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M Neale

Showing results (271-280 of 551) with videos related to

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Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 4, 2005
An IL-7-dependent rebound in thymic T cell output contributes to the bone loss induced by estrogen deficiencyMichaela Robbie Ryan, Rebecca Shepherd, Jennifer K Leavey, et al.
American Journal of Human Genetics|October 2, 2020
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2006
Proinsulin is encoded by an RNA splice variant in human blood myeloid cellsParth Narendran, Alana M Neale, Bo Han Lee, et al.
Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
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 Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2008
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studiesRichard J L Anney, Elaine Kenny, Colm T O'Dushlaine, et al.
American Journal of Human Genetics|March 11, 2014
An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseasesYingleong Chan, Elaine T Lim, Niina Sandholm, et al.
Science (New York, N.Y.)|March 30, 2023
Analysis of genetic dominance in the UK BiobankDuncan S Palmer, Wei Zhou, Liam Abbott, et al.
Pageof 56

Showing results (271-280 of 551) with videos related to

Sort By:
Pageof 56
Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 4, 2005
An IL-7-dependent rebound in thymic T cell output contributes to the bone loss induced by estrogen deficiencyMichaela Robbie Ryan, Rebecca Shepherd, Jennifer K Leavey, et al.
American Journal of Human Genetics|October 2, 2020
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2006
Proinsulin is encoded by an RNA splice variant in human blood myeloid cellsParth Narendran, Alana M Neale, Bo Han Lee, et al.
Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
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 Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2008
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studiesRichard J L Anney, Elaine Kenny, Colm T O'Dushlaine, et al.
American Journal of Human Genetics|March 11, 2014
An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseasesYingleong Chan, Elaine T Lim, Niina Sandholm, et al.
Science (New York, N.Y.)|March 30, 2023
Analysis of genetic dominance in the UK BiobankDuncan S Palmer, Wei Zhou, Liam Abbott, et al.
Pageof 56