Alyssa Ritter
17PUBLICATIONS
91CO-AUTHORS
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Publications (17)
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|May 26, 2025
Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay.Alanna Strong, Caoimhe McKenna, Karen Stals
|Apr 14, 2025
Evaluating the Utility of a New Pathogenicity Predictor for Pediatric Cardiomyopathy.Alyssa L Rippert, Sarah Trackman, Danielle Burstein
|Feb 26, 2025
16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome.Aiko Iwata-Otsubo, Alyssa L Rippert, Jorune Balciuniene
|Jul 27, 2024
Expanding Genetic Counselor Roles: A Model for Global Research Development.Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart
|May 01, 2023
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.Victoria Patterson, Farid Ullah, Laura Bryant
|Feb 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Emily L Griffin, Shannon N Nees, Sarah U Morton
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Frequent Collaborators
7 joint publications
Kosuke Izumi
5 joint publications
Emma C Bedoukian
4 joint publications
Elizabeth Bhoj
2 joint publications
Elizabeth Goldmuntz
2 joint publications
Antonio Vitobello
1 joint publications
Lydia Rockart
1 joint publications
T Blaine Crowley
1 joint publications
Natalie Burrill
1 joint publications
Mary Egan Clark
1 joint publications
Nicole M Engelhardt
