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Benjamin M Neale

Showing results (81-90 of 293) with videos related to

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Cell Genomics|June 29, 2024
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK BiobankFrederik H Lassen, Samvida S Venkatesh, Nikolas Baya, et al.
American Journal of Human Genetics|March 28, 2017
Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human TissuesXuanyao Liu, Hilary K Finucane, Alexander Gusev, et al.
Frontiers in Genetics|February 9, 2023
Ancestry: How researchers use it and what they mean by itBege Dauda, Santiago J Molina, Danielle S Allen, et al.
Nature Genetics|July 6, 2019
Author Correction: Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selectionSteven Gazal, Hilary K Finucane, Nicholas A Furlotte, et al.
Nature Human Behaviour|June 29, 2023
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic lociGianmarco Mignogna, Caitlin E Carey, Robbee Wedow, et al.
Nature Genetics|September 12, 2017
Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selectionSteven Gazal, Hilary K Finucane, Nicholas A Furlotte, et al.
Scientific Reports|September 26, 2020
A data-driven medication score predicts 10-year mortality among aging adultsPaavo Häppölä, Aki S Havulinna, Tõnis Tasa, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Efficient and accurate mixed model association tool for single-cell eQTL analysisWei Zhou, Anna S E Cuomo, Angli Xue, et al.
Cell Genomics|February 13, 2023
Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversityKristin Tsuo, Wei Zhou, Ying Wang, et al.
Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.
Pageof 30

Showing results (81-90 of 293) with videos related to

Sort By:
Pageof 30
Cell Genomics|June 29, 2024
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK BiobankFrederik H Lassen, Samvida S Venkatesh, Nikolas Baya, et al.
American Journal of Human Genetics|March 28, 2017
Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human TissuesXuanyao Liu, Hilary K Finucane, Alexander Gusev, et al.
Frontiers in Genetics|February 9, 2023
Ancestry: How researchers use it and what they mean by itBege Dauda, Santiago J Molina, Danielle S Allen, et al.
Nature Genetics|July 6, 2019
Author Correction: Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selectionSteven Gazal, Hilary K Finucane, Nicholas A Furlotte, et al.
Nature Human Behaviour|June 29, 2023
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic lociGianmarco Mignogna, Caitlin E Carey, Robbee Wedow, et al.
Nature Genetics|September 12, 2017
Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selectionSteven Gazal, Hilary K Finucane, Nicholas A Furlotte, et al.
Scientific Reports|September 26, 2020
A data-driven medication score predicts 10-year mortality among aging adultsPaavo Häppölä, Aki S Havulinna, Tõnis Tasa, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Efficient and accurate mixed model association tool for single-cell eQTL analysisWei Zhou, Anna S E Cuomo, Angli Xue, et al.
Cell Genomics|February 13, 2023
Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversityKristin Tsuo, Wei Zhou, Ying Wang, et al.
Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.
Pageof 30