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Biorxiv : the Preprint Server for Biology
|
April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays
Matthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Cell Metabolism
|
September 3, 2009
T lymphocytes amplify the anabolic activity of parathyroid hormone through Wnt10b signaling
Masakazu Terauchi, Jau-Yi Li, Brahmchetna Bedi, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder
Eric Mick, Alexandre Todorov, Susan Smalley, et al.
Nature Communications
|
December 14, 2025
Complex genetic effects linked to plasma protein abundance in the UK Biobank
Arnor I Sigurdsson, Justus F Gräf, Zhiyu Yang, et al.
Human Molecular Genetics
|
June 26, 2009
Common body mass index-associated variants confer risk of extreme obesity
Chris Cotsapas, Elizabeth K Speliotes, Ida J Hatoum, et al.
Human Molecular Genetics
|
January 8, 2016
Exome arrays capture polygenic rare variant contributions to schizophrenia
A L Richards, G Leonenko, J T Walters, et al.
Bioinformatics (Oxford, England)
|
July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysis
Jacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Biology of Sex Differences
|
March 29, 2025
The impact of childhood maltreatment, HIV status, and their interaction on mental health outcomes and markers of systemic inflammation in women
Amanda Arnold, Heqiong Wang, C Christina Mehta, et al.
Nature Genetics
|
February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics
|
April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
Alexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Page
of 56
Search research articles
Search
Showing results (351-360 of 551) with videos related to
Sort By:
Page
of 56
Biorxiv : the Preprint Server for Biology
|
April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays
Matthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Cell Metabolism
|
September 3, 2009
T lymphocytes amplify the anabolic activity of parathyroid hormone through Wnt10b signaling
Masakazu Terauchi, Jau-Yi Li, Brahmchetna Bedi, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder
Eric Mick, Alexandre Todorov, Susan Smalley, et al.
Nature Communications
|
December 14, 2025
Complex genetic effects linked to plasma protein abundance in the UK Biobank
Arnor I Sigurdsson, Justus F Gräf, Zhiyu Yang, et al.
Human Molecular Genetics
|
June 26, 2009
Common body mass index-associated variants confer risk of extreme obesity
Chris Cotsapas, Elizabeth K Speliotes, Ida J Hatoum, et al.
Human Molecular Genetics
|
January 8, 2016
Exome arrays capture polygenic rare variant contributions to schizophrenia
A L Richards, G Leonenko, J T Walters, et al.
Bioinformatics (Oxford, England)
|
July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysis
Jacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Biology of Sex Differences
|
March 29, 2025
The impact of childhood maltreatment, HIV status, and their interaction on mental health outcomes and markers of systemic inflammation in women
Amanda Arnold, Heqiong Wang, C Christina Mehta, et al.
Nature Genetics
|
February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics
|
April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
Alexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Page
of 56