Asodu Sandeep Sarma

3PUBLICATIONS
156CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesGene mapping
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Publications (3)

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|Sep 30, 2026
A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Mar 21, 2023
A novel homozygous synonymous splicing variant in SELENOI gene causes spastic paraplegia 81.

Asodu Sandeep Sarma, Bathula Siddardha, Pragna Lakshmi T

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Frequent Collaborators

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Dror Sharon

1 joint publications

Bathula Siddardha

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Prajnya Ranganath

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Ashwin Dalal

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Mathieu Quinodoz

1 joint publications

Kim Rodenburg

1 joint publications

Zuzana Cvackova

1 joint publications

Karolina Kaminska

1 joint publications

Suzanne E de Bruijn

1 joint publications

Ana Belén Iglesias-Romero

Frequent Collaborators

2 joint publications

Dror Sharon

1 joint publications

Bathula Siddardha

1 joint publications

Prajnya Ranganath

1 joint publications

Ashwin Dalal

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