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Pediatric Diabetes|January 8, 2022
Improved genetic risk scoring algorithm for type 1 diabetes predictionHui-Qi Qu, Jingchun Qu, Joseph Glessner, et al.
Scientific Reports|August 7, 2021
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patientsJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Communications Biology|July 24, 2021
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported lociHui-Qi Qu, Jingchun Qu, Jonathan Bradfield, et al.
BMC Genomics|May 19, 2022
Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approachYen-Chen A Feng, Ian B Stanaway, John J Connolly, et al.
Experimental Biology and Medicine (Maywood, N.J.)|September 2, 2025
Natural killer cell subpopulations in the peripheral blood of single ventricle/hypoplastic left heart syndrome patients via single-cell RNA sequencingHui-Qi Qu, Kushagra Goel, Kayleigh Ostberg, et al.
American Journal of Human Genetics|June 21, 2023
Studying the impact of translational genomic research: Lessons from eMERGEEllen Wright Clayton, Maureen E Smith, Katherine C Anderson, et al.
Applied Clinical Informatics|May 12, 2021
Infobuttons for Genomic Medicine: Requirements and BarriersLuke V Rasmussen, John J Connolly, Guilherme Del Fiol, et al.
BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.
Neuropsychology|January 19, 2012
Age group and sex differences in performance on a computerized neurocognitive battery in children age 8-21Ruben C Gur, Jan Richard, Monica E Calkins, et al.
Journal of Personalized Medicine|June 2, 2021
Preferences for Updates on General Research Results: A Survey of Participants in Genomic Research from Two InstitutionsCasey Overby Taylor, Natalie Flaks Manov, Katherine D Crew, et al.
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