Mads Vilhelm Hollegaard
Mads Vilhelm Hollegaard
Section of Neonatal Genetics, Dept. Congenital Disorders, Statens Serum Institut
Bekræftet mail på ssi.dk
TitelCiteret afÅr
Biological insights from 108 schizophrenia-associated genetic loci
SWG the Psychiatric Genomics Consortium
Nature 511 (7510), 421-427, 2014
36892014
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Bulik-Sullivan BK, L PR, F HK, R S, Y J, SWGPG Consortium, P N, D M, ...
Nat Genet 47 (3), 291-5, 2015
13382015
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
3862014
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
3702019
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
K Bønnelykke, P Sleiman, K Nielsen, E Kreiner-Møller, JM Mercader, ...
Nature genetics 46 (1), 51, 2014
3602014
Cytokine gene polymorphism in human disease: on-line databases, Supplement 3
MV Hollegaard, JL Bidwell
Genes & Immunity 7 (4), 269-276, 2006
2732006
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, 2017
2572017
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, 2016
2322016
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
M Horikoshi, H Yaghootkar, DO Mook-Kanamori, U Sovio, HR Taal, ...
Nature genetics 45 (1), 76, 2013
2252013
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248-252, 2016
2102016
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
1942011
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
1552019
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
1412016
Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.
E Agerbo, PF Sullivan, BJ Vilhjálmsson, CB Pedersen, O Mors, ...
JAMA Psychiatry, 2015
1372015
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci
AD Børglum, D Demontis, J Grove, J Pallesen, MV Hollegaard, ...
Molecular psychiatry 19 (3), 325-333, 2014
1262014
Common variant at 16p11. 2 conferring risk of psychosis
S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, ...
Molecular psychiatry 19 (1), 108-114, 2014
952014
Common variants associated with general and MMR vaccine–related febrile seizures
B Feenstra, B Pasternak, F Geller, L Carstensen, T Wang, F Huang, ...
Nature genetics 46 (12), 1274, 2014
902014
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
852018
Genome-wide association analyses identify variants in developmental genes associated with hypospadias
F Geller, B Feenstra, L Carstensen, TH Pers, IALM van Rooij, IB Körberg, ...
Nature genetics 46 (9), 957-963, 2014
772014
Genome-wide scans using archived neonatal dried blood spot samples
MV Hollegaard, J Grauholm, A Børglum, M Nyegaard, ...
BMC genomics 10 (1), 297, 2009
732009
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Artikler 1–20