Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders

Frankel, E., Podder, A., Sharifi, M., Pillai, R., Belnap, N., Ramsey, K., Dodson, J., Venugopal, P., Brzezinski, M., Llaci, L., Gerald, B., Mills, G., Sanchez-Castillo, M., Balak, C. D., Szelinger, S., Jepsen, W. M., Siniard, A. L., Richholt, R., Naymik, M., … Rangasamy, S. (2023). Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders. Cells, 12(10), 1437. https://doi.org/10.3390/cells12101437
Authors:
Eric Frankel
Avijit Podder
Megan Sharifi
Roshan Pillai
Newell Belnap
Keri Ramsey
Julian J. Dodson
Pooja Venugopal
Molly Brzezinski
Lorida Llaci
Brittany Gerald
Gabrielle Mills
Meredith Sanchez‐Castillo
Chris Balak
Szabolcs Szelinger
Wayne M. Jepsen
Ashley L. Siniard
Ryan Richholt
Marcus Naymik
Isabelle Schrauwen
David W. Craig
Ignazio S. Piras
Matthew J. Huentelman
Nicholas J. Schork
Vinodh Narayanan
Sampathkumar Rangasamy
Affiliated Authors:
Isabelle Schrauwen
Columbia Affiliation:
Subjects:
Rett Syndrome (MeSH)
Neurodevelopmental Disorders (MeSH)
Molecular Basis of Rett Syndrome and Related Disorders (OpenAlex Topic)
Autism Spectrum Disorders (OpenAlex Topic)
Epigenetic Modifications and Their Functional Implications (OpenAlex Topic)
Author Keywords:
atypical rtt syndrome
methyl-cpg-binding protein 2
neurodevelopmental disorders
overlapping phenotype
protein–protein interaction network
rett syndrome
rett-syndrome-like phenotype
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Publication Type:
Article
Unique ID:
10.3390/cells12101437
PMID:
37408271
DOI:
10.3390/cells12101437
Journal:
Cells
Publication Date:
Data Source:
OpenAlex
Source Link:
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