Author

Balram Gangaram

University of California, San FranciscoORCID 0000-0003-1472-1397Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Boris KereniD· 2 shared Abbey Scott· 1 shared Abigail TurnwaldiD· 1 shared Adeline JacquinetiD· 1 shared Alejandro Iglesias· 1 shared Alexia BourgoisiD· 1 shared Allyn McConkie-Rosell· 1 shared Amanda Carnevale· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Boris KerenORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedMay 13, 2025

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder

María del Rocío Pérez Baca, María Palomares‐Bralo, Michiel Vanhooydonck…·Stephanie Baskin

This study identifies ZFHX4 loss-of-function variants as a cause of a neurodevelopmental disorder with distinctive facial features and brain abnormalities, supported by zebrafish models.

14 citationstop 2%

humanzebrafish

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Genetic & Genomic MedicinemedRxivPreprintJul 22, 2024

Adaptor protein 2 sigma subunit (AP2S1) variants associated with neurodevelopmental disorders

Mark Stevenson, Asha L. Bayliss, Victoria J. Stokes…·Rajesh V. Thakker

The paper identifies AP2S1 variants linked to neurodevelopmental disorders by showing they impair clathrin-mediated endocytosis and disrupt protein interactions.

1 citation

humanstatistical model

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