Bridget Fernandez

About Bridget Fernandez

Bridget Fernandez, With an exceptional h-index of 55 and a recent h-index of 44 (since 2020), a distinguished researcher at University of Southern California, specializes in the field of Human Genetics, Autism Spectrum Disorder.

His recent articles reflect a diverse array of research interests and contributions to the field:

Molecular testing in autism spectrum disorder

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder

Genomic architecture of autism spectrum disorder from comprehensive whole-genome sequence annotation

Genome-wide detection of tandem DNA repeats that are expanded in autism

A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular …

Bridget Fernandez Information

University

Position

Professor of Clinical Pediatrics Keck School of Medicine

Citations(all)

23761

Citations(since 2020)

10011

Cited By

18050

hIndex(all)

55

hIndex(since 2020)

44

i10Index(all)

79

i10Index(since 2020)

68

Email

University Profile Page

Google Scholar

Bridget Fernandez Skills & Research Interests

Human Genetics

Autism Spectrum Disorder

Top articles of Bridget Fernandez

Molecular testing in autism spectrum disorder

2024/1/1

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder

Nature Communications

2022/10/29

A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features

Scientific Reports

2020/7/2

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

2020/7

Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular …

Molecular Genetics & Genomic Medicine

2020/4

Bridget Fernandez
Bridget Fernandez

H-Index: 44

Sean Connors
Sean Connors

H-Index: 13

See List of Professors in Bridget Fernandez University(University of Southern California)