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Nature Genetics
|
July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
Alison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature
|
February 19, 2025
Insufficient evidence for natural selection associated with the Black Death
Alison 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 Death
Alison 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 Biobank
Alison 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 phenotypes
Ronen 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 phenotypes
Ronen 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 estimation
Maxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Cell
|
October 28, 2022
Influences of rare copy-number variation on human complex traits
Margaux 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 cancer
Ronen 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 phenotypes
Margaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.
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Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Nature Genetics
|
July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
Alison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature
|
February 19, 2025
Insufficient evidence for natural selection associated with the Black Death
Alison 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 Death
Alison 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 Biobank
Alison 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 phenotypes
Ronen 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 phenotypes
Ronen 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 estimation
Maxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Cell
|
October 28, 2022
Influences of rare copy-number variation on human complex traits
Margaux 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 cancer
Ronen 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 phenotypes
Margaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.
Page
of 2