Matthew Porteus

Matthew Porteus

Stanford University

H-index: 70

North America-United States

About Matthew Porteus

Matthew Porteus, With an exceptional h-index of 70 and a recent h-index of 51 (since 2020), a distinguished researcher at Stanford University, specializes in the field of Genetic Engineering, stem cells.

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

Functional MRI to Evaluate Inhibition As a Feature of Executive Function in Patients with Sickle Cell Disease Post HSCT: A Pilot Study

TET2 regulates early and late transitions in exhausted CD8+ T-cell differentiation and limits CAR T-cell function

Lineage-tracing hematopoietic stem cell origins in vivo to efficiently make human HLF+ HOXA+ hematopoietic progenitors from pluripotent stem cells

Small-molecule correctors divert CFTR-F508del from ERAD by stabilizing sequential folding states

Epigenetic signature and key transcriptional regulators of human antigen-specific type 1 regulatory T cells

Nuclease-mediated genome editing of primary cells and related kits

Gene correction for scid-x1 in long-term hematopoietic stem cells

Gene regulation in inborn errors of immunity: Implications for gene therapy design and efficacy

Matthew Porteus Information

University

Position

Professor of Pediatrics

Citations(all)

25425

Citations(since 2020)

12750

Cited By

17787

hIndex(all)

70

hIndex(since 2020)

51

i10Index(all)

142

i10Index(since 2020)

120

Email

University Profile Page

Stanford University

Google Scholar

View Google Scholar Profile

Matthew Porteus Skills & Research Interests

Genetic Engineering

stem cells

Top articles of Matthew Porteus

Title

Journal

Author(s)

Publication Date

Functional MRI to Evaluate Inhibition As a Feature of Executive Function in Patients with Sickle Cell Disease Post HSCT: A Pilot Study

Transplantation and Cellular Therapy

Heather Alva

Lara Foland-Ross

Tami John

Matthew H Porteus

Allan L Reiss

2024/2/1

TET2 regulates early and late transitions in exhausted CD8+ T-cell differentiation and limits CAR T-cell function

bioRxiv

Alexander J Dimitri

Amy E Baxter

Gregory M Chen

Caitlin R Hopkins

Geoffrey T Rouin

...

2024

Lineage-tracing hematopoietic stem cell origins in vivo to efficiently make human HLF+ HOXA+ hematopoietic progenitors from pluripotent stem cells

Developmental Cell

Jonas L Fowler

Sherry Li Zheng

Alana Nguyen

Angela Chen

Xiaochen Xiong

...

2024/4/1

Small-molecule correctors divert CFTR-F508del from ERAD by stabilizing sequential folding states

Molecular Biology of the Cell

Celeste Riepe

Magda Wąchalska

Kirandeep K Deol

Anais K Amaya

Matthew H Porteus

...

2024/2/1

Epigenetic signature and key transcriptional regulators of human antigen-specific type 1 regulatory T cells

bioRxiv

Alma-Martina Cepika

Laura Amaya

Colin Waichler

Mansi Narula

Michelle M Mantilla

...

2024

Nuclease-mediated genome editing of primary cells and related kits

2022/1/27

Gene correction for scid-x1 in long-term hematopoietic stem cells

Nature communications

Mara Pavel-Dinu

Volker Wiebking

Beruh T Dejene

Waracharee Srifa

Sruthi Mantri

...

2019/4/9

Gene regulation in inborn errors of immunity: Implications for gene therapy design and efficacy

Hana Y Ghanim

Matthew H Porteus

2024/1/17

Combining Cell-Intrinsic and-Extrinsic Resistance to HIV-1 By Engineering Hematopoietic Stem Cells for CCR5 Knockout and B Cell Secretion of Therapeutic Antibodies

bioRxiv

William N Feist

Sofia E Luna

Kaya Ben-Efraim

Maria V Filsinger Interrante

Nelson A Amorin

...

2024

Engineering inducible signaling receptors to enable erythropoietin-free erythropoiesis

bioRxiv

Aadit P Shah

Kiran R Majeti

Freja K Ekman

Sridhar Selvaraj

Eric Soupene

...

2024

Investigating adverse genomic and regulatory changes caused by replacement of the full-length CFTR cDNA using Cas9 and AAV

Molecular Therapy-Nucleic Acids

Sriram Vaidyanathan

Jenny L Kerschner

Alekh Paranjapye

Vrishti Sinha

Brian Lin

...

2024/2/2

Transient inhibition of 53BP1 increases the frequency of targeted integration in human hematopoietic stem and progenitor cells

Nature Communications

Ron Baik

M Kyle Cromer

Steve E Glenn

Christopher A Vakulskas

Kay O Chmielewski

...

2024/1/2

Genome editing of graft-derived T-cells for post-transplant immunotherapy

2024/2/20

Genetically corrected RAG2-SCID human hematopoietic stem cells restore V(D)J-recombinase and rescue lymphoid deficiency

Blood Advances

Mara Pavel-Dinu

Cameron L Gardner

Yusuke Nakauchi

Tomoki Kawai

Ottavia M Delmonte

...

2024/4/9

Human striatal progenitor cells that contain inducible safeguards and overexpress BDNF rescue Huntington's disease phenotypes in R6/2 mice

bioRxiv

Danielle A Simmons

Sridhar Selvaraj

Tingshuo Chen

Gloria Cao

Talita Sauto Camelo

...

2024

Enhanced Immune Reconstitution and Reduced GvHD Risk with T-allo10 Infusion Post Aβdepleted-HSCT in Pediatric and Young Adult Patients with Hematologic Malignancies

Transplantation and Cellular Therapy

Alice Bertaina

Rosa Bacchetta

David C Shyr

Gopin Saini

Jennifer Lee

...

2024/2/1

A simultaneous knockout knockin genome editing strategy in HSPCs potently inhibits CCR5-and CXCR4-tropic HIV-1 infection

Cell stem cell

Amanda M Dudek

William N Feist

Elena J Sasu

Sofia E Luna

Kaya Ben-Efraim

...

2024/4/4

Gene correction for x-cgd in hematopoietic stem and progenitor cells

2023/11/9

Using Inducible Signaling Receptors to Increase Erythropoietic Output from Genome-Edited Hematopoietic Stem Cells

Blood

Kiran R Majeti

Aadit P Shah

Sofia E Luna

Eric Soupene

Simon N Chu

...

2023/11/28

Crispr-based foxp3 gene engineered t cells and hematopoietic stem cell precursors to treat ipex syndrome patients

2023/3/16

See List of Professors in Matthew Porteus University(Stanford University)