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Nature Neuroscience|December 9, 2022
Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genesJack Humphrey, Sanan Venkatesh, Rahat Hasan, et al.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.Pageof 3