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Alison R Barton

Showing results (1-10 of 18) with videos related to

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Nature Genetics|July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analysesAlison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature|February 19, 2025
Insufficient evidence for natural selection associated with the Black DeathAlison R Barton, Cindy G Santander, Pontus Skoglund, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Insufficient evidence for natural selection associated with the Black DeathAlison R Barton, Cindy G Santander, Pontus Skoglund, et al.
American Journal of Human Genetics|June 1, 2022
A spectrum of recessiveness among Mendelian disease variants in UK BiobankAlison R Barton, Margaux L A Hujoel, Ronen E Mukamel, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Science (New York, N.Y.)|September 23, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Nucleic Acids Research|November 30, 2017
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimationMaxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Cell|October 28, 2022
Influences of rare copy-number variation on human complex traitsMargaux L A Hujoel, Maxwell A Sherman, Alison R Barton, et al.
Cell|August 1, 2023
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancerRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Nature Genetics|March 29, 2024
Protein-altering variants at copy number-variable regions influence diverse human phenotypesMargaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Nature Genetics|July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analysesAlison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature|February 19, 2025
Insufficient evidence for natural selection associated with the Black DeathAlison R Barton, Cindy G Santander, Pontus Skoglund, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Insufficient evidence for natural selection associated with the Black DeathAlison R Barton, Cindy G Santander, Pontus Skoglund, et al.
American Journal of Human Genetics|June 1, 2022
A spectrum of recessiveness among Mendelian disease variants in UK BiobankAlison R Barton, Margaux L A Hujoel, Ronen E Mukamel, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Science (New York, N.Y.)|September 23, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Nucleic Acids Research|November 30, 2017
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimationMaxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Cell|October 28, 2022
Influences of rare copy-number variation on human complex traitsMargaux L A Hujoel, Maxwell A Sherman, Alison R Barton, et al.
Cell|August 1, 2023
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancerRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Nature Genetics|March 29, 2024
Protein-altering variants at copy number-variable regions influence diverse human phenotypesMargaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.
Pageof 2