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Jacqueline I Goldstein

Showing results (1-10 of 19) with videos related to

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Bioinformatics (Oxford, England)|December 24, 2024
The scalable variant call representation: enabling genetic analysis beyond one million genomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million GenomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Nature Genetics|September 17, 2013
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degenerationJohanna M Seddon, Yi Yu, Elizabeth C Miller, et al.
Bioinformatics (Oxford, England)|July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysisJacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Nature Genetics|January 5, 2024
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetesAmanda Elliott, Raymond K Walters, Matti Pirinen, et al.
Nature Genetics|May 16, 2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disordersDaniel J Weiner, Emilie M Wigdor, Stephan Ripke, et al.
Nature Genetics|September 18, 2025
Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effectsKonrad J Karczewski, Rahul Gupta, Masahiro Kanai, et al.
Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomesKatherine R Chao, Lily Wang, Ruchit Panchal, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|December 24, 2024
The scalable variant call representation: enabling genetic analysis beyond one million genomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million GenomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Nature Genetics|September 17, 2013
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degenerationJohanna M Seddon, Yi Yu, Elizabeth C Miller, et al.
Bioinformatics (Oxford, England)|July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysisJacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Nature Genetics|January 5, 2024
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetesAmanda Elliott, Raymond K Walters, Matti Pirinen, et al.
Nature Genetics|May 16, 2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disordersDaniel J Weiner, Emilie M Wigdor, Stephan Ripke, et al.
Nature Genetics|September 18, 2025
Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effectsKonrad J Karczewski, Rahul Gupta, Masahiro Kanai, et al.
Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomesKatherine R Chao, Lily Wang, Ruchit Panchal, et al.
Pageof 2