Pritha Bisarad

5PUBLICATIONS

46CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsNeurology and neuromuscular diseasesInfant and child healthBiomolecular modelling and design

Get your video featured.

Publish with JoVE

Get your video featured.

Publish with JoVE

Publications (5)

Sort by Publication Date:

|Jul 16, 2026

Heterozygous RNF13 Truncating Variants Are Associated With Developmental and Epileptic Encephalopathy.

|Mar 20, 2026

Expanding the Phenotypic Spectrum of the Recurrent De Novo FBXO31 p.Asp334Asn Variant: Evidence for a Novel Neurodevelopmental Disorder (Kruer Syndrome).

Carolina I Galaz-Montoya, Sara A Lewis, Maureen K Galindo

|Nov 24, 2025

Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.

Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore

|Sep 21, 2024

Novel KIF26A variants associated with pediatric intestinal pseudo-obstruction (PIPO) and brain developmental defects.

Mohammad Sadegh Shams Nosrati, Alireza Doustmohammadi, Mariasavina Severino

|Aug 12, 2024

Predicting monoclonal antibody binding sequences from a sparse sampling of all possible sequences.

Pritha Bisarad, Laimonas Kelbauskas, Akanksha Singh

Pageof 1

Frequent Collaborators

Peter T Skidmore

Akanksha Singh

Alexander T Taguchi

Neal W Woodbury

Mahdi Zafari

Alexander Joachim

Marcello Scala

Yung-Chun Wang

Carolina I Galaz-Montoya

1 joint publications

Sara A Lewis

Frequent Collaborators

Peter T Skidmore

Akanksha Singh

Alexander T Taguchi

Neal W Woodbury