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Sampathkumar Rangasamy

7PUBLICATIONS
14CO-AUTHORS
NeurogeneticsAdolescent healthNeurology and neuromuscular diseasesGene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)
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Journal

Publications (7)

Sort by Publication Date:
|Jul 26, 2023
Inherited CSNK2A1 variants in families with Okur-Chung neurodevelopmental syndrome.

Newell Belnap, Aiai Price-Smith, Keri Ramsey

|Jul 06, 2023
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders.

Eric Frankel, Avijit Podder, Megan Sharifi

|Jan 07, 2022
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.

Keri Ramsey, Newell Belnap, Anna Bonfitto

|Aug 06, 2020
Congenital myasthenic syndrome caused by a frameshift insertion mutation in <i>GFPT1</i>.

Szabolcs Szelinger, Jonida Krate, Keri Ramsey

|Apr 17, 2020
Genotypes and Phenotypes: A Search for Influential Genes in Diabetic Retinopathy.

Andrea P Cabrera, Rushi N Mankad, Lauren Marek

|Jan 18, 2020
Do Genomic Factors Play a Role in Diabetic Retinopathy?

Andrea P Cabrera, Finny Monickaraj, Sampathkumar Rangasamy

Pageof 2

Frequent Collaborators

2 joint publications

Vinodh Narayanan

2 joint publications

Isabelle Schrauwen

2 joint publications

Matthew J Huentelman

1 joint publications

Keri Ramsey

1 joint publications

David W Craig

1 joint publications

Sam Hobbs

1 joint publications

Szabolcs Szelinger

1 joint publications

Chris Balak

1 joint publications

Steven A Moore

1 joint publications

Avijit Podder

Frequent Collaborators

2 joint publications

Vinodh Narayanan

2 joint publications

Isabelle Schrauwen

2 joint publications

Matthew J Huentelman

1 joint publications

Keri Ramsey

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