Junjie Chen

Ministry Of Education Key Laboratory Of Child Development And Disorders, Chongqing Key Laboratory Of Child Infection And Immunity
Chongqing, China

Last Updated: 09/26/2026

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Found 8 publications

An early-onset SLE patient with a novel paternal inherited BACH2 mutation.

An early-onset SLE patient with a novel paternal inherited BACH2 mutation.

Journal: Journal of clinical immunology

Published: February 26, 2023

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: January 20, 2023

Multiple Immune Defects in Two Patients with Novel DOCK2 Mutations Result in Recurrent Multiple Infection Including Live Attenuated Virus Vaccine.

Multiple Immune Defects in Two Patients with Novel DOCK2 Mutations Result in Recurrent Multiple Infection Including Live Attenuated Virus Vaccine.

Journal: Journal of clinical immunology

Published: November 03, 2022

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.

Journal: Frontiers in immunology

Published: June 19, 2022

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: May 27, 2022

A Novel RAC2 Mutation Causing Combined Immunodeficiency.

A Novel RAC2 Mutation Causing Combined Immunodeficiency.

Journal: Journal of clinical immunology

Published: March 01, 2022

Genetic and Functional Identifying of Novel STAT1 Loss-of-Function Mutations in Patients with Diverse Clinical Phenotypes.

Genetic and Functional Identifying of Novel STAT1 Loss-of-Function Mutations in Patients with Diverse Clinical Phenotypes.

Journal: Journal of clinical immunology

Published: February 08, 2022

Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations.

Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations.

Journal: Frontiers in immunology

Published: April 24, 2021

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Last Updated: 09/26/2026