| Title | Author(s) | Year | View Count |
 | Dissecting the genetic heterogeneity of depression through age at onset | Power, RA; Keers, R; Ng, MY; Butler, AW; Uher, R; Cohen-Woods, S; Ising, M; Craddock, N; Owen, MJ; Korszun, A; Jones, L; Jones, I; Gill, M; Rice, JP; Hauser, J; Henigsberg, N; Maier, W; Zobel, A; Mors, O; Placentino, AS; Rietschel, M; Souery, D; Kozel, D; Preisig, M; Lucae, S; Binder, EB; Aitchison, KJ; Tozzi, F; Muglia, P; Breen, G; Craig, IW; Farmer, AE; Müller-Myhsok, B; McGuffin, P; Lewis, CM | 2012 | 41 |
 | Genomewide association scan of suicidal thoughts and behaviour in major depression | Schosser, A; Butler, AW; Ising, M; Perroud, N; Uher, R; Ng, MY; Cohen-Woods, S; Craddock, N; Owen, MJ; Korszun, A; Jones, L; Jones, I; Gill, M; Rice, JP; Maier, W; Mors, O; Rietschel, M; Lucae, S; Binder, EB; Preisig, M; Perry, J; Tozzi, F; Muglia, P; Aitchison, KJ; Breen, G; Craig, IW; Farmer, AE; Mulller-Myhsok, B; McGuffin, P; Lewis, CM | 2011 | 42 |
| Functional impact of global rare copy number variation in autism spectrum disorders | Pinto, D; Pagnamenta, AT; Klei, L; Anney, R; Merico, D; Regan, R; Conroy, J; Magalhaes, TR; Correia, C; Abrahams, BS; Almeida, J; Bacchelli, E; Bader, GD; Bailey, AJ; Baird, G; Battaglia, A; Berney, T; Bolshakova, N; Bölte, S; Bolton, PF; Bourgeron, T; Brennan, S; Brian, J; Bryson, SE; Carson, AR; Casallo, G; Casey, J; Chung, BHY; Cochrane, L; Corsello, C; Crawford, EL; Crossett, A; Cytrynbaum, C; Dawson, G; De Jonge, M; Delorme, R; Drmic, I; Duketis, E; Duque, F; Estes, A; Farrar, P; Fernandez, BA; Folstein, SE; Fombonne, E; Freitag, CM; Gilbert, J; Gillberg, C; Glessner, JT; Goldberg, J; Green, A; Green, J; Guter, SJ; Hakonarson, H; Heron, EA; Hill, M; Holt, R; Howe, JL; Hughes, G; Hus, V; Igliozzi, R; Kim, C; Klauck, SM; Kolevzon, A; Korvatska, O; Kustanovich, V; Lajonchere, CM; Lamb, JA; Laskawiec, M; Leboyer, M; Le Couteur, A; Leventhal, BL; Lionel, AC; Liu, XQ; Lord, C; Lotspeich, L; Lund, SC; Maestrini, E; Mahoney, W; Mantoulan, C; Marshall, CR; Mcconachie, H; Mcdougle, CJ; Mcgrath, J; Mcmahon, WM; Merikangas, A; Migita, O; Minshew, NJ; Mirza, GK; Munson, J; Nelson, SF; Noakes, C; Noor, A; Nygren, G; Oliveira, G; Papanikolaou, K; Parr, JR; Parrini, B; Paton, T; Pickles, A; Pilorge, M; Piven, J; Ponting, CP; Posey, DJ; Poustka, A; Poustka, F; Prasad, A; Ragoussis, J; Renshaw, K; Rickaby, J; Roberts, W; Roeder, K; Roge, B; Rutter, ML; Bierut, LJ; Rice, JP; Salt, J; Sansom, K; Sato, D; Segurado, R; Sequeira, AF; Senman, L; Shah, N; Sheffield, VC; Soorya, L; Sousa, I; Stein, O; Sykes, N; Stoppioni, V; Strawbridge, C; Tancredi, R; Tansey, K; Thiruvahindrapduram, B; Thompson, AP; Thomson, S; Tryfon, A; Tsiantis, J; Van Engeland, H; Vincent, JB; Volkmar, F; Wallace, S; Wang, K; Wang, Z; Wassink, TH; Webber, C; Weksberg, R; Wing, K; Wittemeyer, K; Wood, S; Wu, J; Yaspan, BL; Zurawiecki, D; Zwaigenbaum, L; Buxbaum, JD; Cantor, RM; Cook, EH; Coon, H; Cuccaro, ML; Devlin, B; Ennis, S; Gallagher, L; Geschwind, DH; Gill, M; Haines, JL; Hallmayer, J; Miller, J; Monaco, AP; Nurnberger Jr, JI; Paterson, AD; PericakVance, MA; Schellenberg, GD; Szatmari, P; Vicente, AM; Vieland, VJ; Wijsman, EM; Scherer, SW; Sutcliffe, JS; Betancur, C | 2010 | 62 |
| Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha | Carroll, LS; Williams, NM; Moskvina, V; Russell, E; Norton, N; Williams, HJ; Peirce, T; Georgieva, L; Dwyer, S; Grozeva, D; Greene, E; Farmer, A; McGuffin, P; Morris, DW; Corvin, A; Gill, M; Rujescu, D; Sham, P; Holmans, P; Jones, I; Kirov, G; Craddock, N; O'Donovan, MC; Owen, MJ | 2010 | 108 |
| Population differences in the international multi-centre ADHD gene project | Neale, BM; Sham, PC; Purcell, S; Banaschewski, T; Buitelaar, J; Franke, B; SonugaBarke, E; Ebstein, R; Eisenberg, J; Mulligan, A; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Zhou, K; Asherson, P; Faraone, SV | 2008 | 88 |
| DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage | Chen, W; Zhou, K; Sham, P; Franke, B; Kuntsi, J; Campbell, D; Fleischman, K; Knight, J; Andreou, P; Arnold, R; Altink, M; Boer, F; Boholst, MJ; Buschgens, C; Butler, L; Christiansen, H; Fliers, E; HoweForbes, R; Gabriëls, I; Heise, A; KornLubetzki, I; Marco, R; Medad, S; Minderaa, R; Müller, UC; Mulligan, A; Psychogiou, L; Rommelse, N; Sethna, V; Uebel, H; McGuffin, P; Plomin, R; Banaschewski, T; Buitelaar, J; Ebstein, R; Eisenberg, J; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; SonugaBarke, E; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P | 2008 | 224 |
| Linkage to Chromosome 1p36 for Attention-Deficit/Hyperactivity Disorder Traits in School and Home Settings | Zhou, K; Asherson, P; Sham, P; Franke, B; Anney, RJL; Buitelaar, J; Ebstein, R; Gill, M; Brookes, K; Buschgens, C; Campbell, D; Chen, W; Christiansen, H; Fliers, E; Gabriëls, I; Johansson, L; Marco, R; Mulas, F; Müller, U; Mulligan, A; Neale, BM; Rijsdijk, F; Rommelse, N; Uebel, H; Psychogiou, L; Xu, X; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Manor, I; Miranda, A; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV | 2008 | 208 |
| Population differences in the International Multi-Centre ADHD Gene (IMAGE) project (Genetic Epidemiology DOI: 10.1002/gepi.20265) | Neale, BM; Sham, PC; Purcell, S; Banaschewski, T; Buitelaar, J; Franke, B; SonugaBarke, E; Ebstein, R; Eisenberg, J; Mulligan, A; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Chen, W; Zhou, K; Asherson, P; Faraone, SV | 2008 | 23 |
| The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes | Brookes, K; Xu, X; Chen, W; Zhou, K; Neale, B; Lowe, N; Aneey, R; Franke, B; Gill, M; Ebstein, R; Buitelaar, J; Sham, P; Campbell, D; Knight, J; Andreou, P; Altink, M; Arnold, R; Boer, F; Buschgens, C; Butler, L; Christiansen, H; Feldman, L; Fleischman, K; Fliers, E; HoweForbes, R; Goldfarb, A; Heise, A; Gabriëls, I; KornLubetzki, I; Marco, R; Medad, S; Minderaa, R; Mulas, F; Müller, U; Mulligan, A; Rabin, K; Rommelse, N; Sethna, V; Sorohan, J; Uebel, H; Psychogiou, L; Weeks, A; Barrett, R; Craig, I; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Kuntsi, J; Manor, I; McGuffin, P; Miranda, A; Oades, RD; Plomin, R; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P; Johansson, L | 2006 | 170 |
| Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes (Molecular Psychiatry (2006) 11, (934-953) DOI: 10.1038/sj.mp.4001869) | Brookes, K; Xu, X; Chen, W; Zhou, K; Neale, B; Lowe, N; Anney, R; Franke, B; Gill, M; Ebstein, R; Buitelaar, J; Sham, P; Campbell, D; Knight, J; Andreou, P; Altink, M; Arnold, R; Boer, F; Buschgens, C; Butler, L; Christiansen, H; Feldman, L; Fleischman, K; Fliers, E; HoweForbes, R; Goldfarb, A; Heise, A; Gabriëls, I; KornLubetzki, I; Johansson, L; Marco, R; Medad, S; Minderaa, R; Mulas, F; Müller, U; Mulligan, A; Rabin, K; Rommelse, N; Sethna, V; Sorohan, J; Uebel, H; Psychogiou, L; Weeks, A; Barrett, R; Craig, I; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Kuntsi, J; Manor, I; Mcguffin, P; Miranda, A; Oades, RD; Plomin, R; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P | 2006 | 24 |
| Whole genome linkage scan of recurrent depressive disorder from the depression network study | Mcguffin, P; Knight, J; Breen, G; Brewster, S; Boyd, PR; Craddock, N; Gill, M; Korszun, A; Maier, W; Middleton, L; Mors, O; Owen, MJ; Perry, J; Preisig, M; Reich, T; Rice, J; Rietschel, M; Jones, L; Sham, P; Farmer, AE | 2005 | 34 |
| Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes | Lowe, N; Kirley, A; Hawi, Z; Sham, P; Wickham, H; Kratochvil, CJ; Smith, SD; Lee, SY; Levy, F; Kent, L; Middle, F; Rohde, LA; Roman, T; Tahir, E; Yazgan, Y; Asherson, P; Mil, J; Thapar, A; Payton, A; Todd, RD; Stephens, T; Ebstein, RP; Manor, I; Barr, CL; Wigg, KG; Sinke, RJ; Buitelaar, JK; Smalley, SL; Nelson, SF; Biederman, J; Faraone, SV; Gill, M | 2004 | 40 |
| Familiality of clinical characteristics in schizophrenia | Wickham, H; Walsh, C; Asherson, P; Gill, M; Owen, MJ; Mcguffin, P; Murray, R; Sham, P | 2002 | 40 |
| Familiality of symptom dimensions in schizophrenia | Wickham, H; Walsh, C; Asherson, P; Taylor, C; Sigmundson, T; Gill, M; Owen, MJ; Mcguffin, P; Murray, R; Sham, P | 2001 | 35 |
| A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia | Wright, P; Dawson, E; Donaldson, PT; Underhill, JA; Sham, PC; Zhao, J; Gill, M; Nanko, S; Owen, MJ; Mcguffin, P; Murray, RM | 1998 | 32 |
| Catechol-O-methyltransferase polymorphisms and schizophrenia: A transmission disequilibrium study in multiply affected families | Kunugi, H; Vallada, HP; Sham, PC; Hoda, F; Arranz, MJ; Li, T; Nanko, S; Murray, RM; Mcguffin, P; Owen, M; Gill, M; Collier, DA | 1997 | 32 |
| A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12 | Gill, M; Vallada, H; Collier, D; Sham, P; Holmans, P; Murray, R; Mcguffin, P; Nanko, S; Owen, M; Antonarakis, S; Housman, D; Kazazian, H; Nestadt, G; Pulver, AE; Straub, RE; Maclean, CJ; Walsh, D; Kendler, KS; Delisi, L | 1996 | 33 |
| Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia | Shaikh, S; Collier, DA; Sham, PC; Ball, D; Aitchison, K; Vallada, H; Smith, I; Gill, M; Kerwin, RW | 1996 | 34 |
| Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees | Lim, LCC; Craddock, N; Owen, M; Sham, P; Nöthen, MM; Körner, J; Rietschel, M; Fimmer, R; Propping, P; Mcguffin, P; Murray, R; Gill, M | 1996 | 34 |
| Systematic search for major genes in schizophrenia: Methodological issues and results from chromosome 12 | Dawson, E; Powell, JF; Sham, P; Shaikh, S; Taylor, C; Clements, A; Asherson, P; Sargeant, M; Collier, D; Nanko, S; Whatley, S; Murray, R; Mcguffin, P; Owen, M; Gill, M | 1995 | 25 |
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