Daryl Scott

50PUBLICATIONS
247CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesDisease surveillanceOncology and carcinogenesis not elsewhere classified
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Publications (50)

|Aug 26, 2026
Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

|Jul 15, 2026
SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

|Jun 23, 2026
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants.

|Feb 25, 2026
Non-Isolated Dandy-Walker Malformation: Exome Sequencing Efficacy and Phenotypic Expansions.

Sarah Araji, Xiaonan Zhao, Jill A Rosenfeld

|Sep 05, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).

E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld

|Aug 12, 2025
Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions.

Julia Volpi, Xiaonan Zhao, Nichole Owen

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Frequent Collaborators

17 joint publications

Jill Rosenfeld

6 joint publications

Seema R Lalani

4 joint publications

Alfredo Brusco

4 joint publications

Mahshid S Azamian