Anders Børglum
Anders Børglum
Professor, Director, Aarhus University
Bestätigte E-Mail-Adresse bei biomed.au.dk
Titel
Zitiert von
Zitiert von
Jahr
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
16602009
Genome-wide association study identifies five new schizophrenia loci
S Ripke, AR Sanders, KS Kendler, DF Levinson, P Sklar, PA Holmans, ...
Nature genetics 43 (10), 969, 2011
15862011
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
14352014
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, 2013
13512013
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
9212018
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
6252019
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
5352018
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
5312018
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
5182015
α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
J Mogensen, IC Klausen, AK Pedersen, H Egeblad, P Bross, TA Kruse, ...
The Journal of clinical investigation 103 (10), R39-R43, 1999
4611999
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
4452014
Identification of common genetic risk variants for autism spectrum disorder
J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ...
Nature genetics 51 (3), 431-444, 2019
3872019
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
3542019
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death
M Nyegaard, MT Overgaard, MT Søndergaard, M Vranas, ER Behr, ...
The American Journal of Human Genetics 91 (4), 703-712, 2012
3092012
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552-555, 2016
2712016
Psychiatric genomics: an update and an agenda
PF Sullivan, A Agrawal, CM Bulik, OA Andreassen, AD Børglum, G Breen, ...
American Journal of Psychiatry 175 (1), 15-27, 2018
2642018
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
AJ Schork, WK Thompson, P Pham, A Torkamani, JC Roddey, PF Sullivan, ...
PLoS Genet 9 (4), e1003449, 2013
2512013
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
2292017
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
S Steinberg, S de Jong, OA Andreassen, T Werge, AD Børglum, O Mors, ...
Human molecular genetics 20 (20), 4076-4081, 2011
2132011
Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway
GK Alderton, H Joenje, R Varon, AD Børglum, PA Jeggo, M O'Driscoll
Human molecular genetics 13 (24), 3127-3138, 2004
1992004
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20