Jesse Engreitz, PhD

Jesse Engreitz, PhD

Stanford University

H-index: 35

North America-United States

About Jesse Engreitz, PhD

Jesse Engreitz, PhD, With an exceptional h-index of 35 and a recent h-index of 33 (since 2020), a distinguished researcher at Stanford University, specializes in the field of Human Genetics, Gene Regulation, Heart Disease.

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

Multicenter integrated analysis of noncoding CRISPRi screens

Convergence of coronary artery disease genes onto endothelial cell programs

Variant to gene to function workflow for endothelial cell programs related to CAD

High Shear Stress Reduces ERG Causing Endothelial-Mesenchymal Transition and Pulmonary Arterial Hypertension

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

FlowFISH with PrimeFlow

Oligonucleotide-coupled antibodies for single cell or single complex protein measurements

Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma

Jesse Engreitz, PhD Information

University

Position

; Broad Institute of MIT and Harvard

Citations(all)

13869

Citations(since 2020)

10457

Cited By

7512

hIndex(all)

35

hIndex(since 2020)

33

i10Index(all)

50

i10Index(since 2020)

50

Email

University Profile Page

Stanford University

Google Scholar

View Google Scholar Profile

Jesse Engreitz, PhD Skills & Research Interests

Human Genetics

Gene Regulation

Heart Disease

Top articles of Jesse Engreitz, PhD

Title

Journal

Author(s)

Publication Date

Multicenter integrated analysis of noncoding CRISPRi screens

Nature Methods

David Yao

Josh Tycko

Jin Woo Oh

Lexi R Bounds

Sager J Gosai

...

2024/3/19

Convergence of coronary artery disease genes onto endothelial cell programs

Nature

Gavin R Schnitzler

Helen Kang

Shi Fang

Ramcharan S Angom

Vivian S Lee-Kim

...

2024/2/7

Variant to gene to function workflow for endothelial cell programs related to CAD

Gavin R Schnitzler

Helen Kang

Vivian Lee

Rosa Ma

Ramcharan Angom

...

2024/1/12

High Shear Stress Reduces ERG Causing Endothelial-Mesenchymal Transition and Pulmonary Arterial Hypertension

bioRxiv

Tsutomu Shinohara

Jan-Renier AJ Moonen

Yoon Hong Chun

Yannick C Lee-Yow

Kenichi Okamura

...

2024

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

Circulation: Genomic and Precision Medicine

Mengyao Yu

Andrew R Harper

Matthew Aguirre

Maureen Pittman

Catherine Tcheandjieu

...

2023/4/5

FlowFISH with PrimeFlow

Ronghao Zhou

Jesse Engreitz

2023/12/1

Oligonucleotide-coupled antibodies for single cell or single complex protein measurements

2023/1/10

Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma

bioRxiv

Ashwin R Iyer

Aishwarya Gurumurthy

Rohan Kodgule

Athalee R Aguilar

Travis Saari

...

2023

Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension

Nature Communications

Sarasa Isobe

Ramesh V Nair

Helen Y Kang

Lingli Wang

Jan-Renier Moonen

...

2023/11/21

Rewriting regulatory DNA to dissect and reprogram gene expression

bioRxiv

Gabriella E Martyn

Michael T Montgomery

Hank Jones

Katherine Guo

Benjamin R Doughty

...

2023

CRISPRi-Perturb-seq In Endothelial Cells Links Atherosclerosis Risk Loci To Novel Klf2/4 Regulatory Genes

Arteriosclerosis, Thrombosis, and Vascular Biology

Rajat M Gupta

Gavin R Schnitzler

Helen Kang

Ramcharan Singh Angom

Shi Fang

...

2023/5

An encyclopedia of enhancer-gene regulatory interactions in the human genome

bioRxiv

Andreas R Gschwind

Kristy S Mualim

Alireza Karbalayghareh

Maya U Sheth

Kushal K Dey

...

2023/11/13

Novel mechanism of MYC deregulation in Multiple Myeloma

bioRxiv

Mahshid Rahmat

Kendell Clement

Jean-Baptiste Alberge

Romanos Sklavenitis-Pistofidis

Rohan Kodgule

...

2023

The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

Cell metabolism

Maria C Costanzo

Marcin von Grotthuss

Jeffrey Massung

Dongkeun Jang

Lizz Caulkins

...

2023/4/4

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases

Nature genetics

Elle M Weeks

Jacob C Ulirsch

Nathan Y Cheng

Brian L Trippe

Rebecca S Fine

...

2023/8

Multimodal readouts for quantifying and sequencing nucleic acids in single cells

2023/3/23

Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes

Circulation: Genomic and Precision Medicine

Mengyao Yu

Matthew Aguirre

Meiwen Jia

Ketrin Gjoni

Aldo Cordova-Palomera

...

2023/4/7

Methods for identification and modification of lncRNA associated with target genotypes and phenotypes

2023/2/28

Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity

Nature genetics

Steven Gazal

Omer Weissbrod

Farhad Hormozdiari

Kushal K Dey

Joseph Nasser

...

2022/6

Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics

Nature genetics

Karthik A Jagadeesh

Kushal K Dey

Daniel T Montoro

Rahul Mohan

Steven Gazal

...

2022/10

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