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Human Genetics|July 24, 2002
Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sampleStephanie M Fullerton, Andrew G Clark, Kenneth M Weiss, et al.Journal of the American Geriatrics Society|September 18, 2018
Cumulative Antidepressant Use and Risk of Dementia in a Prospective Cohort StudyLaura Heath, Shelly L Gray, Denise M Boudreau, et al.Plos One|August 25, 2018
Vitamin D levels, brain volume, and genetic architecture in patients with psychosisAkiah Ottesen Berg, Kjetil N Jørgensen, Mari Nerhus, et al.Molecular Genetics & Genomic Medicine|November 28, 2017
Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family RegistryMercy Y Laurino, Anjali R Truitt, Lederle Tenney, et al.Public Health Genomics|September 30, 2024
"I Didn't Have to Worry about It": Patient and Family Experiences with Health System Involvement in Notifying Relatives of Genetic Test ResultsPaula Rae Blasi, Jamilyn M Zepp, Aaron Scrol, et al.European Journal of Human Genetics : EJHG|September 26, 2023
Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patientsNandana D Rao, Kristine M King, Jailanie Kaganovsky, et al.American Journal of Human Genetics|March 14, 2002
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locusStephanie M Fullerton, Angelika Bartoszewicz, Gustavo Ybazeta, et al.The Yale Journal of Biology and Medicine|October 3, 2022
Targeting Representation: Interpreting Calls for Diversity in Precision Medicine ResearchSandra Soo-Jin Lee, Stephanie M Fullerton, Caitlin E McMahon, et al.Pilot and Feasibility Studies|August 9, 2022
Feasibility, acceptability, and limited efficacy of health system-led familial risk notification: protocol for a mixed-methods evaluationPaula R Blasi, Aaron Scrol, Melissa L Anderson, et al.Patient Education and Counseling|January 18, 2021
What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?Deborah J Bowen, Sukh Makhnoon, Brian H Shirts, et al.Pageof 14