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Alyssa Ritter

17PUBLICATIONS

91CO-AUTHORS

NeurogeneticsCardiology (incl. cardiovascular diseases)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Molecular targets

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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 <i>ANKRD11</i> 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

Frequent Collaborators

7 joint publications

Kosuke Izumi

5 joint publications

Emma C Bedoukian

4 joint publications

Elizabeth Bhoj

2 joint publications

Elizabeth Goldmuntz

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