Selina S. Dwight

Selina S. Dwight

Stanford University

H-index: 36

North America-United States

About Selina S. Dwight

Selina S. Dwight, With an exceptional h-index of 36 and a recent h-index of 16 (since 2020), a distinguished researcher at Stanford University, specializes in the field of bioinformatics, database, genomics.

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

NGLY1 deficiency natural history study

NGLY1 deficiency: a prospective natural history study

AAV9-NGLY1 gene replacement therapy improves phenotypic and biomarker endpoints in a rat model of NGLY1 deficiency

GlcNAc-Asn is a biomarker for NGLY1 deficiency

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 Registry

Selina S. Dwight Information

University

Position

Biocurator

Citations(all)

57717

Citations(since 2020)

19357

Cited By

45516

hIndex(all)

36

hIndex(since 2020)

16

i10Index(all)

41

i10Index(since 2020)

23

Email

University Profile Page

Stanford University

Google Scholar

View Google Scholar Profile

Selina S. Dwight Skills & Research Interests

bioinformatics

database

genomics

Top articles of Selina S. Dwight

Title

Journal

Author(s)

Publication Date

NGLY1 deficiency natural history study

Molecular Genetics and Metabolism

Bernhard Suter

Julie Thompson

Regina Deck

Selina Dwight

David Weinstein

2024/2/1

NGLY1 deficiency: a prospective natural history study

Human Molecular Genetics

Sandra Tong

Pamela Ventola

Christina H Frater

Jenna Klotz

Jennifer M Phillips

...

2023/9/15

AAV9-NGLY1 gene replacement therapy improves phenotypic and biomarker endpoints in a rat model of NGLY1 deficiency

Molecular Therapy-Methods & Clinical Development

Lei Zhu

Brandon Tan

Selina S Dwight

Brendan Beahm

Matt Wilsey

...

2022/12/8

GlcNAc-Asn is a biomarker for NGLY1 deficiency

J. Biochem.

William F Mueller

Lei Zhu

Brandon Tan

Selina Dwight

Brendan Beahm

...

2022/2

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome medicine

Christine G Preston

Matt W Wright

Rao Madhavrao

Steven M Harrison

Jennifer L Goldstein

...

2022/1/18

NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 Registry

Orphanet Journal of Rare Diseases

Caroline R Stanclift

Selina S Dwight

Kevin Lee

Quirine L Eijkenboom

Matt Wilsey

...

2022/12/17

See List of Professors in Selina S. Dwight University(Stanford University)