Pritha Bisarad

5PUBLICATIONS
46CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsNeurology and neuromuscular diseasesInfant and child healthBiomolecular modelling and design
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Publications (5)

|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

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Frequent Collaborators

2 joint publications

Peter T Skidmore

1 joint publications

Akanksha Singh

1 joint publications

Alexander T Taguchi

1 joint publications

Neal W Woodbury