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European Journal of Human Genetics : EJHG
|
March 31, 2011
Meta-analysis of genome-wide association for migraine in six population-based European cohorts
Lannie Ligthart, Boukje de Vries, Albert V Smith, et al.
Nature Genetics
|
October 6, 2009
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Fernando Rivadeneira, Unnur Styrkársdottir, Karol Estrada, et al.
Annals of Internal Medicine
|
October 21, 2009
Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture
J Brent Richards, Fotini K Kavvoura, Fernando Rivadeneira, et al.
Biological Psychiatry
|
October 23, 2019
Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls
Mariska Bot, Yuri Milaneschi, Tahani Al-Shehri, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 18, 2021
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants
Vincent Damotte, Sven J van der Lee, Vincent Chouraki, et al.
Circulation. Cardiovascular Genetics
|
December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk
Bing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
European Journal of Epidemiology
|
July 28, 2014
Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants
Linda Broer, Julia Raschenberger, Joris Deelen, et al.
Human Molecular Genetics
|
March 24, 2011
Common genetic variants associated with open-angle glaucoma
Wishal D Ramdas, Leonieke M E van Koolwijk, Hans G Lemij, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2025
A rare variant in <i>GPR156</i> associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice
Bradley R Miller, Claudia Gonzaga-Jauregui, Karlla W Brigatti, et al.
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Search research articles
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Showing results (101-110 of 263) with videos related to
Sort By:
Page
of 27
European Journal of Human Genetics : EJHG
|
March 31, 2011
Meta-analysis of genome-wide association for migraine in six population-based European cohorts
Lannie Ligthart, Boukje de Vries, Albert V Smith, et al.
Nature Genetics
|
October 6, 2009
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Fernando Rivadeneira, Unnur Styrkársdottir, Karol Estrada, et al.
Annals of Internal Medicine
|
October 21, 2009
Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture
J Brent Richards, Fotini K Kavvoura, Fernando Rivadeneira, et al.
Biological Psychiatry
|
October 23, 2019
Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls
Mariska Bot, Yuri Milaneschi, Tahani Al-Shehri, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 18, 2021
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants
Vincent Damotte, Sven J van der Lee, Vincent Chouraki, et al.
Circulation. Cardiovascular Genetics
|
December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk
Bing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
European Journal of Epidemiology
|
July 28, 2014
Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants
Linda Broer, Julia Raschenberger, Joris Deelen, et al.
Human Molecular Genetics
|
March 24, 2011
Common genetic variants associated with open-angle glaucoma
Wishal D Ramdas, Leonieke M E van Koolwijk, Hans G Lemij, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2025
A rare variant in <i>GPR156</i> associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice
Bradley R Miller, Claudia Gonzaga-Jauregui, Karlla W Brigatti, et al.
Page
of 27