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Human Genomics|May 26, 2020
Gene X environment: the cellular environment governs the transcriptional response to environmental chemicalsAndreanna Burman, Rolando Garcia-Milian, Shannon WhirledgeHuman Genomics|August 5, 2022
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variantsAnjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, et al.Human Genomics|August 22, 2022
SCP2 variant is associated with alterations in lipid metabolism, brainstem neurodegeneration, and testicular defectsMelanie Galano, Shereen Ezzat, Vassilios PapadopoulosHuman Genomics|May 8, 2021
An application of slow feature analysis to the genetic sequences of coronaviruses and influenza virusesAnastasios A Tsonis, Geli Wang, Lvyi Zhang, et al.Human Genomics|June 10, 2015
Complement regulator CD46: genetic variants and disease associationsM Kathryn Liszewski, John P AtkinsonHuman Genomics|June 25, 2015
Genomics in the renal clinic - translating nephrogenetics for clinical practiceAndrew Mallett, Christopher Corney, Hugh McCarthy, et al.Human Genomics|June 17, 2015
Clinical application of next-generation sequencing for Mendelian diseasesSaumya Shekhar Jamuar, Ene-Choo TanHuman Genomics|June 7, 2020
Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in ChinaYanhui Liu, Hailiang Liu, Yi He, et al.Human Genomics|June 12, 2020
Whole-genome sequencing of Chinese centenarians reveals important genetic variants in aging WGS of centenarian for genetic analysis of agingShuhua Shen, Chao Li, Luwei Xiao, et al.Human Genomics|November 11, 2022
De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathiesNirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, et al.Pageof 112