Last Updated: 09/26/2026
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Found 77 publications
Perceptions of family health history in an East Baltimore community.
Journal: Journal of community genetics
Published: January 27, 2025
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 13, 2025
The 2023 medical genetics workforce in the United States.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 24, 2024
Community-driven partnerships with Community-Engaged Research teams bring resources and reliable information to Baltimore residents.
Journal: Journal of clinical and translational science
Published: December 31, 2023
Palliative care and genetics: personalized medicine for the patient and family.
Journal: European journal of human genetics : EJHG
Published: July 24, 2023
Feasibility of the Genetic Information Assistant Chatbot to Provide Genetic Education and Study Genetic Test Adoption Among Pancreatic Cancer Patients at Johns Hopkins Hospital.
Journal: AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science
Published: June 23, 2023
Latina immigrants' breast and colon cancer causal attributions: genetics is key.
Journal: Journal of community genetics
Published: February 02, 2023
Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndrome.
Journal: Journal of child health care : for professionals working with children in the hospital and community
Published: September 21, 2022
The 2019 medical genetics workforce: A focus on laboratory geneticists.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 06, 2022
Vascular aneurysms in Ehlers-Danlos syndrome subtypes: A systematic review.
Journal: Clinical genetics
Published: July 27, 2022
Successful Treatment of Refractory Orthostatic Intolerance (OI) With Droxidopa.
Journal: Clinical pediatrics
Published: June 09, 2022
Case report of bilateral ovarian fibromas associated with de novo germline variants in PTCH1 and SMARCA4.
Journal: Molecular genetics & genomic medicine
Published: April 11, 2022
Last Updated: 09/26/2026