Jariya Upadia

8PUBLICATIONS
5CO-AUTHORS
Disease surveillanceGene expression (incl. microarray and other genome-wide approaches)Personality and individual differencesImmunogenetics (incl. genetic immunology)Developmental genetics (incl. sex determination)
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Publications (8)

|Dec 24, 2025
Expanded Newborn Screening for Inborn Errors of Metabolism at a Single Center in Louisiana (2005-2024): Outcomes.

Jariya Upadia, Grace Noh, Kea Crivelly

|Jan 22, 2025
Diverse Clinical Presentation of RAC1-Related Intellectual Developmental Disorder.

Jariya Upadia, Jiao Liu, Caide Bier

|Jun 12, 2024
Subtelomeric microdeletion in chromosome 20p13 associated with short stature.

J Liu, Y Li, H C Andersson

|Mar 01, 2022
Genotype-phenotype correlation in IARS2-related diseases: A case report and review of literature.

Jariya Upadia, Yuwen Li, Nicolette Walano

|Nov 12, 2021
HSD10 disease in a female: A case report and review of literature.

Jariya Upadia, Nicolette Walano, Grace S Noh

|Sep 15, 2018
A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13C.

Jariya Upadia, Patrick R Gonzales, T Prescott Atkinson

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