Qing Zhou

发表

Brain volumetric MRI study of extremely low gestational age newborns (ELGANs) at 9 to 10 years of age

Qing Zhou, 2015 .

RIPK1-Associated Inborn Errors of Innate Immunity

Qing Zhou, I. Aksentijevich, Jiahui Zhang, 2021, Frontiers in Immunology.

Deficiency of Adenosine Deaminase 2 in Adults and Children: Experience From India

Zhengping Huang, Sanjay Jain, V. Negi, 2020, Arthritis & rheumatology.

Human adenosine deaminases ADA1 and ADA2 bind to different subsets of immune cells

A. Zavialov, Yuanan Lu, Qing Zhou, 2017, Cellular and Molecular Life Sciences.

Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2).

R. Geha, J. Chou, G. Lefranc, 2020, The Journal of allergy and clinical immunology.

Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance

D. Kastner, J. Chiorini, N. Sobreira, 2020, Journal of Clinical Immunology.

Comprehensive analysis of ADA2 genetic variants and estimation of carrier frequency driven by a function-based approach.

L. Henderson, A. O’Donnell-Luria, Zhengping Huang, 2021, The Journal of allergy and clinical immunology.

Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

J. Mullikin, E. Remmers, D. Kastner, 2016, Proceedings of the National Academy of Sciences.

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study

G. Damonte, M. Severino, A. Martini, 2017, Annals of the rheumatic diseases.

[Identification of a novel JAG1 mutation in a family affected by Alagille syndrome].

Qing Zhou, Ying Cheng, Li Guo, 2016, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAK

J. B. Oliveira, J. Orange, Chi A. Ma, 2013, Proceedings of the National Academy of Sciences.

Supplemental Data Additive Loss-of-Function Mutations in Proteasome-Subunit-Genes induce Type-I-interferon production in CANDLE / PRAAS

E. Remmers, A. Mégarbané, K. Rother, 2015 .

Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors

W. C. Owen, M. Hafner, A. Šedivá, 2018, Annals of the rheumatic diseases.

TNF-inhibition in vasculitis management in adenosine deaminase 2 deficiency (DADA2).

J. Burnham, D. Kastner, S. Rosenzweig, 2021, The Journal of allergy and clinical immunology.

Analysis of point mutation in site 1896 of HBV precore and its detection in the tissues and serum of HCC patients.

Y. Wang, Qing Zhou, Hu Liu, 2000, World journal of gastroenterology.

The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation

D. Kastner, Qing Zhou, I. Aksentijevich, 2017, Nature Immunology.

Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.

E. Remmers, D. Kastner, A. Mégarbané, 2016, Journal of Clinical Investigation.

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.

Qing Zhou, Susan Moir, Matilda Katan, 2012, American journal of human genetics.

NF-κB Pathway in Autoinflammatory Diseases: Dysregulation of Protein Modifications by Ubiquitin Defines a New Category of Autoinflammatory Diseases

Qing Zhou, I. Aksentijevich, 2017, Front. Immunol..

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early onset autoinflammatory syndrome

J. Mullikin, Yuan Zhang, D. Kastner, 2015, Nature Genetics.

A dominant autoinflammatory disease caused by non-cleavable variants of RIPK1

Junying Yuan, Wanjin Li, Jinqiao Sun, 2019, Nature.

New Horizons in the Genetic Etiology of Systemic Lupus Erythematosus and Lupus-Like Disease: Monogenic Lupus and Beyond

Qing Zhou, E. Demirkaya, I. Aksentijevich, 2020, Journal of clinical medicine.

Brief Report: Deficiency of Complement 1r Subcomponent in Early‐Onset Systemic Lupus Erythematosus: The Role of Disease‐Modifying Alleles in a Monogenic Disease

E. Remmers, D. Kastner, M. Gadina, 2017, Arthritis & rheumatology.

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

Alexander F. Wilson, A. F. Wilson, J. Mullikin, 2013, Proceedings of the National Academy of Sciences.

Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.

E. Remmers, D. Kastner, A. Mégarbané, 2015, The Journal of clinical investigation.

Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome

Y. Wang, J. Hejtmancik, J. Hejtmancik, 2015, BMC Medical Genetics.

Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance

D. Kastner, J. Chiorini, N. Sobreira, 2020, Journal of Clinical Immunology.

Novel ADA2 Compound Heterozygous Mutations Resulting in Deficiency of Adenosine Deaminase 2 in a Pair of Siblings

Jun Wang, Qing Zhou, Rong-Jun Zheng, 2021, Journal of Clinical Immunology.

Early-onset stroke and vasculopathy associated with mutations in ADA2.

J. Mullikin, H. Kong, V. Pascual, 2014, The New England journal of medicine.

Interstitial Lung Disease and Psoriasis in a Child With Aicardi-Goutières Syndrome

Jun Wang, Qing Zhou, Shihao Wang, 2020, Frontiers in Immunology.

Erratum: Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type i IFN production (Journal of Clinical Investigation (2015) 125:11 (4196-4211) DOI: 10.1172/JCI81260)

E. Remmers, D. Kastner, A. Mégarbané, 2016 .

Treatment Strategies for Deficiency of Adenosine Deaminase 2.

D. Kastner, C. Toro, A. Soldatos, 2019, The New England journal of medicine.

Adenosine deaminase 2 deficiency presenting as spastic paraplegia and systemic vasculitis

Qing Zhou, I. Aksentijevich, F. Poswar, 2016, Journal of Neurology.

Disrupted N-linked glycosylation as a disease mechanism in deficiency of ADA2.

Todd W. Lyons, L. Notarangelo, S. Pai, 2018, The Journal of allergy and clinical immunology.

Cryopyrin-associated Periodic Syndrome Caused by a Myeloid-Restricted Somatic NLRP3 Mutation

E. Remmers, D. Kastner, A. Walts, 2015 .

A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.

Xiao-yan Xiong, Y. Wang, Xuejun Zhang, 2003, Journal of dermatological science.

Novel mutation of TCIRG1 and clinical pictures of two infantile malignant osteopetrosis patients

Zhiyun Yang, Bin Hu, Yiming Wang, 2011, Journal of Bone and Mineral Metabolism.

The point mutation of p53 gene exon7 in hepatocellular carcinoma from Anhui Province, a non HCC prevalent area in China.

Y. Wang, Qing Zhou, S. Gui, 2002, World journal of gastroenterology.