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Bendik Slagsvold Winsvold
Bendik Slagsvold Winsvold
Dpt of Neurology and Dpt of Research, Innovation and Education, Oslo University Hospital
在 medisin.uio.no 的电子邮件经过验证
标题
引用次数
引用次数
年份
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ...
Nature genetics 51 (2), 237-244, 2019
15312019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13682018
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ...
Nature genetics 53 (6), 817-829, 2021
8232021
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
7432016
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
DP Wightman, IE Jansen, JE Savage, AA Shadrin, S Bahrami, D Holland, ...
Nature genetics 53 (9), 1276-1282, 2021
5572021
Genome-wide meta-analysis identifies new susceptibility loci for migraine
V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ...
Nature genetics 45 (8), 912-917, 2013
4652013
Genome-wide association analysis identifies susceptibility loci for migraine without aura
T Freilinger, V Anttila, B De Vries, R Malik, M Kallela, GM Terwindt, ...
Nature genetics 44 (7), 777-782, 2012
4122012
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3482022
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ...
Cell 184 (18), 4784-4818. e17, 2021
3022021
Biological and clinical insights from genetics of insomnia symptoms
JM Lane, SE Jones, HS Dashti, AR Wood, KG Aragam, VT van Hees, ...
Nature genetics 51 (3), 387-393, 2019
2912019
Stroke genetics informs drug discovery and risk prediction across ancestries
A Mishra, R Malik, T Hachiya, T Jürgenson, S Namba, DC Posner, ...
Nature 611 (7934), 115-123, 2022
2112022
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
MK Bakker, RAA van der Spek, W van Rheenen, S Morel, R Bourcier, ...
Nature genetics 52 (12), 1303-1313, 2020
2022020
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
H Hautakangas, BS Winsvold, SE Ruotsalainen, G Bjornsdottir, ...
Nature genetics 54 (2), 152-160, 2022
2012022
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
H Wang, JM Lane, SE Jones, HS Dashti, HM Ollila, AR Wood, ...
Nature communications 10 (1), 3503, 2019
1632019
Genetic diversity fuels gene discovery for tobacco and alcohol use
GRB Saunders, X Wang, F Chen, SK Jang, M Liu, C Wang, S Gao, ...
Nature 612 (7941), 720-724, 2022
1582022
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
1462022
Headache, migraine and cardiovascular risk factors: the HUNT study
BS Winsvold, K Hagen, AH Aamodt, LJ Stovner, J Holmen, JA Zwart
European journal of neurology 18 (3), 504-511, 2011
1312011
Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants
R Malik, T Freilinger, BS Winsvold, V Anttila, J Vander Heiden, M Traylor, ...
Neurology 84 (21), 2132-2145, 2015
1292015
Genetic markers of human evolution are enriched in schizophrenia
S Srinivasan, F Bettella, M Mattingsdal, Y Wang, A Witoelar, AJ Schork, ...
Biological psychiatry 80 (4), 284-292, 2016
1252016
Common variant burden contributes to the familial aggregation of migraine in 1,589 families
P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ...
Neuron 98 (4), 743-753. e4, 2018
962018
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