Seema R Lalani

21PUBLICATIONS
96CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Autonomic nervous systemNeurology and neuromuscular diseasesMajor global burdens of disease
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Publications (21)

|Aug 26, 2026
Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

|Sep 09, 2024
Project GIVE: using a virtual genetics service platform to reduce health inequities and improve access to genomic care in an underserved region of Texas.

Blake Vuocolo, Roberta Sierra, Daniel Brooks

|Jul 02, 2024
Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.

Adam S Potter, Christina Y Miyake, Claudia Gonzaga-Jauregui

|Apr 22, 2024
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim

|Mar 28, 2024
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis.

Christian M Parobek, Roni Zemet, Matthew A Shanahan

|Mar 12, 2024
Intracranial calcifications simulating Aicardi-Goutières syndrome in PARS2-related mitochondrial disease.

Amanda Gerard, Elizabeth Mizerik, Carrie A Mohila

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Frequent Collaborators

6 joint publications

Daryl A Scott

4 joint publications

Jill A Rosenfeld

3 joint publications

Pengfei Liu

3 joint publications

Lindsay C Burrage