Suma P Shankar

7PUBLICATIONS
46CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Other Asian languages (excl. South-East Asian)Cancer geneticsOptical technologyDevelopmental genetics (incl. sex determination)
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Publications (7)

|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour

|Apr 13, 2023
Prader-Willi and Angelman Syndromes: Mechanisms and Management.

Van K Ma, Rong Mao, Jessica N Toth

|Aug 05, 2022
Atypical presentation of Angelman syndrome with intact expressive language due to low-level mosaicism.

Ruchi Punatar, Alena Egense, Rong Mao

|Oct 06, 2021
Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development.

Suma P Shankar, Reshmitha Fallurin, Tonya Watson

|Jan 12, 2021
The evolving role of genetics in ophthalmology.

Natario L Couser, Brian P Brooks, Arlene V Drack

|Jul 29, 2018
Is exon 8 the most critical or the only dispensable exon of the VCAN gene? Insights into VCAN variants and clinical spectrum of Wagner syndrome.

Arunkanth Ankala, Nieraj Jain, Baker Hubbard

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