UCL School of Life and Medical Sciences

2013

• Kandaswamy R, McQuillin A, Sharp SI, Fiorentino A, Anjorin A, Blizard RA, Curtis D, Gurling HM (2013). Genetic Association, Mutation Screening, and Functional Analysis of a Kozak Sequence Variant in the Metabotropic Glutamate Receptor 3 Gene in Bipolar Disorder.. JAMA Psychiatry, , 1 - 8. doi:10.1001/jamapsychiatry.2013.38

2012

• Rizig MA, McQuillin A, Ng A, Robinson M, Harrison A, Zvelebil M, Hunt SP, Gurling HM (2012). A gene expression and systems pathway analysis of the effects of clozapine compared to haloperidol in the mouse brain implicates susceptibility genes for schizophrenia.. J Psychopharmacol, 26(9), 1218 - 1230. doi:10.1177/0269881112450780
• Dedman A, McQuillin A, Kandaswamy R, Sharp S, Anjorin A, Gurling H (2012). Sequencing of the ANKYRIN 3 gene (ANK3) encoding ankyrin G in bipolar disorder reveals a non-conservative amino acid change in a short isoform of ankyrin G.. Am J Med Genet B Neuropsychiatr Genet, 159B(3), 328 - 335. doi:10.1002/ajmg.b.32030
• Szyszka P, Sharp SI, Dedman A, Gurling HM, McQuillin A (2012). A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia.. Psychiatr Genet, 22(3), 150 - 151. doi:10.1097/YPG.0b013e32834accbe
• Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Johnston JA, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Kölsch H, Heun R, Schürmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Davies G, Harris SE, Starr JM, Deary IJ, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Jones L, Holmans PA, O'Donovan MC, Owen MJ, Williams J (2012). The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.. J Alzheimers Dis, 28(2), 377 - 387. doi:10.3233/JAD-2011-110824
• Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, Brayne C, Gill M, Lawlor B, Lynch A, Craig D, McGuinness B, Johnston J, Holmes C, Livingston G, Bass NJ, Gurling H, McQuillin A, GERAD Consortium , National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group , Holmans P, Jones L, Devlin B, Klei L, Barmada MM, Demirci FY, DeKosky ST, Lopez OL, Passmore P, Owen MJ, O'Donovan MC, Mayeux R, Kamboh MI, Williams J (2012). Genome-wide association study of Alzheimer's disease with psychotic symptoms.. Mol Psychiatry, 17(12), 1316 - 1327. doi:10.1038/mp.2011.125
• Kandaswamy R, McQuillin A, Curtis D, Gurling H (2012). Tests of linkage and allelic association between markers in the 1p36 PRKCZ (protein kinase C zeta) gene region and bipolar affective disorder.. Am J Med Genet B Neuropsychiatr Genet, 159B(2), 201 - 209. doi:10.1002/ajmg.b.32014

2011

• Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (2011). Genome-wide association study identifies five new schizophrenia loci.. Nat Genet, 43(10), 969 - 976. doi:10.1038/ng.940
• McQuillin A, Bass N, Anjorin A, Lawrence J, Kandaswamy R, Lydall G, Moran J, Sklar P, Purcell S, Gurling H (2011). Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.. Eur J Hum Genet, 19(5), 588 - 592. doi:10.1038/ejhg.2010.221
• Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, Chapman J, Jones N, Abraham R, Ivanov D, Pahwa JS, Moskvina V, Dowzell K, Thomas C, Stretton A, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuiness B, Todd S, Johnston JA, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Livingston G, Bass NJ, Gurling H, McQuillin A, Jones L, Holmans PA, O'Donovan M, Owen MJ, Williams J (2011). No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.. Am J Med Genet B Neuropsychiatr Genet, 156B(7), 764 - 771. doi:10.1002/ajmg.b.31216
• Lydall GJ, Saini J, Ruparelia K, Montagnese S, McQuillin A, Guerrini I, Rao H, Reynolds G, Ball D, Smith I, Thomson AD, Morgan MY, Gurling HM (2011). Genetic association study of GABRA2 single nucleotide polymorphisms and electroencephalography in alcohol dependence.. Neurosci Lett, 500(3), 162 - 166. doi:10.1016/j.neulet.2011.05.240
• Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, Ivanov D, Widdowson C, Chapman J, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Beaumont H, Warden D, Wilcock G, Love S, Kehoe PG, Hooper NM, Vardy ER, Hardy J, Mead S, Fox NC, Rossor M, Collinge J, Maier W, Jessen F, Rüther E, Schürmann B, Heun R, Kölsch H, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Gallacher J, Hüll M, Rujescu D, Giegling I, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Pankratz VS, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Dickson DW, Graff-Radford NR, Petersen RC, Alzheimer's Disease Neuroimaging Initiative , van Duijn CM, Breteler MM, Ikram MA, DeStefano AL, Fitzpatrick AL, Lopez O, Launer LJ, Seshadri S, CHARGE consortium , Berr C, Campion D, Epelbaum J, Dartigues JF, Tzourio C, Alpérovitch A, Lathrop M, EADI1 consortium , Feulner TM, Friedrich P, Riehle C, Krawczak M, Schreiber S, Mayhaus M, Nicolhaus S, Wagenpfeil S, Steinberg S, Stefansson H, Stefansson K, Snaedal J, Björnsson S, Jonsson PV, Chouraki V, Genier-Boley B, Hiltunen M, Soininen H, Combarros O, Zelenika D, Delepine M, Bullido MJ, Pasquier F, Mateo I, Frank-Garcia A, Porcellini E, Hanon O, Coto E, Alvarez V, Bosco P, Siciliano G, Mancuso M, Panza F, Solfrizzi V, Nacmias B, Sorbi S, Bossù P, Piccardi P, Arosio B, Annoni G, Seripa D, Pilotto A, Scarpini E, Galimberti D, Brice A, Hannequin D, Licastro F, Jones L, Holmans PA, Jonsson T, Riemenschneider M, Morgan K, Younkin SG, Owen MJ, O'Donovan M, Amouyel P, Williams J (2011). Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.. Nat Genet, 43(5), 429 - 435. doi:10.1038/ng.803
• Kasiakogia-Worlley K, McQuillin A, Lydall GJ, Patel S, Kottalgi G, Gunwardena P, Cherian R, Rao H, Hillman A, Gobikrishnan N, Douglas E, Qureshi SY, Jauhar S, Ball D, Okane A, Owens L, Dedman A, Sharp SI, Kandaswamy R, Guerrini I, Thomson AD, Smith I, Dar K, Morgan MY, Gurling HM (2011). Lack of allelic association between markers at the DRD2 and ANKK1 gene loci with the alcohol-dependence syndrome and criminal activity.. Psychiatr Genet, 21(6), 323 - 324. doi:10.1097/YPG.0b013e3283458a68
• Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, van den Bussche H, Heuser I, Peters O, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Rüther E, Carrasquillo MM, Pankratz VS, Younkin SG, Hardy J, O'Donovan MC, Owen MJ, Williams J (2011). Correction: genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.. PLoS One, 6(2), - . doi:10.1371/annotation/a0bb886d-d345-4a20-a82e-adce9b047798
• Pereira AC, McQuillin A, Puri V, Anjorin A, Bass N, Kandaswamy R, Lawrence J, Curtis D, Sklar P, Purcell SM, Gurling HM (2011). Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder.. Am J Med Genet B Neuropsychiatr Genet, 156(2), 177 - 187. doi:10.1002/ajmg.b.31153
• Curtis D, Vine AE, McQuillin A, Bass NJ, Pereira A, Kandaswamy R, Lawrence J, Anjorin A, Choudhury K, Datta SR, Puri V, Krasucki R, Pimm J, Thirumalai S, Quested D, Gurling HM (2011). Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.. Psychiatr Genet, 21(1), 1 - 4. doi:10.1097/YPG.0b013e3283413382
• Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS, GROUP investigators , International Schizophrenia Consortium (2011). GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.. Mol Psychiatry, 16(11), 1117 - 1129. doi:10.1038/mp.2010.96
• Psychiatric GWAS Consortium Bipolar Disorder Working Group (2011). Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.. Nat Genet, 43(10), 977 - 983. doi:10.1038/ng.943
• Hamshere ML, O'Donovan MC, Jones IR, Jones L, Kirov G, Green EK, Moskvina V, Grozeva D, Bass N, McQuillin A, Gurling H, St Clair D, Young AH, Ferrier IN, Farmer A, McGuffin P, Sklar P, Purcell S, Holmans PA, Owen MJ, Craddock N (2011). Polygenic dissection of the bipolar phenotype. BRIT J PSYCHIAT, 198(4), 284 - 288. doi:10.1192/bjp.bp.110.087866
• Rapp GE, Pineda-Trujillo N, McQuillin A, Tonetti M (2011). Genetic power of a Brazilian three-generation family with generalized aggressive periodontitis. II.. Braz Dent J, 22(1), 68 - 73.
• Ingason A, Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD, Kristinsson KT, le Roux L, Gustafsson O, Craddock N, Möller HJ, McQuillin A, Muglia P, Cichon S, Rietschel M, Ophoff RA, Djurovic S, Andreassen OA, Pietiläinen OP, Peltonen L, Dempster E, Collier DA, St Clair D, Rasmussen HB, Glenthøj BY, Kiemeney LA, Franke B, Tosato S, Bonetto C, Saemundsen E, Hreidarsson SJ, GROUP Investigators , Nöthen MM, Gurling H, O'Donovan MC, Owen MJ, Sigurdsson E, Petursson H, Stefansson H, Rujescu D, Stefansson K, Werge T (2011). Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.. Am J Psychiatry, 168(4), 408 - 417. doi:10.1176/appi.ajp.2010.09111660
• Lydall GJ, Bass NJ, McQuillin A, Lawrence J, Anjorin A, Kandaswamy R, Pereira A, Guerrini I, Curtis D, Vine AE, Sklar P, Purcell SM, Gurling HM (2011). Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder.. Psychiatr Genet, 21(6), 294 - 306. doi:10.1097/YPG.0b013e32834915c2

2010

• Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, Heun R, Kölsch H, van den Bussche H, Heuser I, Peters O, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Rüther E, Carrasquillo MM, Pankratz VS, Younkin SG, Hardy J, O'Donovan MC, Owen MJ, Williams J (2010). Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.. PLoS One, 5(11), e13950 - . doi:10.1371/journal.pone.0013950
• Perlis RH, Huang J, Purcell S, Fava M, Rush AJ, Sullivan PF, Hamilton SP, McMahon FJ, Schulze TG, Potash JB, Zandi PP, Willour VL, Penninx BW, Boomsma DI, Vogelzangs N, Middeldorp CM, Rietschel M, Nöthen M, Cichon S, Gurling H, Bass N, McQuillin A, Hamshere M, Wellcome Trust Case Control Consortium Bipolar Disorder Group , Craddock N, Sklar P, Smoller JW (2010). Genome-wide association study of suicide attempts in mood disorder patients.. Am J Psychiatry, 167(12), 1499 - 1507. doi:10.1176/appi.ajp.2010.10040541
• Datta SR, McQuillin A, Rizig M, Blaveri E, Thirumalai S K, G L, J B, N J P, V C, K P, J C, C F, G W, N C, D Z, M P, A K, R SC, D G, D HM (2010). A threonine to isoleucine mis-sense mutation in the pericentriolar material 1 (PCM1) gene is strongly associated with schizophrenia.. Molecular Psychiatry, , - .
• Rapp GE, Pineda-Trujillo N, McQuillin A, Tonetti M (2010). Genetic power of a Brazilian three-generation family with generalized aggressive periodontitis.. Braz Dent J, 21(2), 137 - 141.
• Lydall GJ, McQuillin A, Guerrini I, O'Kane A, Jauhar S, Patel S, Qureshi S, Gobikrishnan B, Douglas E, Hillman A, Kottalgi G, Reynolds G, Cherian R, Thomson AD, Ball D, Smith I, Rao H, Cook C, Morgan MY, Gurling HMD (2010). MAPPING OF SUSCEPTIBILITY GENES EXPLAINING THE COMORBIDITY BETWEEN THE ALCOHOL DEPENDENCE SYNDROME AND BIPOLAR AFFECTIVE DISORDER.

2009

• Rapp G, McQuillin A, Brett PM, Tonetti MS, Donos N (2009). Evidence of linkage on 1022-23.2 to periodontitis in Brazilian families.
• Ng MYM, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah H, P A E, M W, D B W, N M L, C M, B J B, L M, M S, P G, D L A, G L, B F, M D G, H M D G, P V L, E M, H B, W W, E M F, P T, M T H, H-G O, Y K, K S W, B F, A W, D O, A P, L N, G L, V K L, K Y P, G D, D S, S G O, M J OD, M C N, N H, E nRaventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Basset AS, Roy M-A, Mérette C, Pato CN, Pato MT, LouwRoos J, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, KarayiorgouM LM (2009). Meta-analysis of 32 genomewide linkage studies of schizophrenia. Molecular Psychiatry, 14(8), 774 - 785.
• International Schizophrenia Consortium P, S M W, N R S, J L V, P M O, M C S, P F S, P (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.. Nature, 460(7256), 748 - 752.
• Bass NJ, Datta SR, McQuillin A, Puri V, Choudhury K, Thirumalai S, Lawrence J, Quested D, Pimm J, Curtis D, Gurling HM (2009). Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia.. Behavioral and Brain Functions, 5, 28 - .
• Hennah W, Thomson P, McQuillin A, Bass N, Loukola A, Anjorin A, Blackwood D, Curtis D, Deary IJ, Harris SE, Isometsä ET, Lawrence J, Lönnqvist J, Muir W, Palotie A, Partonen T, Paunio T, Pylkkö E, Robinson M, Soronen P, Suominen K, Suvisaari J, Thirumalai S, St Clair D, Gurling H, Peltonen L, Porteous D (2009). DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.. Mol Psychiatry, 14(9), 865 - 873. doi:10.1038/mp.2008.22
• Perlis RH, Smoller JW, Ferreira MA, McQuillin A, Bass N, Lawrence J, Sachs GS, Nimgaonkar V, Scolnick EM, Gurling H, Sklar P, Purcell S (2009). A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder.. American Journal of Psychiatry, 166(6), 718 - 725.
• Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schurmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JSK, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J (2009). Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nature Genetics, 41(10), 1088 - 1093. doi:10.1038/ng.440
• Sharp SI, McQuillin A, Gurling HM (2009). Genetics of attention-deficit hyperactivity disorder (ADHD).. Neuropharmacology, 57, 590 - 600.
• Vine AE, McQuillin A, Bass NJ, Pereira A, Kandaswamy R, Robinson M, Lawrence J, Anjorin A, Sklar P, Gurling HM, Curtis D (2009). No evidence for excess runs of homozygosity in bipolar disorder.. Psychiatric Genetics, 19(4), 165 - 170.

2008

• Knapp S, Hosie AM, Anstee QM, Thomos P, Mortensen M, Martinez A, Tymowska-Lalanne Z, McQuillin A, Gurling HM, Morgan MY, Kuo YT, Herlihy A, Bell JD, Robinson I, Fisher E, Brown S, Stephens D, Smart TG, Thomas HC (2008). IDENTIFICATION OF A MODEL OF ALCOHOL PREFERENCE AND ITS SIMILARITY TO HUMAN ALCOHOLISM.
• Sklar P, Smoller J, Fan J, Ferreira M, Perlis R, Chambert K, Nimgaonkar V, McQueen MB, Faraone SV, Kirby A, deBakker PIK, Ogdie MN, Thase ME, Sachs GS, Todd-Brown K, Gabriel SB, Sougnez C, Gates C, Blumenstiel B, Defelice M, Ardlie K, Franklin J, Muir WJ, McGhee KA, MacIntyre DA, McLean A, VanBeck M, McQuillin A, Bass NJ, Robinson M, Lawrence J, Anjorin A, Curtis D, Scolnick EM, Daly MJ, Blackwood DH, Gurling HM, Purcell SM (2008). Whole-genome association study of bipolar disorder. Molecular Psychiatry, 13(6), 558 - 569. doi:10.1038/sj.mp.4002151
• Puri V, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass NJ, Moorey H, Fountoulaki G, Kar Ray M, Sule A, Curtis D, Gurling HMD (2008). Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia. European Journal of Human Genetics, , - .
• Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, Sule A, Curtis D, St Clair D, Gurling H (2008). Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.. Eur J Hum Genet, 16(10), 1275 - 1282. doi:10.1038/ejhg.2008.76
• Hennah W, Thomson P, McQuillin A, Bass N, Loukola A, Anjorin A, Blackwood D, Curtis D, Deary IJ, Harris E, Isometsä ET, Lawrence , Lönnqvist J, Muir M, Palotie A, Partonen T, Paunio T, Pylkkö E, Robinson M, Soronen P, Suominen K, Suvisaari J, Thirumalai S, StClair D, Gurling H, Peltonen L, P D DA (2008). Heterogeneity and Interplay in Schizophrenia and Bipolar Disorder. Molecular Psychiatry, , - .
• Ferreira MOD, M Meng YAJI, A Ruderfer1 DMJ, L Fan J Kirov GPRG, E Smoller JWG, D Stone JN, I Chambert KH, M L Nimgaonkar VM, V Thase MEC, S Sachs GSF, J Gordon-Smith KA, K G Gabriel SBF, C Blumenstiel BD, M Breen GG, M Morris DWE, A Muir WJM, K Williamson RM, D J McLean ASC, D VanBeck MP, A Kandaswamy RM, A Collier DAB, N J Young AHL, J Ferrier JNA, A Farmer AC, D Scolnick EM, P Daly MJC, A P Holmans PAB, D H Gurling HMO, M J Purcell SHS, P Craddock N (2008). Collaborative genome-wide association analysis of 10,596 individuals supports a role for Ankyrin-G (ANK3) and the alpha-1C subunit of the L-type voltage-gated calcium channel (CACNA1C) in bipolar disorder. Nature Genetics, 40(9), 1056 - 1058.
• Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DH, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, Sullivan PF, Sklar P, Ruderfer DM, Korn J, Kirov GK, Macgregor S, McQuillin A, Morris DW, O'Dushlaine CT, Daly MJ, Visscher PM, Holmans PA, Hultman CM, Kirov GK, Lichtenstein P, Pato CN, Scolnick EM, St Clair D, Nikolov I, Norton N, Williams H, Toncheva D, Milanova V, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Curtis D, Crombie C, Fraser G, Leh Kwan S, Walker N, Muir WJ, McGhee KA, Pickard B, Malloy P, Maclean AW, Van Beck M, Visscher PM, Macgregor S, Pato MT, Medeiros H, Middleton F, Carvalho C, Morley C, Fanous A, Conti D, Knowles JA, Paz Ferreira C, Macedo A, Helena Azevedo M, Pato CN, Ruderfer DM, Korn J, McCarroll SA (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature, 445, 237 - 241.
• McQuillin A, Bass NJ, Choudhury K, Puri V, Kosmin M, Lawrence J, Curtis D, Gurling HMD (2008). Replication and combined genetic analyses show that a non conservative amino acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar and unipolar affective disorders. Molecular Psychiatry, , - .

2007

• Gurling HMD, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, Curtis D, Blackwood D, Muir W, Malhotra AK, Buchanan RW, Good CD, Frackowiak RSJ, Dolan RJ (2007). Gene-brain structure relationships: arbitrary assumptions of heterogeneity generate unfalsifiable claims - In reply. ARCH GEN PSYCHIAT, 64(9), 1098 - 1099.
• Guerrini I, McQuillin A, Thomson AD, Gurling HMD (2007). Genetic linkage supports the presence oftwo susceptibility loci on chromosome 1p22.1-11.2 and 1q21.3-24.2 in alcoholism.
• Puri V, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Moorey H, Morgan J, Punukollu B, Kandasami G, Curtis D, Gurling H (2007). Fine mapping by genetic association implicates the chromosome 1q23.3 Gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene. Biological Psychiatry, 61(7), 873 - 879. doi:10.1016/j.biopsych.2006.06.014
• Datta SR, McQuillin A, Puri V, Choudhury K, Thirumalai S, Lawrence J, Pimm J, Bass N, Lamb G, Moorey H, Morgan J, Punukollu B, Kandasami G, Kirwin S, Sule A, Quested D, Curtis D, Gurling HM (2007). Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia.. Behavioral and Brain Functions, 3(50), - .
• McQuillin A, Rizig AM, Gurling H (2007). A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder. Pharmacogenetics and Genomics, 17(8), 605 - 617.
• Choudhury K, McQuillin A, Thirumalai S, Lawrence J, Krasucki R, Puri V, Datta S, Quested D, Bass N, Pimm J, Kandasami G, Morgan J, Punukollu B, Nadeem H, Curtis D, Gurling H (2007). A genetic association study implicates the chromosome 11q23.3 gene FXYD6 encoding phopshohippolin in susceptibility to schizophrenia in University College London and Aberdeen case control samples. The American Journal of Human Genetics, 80(4), 664 - 672.
• Gurling H, Pimm J, McQuillin A (2007). Replication of genetic association studies between markers at the Epsin 4 gene locus and schizophrenia in two Han Chinese samples. Schizophrenia Research, 89(1-3), 357 - 359.
• Choudhury K, McQuillin A, Puri V, Pimm J, Datta S, Thirumalai S, Krasucki R, Lawrence J, Bass NJ, Quested D, Crombie C, Fraser G, Walker N, Nadeem H, Johnson S, Curtis D, St Clair D, Gurling HM (2007). A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia.. Am J Hum Genet, 80(4), 664 - 672. doi:10.1086/513475

2006

• McQuillin A, Rizig M, Gurling H (2006). A microarray gene expression study of the effects lithium carbonate on mouse brain mRNA in order to understand the neurobiology of mood stabilisation and treatment of bipolar affective disorder.
• Kandaswamy R, Bass N, Choudhury K, Puri V, Mcquillin A, Lawrence J, Curtis D, Gurling H (2006). Fine mapping of a new bipolar and unipolar affective disorder locus on chromosome 1p36.
• Pereira ACP, McQuillin A, Mors O, Olsen IM, Puri V, Choudhury K, Bass NJ, Gurling HM (2006). Detection and characterisation of the bipolar susceptibility gene Slynar in the mouse.
• Choudhury K, McQuillin A, Puri V, Thirumalai S, Lawrence J, Krasucki R, Datta SR, Bass NJ, Pimm J, Curtis D, Gurling HMD (2006). A genetic association study implicates the chromosome 11q23.3 gene FXYD6 in susceptibility to schizophrenia.
• Bass N, McQuillin A, Lawrence J, Choudhury K, Puri V, Kalsi G, Curtis D, Gurling H (2006). Failure to confirm allelic association between COMT and bipolar disorder in a large UK sample.
• Gurling HM, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, Curtis D, Blackwood D, Muir W, Malhotra AK, Buchanan RW, Good CD, Frackowiak RS, Dolan RJ (2006). Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Archives of General Psychiatry, 63(8), 844 - 854. doi:10.1001/archpsyc.63.8.844
• Rizig MA, McQuillin A, Puri V, Choudhury K, Datta S, Thirumalai S, Lawrence J, Quested D, Pimm J, Bass N, Lamb G, Moorey H, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Kandasami G, Curtis D, Gurling H (2006). Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141(3), 296 - 300. doi:10.1002/ajmg.b.30288
• Puri V, McQuillin A, Thirumalai S, Lawrence J, Krasucki R, Choudhury K, Datta S, Kerwin S, Quested D, Bass N, Pimm J, Lamb G, Moorey H, Kandasami G, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Nadeem H, Curtis D, Gurling HM (2006). Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British Sample.. Biological Psychiatry, 59(2), 195 - 197. doi:10.1016/j.biopsych.2005.08.015
• McQuillin A, Bass NJ, Kalsi G, Lawrence J, Puri V, Choudhury K, Detera-Wadleigh SD, Curtis D, Gurling HMD (2006). Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3. Molecular Psychiatry, 11(2), 134 - 142. doi:10.1038/sj.mp.4001759
• Kalsi G, McQuillin A, Degn B, Lundorf MD, Bass NJ, Lawrence J, Choudhury K, Puri V, Nyegaard M, Curtis D, Mors O, Kruse T, Kerwin S, Gurling HMD (2006). Identification of the Slynar gene (AY070435) and related brain expressed sequences as a candidate gene for susceptibility to affective disorders through allelic and haplotypic association with bipolar disorder on chromosome 12q24. American Journal of Psychiatry, 163(10), 1767 - 1776. doi:10.1176/appi.ajp.163.10.1767

2005

• McQuillin A, Kalsi G, Degn B, Lundorf MD, Bass NJ, Lawrence J, Choudhury K, Puri VH, Nyegaard M, Curtis D, Mors O, Kruse T, Gurling HM (2005). Allelic and haplotypic association with bipolar disorder implicates a 300 kilobase region on chromosome 12q24.3 containing novel brain expressed gene sequences.
• Bass N, McQuillin A, Lawrence J, Choudhury , Puri V, Kalsi G, Curtis D, Gurling HM (2005). Evidence of allelic association of bipolar disorder with two genes P2RX7 and AY070435 6 MB apart on 12q24.
• Choudhury KH, Rizig MA, McQuillin A, Puri V, Datta SR, Thirumalai S, Lawrence J, Bass N, Curtis D, Gurling HM (2005). Genetic association and gene expression studies implicate the chromosome 11q23.3 gene FXYD2 in susceptibility to schizophrenia.
• Datta SR, McQuillin A, Rizig MA, Puri V, Choudhury KH, Thirumalai S, Lawrence J, Bass N, Curtis D, Gurling HM (2005). Detection of potential aetiological base pair changes causing genetic susceptibility to schizophrenia in the pericentriolar material 1 (PCM1) gene on chromosome 8p22 supports evidence from allelic association.
• Puri V, Rizig MA, McQuillin A, Choudhury KH, Datta SR, Thirumalai S, Lawrence J, Bass N, Moorey H, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Gurling H (2005). Failure to confirm association between schizophrenia and markers on chromosome 1q23.3 at the RGS4 and CAPON genes.
• Guerrini I, Cook CCH, Kest W, Devitgh A, McQuillin A, Curtis D, Gurling HMD (2005). Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2. BMC Genetics, 6(art.11), - . doi:10.1186/1471-2156-6-11
• Guerrini I, Thomson AD, Cook CC, McQuillin A, Sharma V, Kopelman M, Reynolds G, Jauhar P, Harper C, Gurling HM (2005). Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 137B(1), 17 - 19. doi:10.1002/ajmg.b.30194
• Rizig M, Gurling H, McQuillin A, Stephen HP (2005). A gene expression study of clozapine compared to haloperidol and how these drugs interact with genes implicated in schizophrenia.
• Pimm J, McQuillin A, Thirumalai S, Lawrence J, Quested D, Bass N, Lamb G, Moorey H, Datta SR, Kalsi G, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Curtis D, Gurling H (2005). The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia.. The American Journal of Human Genetics, 76(5), 902 - 907.

2004

• McQuillin A, Bass N, Kalsi G, Lawrence J, Smyth C, Curtis D, Gurling HMD (2004). Resequencing of the TRPM2 and TSPEAR genes provides additional SNPs in the 21q22.3 region of chromosome 21 that show strengthened allelic and haploptypic association with bipolar disorder.
• Puri V, Rizig MA, Datta SR, McQuillin A, Thirumalai S, Pimm J, Moorey H, Quested D, Kalsi G, Bass N, Lawrence J, Curtis D, Gurling HMD (2004). Fine mapping of the chromosome 1q23-24.2 schizophrenia susceptibility region near the RGS4 D1S196 and Capon loci.
• Curtis D, Brett P, Dearlove AM, McQuillin A, Kalsi G, Robertson MM, Gurling HMD (2004). Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13. Psychiatric Genetics, 14(2), 83 - 87.
• Buttenschon HN, Mors O, Ewald H, McQuillin A, Kalsi G, Lawrence J, Gurling H, Kruse TA (2004). No Association between a neuronal nitric oxide synthase (NOSI) gene polymorphism on chromosome 12q24 and bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, (124B), 73 - 75.
• Rizig MA, McQuillin A, Datta SR, Pimm J, Thirumalai S, Moorey H, Quested DD, Kalsi G, Bass N, Lawrence J, Curtis D, Hubank M, Hunt SP, Gurling HMD (2004). A microarray gene expression and genetic association study of the RGS4 gene in schizophrenia.
• Rizig MA, McQuillin A, Hubank M, Hunt SP, Gurling HMD (2004). A microarray gene expression study of the side effects of the antipsychotic drugs clozapine and haloperidol: Antipsychotic metabolic signatures in the right side of the mouse brain as model for the treatment of schizophrenia.
• Rizig M, McQuillin A, Hubank M, Hunt S, Gurling H (2004). The molecular pharmacology behind the antipsychotic and antimanic effects of clozapine: microarray gene expression profiles of the conventional antipsychotic drug haloperidol compared with the atypical antipsychotic clozapine.
• Choudhury K, Puri V, McQuillin A, Kalsi G, Bass N, Lawrence J, Curtis D, Gurling HMD (2004). Attempted confirmation of the fine mapping of a putative bipolar susceptibility locus on chromosome 4P16.1 at the PPP2R2C gene locus.

2003

• Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lonnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoega T, Helgason T (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.. The American Journal of Human Genetics, 73(1), 34 - 48.
• Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lonnqvist J, Nothen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.. The American Journal of Human Genetics, 73(1), 49 - 62.
• Carbonell J, Allen R, Kalsi G, McQuillin A, Livingston G, Katona C, Walker Z, Rands G, Stevens T, Crossan I, Curtis D, Gurling H (2003). Variations in the DCP1 gene, encoding the angiotensin converting enzyme ACE, is not associated with increased susceptibility to Alzheimer's disease. Psychiatric Genetics, 13, 47 - 50.
• Curtis D, Kalsi G, Brynjolfsson J, McInnis M, O'Neill J, Smyth C, Moloney E, Murphy P, McQuillin A, Petursson H, Gurling H (2003). Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q.. Psychiatric Genetics, 13(2), 77 - 84.

2002

• Kalsi G, Lawrence J, Mcquillin A, Curtis D, Bass N, Gurling HMD (2002). X linkage in bipolar disorder: Allelic association studies of the Xq26-28 region implicate the G6PD locus and flanking region but not the a3 subunit of the GABA receptor gene (GABRA3) in a UK bipolar case-control sample.
• Kalsi G, Rizig MAA, Theobald S, Mcquillin A, Bass N, Curtis D, Pickard B, Blackwood D, Gurling HMD (2002). An allelic association study in a UK case-control sample testing the schizophrenia susceptibility locus on chromosome 1q21-22.
• Rizig MA, McQuillin A, Fletcher D, Hubank M, Hunt SP, Gurling HMD (2002). Differences in mouse brain microarray detected gene expression profiles in response to the antipsychotic drugs Clozapine and haloperidol: What gene expression pathways mediate clozapine's superior clinical efficacy?.
• Blaveri E, Critchley HD, Gurling HMD, O'Daly O, Kalsi G, Datta SR, McQuillin A, Moorey H, Quested D, Curtis D, Lawrence J, Bass N, Good CD, Frackowiak RS, Dolan R (2002). Genetic markers showing linkage disequilibrium with a chromosome 8p22 schizophrenia susceptibility locus near the pericentriolar material gene (PCM1) are associated with reduced left orbitofrontal cortex grey matter volume and other cerebral morphology changes at MRI compared to non chromosome 8p22 associated schizophrenics..
• McQuillin A, Kalsi G, Lawrence J, Smyth C, Curtis D, Bass NJ, Gurling HMD (2002). Positive allelic association of the marker d21sl71 with bipolar disorder identifies TRPC7, a calcium channel protein on chromosome 21 at 21q22.3, as being a candidate gene for increasing genetic susceptibility to bipolar and related unipolar affective disorders..
• McQuillin A, Kalsi G, Moorey H, Lamb G, Mayet S, Quested D, Baker P, Curtis D, Gurling HM (2002). A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia. EUR J HUM GENET, 10(8), 491 - 494. doi:10.1038/sj/ejhg.5200837
• Jorgensen TH, Degn B, Wang AG, Vang M, Gurling H, Kalsi G, McQuillin A, Kruse TA, Mors O, Ewald H (2002). Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands. European Journal of Human Genetics, 10, 381 - 387.
• Guerrini I, Cook CH, Kest W, Devitgh A, McQuillin A, Curtis D, Gurling HMD (2002). Genome scan of alcoholism in multiplex British families supports the presence of susceptibility loci on chromosome 1p and 1q.
• Gurling HMD, Blaveri E, Datta S, Kalsi G, McQuillin A, Moorey H, Quested D, Lamb G, Lawrence J, Chowdhury U, Bass N, O'Daly O, Curtis D, Critchley HD, Good CD, Frackowiak RSJ, Dolan R (2002). Genetic markers showing linkage disequilibrium with a chromosome 8p22 schizophrenia susceptibility locus near the pericentriolar material gene (PCM1) are associated with reduced left orbitofrontal cortex grey matter volume and other cerebral morphology changes at MRI compared to non chromosome 8p22 associated schizophrenics.
• Bass N, McQuillin A, Lawrence J, Darragh N, Kalsi G, Curtis D, Gurling HMD (2002). Investigation of the gene encoding tryptophan hydroxylase (TPH) and suicide behaviour in bipolar affective disorder shows allelic association with poor pre-morbid social and work adjustment and with violent suicide.
• McQuillin A, Kalsi G, Lawrence J, Smyth C, Curtis D, Bass N, Gurling HMD (2002). Positive allelic association of the marker D21S171 with bipolar disorder identifies TRPC7, a calcium channel protein on chromosome 21 at 21q22.3, as being a candidate gene for increasing susceptibility to bipolar and related unipolar affective disorders.
• Kalsi G, Mcquillin A, Curtis D, Bass N (2002). Allelic association study investigating GABRA3 and markers in G6PD region in a UK bipolar case-control sample..

2001

• Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D (2001). Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.. The American Journal of Human Genetics, 68(3), 661 - 673.
• McQuillin A, Kalsi G, Moorey H, Lamb G, Mayet S, Quested D, Gurling H (2001). Exon 11 of the chromosome 22 gene WKL1, previously shown to exhibit a base pair mutation in rare cases of schizophrenia, was found to contain an insertion/deletion polymorphism, affecting the receptor channel amino acid sequence..
• Guerrini I, Cook CCH, Kest W, Devitgh A, McQuillin A, Kalsi G, Curtis D, Gurling HMD (2001). Systematic genome scan of alcoholism using genetic linkage analysis in multiplex British families supports the presence of susceptibility loci on chromosome 1p and 16p..
• Blaveri E, Kalsi G, Lawrence J, Quested D, Moorey H, Lamb G, Kohen D, Shiwach R, Chowdhury U, Curtis D, McQuillin A, Gramoustianou ES, Gurling HM (2001). Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1). European Journal of Human Genetics, 9, 469 - 472.

2000

• Guerrini I, Cook CC, Kest W, Devitgh A, McQuillin A, Holmes D, Turner A, Curtis D, Gurling HMD (2000). Report of a total genome scan for genes increasing susceptibility to alcoholism by genetic linkage analysis in multiplex British families..
• Degn B, Lundorf MD, Bruun TG, McQuillin A, Lawrence J, Curtis D, Kalsi G, Chen A, Mors O, Kruse TA, Gurling H, Ewald H (2000). A search for the risk allele for bipolar affective disorder on chromosome 12q24.2..

1999

• McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Hannesdottir S, Gurling H (1999). Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder. Psychological Medicine, 29(6), 1449 - 1454.
• McQuillin A, Lawrence J, Kalsi G, Chen A, Gurling H, Curtis D (1999). No allelic association between bipolar affective disorder and the tryptophan hydroxylase gene. Archives of General Psychiatry, 56(1), 99 - 101.
• Murray KD, McQuillin A, Stewart L, Etheridge CJ, Cooper RG, Miller AD, Gurling HM (1999). Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon.. Gene Therapy, 6(2), 190 - 197.
• Kalsi G, McQuillin A, Lawrence J, Curtis D, Gurling HMD (1999). Positive allelic association between bipolar affective disorder and G6PD polymorphisms on chromosome Xq28..
• Degn B, Bruun TG, McQuillin A, Lawrence J, Curtis D, Kalsi G, Chen A, Kruse TA, Mors O, Gurling H, Ewald H (1999). Association study between patients with bipolar disorder and markers from the candidate region on chromosome 12q24.2-12q24.3..
• Curtis D, Kalsi G, McQuillin A, Lawrence J, Murphy P, Brynjolfsson T, McInnis M, Sigmundsson T, Petursson H, Gurling HMD (1999). Genome wide parametric genetic linkage analysis of bipolar and related unipolar affective disorders (manic depression) implicates chromosomes 1 and 12..
• Gurling HMD, Kalsi G, Blaveri E, McQuillin A, Read T, Murphy P, Butler R, Brynjolfsson J, Sigmundsson T, Petursson H, Curtis D (1999). Initial genome wide parametric genetic linkage analysis of schizophrenia and schizophrenia spectrum disorders finds lod scores above 3.00 on four chromosomes at 1Q22-23, 5Q22-35, 8P21-23 and 11Q14-24. a further lod above 3.00 at 4Q21-31 was found within a single family..
• Blaveri K, Kalsi G, McQuillin A, Quested D, Read T, Murphy P, Brynjolfsson J, Sigmundsson T, Petursson H, Curtis D, Gurling HMD (1999). Linkage and allelic association studies of the 8p schizophrenia locus..
• Detera-Wadleigh SD, Barden N, Craddock N, Ewald H, Foroud T, Kelsoe J, McQuillin A (1999). Chromosomes 12 and 16 Workshop.
• McQuillin A, Lawrence J, Kalsi G, Smyth C, Curtis D, Gurling HMD (1999). An allelic association study of multiple polymorphic markers in the chromosome 21q22.3 region implicated in bipolar affective disorder..

1998

• McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Gurling HMD (1998). No linkage found between chromosome 11p15.5 markers and manic-depressive illness..
• McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Gurling HMD (1998). No allelic association between bipolar affective disorder and the tryptophan hydroxylase gene (TPH)..
• McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Gurling HMD (1998). An allelic association study of candidate genes in the chromosome 21q22.3 region implicated in bipolar affective disorder.

1997

• Murray KD, McQuillin A, Gurling HMD (1997). Cationic liposome-mediated transfection of postmitotic ND7 and dorsal root ganglion neurons.. AM J MED GENET, 74(6), 603 - 603.
• McQuillin A, Murray K, Stuart L, Etheridge CJ, Cooper RG, Miller AD, Gurling HMD (1997). Intrathecal administration of cationic liposome vectors for gene delivery to the central nervous system..
• McQuillin A, Murray KD, Etheridge CJ, Stewart L, Cooper RG, Brett PM, Miller AD, Gurling HM (1997). Optimization of liposome mediated transfection of a neuronal cell line.. Neuroreport, 8(6), 1481 - 1484.

• Nyegaard M, Severinsen JE, Als TD, Hedemand A, Straarup S, Nordentoft M, McQuillin A, Bass N, Lawrence J, Thirumalai S, Pereira AC, Kandaswamy R, Lydall GJ, Sklar P, Scolnick E, Purcell S C, D G, H M M, P B M, O B, A D (). Support of association between BRD1 and both schizophrenia and bipolar affective disorder.. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, , - .