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Genome Medicine|January 18, 2022
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelinesChristine G Preston, Matt W Wright, Rao Madhavrao, et al.Contemporary Clinical Trials|August 11, 2019
Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness studyXin Niu, Laura M Amendola, Ragan Hart, et al.Nature Genetics|November 25, 2025
Recommendations for responsible use of population descriptors in polygenic risk score developmentJohanna L Smith, Clement A Adebamowo, Sally N Adebamowo, et al.AJOB Empirical Bioethics|September 22, 2018
Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental surveyArmand H Matheny Antommaria, Kyle B Brothers, John A Myers, et al.American Journal of Human Genetics|May 13, 2014
Return of genomic results to research participants: the floor, the ceiling, and the choices in betweenGail P Jarvik, Laura M Amendola, Jonathan S Berg, et al.American Journal of Human Genetics|April 30, 2026
Navigating data sharing in researchAnna C F Lewis, Ellen W Clayton, Hana Bangash, et al.American Journal of Human Genetics|May 21, 2019
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine ResearchCarol R Horowitz, Lori A Orlando, Anne M Slavotinek, et al.BMC Medical Research Methodology|November 25, 2016
Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutionsMaureen E Smith, Saskia C Sanderson, Kyle B Brothers, et al.American Journal of Human Genetics|April 30, 2024
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE NetworkAnna C F Lewis, Rex L Chisholm, John J Connolly, et al.Nature|April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversityTing Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.Pageof 14