Search research articles
Contact Us
Filters
Showing results (281-290 of 370) with videos related to
Page
of 37
Sort By:
The Lancet. Diabetes & Endocrinology
|
December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
Amand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
Biological Psychiatry
|
February 5, 2015
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium
Stéphanie Debette, Carla A Ibrahim Verbaas, Jan Bressler, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 15, 2024
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
Nora I Strom, Brad Verhulst, Silviu-Alin Bacanu, et al.
JAMA Psychiatry
|
October 31, 2019
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
, Dennis van der Meer, Ida E Sønderby, et al.
Circulation
|
August 24, 2013
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Maria Sabater-Lleal, Jie Huang, Daniel Chasman, et al.
Journal of the American Society of Nephrology : JASN
|
September 14, 2013
Common variants in Mendelian kidney disease genes and their association with renal function
Afshin Parsa, Christian Fuchsberger, Anna Köttgen, et al.
Archives of General Psychiatry
|
August 8, 2012
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers
Sarah M Hartz, Susan E Short, Nancy L Saccone, et al.
Nature Communications
|
January 30, 2024
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Rosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, et al.
Nature Communications
|
January 11, 2020
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia Shah, Albert Henry, Carolina Roselli, et al.
Nature Genetics
|
April 30, 2024
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Jacob M Keaton, Zoha Kamali, Tian Xie, et al.
Page
of 37
Search research articles
Search
Showing results (281-290 of 370) with videos related to
Sort By:
Page
of 37
The Lancet. Diabetes & Endocrinology
|
December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
Amand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
Biological Psychiatry
|
February 5, 2015
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium
Stéphanie Debette, Carla A Ibrahim Verbaas, Jan Bressler, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 15, 2024
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
Nora I Strom, Brad Verhulst, Silviu-Alin Bacanu, et al.
JAMA Psychiatry
|
October 31, 2019
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
, Dennis van der Meer, Ida E Sønderby, et al.
Circulation
|
August 24, 2013
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Maria Sabater-Lleal, Jie Huang, Daniel Chasman, et al.
Journal of the American Society of Nephrology : JASN
|
September 14, 2013
Common variants in Mendelian kidney disease genes and their association with renal function
Afshin Parsa, Christian Fuchsberger, Anna Köttgen, et al.
Archives of General Psychiatry
|
August 8, 2012
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers
Sarah M Hartz, Susan E Short, Nancy L Saccone, et al.
Nature Communications
|
January 30, 2024
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Rosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, et al.
Nature Communications
|
January 11, 2020
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia Shah, Albert Henry, Carolina Roselli, et al.
Nature Genetics
|
April 30, 2024
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Jacob M Keaton, Zoha Kamali, Tian Xie, et al.
Page
of 37