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The Journal of Clinical Investigation|January 27, 2015
Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminusMarta Byrska-Bishop, Daniel VanDorn, Amy E Campbell, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 10, 2012
Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cellsStella T Chou, Marta Byrska-Bishop, Joanna M Tober, et al.
Nature Genetics|July 27, 2021
Recent ultra-rare inherited variants implicate new autism candidate risk genesAmy B Wilfert, Tychele N Turner, Shwetha C Murali, et al.
Cell|September 2, 2022
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosMarta Byrska-Bishop, Uday S Evani, Xuefang Zhao, et al.
Nature Biotechnology|September 10, 2021
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing StudyJonathan Foox, Scott W Tighe, Charles M Nicolet, et al.
Iscience|January 17, 2022
Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19Nikhil Shri Sahajpal, Chi-Yu Jill Lai, Alex Hastie, et al.
Nature Communications|January 8, 2025
Small variant benchmark from a complete assembly of X and Y chromosomesJustin Wagner, Nathan D Olson, Jennifer McDaniel, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discoveryJack Humphrey, Ali Oku, Marta Byrska-Bishop, et al.
Human Genomics|July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autismEvin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.
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