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Nature Medicine
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January 23, 2021
Author Correction: The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature Medicine
|
May 29, 2020
The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Gastroenterology
|
August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition
Dalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Nature
|
June 8, 2007
Replicating genotype-phenotype associations
, Stephen J Chanock, Teri Manolio, et al.
Science (New York, N.Y.)
|
January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature Communications
|
June 27, 2022
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, 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.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
Benjamin M Neale, Sarah E Medland, Stephan Ripke, et al.
Nature Communications
|
December 17, 2021
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer
Wei Zhou, Ben Brumpton, Omer Kabil, et al.
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of 15
Search research articles
Search
Showing results (121-130 of 149) with videos related to
Sort By:
Page
of 15
Nature Medicine
|
January 23, 2021
Author Correction: The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature Medicine
|
May 29, 2020
The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Gastroenterology
|
August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition
Dalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Nature
|
June 8, 2007
Replicating genotype-phenotype associations
, Stephen J Chanock, Teri Manolio, et al.
Science (New York, N.Y.)
|
January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature Communications
|
June 27, 2022
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, 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.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
Benjamin M Neale, Sarah E Medland, Stephan Ripke, et al.
Nature Communications
|
December 17, 2021
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer
Wei Zhou, Ben Brumpton, Omer Kabil, et al.
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of 15