Stephen B Montgomery

Stephen B Montgomery

Stanford University

H-index: 74

North America-United States

About Stephen B Montgomery

Stephen B Montgomery, With an exceptional h-index of 74 and a recent h-index of 63 (since 2020), a distinguished researcher at Stanford University, specializes in the field of Genetics, genomics and gene regulation.

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

regionalpcs: improved discovery of DNA methylation associations with complex traits

Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signatures

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation

RNA Sequencing in Disease Diagnosis

Genetic architecture of cardiac dynamic flow volumes

Impact of genome build on RNA-seq interpretation and diagnostics

Stephen B Montgomery Information

University

Position

Associate Professor Pathology and Genetics

Citations(all)

58446

Citations(since 2020)

31421

Cited By

38573

hIndex(all)

74

hIndex(since 2020)

63

i10Index(all)

137

i10Index(since 2020)

126

Email

University Profile Page

Stanford University

Google Scholar

View Google Scholar Profile

Stephen B Montgomery Skills & Research Interests

Genetics

genomics and gene regulation

Top articles of Stephen B Montgomery

Title

Journal

Author(s)

Publication Date

regionalpcs: improved discovery of DNA methylation associations with complex traits

bioRxiv

Tiffany Eulalio

Min Woo Sun

Olivier Gevaert

Michael D Greicius

Thomas J Montine

...

2024/1/1

Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signatures

Cell Genomics

Venugopalan D Nair

Hanna Pincas

Gregory R Smith

Elena Zaslavsky

Yongchao Ge

...

2024/5/1

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv

Tanner D Jensen

Bohan Ni

Chloe Reuter

John E Gorzynski

Sarah Fazal

...

2024

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv

Yuyang Chen

Ruebena Dawes

Hyung Chul Kim

Sarah L Stenton

Susan Walker

...

2024/4/8

Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation

medRxiv

Jonas A Gustafson

Sophia B Gibson

Nikhita Damaraju

Miranda PG Zalusky

Kendra Hoekzema

...

2024

RNA Sequencing in Disease Diagnosis

Craig Smail

Stephen B Montgomery

2024/2/15

Genetic architecture of cardiac dynamic flow volumes

Nature Genetics

Bruna Gomes

Aditya Singh

Jack W O’Sullivan

Theresia M Schnurr

Pagé C Goddard

...

2024/2

Impact of genome build on RNA-seq interpretation and diagnostics

medRxiv

Rachel A Ungar

Pagé C Goddard

Tanner D Jensen

Fabien Degalez

Kevin S Smith

...

2024/1/12

Single-cell multi-omics map of human foetal blood in Down's Syndrome

bioRxiv

Andrew R Marderstein

Marco De Zuani

Haoliang Xue

Jon Bezney

Shuo Wong

...

2023

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv

Marianne K DeGorter

Pagé C Goddard

Emre Karakoc

Soumya Kundu

Stephanie M Yan

...

2023/11/6

Africa-specific human genetic variation near CHD1L associates with HIV-1 load

Nature

Paul J McLaren

Immacolata Porreca

Gennaro Iaconis

Hoi Ping Mok

Subhankar Mukhopadhyay

...

2023/8/31

P643: Transcriptome sequencing increases yield of Mendelian disease diagnosis

Genetics in Medicine Open

Devon Bonner

Rachel Ungar

Page Goddard

Jennefer Kohler

Chloe Reuter

...

2023/1/1

Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases

Nature Genetics

Margaret G Guo

David L Reynolds

Cheen E Ang

Yingfei Liu

Yang Zhao

...

2023/11

Beyond the exome: what’s next in diagnostic testing for Mendelian conditions

Monica H Wojcik

Chloe M Reuter

Shruti Marwaha

Medhat Mahmoud

Michael H Duyzend

...

2023/8/3

The functional impact of rare variation across the regulatory cascade

Cell Genomics

Taibo Li

Nicole Ferraro

Benjamin J Strober

Francois Aguet

Silva Kasela

...

2023/10/11

Molecular quantitative trait loci

François Aguet

Kaur Alasoo

Yang I Li

Alexis Battle

Hae Kyung Im

...

2023/1/25

The mitochondrial multi-omic response to exercise training across tissues

bioRxiv

David Amar

Nicole R Gay

David Jimenez-Morales

Pierre M Jean Beltran

Megan E Ramaker

...

2023/1/13

Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exercise

bioRxiv

Aliza B Rubenstein

Gregory R Smith

Zidong Zhang

Xi Chen

Toby L Chambers

...

2023/9/28

Organ aging signatures in the plasma proteome track health and disease

Nature

Hamilton Se-Hwee Oh

Jarod Rutledge

Daniel Nachun

Róbert Pálovics

Olamide Abiose

...

2023/12/7

Multi-omic identification of key transcriptional regulatory programs during endurance exercise training

bioRxiv

Gregory R Smith

Bingqing Zhao

Malene E Lindholm

Archana Raja

Mark Viggars

...

2023/1/12

See List of Professors in Stephen B Montgomery University(Stanford University)