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Behavior Genetics|June 7, 2008
Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriersJessica Ezzell Hunter, Emily Graves Allen, Ann Abramowitz, et al.Journal of Genetic Counseling|October 15, 2025
Patient-initiated lifestyle changes following receipt of genetic test results in a predominantly marginalized populationMarian J Gilmore, Hannah E Frawley, Elizabeth Shuster, et al.Frontiers in Psychiatry|October 18, 2021
Predictors of Comorbid Conditions in Women Who Carry an <i>FMR1</i> PremutationEmily Graves Allen, Krista Charen, Heather S Hipp, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2019
Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disordersRyan S Paquin, Kathleen F Mittendorf, Megan A Lewis, et al.Hereditary Cancer in Clinical Practice|April 19, 2022
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare systemPhilip R Crain, Jamilyn M Zepp, Sara Gille, et al.Journal of Patient-Centered Research and Reviews|November 7, 2022
Should Health Systems Share Genetic Findings With At-Risk Relatives When the Proband Is Deceased? Interviews With Individuals Diagnosed With Lynch SyndromeJessica Ezzell Hunter, Jennifer L Schneider, Alison J Firemark, et al.Journal of Genetic Counseling|July 17, 2025
Primary care patient and clinician attitudes about population genomic screening, informed decision-making needs, and the potential for Chatbot technologyRebecca R Moultrie, Sara M Andrews, Kristi M Williams, et al.The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|March 8, 2023
An Examination of the Ethical and Legal Limits in Implementing "Traceback Testing" for Deceased PatientsJessica Martucci, Yolanda Prado, Alan F Rope, et al.Plos One|April 2, 2011
Evaluating gene expression in C57BL/6J and DBA/2J mouse striatum using RNA-Seq and microarraysDaniel Bottomly, Nicole A R Walter, Jessica Ezzell Hunter, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 11, 2012
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphismsJessica Ezzell Hunter, Mary Leslie, Gloria Novak, et al.Pageof 5