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American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2026
A scalable approach to resolving variants of uncertain significance
Malvika Tejura, Yile Chen, Abbye E McEwen, et al.
Cell Genomics
|
November 1, 2024
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
Victor Borda, Douglas P Loesch, Bing Guo, et al.
Science Advances
|
May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes
Joshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Nature Communications
|
December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Jonas B Nielsen, Oren Rom, Ida Surakka, et al.
Nature Communications
|
May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
Science Advances
|
April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Tetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.
Nature
|
October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature
|
March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Page
of 18
Search research articles
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Showing results (161-170 of 172) with videos related to
Sort By:
Page
of 18
American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2026
A scalable approach to resolving variants of uncertain significance
Malvika Tejura, Yile Chen, Abbye E McEwen, et al.
Cell Genomics
|
November 1, 2024
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
Victor Borda, Douglas P Loesch, Bing Guo, et al.
Science Advances
|
May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes
Joshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Nature Communications
|
December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Jonas B Nielsen, Oren Rom, Ida Surakka, et al.
Nature Communications
|
May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
Science Advances
|
April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Tetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.
Nature
|
October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature
|
March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Page
of 18