Vidar M Steen
Vidar M Steen
University of Bergen
Verifisert e-postadresse på helse-bergen.no
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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
10542018
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
G Davies, A Tenesa, A Payton, J Yang, SE Harris, D Liewald, X Ke, ...
Molecular psychiatry 16 (10), 996-1005, 2011
7382011
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224-229, 2015
6722015
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
6062012
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
JE Savage, PR Jansen, S Stringer, K Watanabe, J Bryois, CA De Leeuw, ...
Nature genetics 50 (7), 912-919, 2018
5652018
Nomenclature for human CYP2D6 alleles.
AK Daly, J Brockmöller, F Broly, M Eichelbaum, WE Evans, FJ Gonzalez, ...
Pharmacogenetics 6 (3), 193-201, 1996
5651996
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ...
Brain imaging and behavior 8 (2), 153-182, 2014
4792014
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N= 53 949)
G Davies, N Armstrong, JC Bis, J Bressler, V Chouraki, S Giddaluru, ...
Molecular psychiatry 20 (2), 183-192, 2015
3502015
Dopamine D3-receptor gene variant and susceptibility to tardive dyskinesia in schizophrenic patients
VM Steen, R Løvlie, T MacEwan, RG McCreadie
Molecular psychiatry 2 (2), 139-145, 1997
3341997
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
G Davies, M Lam, SE Harris, JW Trampush, M Luciano, WD Hill, ...
Nature communications 9 (1), 1-16, 2018
3072018
Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism
B Lerer, RH Segman, H Fangerau, AK Daly, VS Basile, R Cavallaro, ...
Neuropsychopharmacology 27 (1), 105-119, 2002
2962002
Detection of the poor metabolizer-associated CYP2D6 (D) gene deletion allele by long-PCR technology.
VM Steen, OA Andreassen, AK Daly, T Tefre, AL Børresen, JR Idle, ...
Pharmacogenetics 5 (4), 215-223, 1995
2911995
A genome-wide association study of anorexia nervosa
V Boraska, CS Franklin, JAB Floyd, LM Thornton, LM Huckins, L Southam, ...
Molecular psychiatry 19 (10), 1085-1094, 2014
2902014
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
L Athanasiu, M Mattingsdal, AK Kähler, A Brown, O Gustafsson, I Agartz, ...
Journal of psychiatric research 44 (12), 748-753, 2010
2422010
Ultrarapid metabolizers of debrisoquine: characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene
R Løvlie, AK Daly, A Molven, JR Idle, VM Steen
Febs Letters 392 (1), 30-34, 1996
2421996
Novel genetic loci associated with hippocampal volume
DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ...
Nature communications 8 (1), 1-12, 2017
2012017
Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
T Lencz, E Knowles, G Davies, S Guha, DC Liewald, JM Starr, S Djurovic, ...
Molecular psychiatry 19 (2), 168-174, 2014
1982014
Obesity, dyslipidemia, and diabetes with selective serotonin reuptake inhibitors: the Hordaland Health Study.
MB Raeder, I Bjelland, SE Vollset, VM Steen
Journal of Clinical Psychiatry 67 (12), 1974-1982, 2006
1972006
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), 2020
1932020
Mutations in ABHD12 cause the neurodegenerative disease PHARC: an inborn error of endocannabinoid metabolism
T Fiskerstrand, DHB Brahim, S Johansson, A M'zahem, BI Haukanes, ...
The American Journal of Human Genetics 87 (3), 410-417, 2010
1892010
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Artikler 1–20