Brian Shayota

5PUBLICATIONS
31CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Rheumatology and arthritisNeonatologyCentral nervous systemSocial epidemiology
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Publications (5)

|Aug 31, 2026
Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIa.

|Sep 05, 2020
Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form.

Brian J Shayota, Chaofan Zhang, Roman J Shypailo

|Oct 01, 2019
Characterization of the renal phenotype in RMND1-related mitochondrial disease.

Brian J Shayota, Nhon T Le, Nasim Bekheirnia

|Sep 15, 2019
Loss of CLTRN function produces a neuropsychiatric disorder and a biochemical phenotype that mimics Hartnup disease.

Nishitha R Pillai, Delia Yubero, Brian J Shayota

|Mar 09, 2019
Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency.

Brian J Shayota, Claudia Soler-Alfonso, Mir Reza Bekheirnia

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Frequent Collaborators

1 joint publications

Claudia Soler-Alfonso

1 joint publications

Sarah H Elsea

1 joint publications

Nishitha R Pillai

1 joint publications

Daryl A Scott