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Personalized Medicine|October 7, 2020
Engaging community stakeholders in research on best practices for clinical genomic sequencingIda Griesemer, Brooke S Staley, Alexandra F Lightfoot, et al.European Heart Journal|April 10, 2024
Invasive vs. conservative management of older patients with non-ST-elevation acute coronary syndrome: individual patient data meta-analysisChristos P Kotanidis, Gregory B Mills, Bjørn Bendz, et al.JACC. Heart Failure|June 27, 2024
Randomized Trial of Cholesterol Lowering With Evolocumab for Cardiac Allograft Vasculopathy in Heart Transplant RecipientsKaspar Broch, Karl B Lemström, Finn Gustafsson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findingsKurt D Christensen, Barbara A Bernhardt, Gail P Jarvik, et al.Schizophrenia Research|September 18, 2020
Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndromeMatthew K Harner, Maya Lichtenstein, Martilias Farrell, et al.Nature Genetics|December 6, 2011
Dnmt3a is essential for hematopoietic stem cell differentiationGrant A Challen, Deqiang Sun, Mira Jeong, et al.Translational Psychiatry|February 19, 2020
Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literatureMartilias Farrell, Maya Lichtenstein, Matthew K Harner, et al.Journal of Clinical and Translational Science|April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research coreKimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.Circulation. Cardiovascular Genetics|June 15, 2017
Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular DiseaseGloria T Haskell, Brian C Jensen, Leigh Ann Samsa, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 22, 2013
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencingRobert C Green, Jonathan S Berg, Wayne W Grody, et al.Pageof 56