Sheng Chih Jin

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Assistant Professor

Washington University School of Medicine

United States

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Recent Grants

Grant: Close

K99/R00 Pathway to Independence Award

Open Date: 2019-04-01

Close Date:

Grant: Close

American Heart Association Postdoctoral Fellowship

Open Date: 2018-07-01

Close Date: 2019-04-01

Grant: Close

James Hudson Brown - Alexander Brown Coxe Postdoctoral Fellowships

Open Date: 2015-07-01

Close Date: 2016-07-01

Grant: Close

Howard Hughes Medical Institute Postdoctoral Fellowship

Open Date: 2014-09-01

Close Date: 2015-07-01

Articles (11)

Year:

2024

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (5)

Stefan Barakat

Associate professor

Erasmus MC

NETHERLANDS

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Amy Stiegler

Yale University

UNITED STATES

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Jungmin Choi

Associate Professor

Korea University

SOUTH KOREA

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Elif Eroglu

Karolinska Institutet

SWEDEN

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Christopher Walsh

Chief

Boston Children's Hospital

UNITED STATES

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Sheng Chih Jin

Research Interests

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Recent Grants

Articles (11)

Potential clinical applications of advanced genomic analysis in cerebral palsy

A neural stem cell paradigm of pediatric hydrocephalus.

De novo mutations in the BMP signaling pathway in lambdoid craniosynostosis.

Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesis.

Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease.

Quantifying concordant genetic effects of de novo mutations on multiple disorders.

Mutation spectrum of congenital heart disease in a consanguineous Turkish population

Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia.

Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.

Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus.

Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors

Collaborators (5)

Stefan Barakat

Amy Stiegler

Jungmin Choi

Elif Eroglu

Christopher Walsh

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