Dr Tom Jacques

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Personal Profile

Name: Tom Jacques Email: t.jacques@ucl.ac.uk
Title: Dr Tel: 02078298663
Department: ICH Development Bio & Cancer Prog Fax: 02078314366
Position: Clinical Senior Lecturer Address: Institute of Child Health UCL, 30 Guildford Street, London, WC1N 1EH
Research Domain: Basic Life Sciences, Cancer, Neuroscience, Personalised Medicine, Populations & Lifelong Health, Reproduction & Development, Stem Cells & Regenerative Medicine (Frontier Disciplines) Web Page: Personal Web Page

Profile

Research Description

The aim of our group is to understand the development of paediatric brain diseases and in particular the roles of neural stem cells in these diseases. We have focussed on brain tumours and epilepsy. Recent highlights include demonstrating how initial mutations cause different types of tumour in the brain and the isolation of a pathological stem cell from a human malformation of cortical development.


Keywords: Brain, Brain Tumour, Cancer, Epilepsy,  Focal Cortical Dysplasia, Morphology, Neural stem cells, Neuroanatomy, Neurogenesis,Neuropathology, Progenitors, Stem cells, Temporal lobes

Conditions: Astrocytoma, Brain tumours in children, Focal Cortical Dysplasia, Epilepsy

Methods: Cell culture, Confocal microscopy, Gene expression profiling - tissue level, Histology, Immunohistochemistry, light microscopic techniques, Time-lapse imaging, Stereological analysis

Research Activities

Neuropathology

Neuropathology of Stem Cells in Children

Neuropathology studies in epilepsy

Education Description

UCL Collaborators

Dr Janice Holton; Prof Faraneh Vargha-Khadem; Prof Sebastian Brandner; Dr Maria Thom

External Collaborators

Publications

    2015

    • Jacques TS, Harding, B. (2015). Metabolic and neurodegenerative diseases of childhood. In Love, S. , Perry A, Ironside J, Budka H (Ed.), Greenfield's Neuropathology (pp. - ). : CRC Press.

    2014

    • Wedatilake Y, Plagnol V, Anderson G, Paine S, Clayton P, Jacques TS, Rahman S (2014). Tubular aggregates caused by SERAC1 mutations in a patient with a mitochondrial encephalopathy. Neuropathology and Applied Neurobiology, , - . doi:10.1111/nan.12190
    • Paine SML, Willsher AR, Nicholson SL, Sebire NJ, Jacques TS (2014). Characterisation of a population of neural progenitor cells in the infant hippocampus. Neuropathology and Applied Neurobiology, 40(5), 544 - 550. doi:10.1111/nan.12065
    • Jacques TS (2014). Book review: Muscle Disease: Pathology and Genetics. Neuromuscular Disorders, 24(8), 746 - 746. doi:10.1016/j.nmd.2014.05.002
    • Hersheson J, Burke D, Clayton R, Mills PB, Anderson G, Jacques TS, Wood N, Gissen P, Clayton P, Fearnley J, Mole SE, Houlden H (2014). Cathepsin D deficiency causes juvenile-onset ataxia and distinctive muscle pathology. Neurology, , - .
    • Hill R, Kuijper S, Lindsey J, Schwalbe E, Barker K, Boult J, Williamson D, Ahmad Z, Hallsworth A, Ryan S, Poon E, Robinson S, Ruddle R, Raynaud F, Howell L, Kwok C, Joshi A, Nicholson SL, Crosier S, Wharton S, Robson K, Michalski A, Hargrave D, Jacques T, Pizer B, Bailey S, Swartling F, Petrie K, Weiss W, Chesler L, Clifford S (2014). MYC And TP53 defects emerge and interact at medulloblastoma relapse, define rapidly progressive disease and can be targeted therapeutically.
    • Karakoula K, Jacques TS, Phipps KP, Harkness W, Thompson D, Harding BN, Darling JL, Warr TJ (2014). Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma. Cancer Letters, 346(1), 34 - 44. doi:10.1016/j.canlet.2013.12.005
    • Fouladi M, Bartels U, Warren K, Hassal T, Baugh J, Kirkendall J, Doughman R, Leach J, Jones B, Miles L, Hawkins C, Bouffet E, Hargrave D, Grill J, Jones C, Jacques T, Savage S, Goldman S, Leary S, Packer R, Saunders D, Wesseling P, Varlet P, van Vuurden D (2014). Establishment of an international diffuse intrinsic pontine glioma (DIPG) registry.
    • Paine SML, Sebire NJ, Mills K, Sirkas E, Anderson GW, Kiho L, Males A, Jacques TS (2014). Perinatal lethal Gaucher disease: Diagnosis by mass spectrometry in a fetal case.
    • Eggens VRC, Barth PG, Niermeijer J-MF, Berg JN, Darin N, Dixit A, Fluss J, Foulds N, Fowler D, Hortobagyi T, Jacques T, King MD, Makrythanasis P, Mate A, Nicoll JAR, O'Rourke D, Price S, Williams AN, Wilson L, Suri M, Sztriha L, Dijns-de Wissel MB, van Meegen MT, van Ruissen F, Aronica E, Troost D, Majoie CBLM, Marquering HA, Poll-The BT, Baas F (2014). EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. Orphanet Journal of Rare Diseases, 9, - . doi:10.1186/1750-1172-9-23
    • Grech-Sollars M, Saunders DE, Phipps KP, Kaur R, Paine SML, Jacques TS, Clayden JD, Clark CA (2014). Challenges for the functional diffusion map in pediatric brain tumors. Neuro-Oncology, 16(3), 449 - 456. doi:10.1093/neuonc/not197
    • Scerif F, Picker SR, Leung J, Yasin SA, Virasami A, Harkness W, Hubank M, Guillemot F, Paine SML, Cross JH, Jacques TS (2014). Understanding the molecular pathology underlying paediatric Focal Cortical Dysplasia.
    • Jacques TS, Andersen G, Hersheson J, Burke D, Clayton R, Mills P, Wood N, Gissen P, Clayton P, Fearnley J, Mole SE, Houlden H (2014). Distinctive muscle pathology in patients with mutations in the Cathepsin D gene.
    • Tansley SL, Betteridge ZE, Gunawardena H, Jacques TS, Owens CM, Pilkington C, Arnold K, Yasin S, Moraitis E, Wedderburn LR, McHugh NJ (2014). Anti-MDA5 autoantibodies in juvenile dermatomyositis identify a distinct clinical phenotype: a prospective cohort study.. Arthritis Research and Therapy, 16(4), R138 - . doi:10.1186/ar4600
    • de Kock L, Sabbaghian N, Plourde F, Srivastava A, Weber E, Bouron-Dal Soglio D, Hamel N, Kelsey MM, Park SH, Deal CL, Choi JH, Dishop MK, Esbenshade A, Kuttesch JF, Jacques TS, Perry A, Leichter H, Maeder P, Brundler MA, Warner J, Neal J, Zacharin M, Korbonits M, Cole T, Traunecker H, McLean TW, Rotondo F, Lepage P, Albrecht S, Horvath E, Kovacs K, Priest JR, Foulkes WD (2014). Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations.. Acta Neuropathologica, 128(1), 111 - 122. doi:10.1007/s00401-014-1285-z
    • Kelberman D, Islam L, Lakowski J, Bacchelli C, Chanudet E, Lescai F, Patel A, Stupka E, Buck A, Wolf S, Beales PL, Jacques TS, Bitner-Glindzicz M, Liasis A, Lehmann OJ, Kohlhase J, Nischal KK, Sowden JC (2014). Mutation of SALL2 causes recessive ocular coloboma in humans and mice.. Human Molecular Genetics, 23, 2511 - 2526. doi:10.1093/hmg/ddt643
    • Paine SML, Jacques TS, Sebire NJ (2014). Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies. Neuropathology and Applied Neurobiology, 40(5), 520 - 543.
    • Brown JR, Morfopoulou S, Hubb J, Emmett WA, Ip W, Shah D, Brooks T, Paine SML, Anderson G, Virasami A, Tong CYW, Clark DA, Plagnol V, Jacques TS, Qasim W, Hubank M, Breuer J (2014). Astrovirus VA1/HMO-C: an increasingly recognised neurotropic pathogen in immunocompromised patients. Clinical Infectious Diseases, , - .

    2013

    • Paine SML, Ternier J, Thompson DNP, Mazumder A, Manka K, Craig F, Hargrave D, Jacques TS (2013). Rhabdoid meningioma in a young child: post-mortem findings of a widely disseminated and aggressive tumour.
    • McTague A, Appleton R, Avula S, Cross JH, King MD, Jacques TS, Bhate S, Cronin A, Curran A, Desurkar A, Farrell MA, Hughes E, Jefferson R, Lascelles K, Livingston J, Meyer E, McLellan A, Poduri A, Scheffer IE, Spinty S, Kurian MA, Kneen R (2013). Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.. Brain, 136(Pt 5), 1578 - 1591. doi:10.1093/brain/awt073
    • 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
    • Sebire NJ, Miller S, Jacques TS, Taylor AM, Rennie JM, Kendall G, Chitty LS (2013). Post-mortem apparent resolution of fetal ventriculomegaly: evidence from magnetic resonance imaging.. Prenatal Diagnosis, 33(4), 360 - 364. doi:10.1002/pd.4065
    • Coras R, Bluemcke I, Thom M, Aronica E, Armstrong D, Bartolomei F, Bernasconi A, Bernasconi N, Bien CG, Cendes F, Cross HJ, Jacques TS, Kahane P, Gary MW, Miyata H, Moshe SL, Oz B, Ozkara C, Perucca E, Sisodiya S, Wiebe S, Spreafico R (2013). International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A task force report from the ILAE commission on diagnostic methods.
    • Scoto M, Cullup T, Cirak S, Yau S, Manzur AY, Feng L, Jacques TS, Anderson G, Abbs S, Sewry C, Jungbluth H, Muntoni F (2013). Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. European Journal of Human Genetics, 21(11), 1249 - 1252. doi:10.1038/ejhg.2013.31
    • Schwalbe EC, Hayden JT, Rogers HA, Miller S, Lindsey JC, Hill RM, Nicholson S-L, Kilday J-P, Adamowicz-Brice M, Storer L, Jacques TS, Robson K, Lowe J, Williamson D, Grundy RG, Bailey S, Clifford SC (2013). Histologically defined central nervous system primitive neuro-ectodermal tumours (CNS-PNETs) display heterogeneous DNA methylation profiles and show relationships to other paediatric brain tumour types. Acta Neuropathologica, 126(6), 943 - 946. doi:10.1007/s00401-013-1206-6
    • Paine SML, Kempski H, Harkness W, Mazumder A, Mankad K, Craig F, Hargrave D, Jacques TS (2013). Post-mortem findings in embryonal tumour with abundant neuropil and true rosettes (ETANTR): implications for biopsy diagnosis.
    • Paine SML, Bell DNR, Melchionda V, Weereratne C, Harrison S, Vargha-Khadem F, Harkness W, Cross JH, Harding BN, Pizarro L, Jacques TS (2013). Patterns of hippocampal sclerosis in children.
    • Hollingworh MA, Paine SML, Latak K, Ganapathi A, Miller K, Becherini F, Cross JH, Harkness W, Harding BN, Jacques TS (2013). The balloon cell vascular niche: anatomical evidence of a stem cell-blood vessel relationship in epilepsy-associated malformations of cortical development.
    • Clifford S, Crosier S, Nicholson S, Robson K, Jacques TS, Wharton S, Bown N, Michalski A, Pizer B (2013). A national feasibility study of real-time central pathology review (CPR) and molecular diagnostics for medulloblastoma.
    • Andoniadou CL, Matsushima D, Mousavy Gharavy SN, Signore M, Mackintosh AI, Schaeffer M, Gaston-Massuet C, Mollard P, Jacques TS, Le Tissier P, Dattani MT, Pevny LH, Martinez-Barbera JP (2013). Sox2(+) stem/progenitor cells in the adult mouse pituitary support organ homeostasis and have tumor-inducing potential. Cell Stem Cell, 13(4), 433 - 445. doi:10.1016/j.stem.2013.07.004
    • Varsani H, Charman SC, Li CK, Marie SK, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith AM, Jacques TS, Lundberg IE, Minetti C, Nennesmo I, Rushing EJ, Sallum AM, Sewry C, Pilkington CA, Holton JL, Wedderburn LR, the UK Juvenile Dermatomyositis Research Group (2013). Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease.. Annals of Rheumatic Disease, , - . doi:10.1136/annrheumdis-2013-203396
    • Barba C, Jacques T, Kahane P, Polster T, Isnard J, Leijten FSS, Ozkara C, Tassi L, Giordano F, Castagna M, John A, Öz B, Salon C, Streichenberger N, Cross JH, Guerrini R (2013). Epilepsy surgery in Neurofibromatosis Type 1. Epilepsy Research, 105(3), 384 - 395. doi:10.1016/j.eplepsyres.2013.02.021
    • Yasin S, Ali A, Tata M, Picker S, Anderson G, Latimer-Bowman E, Nicholson S, Harkness W, Cross JH, Paine SL, Jacques T (2013). mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis. Acta Neuropathologica, 126, 207 - 218. doi:10.1007/s00401-013-1135-4
    • Yasin S, Ali A, Tata M, Picker SR, Anderson G, Nicholson SL, Cross JH, Harkness W, Paine SML, Jacques TS (2013). mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: Evidence from focal cortical dysplasia and tuberous sclerosis.
    • Blümcke I, Thom M, Aronica E, Armstrong DD, Bartolomei F, Bernasconi A, Bernasconi N, Bien CG, Cendes F, Coras R, Cross JH, Jacques TS, Kahane P, Mathern GW, Miyata H, Moshé SL, Oz B, Ozkara C, Perucca E, Sisodiya S, Wiebe S, Spreafico R (2013). International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods.. Epilepsia, 54, 1315 - 1329. doi:10.1111/epi.12220
    • Jethwa H, Jacques TS, Gunny R, Wedderburn LR, Pilkington C, Manzur AY (2013). Limb girdle muscular dystrophy type 2B masquerading as inflammatory myopathy: case report.. Pediatric Rheumatology Online Journal, 11(1), 19 - . doi:10.1186/1546-0096-11-19
    • Thurston B, Gunny R, Anderson G, Paine S, Thompson D, Jacques T, Ternier J (2013). Fourth ventricle rosette-forming glioneuronal tumour in children: An unusual presentation in an 8-year-old patient, discussion and review of the literature. Child's Nervous System, 29(5), 839 - 847. doi:10.1007/s00381-012-1993-4
    • Dlamini N, Josifova DJ, Paine SML, Wraige E, Pitt M, Murphy AJ, King A, Buk S, Smith F, Abbs S, Sewry C, Jacques TS, Jungbluth H (2013). Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene. Neuromuscular Disorders, 23(5), 391 - 398. doi:10.1016/j.nmd.2013.02.001
    • Henriquez NV, Forshew T, Tatevossian R, Ellis M, Richard-Loendt A, Rogers HA, Jacques TS, Garcia Reitboeck P, Pearce K, Sheer D, Grundy RG, Brandner S (2013). Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumour propagation in vitro.. Cancer Research, 73, 5834 - 5844. doi:10.1158/0008-5472.CAN-13-1299

    2012

    • Phipps KP, Gumley D, Jacques TS, Hargrave D, Saunders D, Michalski A (2012). Neuropsychological and survival outcomes of 31 children under 36 months at diagnosis with central nervous system primitive neuroectodermal tumours treated with dose intensive chemotherapy and irradiation at a single centre.
    • Winder-Rhodes SE, Garcia-Reitböck P, Ban M, Evans JR, Jacques TS, Kemppinen A, Foltynie T, Williams-Gray CH, Chinnery PF, Hudson G, Burn DJ, Allcock LM, Sawcer SJ, Barker RA, Spillantini MG (2012). Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome. Movement Disorders, 27(2), 312 - 315. doi:10.1002/mds.24029
    • Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling J, Warr T (2012). Expression of BEX1 is down-regulated by hypermethylation in paediatric ependymoma.
    • Tirabosco R, Jacques T, Berisha F, Flanagan AM (2012). Assessment of integrase interactor 1 (INI-1) expression in primary tumours of bone. Histopathology, 61, 1245 - 1247.
    • Paine SML, Munot P, Carmichael J, Das K, Weber MA, Prabhakar P, Jacques TS (2012). The neuropathological consequences of CDKL5 mutation. Neuropathology and Applied Neurobiology, 38, 744 - 747.
    • Kinsler VA, Paine SML, Anderson GW, Wijesekara DS, Sebire NJ, Chong WK, Harkness W, Aylett SE, Jacques TS (2012). Neuropathology of neurocutaneous melanosis: Histological foci of melanotic neurones and glia may be undetectable on MRI. Acta Neuropathologica, 123(3), 453 - 456. doi:10.1007/s00401-012-0945-0
    • Barba C, Jacques TS, Kahane P, Polster T, Isnard J, Leijten FSS, Ozkara C, Tassi L, Giordano F, Castagna M, John A, Oz B, Streichenberger N, Salon C, Guerrini R, Cross H (2012). Epilepsy surgery in Neurofibromatosis type I.
    • Holme H, Ghara N, Jacques TS, Humphries P, Daw S, Shankar A (2012). A Isolated intracranial relapse of Hodgkin lymphoma in a child. International Journal of Case Reports and Images, 3(10), 12 - 15.
    • Apps J, Hasan F, Campus O, Behjati S, Jacques T, Sebire N, J A (2012). The immune environment of paediatric solid malignancies; evidence from an immunohistochemical study of clinical cases. Fetal and Pediatric Pathology, In press, - .
    • Munot P, Saunders DE, Milewicz DM, Regalado ES, Ostergaard JR, Braun KP, Kerr T, Lichtenbelt KD, Philip S, Rittey C, Jacques TS, Cox TC, Ganesan V (2012). A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations.. Brain, 135(Pt 8), 2506 - 2514. doi:10.1093/brain/aws172
    • Andoniadou CL, Gaston-Massuet C, Reddy R, Schneider RP, Blasco MA, Le Tissier P, Jacques TS, Pevny LH, Dattani MT, Martinez-Barbera JP (2012). Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma.. Acta Neuropathologica, 124(2), 259 - 271. doi:10.1007/s00401-012-0957-9
    • D'Argenzio L, Colonnelli MC, Harrison S, Jacques TS, Harkness W, Scott RC, Cross JH (2012). Seizure outcome after extratemporal epilepsy surgery in childhood.. Developmental Medicine and Child Neurology, 54(11), 995 - 1000. doi:10.1111/j.1469-8749.2012.04381.x
    • Coras R, de Boer OJ, Armstrong D, Becker A, Jacques TS, Miyata H, Thom M, Vinters HV, Spreafico R, Oz B, Marucci G, Pimentel J, Mühlebner A, Zamecnik J, Buccoliero AM, Rogerio F, Streichenberger N, Arai N, Bugiani M, Vogelgesang S, Macaulay R, Salon C, Hans V, Polivka M, Giangaspero F, Fauziah D, Kim JH, Liu L, Dandan W, Gao J, Lindeboom B, Blümcke I, Aronica E (2012). Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias.. Epilepsia, 53(8), 1341 - 1348. doi:10.1111/j.1528-1167.2012.03508.x
    • Paine SML, Grünewald S, Jacques TS (2012). Antenatal neurodevelopmental defects in ornithine transcarbamylase deficiency. Neuropathology and Applied Neurobiology, 38(5), 509 - 512. doi:10.1111/j.1365-2990.2012.01262.x
    • Pryce JW, Paine SML, Weber MA, Harding B, Jacques TS, Sebire NJ (2012). Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI). Journal of Clinical Pathology, 65(3), 257 - 261. doi:10.1136/jclinpath-2011-200264
    • Crosier S, Nicholson SL, Robson K, Jacques TS, Wharton S, Bown N, Michalski A, Pizer B, Clifford S (2012). A national feasibility study of real-time central pathology review and molecular diagnostics for medulloblastoma.

    2011

    • Kelberman D, Islam L, Jacques TS, Russell-Eggitt I, Bitner-Glindzicz M, Khaw PT, Nischal KK, Sowden JC (2011). CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.. Ophthlamology, 118(9), 1865 - 1873.
    • Thayyil S, Robertson NJ, Gunny R, Chong WK, Chitty LS, Jacques TS, Sebire NJ, Taylor AM (2011). Less invasive autopsy by postmortem MR imaging of brain and spinal cord in fetuses, newborns and children.
    • Jeyapalan JN, Mumin MA, Forshew T, Lawson ARJ, Tatevossian RG, Jacques TS, Sheer D (2011). MicroRNA Expression In Paediatric Brain Tumours.
    • Wedderburn LR, Varsani H, Charman SC, Marie S, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith A, Jacques TS, Lundberg IE, Minetti C, Nenesmo I, Rushing EJ, Sewry C, Pilkington CA, Holton JL (2011). Validation and clinical testing of a standardised assessment of juvenile dermatomyositis muscle biopsy.
    • D'Argenzio L, Colonnelli MC, Harrison S, Jacques TS, Harkness W, Vargha-Khadem F, Scott RC, Cross JH (2011). Cognitive outcome after extratemporal epilepsy surgery in childhood.. Epilepsia, 52(11), 1966 - 1972. doi:10.1111/j.1528-1167.2011.03272.x
    • Kelberman D, Islam L, Holder SE, Jacques TS, Calvas P, Hennekam RC, Nischal KK, Sowden JC (2011). Digenic inheritance of mutations in FOXC1 and PITX2: Correlating transcription factor function and Axenfeld-Rieger disease severity. Human Mutation, 32(10), 1144 - 1152. doi:10.1002/humu.21550
    • Moody H, Male A, Scott R, Jacques T, Offiah A, Rennie J, Jackson M (2011). Unusual antenatal presentation of Zellweger syndrome confirmed biochemically in a second affected fetus.
    • Gaston-Massuet C, Andoniadou CL, Signore M, Jayakody SA, Charolidi N, Kyeyune R, Vernay B, Jacques TS, Taketo MM, Le Tissier P, Dattani MT, Martinez-Barbera JP (2011). Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans.. Proceedings of the National Academy of Sciences of USA, 108(28), 11482 - 11487. doi:10.1073/pnas.1101553108
    • Jacques TS, Harkness W (2011). Ganglioglioma, dysembryoplastic neuroepithelial tumours, and related tumours. In Shorvon SD, Andermann F, Guerrini R (Ed.), The Causes of Epilepsy (pp. - ). : Cambridge Univ Pr.
    • Menghi F, Jacques TS, Barenco M, Schwalbe EC, Clifford SC, Hubank M, Ham J (2011). Genome-wide analysis of alternative splicing in medulloblastoma identifies splicing patterns characteristic of normal cerebellar development. Cancer Research, 71(6), 2045 - 2055. doi:10.1158/0008-5472.CAN-10-2519
    • Nicholson SL, Robson DK, Wharton SB, Jacques TS, Michalski AM, Pizer B, Bown NP, Clifford SC (2011). A feasibility study of real-time central pathology review (CPR) and molecular diagnostics for medulloblastoma in the United Kingdom.
    • 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.
    • Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A, Jacques TS, Avanzini G, Barkovich AJ, Battaglia G, Becker A, Cepeda C, Cendes F, Colombo N, Crino P, Cross JH, Delalande O, Dubeau F, Duncan J, Guerrini R, Kahane P, Mathern G, Najm I, Ozkara C, Raybaud C, Represa A, Roper SN, Salamon N, Schulze-Bonhage A, Tassi L, Vezzani A, Spreafico R (2011). The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission(1). Epilepsia, 52(1), 158 - 174. doi:10.1111/j.1528-1167.2010.02777.x
    • Presneau N, Shalaby A, Ye H, Pillay N, Halai D, Idowu B, Tirabosco R, Whitwell D, Jacques TS, Kindblom LG, Brüderlein S, Möller P, Leithner A, Liegl B, Amary FM, Athanasou NN, Hogendoorn PC, Mertens F, Szuhai K, Flanagan AM (2011). Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.. Journal of Pathology, 223, 327 - 335. doi:10.1002/path.2816
    • 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

    2010

    • Ye H, Shalaby A, Presneau N, Pillay N, Idowu B, Halai D, Tirabosco R, Jacques T, Mertens F, Szuhai K, Kindblom L, Hogendoom P, Flanagan AM (2010). Genetic abnormalities of the transcription factor T (Brachyury) in sporadic chordomas.
    • Pryce J, Weber MA, Malone M, Jacques TS, Ashworth MT, Sebire NJ (2010). Autopsy findings in paediatric sickle cell disease. doi:10.1002/path.2770
    • Shalaby A, Ye H, Diss T, Whitwell D, Jacques T, Tirabosco R, Presneau N, Flanagan A (2010). Epidermal growth factor receptor as a potential therapeutic target in chordomas.
    • Shalaby A, Presneau N, Pillay N, Ye H, Idowu B, Halai D, Tirabosco R, Jacques T, Mertens F, Szuhai K, Kindblom L, Hogendoorn P, Flanagan A (2010). In vivo and in vitro implications of the transcription factor T (Brachyury) in pathogenesis of sporadic chordomas.
    • Lawson ARJ, Tatevossian RG, Phipps KP, Picker SR, Michalski A, Sheer D, Jacques TS, Forshew T (2010). RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort. Acta Neuropathologica, 120(2), 271 - 273. doi:10.1007/s00401-010-0693-y
    • Wedderburn LR, Varsani H, Charman SC, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith A, Jacques TS, Lundberg IE, Marie S, Minetti C, Nenesmo I, Rushing EJ, Sewry C, Pilkington CA, Holton JL, UK JDM Res Grp (2010). Validation of a histopathological score tool for the measurement of severity in muscle biopsies from patients with juvenile dermatomyositis.
    • Yasin SA, Anderson G, Cross JH, Harkness W, Harding BN, Ham J, Jacques TS (2010). Balloon cells in focal cortical dysplasia: progenitor cells with structural and cell cycle defects.
    • Henriquez NV, Swales A, Jacques TS, Brandner S (2010). Gene expression profiling of brain tumours in a mouse model: insights into tumour-type specific transcripteome networks.
    • Sewry CA, Holton JH, Dick DJ, Jacques TS, Muntoni F, Hanna MG (2010). Zebra body myopathy resolved.
    • Jacques TS, Sebire NJ (2010). The impact of article titles on citation hits: an analysis of general and specialist medical journals. Journal of the Royal Society of Medicine-Short Reports, 1, 2 - . doi:10.1258/shorts.2009.100020
    • Jacques TS, Swales A, Brzozowski MJ, Henriquez NV, Linehan JM, Mirzadeh Z, O' Malley C, Naumann H, Alvarez-Buylla A, Brandner S (2010). Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes.. The EMBO Journal, 29(1), 222 - 235. doi:10.1038/emboj.2009.327
    • Pryce J, Weber MA, Jacques TS, Malone M, Ashworth MT, Sebire NJ (2010). Autopsy findings in neonatal deaths:>500 consecutive cases from a specialist paediatric centre. doi:10.1002/path.2770
    • Wijesekara DS, Chong WK, Jacques TS, Aylett SE (2010). Seizures And Neurological Outcome In Patients With Congenital Melanocytic Naevi (Cmn) And Central Nervous System (Cns) Melanosis.
    • Yasin SA, Latak K, Becherini F, Ganapathi A, Miller K, Campos O, Picker SR, Bier N, Smith M, Thom M, Anderson G, Cross JH, Harkness W, Harding B, Jacques TS (2010). Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell. Acta Neuropathologica, , - . doi:10.1007/s00401-010-0677-y
    • Nicholson S, Robson D, Jacques T, Wharton S, Michalski A, Pizer B, Bown N, Clifford S (2010). Establishment of real-time centralised pathology review (CPR) and molecular diagnostics for medulloblastoma in the United Kingdom.
    • Cohen NR, Scott R, Jacques TS (2010). Pontosubicular necrosis in early neonatal death.
    • Yasin SA, Harkness W, Cross JH, Cohen NR, Jacques TS (2010). Subependymal Giant Cell Astrocytoma (SEGA) cells respond to rapamycin in vitro.
    • Wedderburn LR, Varsani H, Charman SC, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith A, Jacques TS, Lundberg IE, Marie S, Minetti C, Nennesmo I, Rushing E, Sewry CA, Pilkington CA, Holton JL (2010). Validation of a histopathological score tool for the measurement of severity in muscle biopsies from patients with juvenile dermatomyositis.
    • Bossley C, Hogg C, Stoneham S, Jacques TS, Bush A (2010). A fatal case of cough. Pediatric Pulmonology, 45(2), 205 - 207.
    • Kristiansen M, Hughes R, Patel P, Jacques TS, Clark AR, Ham J (2010). Mkp1 is a c-Jun target gene that antagonizes JNK-dependent apoptosis in sympathetic neurons. Journal of Neuroscience, 30(32), 10820 - 10832. doi:10.1523/​JNEUROSCI.2824-10.2010

    2009

    • Potter NE, Phipps K, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Thomas DGT, Rees J, Darling JL, Warr TJ (2009). Astrocytoma derived short-term cell cultures retain molecular signatures characteristic of the tumour in situ. Experimental Cell Research, 315(16), 2835 - 2846. doi:10.1016/j.yexcr.2009.06.003
    • Cohen NR, Gunny R, Harkness W, Michalski A, Harding B, Jacques TS (2009). Rapamycin induces a clinical and pathological response in subependymal giant cell astrocytoma.
    • Yasin S, Miller K, Campos O, Gunny R, Harkness W, Cross JH, Harding B, Jacques TS (2009). Isolation of a proliferative progenitor cell from a case of epilepsy-associated ‘perivascular oligodendrocyte hyperplasia’.
    • Cohen NR, Phipps K, Harding B, Jacques TS (2009). Is CSF cytology a useful diagnostic procedure in staging paediatric CNS tumours?. Cytopathology, 20(4), 256 - 260.
    • Menghi F, Jacques TS, Gibson S, Hubank M, Ham J (2009). Global analysis of gene expression and splicing in human medulloblastomas.
    • Sebire N, Malone M, Ashworth M, Jacques TS (2009). Diagnostic pediatric surgical pathology.
    • Macleod M, Harding B, Chong WK, Desai N, Cross JH, Harkness W, Jacques TS (2009). A re-evaluation of the clinical and pathological features of malformations of cortical development associated with epilepsy in children.
    • Thayyil S, Robertson NJ, Scales A, Weber MA, Jacques TS, Sebire NJ, Taylor A (2009). Prospective parental consent for autopsy research following sudden unexpected childhood deaths: a successful model. Archives of Disease in Childhood, 94(5), 354 - 358. doi:10.1136/adc.2008.150904
    • Jacques T, Yasin S, Latak K, Ganapathi A, Becherini F, Miller K, Campos O, Cross H, Harkness W, Harding B (2009). Isolation and characterisation of an undifferentiated balloon cell from focal cortical dysplasia.
    • Robertson L, Parker M, Al-Adnani M, M Jacques TS (2009). Detailed neuropathological findings in a case of Galloway-Mowat Syndrome.
    • Henriquez N, Jacques TS, Swales A, Brandner S (2009). Stem cells, progenitor cells and brain tumours: how related are they?.
    • Yasin S, Farndon SJ, Miller K, Campos O, Cross JH, Harkness W, Harding B, Jacques TS (2009). Identification of a proliferating progenitor cell in angiocentric glioma.
    • Warr TJ, Karakoula K, Phipps K, Harkness W, Hayward R, Thompson D, Jacques T, Thomas DGT (2009). Epigenetic silencing of gene expression in pediatric intracranial ependyoma. doi:10.1215/15228517-2009-034
    • Trotz M, Weber MA, Jacques TS, Malone M, Sebire NJ (2009). Disseminated langerhans cell histiocytosis-related sudden unexpected death in infancy. Fetal and Pediatric Pathology, 28(1), 39 - 44.
    • Yasin S, Latak K, Farndon SJ, Miller K, Campos O, Cross JH, Harkness W, Harding B, Jacques TS (2009). Characterisation of an undifferentiated balloon cell from focal cortical dysplasia.
    • Stacpoole SRL, Phadke R, Jacques TS, Revesz T, Plant GT (2009). Vacuolar myelopathy associated with optic neuropathy in an HIV-negative, immunosuppressed liver transplant recipient. Journal of Neurology, Neurosurgery and Psychiatry, 80(5), 581 - 583. doi:10.1136/jnnp.2008.150292

    2008

    • Jacques TS, Miller K, Rampling D, Gatscher S, Harding B (2008). Peritoneal dissemination of a malignant glioma. Cytopathology, , - .
    • Apostolidis A, Jacques TS, Freeman A, Kalsi V, Popat R, Gonzales G, Datta SN, Ghazi-Noori S, Elneil S, Dasgupta P, Fowler CJ (2008). Histological changes in the urothelium and suburothelium of human overactive bladder following intradetrusor injections of botulinum neurotoxin type A for the treatment of neurogenic or idiopathic detrusor overactivity. European Urology, 53(6), 1245 - 1253. doi:10.1016/j.eururo.2008.02.037
    • Karakoula K, Suarez-Merino B, Ward S, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Beck J, Thomas DGT, Warr TJ (2008). Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13. Genes, Chromosomes and Cancer, 47(11), 1005 - 1022. doi:10.1002/gcc.20607
    • Potter N, Karakoula A, Phipps KP, Harkness W, Hayward R, Thompson DN, Jacques TS, Harding B, Thomas DG, Palmer RW, Rees J, Darling J, Warr TJ (2008). Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma. Neoplasia, 10(8), 757 - 772. doi:10.1593/neo.07914
    • Fowler DJ, Harding B, Jacques TS (2008). A protocol for rapid high yield neuropathology in paediatric autopsy practice: the GOSH protocol.
    • Forrest K, Harding B, Jacques TS (2008). Cerebral angiopathy associated with neuroectodermal and skeletal dysplasia.
    • Cohen NR, Phipps K, Harding B, Jacques TS (2008). CSF cytology in paediatric practice: an important staging investigation in the absence of MRI-proven leptomeningeal spread.
    • Swales A, Naumann H, Cuadrado P, Jacques T, Brandner S (2008). Neural stem cells differentially govern tumorigenesis within the brain dependent on their early genetic profile.
    • Jacques T, Harding B (2008). New developments in “shaken baby syndrome”. Advances in Clinical Neuroscience and Rehabilitation, 8, 24 - 25.
    • Cuadrado PMR, Naumann H, Jacques TS, Brandner S (2008). Wnt signalling in neural stem cell differentiation and tumorigenesis in the CNS.
    • Hassan HM, McAndrew PT, Yagan A, Jacques TS, Hayward R (2008). Mature orbital teratoma presenting as a recurrent orbital cellulitis with an ectopic tooth and sphenoid malformation-a case report. Orbit, 27(4), 309 - 12. doi:10.1080/01676830802222902
    • Latak K, Yasin S, Cross JH, Harkness W, Harding B, Jacques TS (2008). In vitro isolation of balloon cells from focal cortical dysplasia.
    • Yasin S, Fardon SJ, Miller K, Smyk D, Campos O, Harkness W, Cross JH, Harding B, Jacques TS (2008). A developmental model of low-grade glio-neuronal tumours: identification of progenitor cells in DNETs and related tumours.
    • Yasin S, Latak K, Miller K, Harkness W, Cross JH, Harding B, Jacques TS (2008). In vitro isolation of balloon cells from focal cortical dysplasia.
    • Karakoula K, Potter N, Keir ST, Bigner DD, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Thomas DGT, Warr TJ (2008). Genetic profiling in tumor xenografts from paediatric gliomas by expression and high resolution comparative genomic hybridisation microarrays.
    • Jacques T (2008). Neurobiology from Molecular Basis to Disease. doi:10.1111/j.1365-2990.2008.00990.x

    2007

    • Jacques TS (2007). Adams and Graham's Introduction to Neuropathology (3rd edition). Neuropathology and Applied Neurobiology, 33(5), 591 - 592. doi:10.1111/j.1365-2990.2007.00851.x
    • Weber MA, Jacques TS, Harding B, Malone M, Sebire NJ (2007). Histological examination of the macroscopically normal brain is of limited value in determining the cause of death in SUDI..
    • Weber MA, Jacques TS, Harding B, Malone M, Sebire NJ (2007). The contribution of formal neuropathological examination in paediatric autopsies..
    • Tofaris GK, Revesz T, Jacques TS, Papacostas S, Chataway J (2007). Adult-onset neurodegeneration with brain iron accumulation and cortical alpha-synuclein and tau pathology: a distinct clinicopathological entity. Archives of Neurology, 64(2), 280 - 282. doi:10.1001/archneur.64.2.280
    • Becherini F, Ganapathi A, Latak K, Miller K, Smith M, Thom M, Harkness W, Cross H, Harding B, Jacques TS (2007). Integrin expression identifies progenitor cells in focal cortical dysplasia.. doi:10.1007/s00381-007-0420-8

    2006

    • Fowler DJ, Jacques TS, Gatscher S, Harding B (2006). Paediatric meningiomas, a clinico-pathological study.
    • Fowler DJ, Sebire NJ, Ashworth MT, Weber MA, Jacques TS, Harding BN (2006). Sudden unexpected death in early childhood due to saccular aneurysm-related subarachnoid haemorrhage.
    • Harding B, Benton S, Jacques TS (2006). Mixed neuropathologic features including MELAS- and Leigh-associated lesions in a boy with a DNA point mutation in mitochondrial Complex IND5 gene.
    • Becherini F, Miller K, Smith M, Martinian L, Thom M, Cross H, Harding B, Jacques TS (2006). The pattern of integrin expression by balloon cells distinguishes focal cortical dysplasia from cortical tubers.
    • Jacques TS, Naumann H, Brandner S (2006). A novel role for the tumour suppressor gene, PTEN, in the development of tumours from neural stem cells.
    • Fowler DJ, Sebire NJ, Weber MA, Ashworth M, Jacques TS, Harding B (2006). Sudden unexpected death in early childhood due to saccular aneurysm-related subarachnoid haemorrhage.
    • Apostolidis A, Jacques TS, Freeman A, Ghazi-Noori S, Kalsi V, Popat RB, Gonzales GE, Beckett A, Datta SN, Elneil S, Fowler CJ, Dasgupta P (2006). Histological changes in the superficial layers of the human bladder following injections of botulinum neurotoxin type A (BoNT/A) for the treatment of detrusor overactivity.
    • Apostoliclis A, Jacques TS, Freeman A, Ghazi-Noori S, Kalsi V, Popat R, Gonzales G, Beckett A, Datta S, Elneil S, Dasgupta P, Fowler CJ (2006). Histological changes in the human bladder urothelium and suburothelium following injections of botulinum neurotoxin type a (BoNT/A) for the treatment of neurogenic versus idiopathic detrusor overactivity (NDO/IDO).
    • Jacques TS, Galloway MJ, Scaravilli F (2006). Cerebrospinal fluid findings in central neurocytoma. Cytopathology, 17(5), 301 - 303. doi:10.1111/j.1365-2303.2006.00296.x
    • Jacques TS, Eldridge C, Patel A, Saleem NM, Powell M, Kitchen ND, Thom M, Revesz T (2006). Mixed glioneuronal tumour of the fourth ventricle with prominent rosette formation.. Neuropathology and Applied Neurobiology, 32(2), 217 - 220.
    • Trivedi SG, Newson J, Rajakariar R, Jacques TS, Hannon R, Kanaoka Y, Eguchi N, Colville-Nash P, Gilroy DW (2006). Essential role for hematopoietic prostaglandin D2 synthase in the control of delayed type hypersensitivity. Proceedings Of The National Academy Of Sciences Of The United States Of America, 103(13), 5179 - 5184. doi:10.1073/pnas.0507175103
    • Vujovic S, Henderson S, Presneau N, Odell E, Jacques TS, Tirabosco R, Boshoff C, Flanagan AM (2006). Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas. The Journal of Pathology, 209, 157 - 165.

    2005

    • Clarke AJ, Jacques TS, Galloway MJ, Thom M, Kitchen ND, Plant GT (2005). ALK positive inflammatory myofibroblastic tumour of the pineal region. Journal of Clinical Pathology, 58(9), 981 - 983.
    • Jacques TS, Ikenberg K, Reynolds S, Naumann H, Brandner S (2005). A novel model of tumour formation by neural stem cells.
    • Jacques TS (2005). The 10th Wye Advanced Neuroscience Symposium 6-9th July 2004. doi:10.1111/j.1365-2990.2004.00628.x
    • Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C (2005). Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers. Annals of Neurology, 58(3), 411 - 422. doi:10.1002/ana.20587
    • Nandi M, Miller A, Stidwill R, Jacques TS, Lam AJA, Haworth S, Heales S, Vallance P (2005). Pulmonary hypertension in a GTP-cyclohydrolase 1 deficient mouse. Circulation, 111(16), 2086 - 2090. doi:10.1161/01.CIR.0000163268.32638.F4
    • Tofaris GK, Revesz T, Jacques T, Chataway J (2005). Adult-onset Hallervorden-Spatz syndrome with cortical alpha-synuclein and tau pathology: a distinct clinico-pathological entity?.
    • Apostolidis A, Jacques T, Freeman A, Kalsi V, Popat R, Beckett A, Fowler CJ, Dasgupta P (2005). Suburothelial histopathological changes after intra-detrusor botulinum-A toxin (BTX/A) injections for detrusor overactivity (DO): Short-term result.
    • Pramstaller PP, Jacques TS, Scaravilli F, Hedrich K, Kramer PL, Klein C (2005). Lewy body parkinsonism in a large pedigree with 77 Parkin mutation carriers.

    2004

    • Galloway M, Jacques TS, Scaravilli F (2004). Neuropathology characteristic of paraneoplastic opsoclonus-myoclonus in a patient with lymphoma.
    • Jacques TS, Valentine A, Bradford R, McLaughlin JE (2004). December 2003: A 70-year-old woman with a recurrent meningeal mass. Brain Pathology, 14(2), 229 - 230.
    • Brady CM, Apostolidis A, Yiangou Y, Baecker PA, Ford AP, Freeman A, Jacques TS, Fowler CJ, Anand P (2004). P2X3-immunoreactive nerve fibres in neurogenic detrusor overactivity and the effect of intravesical resiniferatoxin. European Urology, 46(2), 247 - 253.
    • Apostolidis AN, Yiangou Y, Brady CM, Ford AP, Baecker PA, Jacques TS, Freeman A, Fowler CJ, Anand P (2004). Endothelial nitric oxide synthase expression in neurogenic urinary bladders treated with intravesical resiniferatoxin. BJU International, 93(3), 336 - 340.
    • Brady CM, Apostolidis AN, Harper M, Yiangou Y, Beckett A, Jacques TS, Freeman A, Scaravilli F, Fowler CJ, Anand P (2004). Parallel changes in bladder suburothelial vanilloid receptor TRPV1 and pan-neuronal marker PGP9.5 immunoreactivity in patients with neurogenic detrusor overactivity after intravesical resiniferatoxin treatment. BJU International, 93(6), 770 - 776.

    2003

    • Jacques TS, Eldridge C, Powell M, Revesz T (2003). A mixed glial-neuronal tumour of the IVth ventricle with prominent rosette formation.
    • Galloway M, Jacques TS, Scaravilli F (2003). Neuropathology characteristic of paraneoplastic opsoclonus-myoclonus in a patient with lymphoma.
    • Brealey DA, Karyampudi S, Jacques TS, Novelli M, Stidwill R, Taylor V, Smolenski RT, Singer M (2003). Mitochondrial dysfunction in a long-term rodent model of sepsis and organ failure. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology, , - .

    2002

    • Heelan B, Jacques TS, Karim MY, Bunn C (2002). Audit of IgG subclasses in adults and guidelines for their measurement. Allergy and Immunology CPD Bulletin, 2, 52 - 54.
    • Jacques TS, Holton J, Watts PM, Wills AJ, Smith SE, Hanna MG (2002). Tubular aggregate myopathy with abnormal pupils and skeletal deformities. Journal of Neurology, Neurosurgery and Psychiatry, 73(3), 324 - 326.

    1999

    • Ponassi M, Jacques TS, Ciani L, ffrench Constant C (1999). Expression of the rat homologue of the Drosophila fat tumour suppressor gene.. Mechanisms of Development, 80(2), 207 - 212.
    • Jacques TS, Skepper JN, Navaratnam V (1999). Fibroblast growth factor-1 improves survival and regeneration of rat vagal preganglionic neurones following axonal injury. Neuroscience Letters, 276, 197 - 200.

    1998

    • Navaratnam V, Jacques TS, Skepper JN (1998). Ultrastructural and cytochemical study of neurones in the rat dorsal motor nucleus of the vagus after axon crush. Microscopy Research and Techniques, 42, 334 - 344.
    • Jacques TS, Relvas J, Nishimura S, Pytela R, Edwards G, Streuli CH, ffrench-Constant C (1998). Neural precursor cell chain migration and division are regulated through different β1 integrins. Development, 126, 3167 - 3177.

    1997

    • Jefferson S, Jacques TS, Kiernan BW, Scott-Drew S, Milner R, ffrench-Constant C (1997). Inhibition of oligodendrocyte precursor mobility by oligodendrocyte processes: implications for transplantation based approaches to multiple sclerosis. Multiple Sclerosis, 3, 162 - 167.
    • Ponassi M, Jacques T, ffrench-Constant C (1997). Expression of the protocadherin tumour suppressor gene fat in neuroepithelial cells within the developing rat brain.

    • Jacques TS (). Pathology of epilepsy in the ISPN Guide to Paediatric Neurosurgery.
    • Jeyapalan J, Patel SN, Forshew T, Lawson ARJ, Tatevossian RG, Corbett-Jones T, Mumin MA, Picker SR, Phipps K, Michalski A, Jacques TS, Sheer D (). MicroRNA signatures in a broad cohort of paediatric brain tumours.
    • Paine SML, Shanmuganathan M, Jeelani NUO, Jacques TS (). A highly unusual congenital developmental neuroepithelial cyst of the orbit.
    • Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Darling JL, Warr TJ (). Epigenetic genome-wide analysis identifies BEX1 as a candidate tumor suppressor gene in pediatric ependymoma.
    • Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling JL, Thomas DG, Warr TJ (). Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation. Journal of Neuro-oncology, , - .