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David A Collier
David A Collier
Independent Consultant
Verified email at kcl.ac.uk
Title
Cited by
Cited by
Year
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
1958 Birth Cohort Controls Jones Richard W. 18 McArdle Wendy L. 18 Ring ...
nature 447 (7145), 661-678, 2007
92562007
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
72882014
Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ...
nature 455 (7210), 232-236, 2008
3595*2008
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
23032013
Genome-wide association study identifies five new schizophrenia loci
Nature genetics 43 (10), 969-976, 2011
19662011
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150-1159, 2013
17272013
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
14852011
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
AF Pardiñas, P Holmans, AJ Pocklington, V Escott-Price, S Ripke, ...
Nature genetics 50 (3), 381-389, 2018
14442018
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
1958 Birth Cohort Controls: Jones Richard W 18 McArdle Wendy L 18 Ring Susan ...
Nature genetics 39 (11), 1329-1337, 2007
14192007
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
MAR Ferreira, MC O'Donovan, YA Meng, IR Jones, DM Ruderfer, L Jones, ...
Nature genetics 40 (9), 1056-1058, 2008
14062008
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
12992015
Percutaneous coronary intervention in stable angina (ORBITA): a double-blind, randomised controlled trial
R Al-Lamee, D Thompson, HM Dehbi, S Sen, K Tang, J Davies, T Keeble, ...
The Lancet 391 (10115), 31-40, 2018
10062018
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
9912019
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
9762022
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
8792017
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.
DA Collier, G Stöber, T Li, A Heils, M Catalano, D Di Bella, MJ Arranz, ...
Molecular psychiatry 1 (6), 453-460, 1996
8781996
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
A Helgadottir, G Thorleifsson, KP Magnusson, S Grétarsdottir, ...
Nature genetics 40 (2), 217-224, 2008
8532008
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
S Nejentsev, JMM Howson, NM Walker, J Szeszko, SF Field, HE Stevens, ...
Nature 450 (7171), 887-892, 2007
6912007
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
6862021
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
6382014
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