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Nature
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April 8, 2026
Population-scale repeat expansions elucidate disease risk and brain atrophy
Vijay Kumar Pounraja, Jae Hoon Sul, Joseph Herman, et al.
Iscience
|
January 17, 2022
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry
Nicholas W Bateman, Christopher M Tarney, Tamara S Abulez, et al.
Science (New York, N.Y.)
|
December 14, 2011
A SUMOylation-dependent transcriptional subprogram is required for Myc-driven tumorigenesis
Jessica D Kessler, Kristopher T Kahle, Tingting Sun, et al.
Cell
|
March 8, 2011
Activation of multiple proto-oncogenic tyrosine kinases in breast cancer via loss of the PTPN12 phosphatase
Tingting Sun, Nicola Aceto, Kristen L Meerbrey, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individuals
Jack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 2020
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population
Michael D Kessler, Douglas P Loesch, James A Perry, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
Biorxiv : the Preprint Server for Biology
|
May 22, 2023
A deep catalog of protein-coding variation in 985,830 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participants
Joshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Nature
|
May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Page
of 23
Search research articles
Search
Showing results (211-220 of 229) with videos related to
Sort By:
Page
of 23
Nature
|
April 8, 2026
Population-scale repeat expansions elucidate disease risk and brain atrophy
Vijay Kumar Pounraja, Jae Hoon Sul, Joseph Herman, et al.
Iscience
|
January 17, 2022
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry
Nicholas W Bateman, Christopher M Tarney, Tamara S Abulez, et al.
Science (New York, N.Y.)
|
December 14, 2011
A SUMOylation-dependent transcriptional subprogram is required for Myc-driven tumorigenesis
Jessica D Kessler, Kristopher T Kahle, Tingting Sun, et al.
Cell
|
March 8, 2011
Activation of multiple proto-oncogenic tyrosine kinases in breast cancer via loss of the PTPN12 phosphatase
Tingting Sun, Nicola Aceto, Kristen L Meerbrey, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individuals
Jack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 2020
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population
Michael D Kessler, Douglas P Loesch, James A Perry, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
Biorxiv : the Preprint Server for Biology
|
May 22, 2023
A deep catalog of protein-coding variation in 985,830 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participants
Joshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Nature
|
May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Page
of 23