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Research Square|November 24, 2025
Expanding the Genetic Landscape of Craniofacial Anomalies Through Transcriptome-Wide Association StudiesElly Brokamp, Alexandra Scalici, Tyne Miller-Fleming, et al.Lupus Science & Medicine|November 14, 2022
Ancestry, ACKR1 and leucopenia in patients with systemic lupus erythematosusCecilia P Chung, Gul Karakoc, Ge Liu, et al.Plos One|November 17, 2015
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, TexasEric L Brown, Jennifer E Below, Rebecca S B Fischer, et al.Journal of the American Heart Association|May 15, 2025
Circulating Proteomics Identifies a Dynamic Profile of Hepatic Steatosis During Metabolic InterventionBassim El-Sabawi, Kahraman Tanriverdi, Priya Gajjar, et al.The Journal of Infectious Diseases|October 31, 2002
Intercontinental circulation of human influenza A(H1N2) reassortant viruses during the 2001-2002 influenza seasonXiyan Xu, Catherine B Smith, Bruce A Mungall, et al.Cell Genomics|November 7, 2022
Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies: Lessons from the Global Biobank Meta-analysis InitiativeArjun Bhattacharya, Jibril B Hirbo, Dan Zhou, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autismSoo-Jeong Kim, Camille W Brune, Emily O Kistner, et al.The Journal of Clinical Endocrinology and Metabolism|April 5, 2002
Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndromeDavid A Ehrmann, Peter E H Schwarz, Manami Hara, et al.Pharmacogenomics|April 21, 2009
Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell linesShiwei Duan, R Stephanie Huang, Wei Zhang, et al.Research Square|October 4, 2023
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT SyndromeMegan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.Pageof 52