Jing Yang

发表

Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity that may underly population disparities in this disease

Jiangshan J. Shen, P. Sham, Xuejun Zhang, 2020, bioRxiv.

HLAreporter: a tool for HLA typing from next generation sequencing data

P. Sham, Y. Lau, Y. Zhang, 2015, Genome Medicine.

Identification of ST3AGL4, MFHAS1, CSNK2A2 and CD226 as loci associated with systemic lupus erythematosus (SLE) and evaluation of SLE genetics in drug repositioning

Jiangshan J. Shen, Xuejun Zhang, Y. Lau, 2018, Annals of the rheumatic diseases.

Title EFIN : predicting the functional impact of nonsynonymous singlenucleotide polymorphisms in human genome

Y. Lau, B. Chung, Jing Yang, 2014 .

Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations

Jiangshan J. Shen, P. Sham, S. Cherny, 2015, Annals of the rheumatic diseases.

Excessive deubiquitination of NLRP3-R779C variant contributes to very-early-onset inflammatory bowel disease development.

Y. Lau, J. Cui, S. Masters, 2020, Journal of Allergy and Clinical Immunology.

Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity

Chung Y. Wong, Tong-Xin Chen, Y. Chien, 2022, Frontiers in Immunology.

Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease

Chung Y. Wong, D. Lung, Tong-Xin Chen, 2022, Frontiers in Immunology.

Application of Flow Cytometry in the Diagnostics Pipeline of Primary Immunodeficiencies Underlying Disseminated Talaromyces marneffei Infection in HIV-Negative Children

Y. Lau, Jing Yang, Wanling Yang, 2019, Front. Immunol..

RASGRP1 mutation in autoimmune lymphoproliferative syndrome‐like disease

A. Fischer, Y. Lau, Jing Yang, 2017, The Journal of allergy and clinical immunology.

Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.

P. Sham, P. Tam, S. Cherny, 2013, American journal of human genetics.

Identification of Regulatory Modules That Stratify Lupus Disease Mechanism through Integrating Multi-Omics Data

Jiangshan J. Shen, Y. Lau, Yongfei Wang, 2019, Molecular therapy. Nucleic acids.

EFIN: predicting the functional impact of nonsynonymous single nucleotide polymorphisms in human genome

Wanling Yang, Jing Yang, Y. Lau, 2014, BMC Genomics.

Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE

Jiangshan J. Shen, Xuejun Zhang, Y. Lau, 2018, Arthritis Research & Therapy.

Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups

Jiangshan J. Shen, P. Sham, Xuejun Zhang, 2021, Nature Communications.

Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.

Jiangshan J. Shen, P. Sham, P. Tam, 2015, Human molecular genetics.

Gene‐Based Meta‐Analysis of Genome‐Wide Association Study Data Identifies Independent Single‐Nucleotide Polymorphisms in ANXA6 as Being Associated With Systemic Lupus Erythematosus in Asian Populations

P. Sham, S. Cherny, Liangdan Sun, 2015, Arthritis & rheumatology.

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families

A. Bousfiha, Y. Lau, M. Barbouche, 2019, Journal of Clinical Immunology.

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, J. Casanova, 2022, medRxiv.

Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.

P. Sham, P. Tam, S. Cherny, 2014, Human molecular genetics.

ELF1 is associated with systemic lupus erythematosus in Asian populations.

P. Sham, P. Tam, P. Kwan, 2011, Human molecular genetics.

Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.

Y. Lau, Jian Li, Yongfei Wang, 2021, Rheumatology.

Accurate HLA Typing at High-Digit Resolution from NGS Data

Yan Zhang, Yazhi Huang, Pak C. Sham, 2015 .

Title HLAreporter : a tool for HLA typing from next generationsequencing data

P. Sham, Y. Lau, Y. Zhang, 2015 .

Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population

P. Tam, Y. Lau, B. Chung, 2021, PLoS genetics.

Epistatic Interaction between Genetic Variants in Susceptibility Gene ETS1 Correlates with IL‐17 Levels in SLE Patients

Y. Lau, P. Lee, T. Chan, 2013, Annals of human genetics.

Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus

Jiangshan J. Shen, P. Sham, P. Tam, 2015, Arthritis Research & Therapy.

Title Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22 q 11 . 21 as associated with systemic lupus erythematosus

Jiangshan J. Shen, P. Sham, P. Tam, 2015 .

NGS4THAL, a one-stop molecular diagnosis and carrier screening tool for thalassemia and other hemoglobinopathies by next-generation sequencing.

Yu-Lung Lau, Godfrey Chi-Fung Chan, Nattiya Hirankarn, 2021, The Journal of molecular diagnostics : JMD.

NF‐E2 mutation as a novel cause for inherited thrombocytopenia

Y. Lau, P. Lee, Jing Yang, 2020, British journal of haematology.

Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia.

Y. Lau, M. Barbouche, Jing Yang, 2017, The Journal of allergy and clinical immunology.

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families

A. Bousfiha, Y. Lau, M. Barbouche, 2019, Journal of Clinical Immunology.

Association of CD247 with systemic lupus erythematosus in Asian populations

S. Cherny, P. Sham, Y. Lau, 2012, Lupus.

Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese

P. Sham, P. Tam, S. Cherny, 2011, Genes and Immunity.

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, W. Wasserman, 2023, The Journal of experimental medicine.

HLAreporter: a tool for HLA typing from next generation sequencing data

P. Sham, Y. Lau, Y. Zhang, 2015, Genome Medicine.

Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease

Jing Yang, Wanling Yang, W. Tu, 2012, Genes and Immunity.