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Nature Communications
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February 21, 2018
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
Laura J Corbin, Vanessa Y Tan, David A Hughes, et al.
Nature Genetics
|
September 4, 2007
A common variant of HMGA2 is associated with adult and childhood height in the general population
Michael N Weedon, Guillaume Lettre, Rachel M Freathy, et al.
American Journal of Human Genetics
|
September 3, 2016
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Anubha Mahajan, Aylin R Rodan, Thu H Le, et al.
American Journal of Human Genetics
|
October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder
Michael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Nature Genetics
|
April 9, 2008
Genome-wide association analysis identifies 20 loci that influence adult height
Michael N Weedon, Hana Lango, Cecilia M Lindgren, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Nature Genetics
|
July 22, 2024
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Atherosclerosis
|
October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation
Rona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.
Science (New York, N.Y.)
|
April 17, 2007
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Timothy M Frayling, Nicholas J Timpson, Michael N Weedon, et al.
Plos Genetics
|
December 20, 2018
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
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of 62
Search research articles
Search
Showing results (271-280 of 619) with videos related to
Sort By:
Page
of 62
Nature Communications
|
February 21, 2018
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
Laura J Corbin, Vanessa Y Tan, David A Hughes, et al.
Nature Genetics
|
September 4, 2007
A common variant of HMGA2 is associated with adult and childhood height in the general population
Michael N Weedon, Guillaume Lettre, Rachel M Freathy, et al.
American Journal of Human Genetics
|
September 3, 2016
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Anubha Mahajan, Aylin R Rodan, Thu H Le, et al.
American Journal of Human Genetics
|
October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder
Michael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Nature Genetics
|
April 9, 2008
Genome-wide association analysis identifies 20 loci that influence adult height
Michael N Weedon, Hana Lango, Cecilia M Lindgren, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Nature Genetics
|
July 22, 2024
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Atherosclerosis
|
October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation
Rona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.
Science (New York, N.Y.)
|
April 17, 2007
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Timothy M Frayling, Nicholas J Timpson, Michael N Weedon, et al.
Plos Genetics
|
December 20, 2018
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
Page
of 62