Gang Chen

发表

Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population

Yan Wang, Hui Li, Sen Yang, 2011, Nature Genetics.

Variation at HLA‐DPB1 is associated with dermatomyositis in Chinese population

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, The Journal of dermatology.

Exome-wide association study identifies four novel loci for systemic lupus erythematosus in Han Chinese population

Liangdan Sun, X. Zuo, Xuejun Zhang, 2017, Annals of the rheumatic diseases.

Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genes

M. Pittelkow, S. Yang, M. Gao, 2014, Clinical and experimental dermatology.

The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes

G. Gao, Wei Liu, Huai-Dong Song, 2018, European journal of endocrinology.

Uterus globulin associated protein 1 (UGRP1) is a potential marker of progression of Graves' disease into hypothyroidism

Ping Wang, Yue Chen, Huai-Dong Song, 2019, Molecular and Cellular Endocrinology.

Association of the variant rs2243421 of human DOC-2/DAB2 interactive protein gene (hDAB2IP) with gastric cancer in the Chinese Han population.

Xuejun Zhang, F. Zhou, Marion Schneider, 2013, Gene.

Association analysis of ERBB2 amplicon genetic polymorphisms and STARD3 expression with risk of gastric cancer in the Chinese population.

X. Zuo, Xuejun Zhang, Ji-Feng Wu, 2014, Gene.

Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population

Liangdan Sun, Xuejun Zhang, Yong Cui, 2012, Rheumatology International.

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.

L. Liang, Zhu Chen, G. Ning, 2013, Human molecular genetics.

RobustevidenceforfivenewGraves ’ diseaserisk loci from a staged genome-wide association analysis

L. Liang, Zhu Chen, G. Ning, 2013 .

Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne

Liangdan Sun, X. Zuo, Xuejun Zhang, 2014, Nature Communications.

Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population

Liangdan Sun, X. Zuo, Xuejun Zhang, 2013, PloS one.

Trans-ethnic genome-wide association study of severe COVID-19

Xihong Lin, Xin Jin, Chaolong Wang, 2021, Communications Biology.

Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2018, The Journal of investigative dermatology.

Confirmation by exome sequencing of the pathogenic role of NCSTN mutations in acne inversa (hidradenitis suppurativa).

T. Jiang, Liangdan Sun, X. Zuo, 2011, The Journal of investigative dermatology.

Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC

Ying Wang, Yong Zhang, Yun Li, 2010, Nature Genetics.

Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma

Liangdan Sun, X. Zuo, Jun Wang, 2012, Journal of Medical Genetics.

Fine-mapping analysis of the MHC region for vitiligo based on a new Han-MHC reference panel.

Liangdan Sun, F. Zhou, Sen Yang, 2018, Gene.

CONFLICT OF INTEREST: No conflict of interest.

Sen Yang, Yi Zhou, Huayang Tang, 2013 .

Association analyses identify six new psoriasis susceptibility loci in the Chinese population

James T. Elder, M. Weichenthal, A. Bowcock, 2010, Nature Genetics.

A genome-wide association study identifies two new risk loci for Graves' disease

L. Liang, X. Chu, Zhu Chen, 2011, Nature Genetics.

Author Correction: Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis

Liangdan Sun, X. Zuo, Xuejun Zhang, 2018, Nature Communications.

Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis

Liangdan Sun, X. Zuo, Xuejun Zhang, 2015, Nature Communications.

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity

T. Beaty, I. Ruczinski, Liangdan Sun, 2017, Nature Communications.

DNA methylation profile of psoriatic skins from different body locations.

Xuejun Zhang, F. Zhou, Xiao-dong Zheng, 2019, Epigenomics.

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.

W. Liu, G. Ning, Wei Huang, 2014, Human molecular genetics.

Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease

Huanming Yang, Jian Wang, Qibin Li, 2016, Nature Genetics.

Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6.

Rafael de Cid, Pui-Yan Kwok, Xavier Estivill, 2011, The Journal of investigative dermatology.

Sequencing-based approach identified three new susceptibility loci for psoriasis

Xin Jin, Liangdan Sun, X. Zuo, 2014, Nature Communications.

A large-scale screen for coding variants predisposing to psoriasis

Renhua Wu, Lin Yang, Hui Jiang, 2013, Nature Genetics.

Epigenome-Wide Association Analysis Identified Nine Skin DNA Methylation Loci for Psoriasis.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, The Journal of investigative dermatology.

AURKA Facilitates the Psoriasis-related Inflammation by Impeding Autophagy-mediated AIM2 Inflammasome Suppression.

Liangdan Sun, Y. Sheng, Xiao-dong Zheng, 2021, Immunology letters.

E‐selectin rs5361 and FCGR2A rs1801274 variants were associated with increased risk of gastric cancer in a Chinese population

X. Zuo, Xuejun Zhang, H. Xia, 2012, Molecular carcinogenesis.

Association analysis of genetic variants in microRNA networks and gastric cancer risk in a Chinese Han population

X. Zuo, Xuejun Zhang, F. Zhou, 2012, Journal of Cancer Research and Clinical Oncology.

EZH2 genetic variants affect risk of gastric cancer in the Chinese Han population

Liangdan Sun, X. Zuo, Xuejun Zhang, 2012, Molecular carcinogenesis.

Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.

Wei Li, Hui Zhao, Y. Lv, 2009, Biosensors & bioelectronics.

Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis

Jian Wang, Sen Yang, Jun Wang, 2012, Nature Genetics.

A miRNA-492 binding-site polymorphism in BSG (basigin) confers risk to psoriasis in Central South Chinese population

Liangdan Sun, Juan Su, Gang Chen, 2011, Human Genetics.

Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese

Tian Liu, Yongyong Shi, Zhiqiang Li, 2015, Nature Communications.

Genetic Variants in TEX15 Gene Conferred Susceptibility to Spermatogenic Failure in the Chinese Han Population

X. Zuo, Xuejun Zhang, Xiaojin He, 2012, Reproductive Sciences.

Genetic association of osteopontin (OPN) and its receptor CD44 genes with susceptibility to Chinese gastric cancer patients

X. Zuo, Ji-Feng Wu, F. Zhou, 2014, Journal of Cancer Research and Clinical Oncology.

Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population.

N. Schork, E. Tai, Liangdan Sun, 2016, Journal of psychiatry & neuroscience : JPN.

Knockdown of myosin VI by lentivirus-mediated short hairpin RNA suppresses proliferation of melanoma.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2015, Molecular medicine reports.

Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves’ Disease in a Chinese Han Population

W. Liu, Chang-gui Li, G. Gao, 2013, PloS one.

Association of Genetic Variants of VEGF gene with Gastric Carcinoma Risk

Liangdan Sun, F. Zhou, H. Xia, 2011 .

Genome-Wide Association Study Identifies Variants in PMS1 Associated with Serum Ferritin in a Chinese Population

Jianfeng Xu, Z. Mo, A. Tan, 2014, PloS one.

Six mutations in AAGAB confirm its pathogenic role in Chinese punctate palmoplantar keratoderma patients.

Min Zhang, Liangdan Sun, Jun Wang, 2013, The Journal of investigative dermatology.

A Simple Oligonucleotide Biochip Capable of Rapidly Detecting Known Mitochondrial DNA Mutations in Chinese Patients with Leber’S Hereditary Optic Neuropathy (LHON)

Hui Zhao, Y. Lv, Qinghui Jin, 2011, Disease markers.

Genetic analysis of ADIPOQ variants and gastric cancer risk: a hospital-based case–control study in China

X. Zuo, Xuejun Zhang, Ji-Feng Wu, 2013, Medical Oncology.

A rare variant in COL11A1 is strongly associated with adult height in Chinese Han population.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, Journal of genetics and genomics = Yi chuan xue bao.

Knockdown of asparagine synthetase by RNAi suppresses cell growth in human melanoma cells and epidermoid carcinoma cells

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, Biotechnology and applied biochemistry.

Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis

X. Kong, Peiguang Wang, Hervé Huang, 2022, Frontiers in Genetics.

Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis

Liangdan Sun, X. Zuo, A. Al-Chalabi, 2013, Nature Genetics.

Genomic DNA methylation in HLA-Cw*0602 carriers and non-carriers of psoriasis.

F. Zhou, Xiao-dong Zheng, Gang Chen, 2020, Journal of dermatological science.

Identification of a missense variant in LNPEP that confers psoriasis risk.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2014, The Journal of investigative dermatology.

Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient

Xuejun Zhang, Peiguang Wang, Sen Yang, 2014, The Journal of dermatology.

A Genetic Variant rs1020760at NFKB1 is Associated with Clinical Features of Psoriasis Vulgaris in a Han Chinese Population

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, Annals of human genetics.

A novel splice-site variant of the LAMB3 gene is associated with junctional epidermolysis bullosa

Gang Chen, B. Liang, Mengyun Chen, 2022, EJD. European journal of dermatology.

Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis

Liangdan Sun, X. Zuo, Xuejun Zhang, 2015, Nature Communications.

PRDM9 gene polymorphism may not be associated with defective spermatogenesis in the Chinese Han population

X. Zuo, Xuejun Zhang, Huan Wu, 2013, Systems biology in reproductive medicine.

Combined effect of five single nucleotide polymorphisms related to IL23/Th17 pathway in the risk of psoriasis

X. Zuo, Xuejun Zhang, F. Zhou, 2014, Immunogenetics.

Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne

Liangdan Sun, X. Zuo, Xuejun Zhang, 2014, Nature Communications.

Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis

Qibin Li, T. Jiang, Liangdan Sun, 2012, Journal of Medical Genetics.

Epigenome-Wide Association Analysis Identified Nine Skin DNA Methylation Loci for Psoriasis.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2016, The Journal of investigative dermatology.

PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population.

X. Zuo, Xuejun Zhang, Xiaojin He, 2012, Reproductive biomedicine online.

PRM1 variant RS35576928 (R34S) was associated with defect spermatogenesis in the Chinese han population

X. Zuo, Yunxia Cao, Xiaojin He, 2012 .