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Clinical and Translational Medicine|June 20, 2023
Trans-ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium studyHui-Qi Qu, John J Connolly, Peter Kraft, et al.
Nature Genetics|June 2, 2009
Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancerPeter A Kanetsky, Nandita Mitra, Saran Vardhanabhuti, et al.
Ebiomedicine|February 19, 2026
Interstitial cystitis: a phenotype and rare variant exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Plos One|November 17, 2022
Childhood exposures to environmental chemicals and neurodevelopmental outcomes in congenital heart diseaseJ William Gaynor, Nancy B Burnham, Richard F Ittenbach, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium StudyHuiqi Qu, John J Connolly, Peter Kraft, et al.
American Journal of Human Genetics|April 7, 2023
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsPankhuri Singhal, Yogasudha Veturi, Scott M Dudek, et al.
Pharmacogenetics and Genomics|August 12, 2021
Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel diseaseTanima De, Honghong Zhang, Cristina Alarcon, et al.
JIMD Reports|February 12, 2014
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J Falk, Dong Li, Xiaowu Gai, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 3, 2014
Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritisJustine A Ellis, Katrina J Scurrah, Yun R Li, et al.
JAMA Internal Medicine|June 28, 2021
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American PatientsSara L Van Driest, Noura S Abul-Husn, Joseph T Glessner, et al.
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