Yufeng Shen

Yufeng Shen

Columbia University in the City of New York

H-index: 60

North America-United States

About Yufeng Shen

Yufeng Shen, With an exceptional h-index of 60 and a recent h-index of 51 (since 2020), a distinguished researcher at Columbia University in the City of New York, specializes in the field of Computational Genomics, Genetics.

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

PreMode predicts mode of action of missense variants by deep graph representation learning of protein sequence and structural context

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for …

Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease

Rescuing lung development through embryonic inhibition of histone acetylation

Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A …

Tissue adaptation and clonal segregation of human memory T cells in barrier sites

VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants

A probabilistic graphical model for estimating selection coefficient of missense variants from human population sequence data

Yufeng Shen Information

University

Position

Associate Professor

Citations(all)

19386

Citations(since 2020)

10669

Cited By

12583

hIndex(all)

60

hIndex(since 2020)

51

i10Index(all)

119

i10Index(since 2020)

110

Email

University Profile Page

Columbia University in the City of New York

Google Scholar

View Google Scholar Profile

Yufeng Shen Skills & Research Interests

Computational Genomics

Genetics

Top articles of Yufeng Shen

Title

Journal

Author(s)

Publication Date

PreMode predicts mode of action of missense variants by deep graph representation learning of protein sequence and structural context

bioRxiv

Guojie Zhong

Yige Zhao

Demi Zhuang

Wendy K Chung

Yufeng Shen

2024

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for …

Genetics in Medicine

Mengqi Ma

Mythily Ganapathi

Yiming Zheng

Kai-Li Tan

Oguz Kanca

...

2024/3/21

Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease

Nature Genetics

Feng Xiao

Xiaoran Zhang

Sarah U Morton

Seong Won Kim

Youfei Fan

...

2024/2/20

Rescuing lung development through embryonic inhibition of histone acetylation

Science Translational Medicine

Giangela Stokes

Zhuowei Li

Nicole Talaba

William Genthe

Maria B Brix

...

2024/1/31

Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A …

medRxiv

Khemika K Sudnawa

Wenxing Li

Sean Calamia

Cara H Kanner

Jennifer M Bain

...

2024

Tissue adaptation and clonal segregation of human memory T cells in barrier sites

Nature immunology

Maya ML Poon

Daniel P Caron

Zicheng Wang

Steven B Wells

David Chen

...

2023/2

VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants

Communications Biology

Guojie Zhong

Yoolim A Choi

Yufeng Shen

2023/7/25

A probabilistic graphical model for estimating selection coefficient of missense variants from human population sequence data

medRxiv

Yige Zhao

Guojie Zhong

Jake Hagen

Hongbing Pan

Wendy K Chung

...

2023/12/13

SABRE: Self-Attention Based model for predicting T-cell Receptor Epitope Specificity

bioRxiv

Zicheng Wang

Yufeng Shen

2023

Contribution of previously unrecognized RNA splice-altering variants to congenital heart disease

Circulation: Genomic and Precision Medicine

Min Young Jang

Parth N Patel

Alexandre C Pereira

Jon AL Willcox

Alireza Haghighi

...

2023/6

Rare predicted loss of function alleles in Bassoon (BSN) are associated with obesity

NPJ Genomic Medicine

Na Zhu

Charles A LeDuc

Ilene Fennoy

Blandine Laferrère

Claudia A Doege

...

2023/10/21

P111: Phenotypic insights into newly established moderate effect genes for autism spectrum disorder

Genetics in Medicine Open

Sarah Barns

Chang Shu

Jessica Wright

Alexandra Goler

Jacob Hall

...

2023/1/1

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine

Jodell E Linder

Aimee Allworth

Harris T Bland

Pedro J Caraballo

Rex L Chisholm

...

2023/4/1

Disrupted endosomal trafficking of the Vangl-Celsr polarity complex underlies congenital anomalies in trachea-esophageal morphogenesis

bioRxiv

Nicole A Edwards

Adhish Kashyap

Alissa Warren

Zachary N Agricola

Alan P Kenny

...

2023/10/11

SHINE: protein language model-based pathogenicity prediction for short inframe insertion and deletion variants

Briefings in Bioinformatics

Xiao Fan

Hongbing Pan

Alan Tian

Wendy K Chung

Yufeng Shen

2023/1

Association of Predicted Damaging De Novo Variants on Ventricular Function in Individuals With Congenital Heart Disease

Circulation: Genomic and Precision Medicine

Matthew J Lewis

Alexander Hsieh

Lu Qiao

Renjie Tan

Brigitte Kazzi

...

2023/4

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects

The American Journal of Human Genetics

Florence Petit

Mauro Longoni

Julie Wells

Richard S Maser

Eric L Bogenschutz

...

2023/10/5

Evidence-based assessment of congenital heart disease genes to enable returning results in a genomic study

Circulation: Genomic and Precision Medicine

Emily L Griffin

Shannon N Nees

Sarah U Morton

Julia Wynn

Nihir Patel

...

2023/4

Site-specific development and progressive maturation of human tissue-resident memory T cells over infancy and childhood

Immunity

Thomas J Connors

Rei Matsumoto

Shivali Verma

Peter A Szabo

Rebecca Guyer

...

2023/8/8

Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk

The American Journal of Human Genetics

Jon AL Willcox

Joshua T Geiger

Sarah U Morton

David McKean

Daniel Quiat

...

2022/5/5

See List of Professors in Yufeng Shen University(Columbia University in the City of New York)

Co-Authors

H-index: 238
Mark Daly

Mark Daly

Harvard University

H-index: 123
Munir Pirmohamed

Munir Pirmohamed

University of Liverpool

H-index: 122
Wendy Chung

Wendy Chung

Columbia University in the City of New York

H-index: 101
Ann Daly

Ann Daly

Newcastle University

H-index: 89
George Hripcsak

George Hripcsak

Columbia University in the City of New York

H-index: 79
Kai Wang

Kai Wang

University of Pennsylvania

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