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Nature Immunology
|
January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function
Taja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, 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.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing
Alba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
The New England Journal of Medicine
|
June 5, 2024
Genome Sequencing for Diagnosing Rare Diseases
Monica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Research Square
|
February 13, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Cell
|
September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Cell
|
September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Ming-Huei Chen, Laura M Raffield, Abdou Mousas, 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.
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of 24
Search research articles
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Showing results (231-240 of 240) with videos related to
Sort By:
Page
of 24
You have reached the last page of results.
This site can display upto 240 results.
Nature Immunology
|
January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function
Taja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, 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.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing
Alba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
The New England Journal of Medicine
|
June 5, 2024
Genome Sequencing for Diagnosing Rare Diseases
Monica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Research Square
|
February 13, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Cell
|
September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Cell
|
September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Ming-Huei Chen, Laura M Raffield, Abdou Mousas, 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 24