460.
Sisodiya S, Duncan J, Eriksson S, Free S, Martinian L, Symms M, Thom M (2006). Correlation of quantitative mri and quantitative neuropathological analysis of white matter in focal epilepsy.
Cavalleri GL, Weale ME, Shianna K, Lynch J, Singh R, Murphy K, Radtke R, McNamara J, Berkovic S, Scheffer I, Mulley J, Wood N, Depondt C, Claeys K, Doherty C, Delanty N, Sisodiya S, Goldstein D (2006). A large scale genetic association study of common forms of epilepsy.
Sen A, Martinian L, Chandler K, Jacobs T, Walker MC, Nikolic M, Thom M, Sisodiya SM (2006). Cyclin dependent kinase 5 causes pathological phosphorylation of the NMDA receptor in hippocampal sclerosis.
Eriksson SH, Free SL, Thom M, Symms MR, Sisodiya SM, Duncan JS (2006). Correlation of quantitative MRI and quantitative neuropathological analysis of grey and white matter in temporal lobe epilepsy.
Kinirons P, Cavalleri GL, Shahwan A, Wood NW, Goldstein DB, Sisodiya SM, Delanty N, Doherty CP (2006). Examining the role of common genetic variation in the gamma 2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs. EPILEPSY RES, 70(2-3), 229 - 238. doi:10.1016/j.eplepsyres.2005.05.009
Sisodiya SM (2006). Lessons from the Mendelian epilepsies. EUR J NEUROL, 13, 1 - 2.
Eriksson SH, Free SL, Thom M, Martinian L, Sisodiya SM (2006). Methodological aspects of 3D and automated 2D analyses of white matter neuronal density in temporal lobe epilepsy (vol 32, pg 260, 2006). NEUROPATH APPL NEURO, 32(4), 460 - 460.
Kinirons P, Cavalleri GL, Shahwan A, Wood NW, Goldstein DB, Sisodiya SM, Delanty N, Doherty CP (2006). Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs. Epilepsy Research, 70(2-3), 229 - 238. doi:10.1016/j.eplepsyres.2006.05.009

2005

Cavalleri GL, Lynch JM, Depondt C, Burley MW, Wood NW, Sisodiya SM, Goldstein DB (2005). Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?. Brain, 128(8), 1832 - 1840.
Sisodiya SM (2005). Genetics of drug resistance.. Epilepsia, 46 Suppl 10, 33 - 38. doi:10.1111/j.1528-1167.2005.00356.x
Sisodiya SM (2005). Genetics of drug resistance in epilepsy. Current Neurology and Neuroscience Reports, 5(4), 307 - 311.
Sisodiya S, Soranzo N, Wood NW, Goldstein DB (2005). Association of genetic loci: replication or not, that is the question. Neurology, 64(11), 1989 - 1989.
Manford M, Sisodiya SM (2005). Frontal lobe epilepsy. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2005: from neuron to NICE. A practical guide to epilepsy. (pp. 153 - 156). : Meritus Communications.
Thom M, Martinian L, Cross H, Harding B, Sisodiya S (2005). Neuronal density and size in focal cortical dysplasia in epilepsy. Neuropathology and Applied Neurobiology, 31(2), 226 - 226.
Thom M, Martinian L, Sisodiya SM, Cross JH, Williams G, Stoeber K, Harkness W, Harding BN (2005). Mcm2 labelling of balloon cells in focal cortical dysplasia. Neuropathology and Applied Neurobiology, 31(6), 580 - 588.
Ragge NK, Lorenz B, Schneider A, Bushby K, Sanctis L, de S, U de S, A C, R O V, A F, S L T, P W, K A S, S M H, V van F, D (2005). SOX2 Anophthalmia syndrome. AM J MED GENET A, 135(1), 1 - 7.
Thom M, Martinian L, Williams G, Stoeber K, Cross H, Harding BN, Sisodiya SM (2005). Geminin expression in balloon cells in focal cortical dysplasia (FCD) type IIB. Epilepsia, 46, 368 - 368.
Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, Thom M, Sen A, Shorvon SD, Sander JW, Wood NW, Goldstein DB (2005). Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin.. Proceedings of the National Academy of Sciences of the United States of America, 102(15), 5507 - 5512. doi:10.1073/pnas.0407346102
Soranzo N, Goldstein DB, Sisodiya SM (2005). The role of common variation in drug transporter genes in refractory epilepsy. Expert Opinion on Pharmacotherapy, 6(8), 1305 - 1312.
Liu RS, Lemieux L, Bell GS, Sisodiya SM, Bartlett PA, Shorvon SD, Sander JW, Duncan JS (2005). Cerebral damage in epilepsy: a population-based longitudinal quantitative MRI study. Epilepsia, 46(9), 1482 - 1494.
Eriksson SH, Free SL, Thom M, Harkness W, Sisodiya SM, Duncan JS (2005). Reliable registration of preoperative MRI with histopathology after temporal lobe resections. Epilepsia, 46(10), 1646 - 1653.
Ragge NK, Brown AG, Poloschek CM, Lorenz B, Henderson RA, Clarke MP, Russell-Eggitt I, Fielder A, Gerrelli D, Martinez-Barbera JP, Ruddle P, Hurst J, Collin JR, Salt A, Cooper ST, Thompson PJ, Sisodiya SM, Williamson KA, Fitzpatrick DR, van Heyningen V, Hanson IM (2005). Heterozygous mutations of OTX2 cause severe ocular malformations.. The American Journal of Human Genetics, 76(6), 1008 - 1022. doi:10.1086/430721
Thom M, Martinian L, Sen A, Cross JH, Harding BN, Sisodiya SM (2005). Cortical neuronal densities and lamination in focal cortical dysplasia. Acta Neuropathologica, 110(4), 383 - 392.
Walker MC, Sisodiya SM (2005). Epilepsy and sleep. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2005: from neuron to NICE. A practical guide to epilepsy. (pp. 177 - 183). : Meritus Communications.
Thom M, Zhou JM, Martinian L, Sisodiya S (2005). Quantitative post-mortem study of the hippocampus in chronic epilepsy: seizures do not inevitably cause neuronal loss. Brain, 128(6), 1344 - 1357. doi:10.1093/brain/awh475
Sisodiya SM (2005). Syncope. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2005: from neuron to NICE. A practical guide to epilepsy. (pp. 173 - 176). : Meritus Communications.
Sen A, Thom M, Martinian T, Dawodu T, Sisodiya SM (2005). Hippocampal malformations do not necessarily evolve into hippocampal sclerosis. Epilepsia, 46(6), 939 - 943.
Sisodiya SM (2005). Genetics of drug resistance. Epilepsia, 46(SUPPL. 10), 33 - 38.
McEvoy A, Sinha S, Thom M, Scott C, Smith S, Walker M, Richardson M, Sisodiya S, Sander JWA, Shorvon S, Duncan JS, Harkness W (2005). Temporal lobe epilepsy surgery: Experience at a single centre over 14 years.
Martinian L, Thom M, Sisodiya S (2005). Expression of multi drug resistance proteins in hippocampal sclerosis (HS) and focal cortical dysplasia (FCD) in patients with refractory epilepsy.
Cavallieri GL, Kinirons P, Shahwan A, McCarthy M, Doherty CP, Wood NW, Sisodiya S, Goldstein DB, Delanty N (2005). Genetic variation in GABAG2 - Lessons to be learned from association studies in two large epilepsy cohorts.
Depondt C, Cavalleri GL, Shorvon SD, Wood NW, Sisodiya SM, Goldstein DB (2005). Association study of five sodium channel genes in epilepsy and antiepileptic drug response.
Sen A, Thom M, Martinian L, Nikolic M, Sisodiya SM (2005). Deregulation of cyclin dependent kinase 5 in hippocampal sclerosis.
Eriksson SH, Free SL, Thom M, Martinian L, Sisodiya SM (2005). Temporal lobe size changes during postoperative tissue preparation.
Sen A, Thom M, Martinian L, Sisodiya SM (2005). Hippocampal malformations need not evolve into hippocampal sclerosis.
Sen A, Thom M, Martinian L, Nikolic M, Sisodiya SM (2005). A case of focal cortical dysplasia and neurofibrillary tangles.
Sen A, Thom M, Martinian L, Nikolic M, Sisodiya SM (2005). Deregulation of cyclin dependent kinase 5 in hippocampal sclerosis.
Eriksson SH, Free SL, Thom M, Martinian L, Sisodiya SM (2005). Density of white matter neurones in temporal lobe epilepsy - correlation of automated 2D and 3D measurements.
Liolitsa D, McKenzie M, Hargreaves I, Heales S, Land J, Sisodiya SM, Wood NW, Duchen MR, Hanna MG (2005). MELAS, a young-onset stroke disorder associated with a homoplasmic ND5 mitochondrial DNA mutation. EUR J NEUROL, 12, 158 - 159.
Thom M, Martinian L, Williams G, Stoeber K, Sisodiya SM (2005). Cell proliferation and granule cell dispersion in human hippocampal sclerosis. Journal of Neuropathology and Experimental Neurology, 64(3), 194 - 201.

2004

Sisodiya SM (2004). Mechanisms of drug resistance in epilepsy. In Shorvon SD, Perucca E, Fish DR, Dodson WE (Ed.), The treatment of epilepsy (pp. 84 - 88). : Blackwell Science.
Goldstein DB, Tate SK, Sisodiya SM (2004). Pharmacogenetics goes genomic (vol 4, pg 937, 2003). NAT REV GENET, 5(1), 76 - +.
Eriksson SH, Nordborg C, Thom M, Sisodiya SM (2004). Microdysgenesis in mesial temporal lobe epilepsy. Annals of Neurology, 55(4), 596 - 597.
Thompson PJ, Mitchell TN, Free SL, Williamson KA, Hanson IM, van Heyningen V, Moore AT, Sisodiya SM (2004). Cognitive functioning in humans with mutations of the PAX6 gene. Neurology, 62(7), 1216 - 1218.
Sisodiya SM (2004). Surgery for focal cortical dysplasia. Brain, 127(11), 2383 - 2384.
Graves TD, Gandhi S, Smith SJ, Sisodiya SM, Conway GS (2004). Misdiagnosis of seizures: insulinoma presenting as adult-onset seizure disorder. Journal of Neurology, Neurosurgery and Psychiatry, 75(8), 1091 - 1092.
Bamiou DE, Musiek FE, Sisodiya SM, Free SL, Mitchell TN, Davies RA (2004). Defective auditory interhemispheric transfer in a patient with a PAX6 mutation. Neurology, 62(3), 489 - 490.
Depondt C, Cock HR, Healy DG, Burley MW, Weinshenker D, Wood NW, Goldstein DB, Sisodiya SM (2004). The -1021C -> T DBH gene variant is not associated with epilepsy or antiepileptic drug response. Neurology, 63(8), 1497 - 1499.
Thom M, Martinian L, Parnavelas JG, Sisodiya SM (2004). Distribution of cortical interneurons in grey matter heterotopia in patients with epilepsy. Epilepsia, 45(8), 916 - 923.
Sisodiya SM (2004). Malformations of cortical development: burdens and insights from important causes of human epilepsy. The Lancet Neurology, 3(1), 29 - 38.
Soranzo N, Cavalleri GL, Weale ME, Wood NW, Depondt C, Marguerie R, Sisodiya SM, Goldstein DB (2004). Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene. Genome Research, 14(7), 1333 - 1344. doi:10.1101/gr.1965304
Sisodiya SM, Sander JW (2004). Epilepsy: management. Medicine (Oxford), 32(10), 52 - 56. doi:10.1383/medc.32.10.52.51494
Bamiou DE, Musiek FE, Sisodiya SM, Free SL, Davies RA, Moore A, van Heyningen V, Luxon LM (2004). Deficient auditory interhemispheric transfer in patients with PAX6 mutations. Annals of Neurology, 56(4), 503 - 509. doi:10.1002/ana.20227
Guerrini R, Mei D, Sisodiya S, Sicca F, Harding B, Takahashi Y, Dorn T, Yoshida A, Campistol J, Kramer G, Moro F, Dobyns WB, Parrini E (2004). Germline and mosaic mutations of FLN1 in men with periventricular heterotopia. Neurology, 63(1), 51 - 56.
Sisodiya SM, Duncan J (2004). Epilepsy: Epidemiology, clinical assessment, investigation and natural history. Medicine, 32(10), 47 - 51.
Goldstein DB, Tate SK, Sisodiya SM (2004). Erratum: Pharmacogenetics goes genomic (Nature Review Genetics (2003) 4 (937-947)). Nature Reviews Genetics, 5(1), 76 - 76.
Depondt C, Cavalleri G, Weale ME, Burly MW, Cock H, Shorvon SD, Sisodiya S, Wood NW, Goldstein DB (2004). Common variation in the SCN1A gene is a risk factor for common forms of epilepsy associated with febrile seizures.
Klinger L, Sisodiya S, Duncan J, Swaminathan R, Shah V, Keen RW (2004). Exposure to anti-epileptic medication in utero and effect on peak bone mineral density.
McKenzie M, Liolitsa D, Sisodiya S, Wood N, Duchen M, Hanna M (2004). A homoplasmic ND5 mutation associated with MELAS: mitochondria as ATP consumers?.
Eriksson SH, Nordborg C, Thom M, Sisodiya SM, Kasper BS (2004). Microdysgenesis in Mesial Temporal Lobe Epilepsy [2] (multiple letters). Annals of Neurology, 55(4), 596 - 597.
Eriksson SH, Free SL, Thom M, Harkness W, Sisodiya SM, Duncan JS (2004). Precise registration of preoperative MRI with histopathology after temporal lobe resections.
Graves TD, Gandhi S, Smith SJM, Sisodiya SM, Conway GS (2004). Misdiagnosis of seizures: insulinoma presenting as adult-onset seizure disorder. J NEUROL NEUROSUR PS, 75(8), 1091 - 1092. doi:10.1136/jnnp.2004.029249
Sisodiya SM (2004). Is refractory epilepsy a disorder of transporter systems?.
Sen A, Thom M, Sisodiya SM (2004). Differential activation of CDK5 in subfields of hippocampal sclerosis.
Sisodiya SM (2004). How to overcome pharmacoresistance by designing drugs that will overcome transport system disorders?.
Sisodiya S (2004). Pharmacogenetics and epilepsy. MIMS Advances in Epilepsy, 11, 2 - 5.

2003

Free SL, Mitchell TN, Williamson KA, Churchill AJ, Shorvon SD, Moore AT, van H, V S, S M (2003). Quantitative MR image analysis in subjects with defects in the PAX6 gene. NeuroImage, 20(4), 2281 - 2290.
Sisodiya S (2003). Pharmacogenetics: Markers of efficacy, intracability and adverse effects.
Mitchell TN, Free SL, Williamson KA, Stevens JM, Churchill AJ, Hanson IM, Shorvon SD, Moore AT, van Heyningen V, Sisodiya SM (2003). Polymicrogyria and absence of pineal gland due to PAX6 mutation. Annals of Neurology, 53(5), 658 - 663. doi:10.1002/ana.10576
Mitchell TN, Free SL, Merschhemke M, Lemieux L, Sisodiya SM, Shorvon SD (2003). Reliable callosal measurement: population normative data confirm sex-related differences. American Journal of Neuroradiology, 24(3), 410 - 418.
Sisodiya S (2003). Drug resistance in epilepsy: not futile, but complex?. The Lancet Neurology, 2(6), 331 - 331.
Liu RSN, Lemieux L, Bell GS, Hammers A, Sisodiya SM, Bartlett PA, Shorvon SD, Sander JWAS, Duncan JS (2003). Progressive neocortical damage in epilepsy. Annals of Neurology, 53(3), 312 - 324. doi:10.1002/ana.10463
Thom M, Seetah S, Sisodiya S, Koepp M, Scaravilli F (2003). Sudden and unexpected death in epilepsy (SUDEP): evidence of acute neuronal injury using HSP-70 and c-Jun immunohistochemistry. Neuropathology and Applied Neurobiology, 29(2), 132 - 143.
Sisodiya SM (2003). Brain malformations in adults. In Trimble MR (Ed.), Learning disability and epilepsy (pp. 65 - 83). : Clarius Press.
Liu RS, Lemieux L, Bell GS, Sisodiya SM, Shorvon SD, Sander JW, Duncan JS (2003). A longitudinal study of brain morphometrics using quantitative magnetic resonance imaging and difference image analysis. NeuroImage, 20(1), 22 - 33. doi:10.1016/S1053-8119(03)00219-2
Manford M, Sisodiya SM (2003). Frontal lobe epilepsy. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2003: from synapse to society. A practical guide to epilepsy (pp. 147 - 150). : Meritus Communications.
Siddiqui A, Kerb R, Weale ME, Brinkmann U, Smith A, Goldstein DB, Wood NW, Sisodiya SM (2003). Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1. New England Journal of Medicine, 348(15), 1442 - 1448. doi:10.1056/NEJMoa021986
Thom M, Harding BN, Lin WR, Martinian L, Cross H, Sisodiya SM (2003). Cajal-Retzius cells, inhibitory interneuronal populations and neuropeptide Y expression in focal cortical dysplasia and microdysgenesis.. Acta Neuropathologica, 105(6), 561 - 569. doi:10.1007/s00401-003-0673-6
Powell HWR, Hart PE, Sisodiya SM (2003). Epilepsy and perisylvian polymicrogyria in a patient with Kabuki syndrome. Developmental Medicine and Child Neurology, 45(12), 841 - 843.
Sisodiya SM (2003). Mechanisms of antiepileptic drug resistance. Current Opinion in Neurology, 16(2), 197 - 201.
Squier W, Salisbury H, Sisodiya S (2003). Stroke in the developing brain and intractable epilepsy: effect of timing on hippocampal sclerosis. Developmental Medicine and Child Neurology, 45(9), 580 - 585.
Goldstein DB, Tate SK, Sisodiya SM (2003). Pharmacogenetics goes genomic. Nature Reviews Genetics, 4(12), 937 - 947.
Aronica E, Gorter JA, van Vliet EA, Spliet WG, van Veelen CW, van Rijen PC, Leenstra S, Ramkema MD, Scheffer GL, Scheper RJ, Sisodiya SM, Troost D (2003). Overexpression of the human major vault protein in gangliogliomas. Epilepsia, 44(9), 1166 - 1175.
Sisodiya SM, Thom M (2003). Widespread upregulation of drug-resistance proteins in fatal human status epilepticus. Epilepsia, 44(2), 261 - 264.
Sisodiya SM (2003). Syncope. In Sander JW, Walker MC, Smalls JE (Ed.), Epilepsy 2003: from synapse to society. A practical guide to epilepsy (pp. 167 - 170). : Meritus Communications.
Goldstein D, Soranzo N, Cavalleri G, Wood N, Sisodiya S (2003). An associated interval approach for identifying candidate causal variants underlying altered activity of the ABCB1 multi-drug resistance gene..
Sisodiya SM, Martinian L, Scheffer GL, van der Valk P, Cross JH, Scheper RJ, Harding BN, Thom M (2003). Major vault protein, a marker of drug resistance, is upregulated in refractory epilepsy. Epilepsia, 44(11), 1388 - 1396.

2002

Mitchell TN, Stevens JM, Free SL, Sander JW, Shorvon SD, Sisodiya SM (2002). Anterior commissure absence without callosal agenesis: a new brain malformation. Neurology, 58(8), 1297 - 1299.
Duncan JS, Sisodiya SM, Smalls JE (2002). Epilepsy 2002: from science to patient - Lecture notes.
Buttery PC, Sisodiya SM (2002). The safety, tolerability and adverse events profile of tiagabine. Reviews in Contemporary Pharmacotherapy, 12(5), 251 - 262.
Sisodiya S (2002). Syncope. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2002: from science to patient - Lecture notes (pp. 157 - 160). : Meritus Communications.
Edwards MJJ, Hargreaves IP, Heales SJR, Jones SJ, Ramachandran V, Bhatia KP, Sisodiya S (2002). N-acetylcysteine and Unverricht-Lundborg disease - Variable response and possible side effects. Neurology, 59(9), 1447 - 1449.
Sisodiya SM, Patsalos PN, Sander JWAS (2002). Carbamazepine toxicity during combination therapy with levetiracetam: a pharmacodynamic interaction. Epilepsy Research, 48(3), 217 - 219.
Thom M, Sisodiya SM, Beckett A, Martinian L, Lin WR, Harkness W, Mitchell TN, Craig J, Duncan JS, Scaravilli F (2002). Cytoarchitectural abnormalities in hippocampal sclerosis. Journal of Neuropathology and Experimental Neurology, 61(6), 510 - 519.
Bastos A, Bernasconi A, Bernasconi N, Duncan J, Lemieux L, Sisodiya SJM (2002). Structural image analysis in epilepsy. Epilepsia, 43(Suppl.), 19 - 24.
Liu RSN, Lemieux L, Bell GS, Sisodiya SM, Bartlett PA, Shorvon SD, Sander JW, Duncan JS (2002). The structural consequences of newly diagnosed seizures. Annals of Neurology, 52(5), 573 - 580. doi:10.1002/ana.10338
Thom M, Sisodiya SM, Lin WR, Mitchell T, Free SL, Stevens J, Scaravilli F (2002). Bilateral isolated hippocampal malformation in temporal lobe epilepsy. Neurology, 58(11), 1683 - 1686.
Liu RS, Lemieux L, Sander JW, Sisodiya SM, Duncan JS (2002). Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy.. Annals of Neurology, 52(6), 861 - 862.
Sisodiya SM, Lin WR, Harding BN, Squier MV, Thom M (2002). Drug resistance in epilepsy: human epilepsy. Novartis Foundation Symposium, 243, 167 - 185.
Sisodiya S (2002). Epilepsy and sleep. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2002: from science to patient - Lecture notes (pp. 161 - 164). : Meritus Communications.
Sisodiya SM, Thom M, Lin WR, Bajaj NP, Cross JH, Harding BN (2002). Abnormal expression of cdk5 in focal cortical dysplasia in humans. Neuroscience Letters, 328(3), 217 - 220.
Manford M, Sisodiya S (2002). Frontal lobe epilepsy. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2002: from science to patient - Lecture notes (pp. 137 - 140). : Meritus Communications.
Sisodiya SM, Lin WR, Harding BN, Squier MV, Thom M (2002). Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy. Brain, 125(1), 22 - 31. doi:10.1093/brain/awf002
Mitchell TN, Free SL, Shorvon SD, Sisodiya SM (2002). A paradigm for exploring the genetic control of brain development and function. J NEUROL NEUROSUR PS, 73(2), 225 - 225.
Liu RSN, Lemieux L, Bell GS, Sisodiya SM, Bartlett PA, Sander JWAS, Shorvon SD (2002). The effect of epilepsy on the brain: Findings of a longitudinal community based quantitative MRI study. J NEUROL NEUROSUR PS, 73(2), 219 - 219.
Mitchell TN, Free SL, Thorn M, Sisodiya SM, Shorvon SD (2002). Quantitative MRI abnormalities with histopathological correlation in refractory epilepsy: A tool to predict surgical outcome?. J NEUROL NEUROSUR PS, 72(1), 135 - 135.

2001

Eriksson SH, Thom M, Heffernan J, Lin WR, Harding BN, Squier MV, Sisodiya SM (2001). Persistent reelin-expressing Cajal-Retzius cells in polymicrogyria. Brain, 124(7), 1350 - 1361.
Sisodiya SM (2001). Epilepsy and sleep. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2001: from science to patient - Lecture notes: 8th Epilepsy Teaching Weekend, September 28-30, 2001, St Anne's College, Oxford (pp. 161 - 164). : Meritus Communications.
Thom M, Sisodiya S, Harkness W, Scaravilli F (2001). Microdysgenesis in temporal lobe epilepsy: a quantitative and immunohistochemical study of white matter neurones. Brain, 124(11), 2299 - 2309. doi:10.1093/brain/124.11.2299
Liu RSN, Lemieux L, Bell GS, Bartlett PA, Sander JWAS, Sisodiya SM, Shorvon SD, Duncan JS (2001). A longitudinal quantitative MRI study of community-based patients with chronic epilepsy and newly diagnosed seizures: methodology and preliminary findings. NeuroImage, 14(1), 231 - 243.
Craig J, Sisodiya SM (2001). Guide to the management of epilepsy in pregnancy. PRESCRIBER, 12(18), 30 - 38.
Sisodiya SM, Lin WR, Squier MV, Thom M (2001). Multidrug-resistance protein 1 in focal cortical dysplasia. The Lancet, 357(9249), 42 - 43. doi:10.1016/S0140-6736(00)03573-X
Sisodiya SM, Fish DR (2001). Structural neuroimaging in the presurgical evaluation of patients with malformations of cortical development and neurocutaneous syndromes. In Luders HO, Youssef G (Ed.), Epilepsy surgery (pp. 239 - 245). : Lippincott, Wilkins and Williams.
Van Paesschen W, Sisodiya S, Connelly A, Duncan JS, Free SL, Raymond AA, Grunewald RA, Revesz T, Shorvon SD, Fish DR, Stevens JM, Johnson CL, Scaravilli F, Harkness WFJ, Jackson GD (2001). Quantitative hippocampal MRI and intractable temporal lobe epilepsy. Neurology, 57(11), S5 - S12.
Sheen VL, Dixon PH, Fox JW, Hong SE, Kinton L, Sisodiya SM, Duncan JS, Dubeau F, Scheffer IE, Schachter SC, Wilner A, Henchy R, Crino P, Kamuro K, DiMario F, Berg M, Kuzniecky R, Cole AJ, Bromfield E, Biber M, Schomer D, Wheless J, Silver K, Mochida GH, Berkovic SF, Andermann F, Andermann E, Dobyns WB, Wood NW, Walsh CA (2001). Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Human Molecular Genetics, 10(17), 1775 - 1783.
Manford M, Sisodiya SM (2001). Frontal lobe epilepsy. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2001: from science to patient - Lecture notes: 8th Epilepsy Teaching Weekend, September 28-30, 2001, St Anne's College, Oxford (pp. 137 - 140). : Meritus Communications.
Van Paesschen W, Sisodiya S, Connelly A, Duncan JS, Free SL, Raymond AA, Grünewald RA, Revesz T, Shorvon SD, Fish DR, Stevens JM, Johnson CL, Scaravilli F, Harkness WFJ, Jackson GD (2001). Quantitative hippocampal MRI and intractable temporal lobe epilepsy. Neurology, 57(11 SUPPL. 4), S5 - S12.
Sisodiya SM (2001). Syncope. In Duncan JS, Sisodiya SM, Smalls JE (Ed.), Epilepsy 2001: from science to patient - Lecture notes: 8th Epilepsy Teaching Weekend, September 28-30, 2001, St Anne's College, Oxford (pp. 157 - 160). : Meritus Communications.
Sisodiya SM, Cross H, Richardson M, Wyllie E, Fish DR (2001). What tests are needed to define the epileptogenic zone in patients with malformations of cortical development?. In Luders HO, Youssef G (Ed.), Epilepsy surgery (pp. 951 - 957). : Lippincott, Wilkins and Williams.
Sisodiya SM, Free SL, Williamson KA, Mitchell TN, Willis C, Stevens JM, Kendall BE, Shorvon SD, Hanson IM, Moore AT, van Heyningen V (2001). PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans. Nature Genetics, 28(3), 214 - 216. doi:10.1038/90042
Donaghy M, Sisodiya SM, Kennett R, McDonald B, Haites N, Bell C (2001). Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation. J NEUROL NEUROSUR PS, 70(2), 277 - 277.

2000

Liu RSN, Lemieux L, Shorvon SD, Sisodiya SJM, Duncan JS (2000). Association between brain size and abstinence from alcohol. The Lancet, 355(9219), 1969 - 1970.
Sisodiya SJM, Sander JWAS (2000). Epilepsy: management. Medicine, 28, 47 - 51.
Donaghy M, Sisodiya SM, Kennett R, McDonald B, Haites N, Bell C (2000). Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation.. J Neurol Neurosurg Psychiatry, 69(6), 799 - 805.
Sisodiya SM, Free SL, Duncan JS, Stevens JM (2000). Bilateral periventricular and subcortical heterotopia in a man with refractory epilepsy. Epilepsia, 41(3), 352 - 354.
Sisodiya SJM, Heffernan J, Harrison PJ, Squier MV, Thom M (2000). Sulcogyral variation in NMDA receptor 2A/B subunit immunoreactivity in human brain. NeuroReport, 11(11), 2601 - 2606.
Sisodiya SJM, Squier MV, Anslow P (2000). Malformations of cortical development. In Oxbury JM, Polkey CE, Duchowny M (Ed.), Intractable focal epilepsy (pp. 99 - 130). : W. B. Saunders.
Thom M, Holton JL, D'Arrigo C, Griffin B, Beckett AAJ, Sisodiya SJM, Alexiou D, Sander JWAS (2000). Microdysgenesis with abnormal cortical myelinated fibres in temporal lobe epilepsy: a histopathological study with calbindin D-28-K immunohistochemistry. Neuropathology and Applied Neurobiology, 26(3), 251 - 257.
Sisodiya SJM, Duncan JS (2000). Epilepsy: epidemiology, clinical assessment, investigation and natural history. Medicine International, 28, 42 - 47.
Sisodiya SJM (2000). Surgery for malformations of cortical development causing epilepsy. Brain, 123, 1075 - 1091.

1999

Sisodiya SM, Marques W, Everitt A, Sander JW (1999). Male monozygotic twins discordant for periventricular nodular heterotopia and epilepsy.. Epilepsia, 40(2), 248 - 250.
Krakow K, Lemieux L, Sisodiya SM, Symms MR, Allen PJ, Duncan JS, Fish DR (1999). Brain activity identified with spike-triggered functional MRI and its spatial relation to different pathologies in lesional epilepsy.
Woermann FG, Free SL, Koepp MJ, Sisodiya SM, Duncan JS (1999). Abnormal cerebral structure in juvenile myoclonic epilepsy demonstrated with voxel-based analysis of MRI.. Brain, 122 ( Pt 11), 2101 - 2108.
Sisodiya SM, Heffernan J, Squier MV (1999). Over-expression of P-glycoprotein in malformations of cortical development.. Neuroreport, 10(16), 3437 - 3441.
Sisodiya SM, Free S, Fish DR, Shorvon SD (1999). Novel magnetic resonance imaging methods for quantifying changes in the cortical ribbon in patients with epilepsy.. Adv Neurol, 81, 81 - 87.
Liu RLSN, Lemieux L, Sisodiya SM, Shorvon SD, Duncan JS (1999). Serial volumetric hippocampal measurements in coregistered scan pairs: Reproducibility in a blinded study.
Baxendale SA, Sisodiya SM, Thompson PJ, Free SL, Kitchen ND, Stevens JM, Harkness WFJ, Fish DR, Shorvon SD (1999). Disproportion in the distribution of gray and white matter - neuropsychological correlates. Neurology, 52, 248 - 252.
Manford M, Sisodiya SJM (1999). Frontal lobe epilepsy. In Duncan JS, Sisodiya SJM, Smalls JE (Ed.), Epilepsy 99. From science to patient. Lecture notes (pp. 139 - 142). : International League Against Epilepsy.
Sisodiya SM, Free SL, Thom M, Everitt AE, Fish DR, Shorvon SD (1999). Evidence for nodular epileptogenicity and gender differences in periventricular nodular heterotopia.. Neurology, 52(2), 336 - 341.
Hannan AJ, Servotte S, Katsnelson A, Sisodiya S, Blakemore C, Squier M, Molnár Z (1999). Characterization of nodular neuronal heterotopia in children.. Brain, 122 ( Pt 2), 219 - 238.
Duncan JS, Sisodiya SJM, Smalls JE (1999). Extratemporal resection, corpus callosotomy and subpial transection. In Duncan JS, Sisodiya SJM, Smalls JE (Ed.), Epilepsy 99. From science to patient. Lecture notes (pp. 405 - 408). : International League Against Epilepsy.

1998

Maudgil DD, Free SL, Sisodiya SM, Lemieux L, Woermann FG, Fish DR, Shorvon SD (1998). Identifying homologous anatomical landmarks on reconstructed magnetic resonance images of the human cerebral cortical surface.. J Anat, 193 ( Pt 4), 559 - 571.
Sisodiya SM, Free SL, Sander JWA, Salmenpera T, Kalviainen R, Partanen K, Pitkanen A (1998). Hippocampal damage caused by seizures in temporal lobe epilepsy (multiple letters) [4]. Lancet, 351(9109), 1132 - 1133.
Woermann FG, Sisodiya SM, Free SL, Duncan JS (1998). Quantitative MRI in patients with idiopathic generalized epilepsy. Evidence of widespread cerebral structural changes. Brain, 121, 1661 - 1667.
Woermann FG, Free SL, Koepp MJ, Sisodiya SM, Duncan JS (1998). Quantitative MRI in patients with juvenile myoclonic epilepsy (JME): An objective voxel based comparison of structural imaging data. NeuroImage, 7(4 PART II), - .
Sisodiya SM, Free SL, Sander JW (1998). Hippocampal damage caused by seizures in temporal lobe epilepsy.. The Lancet, 351(9109), 1132 - 1133.
Sisodiya SM, Free SL, Shorvon SD (1998). Surgical treatment of hypothalamic hamartoma.. Ann Neurol, 43(2), 273 - 275. doi:10.1002/ana.410430222

1997

Sisodiya SM, Moran N, Free SL, Kitchen ND, Stevens JM, Harkness WFJ, Fish DR, Shorvon SD (1997). Correlation of widespread preoperative magnetic resonance imaging changes with unsuccessful surgery for hippocampal sclerosis. Annals of Neurology, 41, 490 - 496.
Sisodiya SM, Free SL, Stevens JM, Fish DR, Shorvon SD (1997). Widespread cerebral structural changes in two patients with gelastic seizures and hypothalamic hamartomata. Epilepsia, 38, 1008 - 1010.
Richardson MP, Friston KJ, Sisodiya SM, Koepp MJ, Ashburner J, Free SL, Brooks DJ, Duncan JS (1997). Cortical grey matter and benzodiazepine receptors in malformations of cortical development. A voxel-based comparison of structural and functional imaging data. Brain, 120, 1961 - 1973.
Sisodiya SM, Free SL (1997). Disproportion of cerebral surface areas and volumes in cerebral dysgenesis: MRI-based evidence for connectional abnormalities. Brain, 120, 271 - 281.
Woermann FG, Sisodiya SM, Koepp M, Free SL, Duncan JS, Shorvon SD (1997). Quantitative MRI in patients with idiopathic generalized epilepsy (IGE): Evidence of widespread cerebral structural changes. NEUROLOGY, 48(3), V2001 - V2001.

1996

Sisodiya S, Free S, Fish D, Shorvon S (1996). MRI-based surface area estimates in the normal adult human brain: evidence for structural organisation.. J Anat, 188 ( Pt 2), 425 - 438.
Free SL, Sisodiya SM, Cook MJ, Fish DR, Shorvon SD (1996). Three-dimensional fractal analysis of the white matter surface from magnetic resonance images of the human brain.. Cereb Cortex, 6(6), 830 - 836.
Sisodiya SM, Stevens JM, Fish DR, Free SL, Shorvon SD (1996). The demonstration of gyral abnormalities in patients with cryptogenic partial epilepsy using three-dimensional MRI.. Arch Neurol, 53(1), 28 - 34.

1995

Sisodiya SM (1995). Wiring, dysmorphogenesis and epilepsy: a hypothesis.. Seizure, 4(3), 169 - 185.
Van Paesschen W, Sisodiya S, Connelly A, Duncan JS, Free SL, Raymond AA, Grünewald RA, Revesz T, Shorvon SD, Fish DR (1995). Quantitative hippocampal MRI and intractable temporal lobe epilepsy.. Neurology, 45(12), 2233 - 2240.
Sisodiya SM, Free SL, Fish DR, Shorvon SD (1995). Increasing the yield from volumetric MRI in patients with epilepsy.. Magn Reson Imaging, 13(8), 1147 - 1152.
Tofts PS, Sisodiya S, Barker GJ, Webb S, MacManus D, Fish F, Shorvon S (1995). MR magnetization transfer measurements in temporal lobe epilepsy: a preliminary study.. AJNR Am J Neuroradiol, 16(9), 1862 - 1863.
Li LM, Fish DR, Sisodiya SM, Shorvon SD, Alsanjari N, Stevens JM (1995). High resolution magnetic resonance imaging in adults with partial or secondary generalised epilepsy attending a tertiary referral unit.. J Neurol Neurosurg Psychiatry, 59(4), 384 - 387.
Sisodiya SM, Free SL, Stevens JM, Fish DR, Shorvon SD (1995). Widespread cerebral structural changes in patients with cortical dysgenesis and epilepsy.. Brain, 118 ( Pt 4), 1039 - 1050.
Raymond AA, Fish DR, Sisodiya SM, Alsanjari N, Stevens JM, Shorvon SD (1995). Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patients.. Brain, 118 ( Pt 3), 629 - 660.
Walker MC, Smith SJ, Sisodiya SM, Shorvon SD (1995). Case of simple partial status epilepticus in occipital lobe epilepsy misdiagnosed as migraine: clinical, electrophysiological, and magnetic resonance imaging characteristics.. Epilepsia, 36(12), 1233 - 1236.

1994

Raymond AA, Fish DR, Stevens JM, Sisodiya SM, Alsanjari N, Shorvon SD (1994). Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy.. J Neurol Neurosurg Psychiatry, 57(10), 1195 - 1202.
Raymond AA, Fish DR, Stevens JM, Cook MJ, Sisodiya SM, Shorvon SD (1994). Association of hippocampal sclerosis with cortical dysgenesis in patients with epilepsy.. Neurology, 44(10), 1841 - 1845.
Bergin PS, Raymond AA, Free SL, Sisodiya SM, Stevens JM (1994). Magnetic resonance volumetry.. Neurology, 44(9), 1770 - 1771.

1993

Sisodiya S, Hoffbrand BI (1993). Hazards of fad diets in patients treated with ACE inhibitors.. Br J Hosp Med, 50(8), 486 - 487.
Corbett EL, Sisodiya S, Sarkar D (1993). Chronic hypothermia and water intoxication associated with a neurodegenerative disease.. Postgrad Med J, 69(818), 937 - 940.

1986

Stern CD, Sisodiya SM, Keynes RJ (1986). Interactions between neurites and somite cells: inhibition and stimulation of nerve growth in the chick embryo.. J Embryol Exp Morphol, 91, 209 - 226.

Caruana Galizia E, Srikantha M, Palmer R, Waters JJ, Lench N, Mackie Ogilvie C, Kasperavičiūtė D, Nashef L, Sisodiya SM (). Array Comparative Genomic Hybridization: Results from an adult population with drug-resistant epilepsy and co-morbidities.. European Journal of Medical Genetics, , - .
Sisodiya SM, Thom M, Martinian LM, Liu JYW (). Immunolabeling recovery in archival, post mortem, human brain tissue using modified antigen retrieval and the catalyzed signal amplification system. Journal of Neuroscience Methods, , - .
Blanc F, Martinian L, Liagakouras I, Catarino C, Sisodiya SM, Thom M (). Investigation of widespread neocortical pathology associated with hippocampal sclerosis in epilepsy: A post mortem study.. Epilepsia, , - .
Chaudhary UJ (). Imaging the interaction: working memory, epileptic discharges and behavioural performance.
Stretton J, Foulkes A, Williams E, Burdett J, Baxendale S, Thompson P, Sisodiya S, Duncan J, Matarin M (). Does the BDNF Val66Met polymorphism influence cognitive function in mTLE..