Alyssa Ritter

18PUBLICATIONS
108CO-AUTHORS
Gene mappingNeurogeneticsCardiology (incl. cardiovascular diseases)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (18)

|Aug 26, 2026
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

|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

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Frequent Collaborators

8 joint publications

Kosuke Izumi

5 joint publications

Emma C Bedoukian

4 joint publications

Elizabeth Bhoj

2 joint publications

Elizabeth Goldmuntz