Wei Huang

Wei Huang, Shu Zheng, Su-zhan Zhang, 2004, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

Zhu Chen, Xiangyin Kong, G. Fu, 2001, Nature Genetics.

Association of Polymorphisms in the Solute Carrier Organic Anion Transporter Family Member 1B1 Gene with Essential Hypertension in the Uyghur Population

Li Jin, Ying Wang, Wenqing Fu, 2010, Annals of human genetics.

The gene for a rare autosomal dominant form of pompholyx maps to chromosome 18q22.1-18q22.3.

Xuejun Zhang, Wei Huang, F. Zhou, 2006, The Journal of investigative dermatology.

Gene expression profiling of porokeratosis

Wei Huang, Haifeng Wang, Zhi-zhong Zheng, 2008, Journal of cutaneous pathology.

Characterization of PIK3CA and PIK3R1 somatic mutations in Chinese breast cancer patients

Xin Hu, Z. Shao, Wei Huang, 2018, Nature Communications.

Inversa acne (hidradenitis suppurativa): a case report and identification of the locus at chromosome 1p21.1-1q25.3.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2006, The Journal of investigative dermatology.

Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo

Liangdan Sun, Xuejun Zhang, Jianjun Liu, 2009, PLoS genetics.

Evidence for two susceptibility loci on chromosomes 22q12 and 6p21-p22 in Chinese generalized vitiligo families.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2007, The Journal of investigative dermatology.

A novel linkage to generalized vitiligo on 4q13-q21 identified in a genomewide linkage analysis of Chinese families.

Wei Li, Xuejun Zhang, Wei Huang, 2005, American journal of human genetics.

A gene for freckles maps to chromosome 4q32-q34.

Xuejun Zhang, Wei Huang, Sen Yang, 2004, The Journal of investigative dermatology.

Identification of a locus for punctate palmoplantar keratodermas at chromosome 8q24.13-8q24.21.

Xuejun Zhang, Wei Huang, Sen Yang, 2004, The Journal of investigative dermatology.

A polymorphism in the promoter region of catalase is associated with blood pressure levels

M. Xiong, Li Jin, Yayun Shen, 2001, Human Genetics.

Association of human aryl hydrocarbon receptor gene polymorphisms with risk of lung cancer among cigarette smokers in a Chinese population

Hongbing Shen, Weiwei Sun, Yi Wang, 2009, Pharmacogenetics and genomics.

Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria.

Xuejun Zhang, Wei Huang, W. Du, 2005, Archives of dermatology.

BMC Medical Genetics

Yi Wang, Wei Huang, Changzheng Dong, 2007 .

Functional polymorphisms, altered gene expression and genetic association link NRH:quinone oxidoreductase 2 to breast cancer with wild-type p53.

L. Fan, Keda Yu, Z. Shao, 2009, Human molecular genetics.

Structure and computation-guided design of a mutation-integrated trimeric RBD candidate vaccine with broad neutralization against SARS-CoV-2

Wei-min Zhou, Zhixin Ma, Wei Huang, 2021, bioRxiv.

Insight into hepatocellular carcinogenesis at transcriptome level by comparing gene expression profiles of hepatocellular carcinoma with those of corresponding noncancerous liver

G. Fu, Zhu Chen, Xin Tai Zhao, 2001, Proceedings of the National Academy of Sciences of the United States of America.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Karsten B. Sieber, Nicholette D. Palmer, Cassandra N. Spracklen, 2019, Nature Genetics.

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

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

Characterization of PIK3CA and PIK3R1 somatic mutations in Chinese breast cancer patients

Xin Hu, Wei Huang, Z. Shao, 2018, Nature Communications.

Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives

Z. Shao, Jiong Wu, G. Di, 2009, Breast Cancer Research and Treatment.

Genomic and Transcriptomic Landscape of Triple-Negative Breast Cancers: Subtypes and Treatment Strategies.

Xin Hu, Leming Shi, Yuanting Zheng, 2019, Cancer cell.

An SNP of the ZBTB38 gene is associated with idiopathic short stature in the Chinese Han population

Wei Wang, X. Chu, Ying Wang, 2013, Clinical endocrinology.

Functional Evaluation of Genetic and Environmental Regulators of P450 mRNA Levels

X. Chu, Wei Huang, Jinxiu Shi, 2011, PloS one.

A haplotype of the catalase gene confers an increased risk of essential hypertension in Chinese Han

Yungang He, Li Jin, Ying Wang, 2010, Human mutation.

Genomic features of rapid versus late relapse in triple negative breast cancer

E. Winer, Leming Shi, B. Ramaswamy, 2021, BMC Cancer.

Linkage disequilibrium sharing and haplotype-tagged SNP portability between populations

Wei Huang, Chenhui Zhang, Ying Wang, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Y-chromosome haplotype distribution in Han Chinese populations and modern human origin in East Asians

Zhu Chen, J. Chu, Wei Huang, 2001, Science in China Series C: Life Sciences.

Y-chromosome evidence for no independent origin of modern human in China

Li Jin, Wei Huang, B. Su, 2001 .

African Origin of Modern Humans in East Asia: A Tale of 12,000 Y Chromosomes

P. Underhill, M. Seielstad, Zhu Chen, 2001, Science.

A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2006, The Journal of investigative dermatology.

Genome-wide scan of Graves' disease: evidence for linkage on chromosome 5q31 in Chinese Han pedigrees.

Li Jin, Xiao-yan Xiong, Y. Shugart, 2003, The Journal of clinical endocrinology and metabolism.

Dissecting linkage disequilibrium in African-American genomes: roles of markers and individuals.

M. Xiong, Shuhua Xu, Yungang He, 2007, Molecular biology and evolution.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Kyle J. Gaulton, Yoonjung Yoonie Joo, Cassandra N. Spracklen, 2020, Nature Genetics.

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.

Fine genetic mapping of the chromosome 11q23.3 region in a Han Chinese population: insights into the apolipoprotein genes underlying the blood lipid-lipoprotein variances.

Wei Huang, Jinxiu Shi, Chenhui Zhang, 2021, Journal of genetics and genomics = Yi chuan xue bao.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Aaron F. McDaid, Yan V. Sun, Cassandra N. Spracklen, 2022 .

Fine Mapping of the Psoriasis Susceptibility Locus PSORS1 Supports HLA-C as the Susceptibility Gene in the Han Chinese Population

Sen Yang, Wei Huang, Wen-Hui Du, 2008, PLoS genetics.

The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives

Z. Shao, Jiong Wu, G. Di, 2009, Breast Cancer Research and Treatment.

Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH)

Xuejun Zhang, Wei Huang, Sen Yang, 2004, Human mutation.

Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.

Xiao-yan Xiong, Xuejun Zhang, Wei Huang, 2003, The Journal of investigative dermatology.

An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves’ disease

X. Chu, Yi Wang, Zhu Chen, 2013, Journal of Medical Genetics.

Gene-Wide Characterization of Common Quantitative Trait Loci for ABCB1 mRNA Expression in Normal Liver Tissues in the Chinese Population

Wei Huang, Jinxiu Shi, Beilan Wang, 2012, PloS one.

Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma.

Wei Huang, Yin Yao Shugart, Timothy J Jorgensen, 2011, Cancer research.

Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population.

Hongbing Shen, Weiwei Sun, Yi Wang, 2008, Lung cancer.

Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations

Ying Wang, Wenqing Fu, Li Jin, 2009, Human mutation.

A molecular signature for the prediction of recurrence in colorectal cancer

P. Wei, Wei Huang, Qifeng Wang, 2015, Molecular Cancer.

Sox17, the canonical Wnt antagonist, is epigenetically inactivated by promoter methylation in human breast cancer

Z. Shao, Wei Huang, De-Yuan Fu, 2010, Breast Cancer Research and Treatment.

Interethnic analyses of blood pressure loci in populations of East Asian and European descent

Cassandra N. Spracklen, Dermot F. Reilly, P. Elliott, 2018, Nature Communications.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Christopher D. Brown, Aaron F. McDaid, Yan V. Sun, 2021, bioRxiv.

Multiple cancer susceptible genes sequencing in BRCA-negative breast cancer with high hereditary risk

Xin Hu, Z. Shao, Wei Huang, 2020, Annals of translational medicine.

The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified

Z. Shao, Jiong Wu, G. Di, 2008, Breast Cancer Research and Treatment.

Follow-up analysis of PSORS9 in 151 Chinese families confirmed the linkage to 4q31-32 and refined the evidence to the families of early-onset psoriasis.

Wei Li, Liangdan Sun, Xuejun Zhang, 2007, The Journal of investigative dermatology.

Systematic evaluation of association between the microsomal glutathione S-transferase 2 common variation and psoriasis vulgaris in Chinese population

Liangdan Sun, Xuejun Zhang, Wei Huang, 2006, Archives of Dermatological Research.

Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma.

Xuejun Zhang, Wei Huang, Sen Yang, 2004, The Journal of investigative dermatology.

Evidence for a major psoriasis susceptibility locus at 6p21(PSORS1) and a novel candidate region at 4q31 by genome-wide scan in Chinese hans.

Li Jin, Xuejun Zhang, Wei Huang, 2002, The Journal of investigative dermatology.

Functional characterization of a promoter polymorphism in APE1/Ref‐1 that contributes to reduced lung cancer susceptibility

Hongbing Shen, Q. Wei, Zhibin Hu, 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Association between polymorphisms in the GSTA4 gene and risk of lung cancer: A case–control study in a Southeastern Chinese population

Hongbing Shen, Weiwei Sun, Yi Wang, 2009, Molecular carcinogenesis.

Genetic susceptibility of lung cancer associated with common variants in the 3′ untranslated regions of the adenosine triphosphate‐binding cassette B1 (ABCB1) and ABCC1 candidate transporter genes for carcinogen export

Hongbing Shen, Q. Wei, G. Jin, 2009, Cancer.

Tagging single nucleotide polymorphisms in MBD4 are associated with risk of lung cancer in a Chinese population.

Hongbing Shen, Weiwei Sun, Ying Wang, 2008, Lung cancer.

Polymorphisms in excision repair cross-complementing group 4 (ERCC4) and susceptibility to primary lung cancer in a Chinese Han population.

Hongbing Shen, Yi Wang, Ying Wang, 2008, Lung cancer.

Tagging single nucleotide polymorphisms in excision repair cross-complementing group 1 (ERCC1) and risk of primary lung cancer in a Chinese population

Hongbing Shen, Yi Wang, Ying Wang, 2007, Pharmacogenetics and genomics.

Frequent epigenetic inactivation of the receptor tyrosine kinase EphA5 by promoter methylation in human breast cancer.

Wei Huang, Wen-Tao Yang, Z. Shao, 2010, Human pathology.

Bioinformatics study indicates possible microRNA-regulated pathways in the differentiation of breast cancer

Xuegong Zhang, Z. Shao, Wei Huang, 2010 .

Tagging Single Nucleotide Polymorphisms in Phosphoinositide-3-Kinase–Related Protein Kinase Genes Involved in DNA Damage “Checkpoints” and Lung Cancer Susceptibility

Hongbing Shen, Weiwei Sun, Ying Wang, 2008, Clinical Cancer Research.

Mitochondrial aldehyde dehydrogenase-2 (ALDH2) Glu504Lys polymorphism contributes to the variation in efficacy of sublingual nitroglycerin.

D. Nebert, Wei Huang, D. Lu, 2006, The Journal of clinical investigation.

A functional polymorphism affecting the APOA5 gene expression is causally associated with plasma triglyceride levels conferring coronary atherosclerosis risk in Han Chinese Population.

Yi Wang, Ying Wang, Wei Huang, 2014, Biochimica et biophysica acta.

Association of the R485K polymorphism of the Factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population

Zhu Chen, Wei Huang, Ding-liang Zhu, 2000, Clinical genetics.

Association between single nucleotide polymorphisms in deoxycytidine kinase and treatment response among acute myeloid leukaemia patients.

Jiong Hu, Yong-mei Zhu, Saijuan Chen, 2004, Pharmacogenetics.

Analysis of genomic admixture in Uyghur and its implication in mapping strategy.

Li Jin, Wei Huang, Shuhua Xu, 2008, American journal of human genetics.

A Genome-Wide Association Study Confirms Previously Reported Loci for Type 2 Diabetes in Han Chinese

Weiqing Wang, G. Ning, Y. Bi, 2011, PloS one.

Exploration of gene–gene interaction effects using entropy-based methods

Yi Wang, Wei Huang, Yixue Li, 2008, European Journal of Human Genetics.

Genetic evidence supports demic diffusion of Han culture

Yungang He, Xianyun Mao, R. Chakraborty, 2004, Nature.

A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.

Jianfang Ma, Wei Huang, S. Chen, 2012, American journal of human genetics.

Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease

Christian R. Tilley, J. Berg, K. Wilhelmsen, 2017, Circulation. Cardiovascular genetics.

Potentially functional polymorphisms of EXO1 and risk of lung cancer in a Chinese population: A case-control analysis.

Hongbing Shen, Weiwei Sun, Hongliang Liu, 2008, Lung cancer.

Single nucleotide polymorphism rs3732860 in the 3′‐untranslated region of CYP8B1 gene is associated with gallstone disease in Han Chinese

Wei Huang, Zhao-yan Jiang, Shi-jie Xu, 2013, Journal of gastroenterology and hepatology.

Polymorphisms in interleukin-15 gene on chromosome 4q31.2 are associated with psoriasis vulgaris in Chinese population.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2007, The Journal of investigative dermatology.

Fine mapping MHC associations in Graves’ disease and its clinical subtypes in Han Chinese

X. Chu, Zhu Chen, Wei Huang, 2018, Journal of Medical Genetics.

Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey

Cassandra N. Spracklen, Jingchun Luo, Ying Wang, 2018, PLoS genetics.

Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population.

Li Jin, Ying Wang, Wenqing Fu, 2011, Genetic testing and molecular biomarkers.

Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia

Xiao-yan Xiong, Xuejun Zhang, Wei Huang, 2003, Archives of Dermatological Research.

Replication of Putative Susceptibility Loci from Genome-Wide Association Studies Associated with Coronary Atherosclerosis in Chinese Han Population

X. Chu, Weiwei Sun, Yi Wang, 2011, PloS one.

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.

X. Chu, Li Jin, Zhi Liu, 2009, Human molecular genetics.

NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study

Daowen Wang, Wei Huang, Y. Gong, 2016, Oncotarget.

Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population

X. Chu, Weiwei Sun, Yi Wang, 2010, Journal of Human Genetics.

A molecular signature for the prediction of recurrence in colorectal cancer

P. Wei, Wei Huang, Xiaoyan Zhou, 2015, Molecular Cancer.

Genetic contribution of GADD45A to susceptibility to sporadic and non-BRCA1/2 familial breast cancers: a systematic evaluation in Chinese populations

L. Fan, Keda Yu, Z. Shao, 2010, Breast Cancer Research and Treatment.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Karsten B. Sieber, M. P. Concas, Nicholette D. Palmer, 2019, Nature Genetics.

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.

Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.

Wei Huang, Jian Fei, Zhi-Min Yuan, 2009, American journal of human genetics.

Linkage analysis of five candidate genes and essential hypertension in 106 Chinese nuclear families

Wei Huang, Gu-liang Wang, Xin He, 2003, Journal of Human Hypertension.

Models for predicting BRCA1 and BRCA2 mutations in Han Chinese familial breast and/or ovarian cancer patients

Wei Huang, Jiong Wu, Z. Shao, 2009, Breast Cancer Research and Treatment.

Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription units

Shuhua Xu, Yayun Shen, Ying Wang, 2003, Proceedings of the National Academy of Sciences of the United States of America.

A functional polymorphism in the promoter region of GSTM1 implies a complex role for GSTM1 in breast cancer

L. Fan, Keda Yu, Z. Shao, 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Genetic variants in MGMT and risk of lung cancer in Southeastern Chinese: a haplotype‐based analysis

Hongbing Shen, Weiwei Sun, Yi Wang, 2007, Human mutation.

Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control study

Hongbing Shen, Ying Wang, Liang Xu, 2007, BMC Cancer.

Polymorphisms in the Two Helicases ERCC2/XPD and ERCC3/XPB of the Transcription Factor IIH Complex and Risk of Lung Cancer: A Case-Control Analysis in a Chinese Population

Hongbing Shen, Yi Wang, Ying Wang, 2006, Cancer Epidemiology Biomarkers & Prevention.

Association of polymorphisms in one-carbon metabolizing genes and lung cancer risk: a case-control study in Chinese population.

Weiwei Sun, Li Jin, Hongbing Shen, 2008, Lung cancer.

Polymorphisms in DNA damage binding protein 2 (DDB2) and susceptibility of primary lung cancer in the Chinese: a case-control study.

Hongbing Shen, Yi Wang, Ying Wang, 2006, Carcinogenesis.

Genetic variants in peroxisome proliferator-activated receptor-gamma gene are associated with risk of lung cancer in a Chinese population.

Hongbing Shen, Weiwei Sun, Ying Wang, 2008, Carcinogenesis.

A multigenic study on breast cancer risk associated with genetic polymorphisms of ER Alpha, COMT and CYP19 gene in BRCA1/BRCA2 negative Shanghai women with early onset breast cancer or affected relatives

Z. Shao, Wei Huang, Zhen Hu, 2007, Journal of Cancer Research and Clinical Oncology.

Angiotensin II type 2 receptor gene polymorphisms and essential hypertension.

Wei Huang, Kui Zhang, Yi Zhang, 2003, Acta pharmacologica Sinica.

Dermatoglyphics from All Chinese Ethnic Groups Reveal Geographic Patterning

Wei Huang, Li Jin, D. Troy Case, 2010, PloS one.

AR-based Technoself Enhanced Learning Approach to Improving Student Engagement

Zhigang Wen, Wei Huang, Li Jin, 2016 .

Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index.

Jingchun Luo, Ying Wang, E. Lange, 2015, American journal of hypertension.

Polymorphisms of CAK genes and risk for lung cancer: a case-control study in Chinese population.

Hongbing Shen, Weiwei Sun, Yi Wang, 2007, Lung cancer.

Two closely linked variations in actin cytoskeleton pathway in a Chinese pedigree with disseminated superficial actinic porokeratosis.

Wei Huang, Shi-jie Xu, Zhi-zhong Zheng, 2005, Journal of the American Academy of Dermatology.

Fine Mapping and Identification of a Candidate Gene SSH1 in Disseminated Superficial Actinic

X. Chu, Ying Wang, Wei Huang, 2004 .

Fine mapping and identification of a candidate gene SSH1 in disseminated superficial actinic porokeratosis

X. Chu, Yi Wang, L. Nie, 2004, Human mutation.

[The association of two single nucleotide polymorphisms in PRKCZ and UTS2 respectively with type 2 diabetes in Han people of northern China].

Yan Shen, Zhu Chen, Wei Huang, 2002, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Genetic variants in GSTM3 gene within GSTM4-GSTM2-GSTM1-GSTM5-GSTM3 cluster influence breast cancer susceptibility depending on GSTM1

L. Fan, Keda Yu, Z. Shao, 2010, Breast Cancer Research and Treatment.

Allelic imbalance regions on chromosomes 8p, 17p and 19p related to metastasis of hepatocellular carcinoma: comparison between matched primary and metastatic lesions in 22 patients by genome-wide microsatellite analysis

Q. Ye, L. Qin, Zeng-chen Ma, 2003, Journal of Cancer Research and Clinical Oncology.

Research Status and Expectation of Intelligent Deformable Wing Aircraft

Ying Wang, Lin Yi, Wei Huang, 2020, IOP Conference Series: Materials Science and Engineering.

Developing a technoself system to improve lifelong learning engagement

Wei Huang, Li Jin, Zhigang Wen, 2015, 2015 IEEE International Conference on Teaching, Assessment, and Learning for Engineering (TALE).

Polymorphic distribution of Y-chromosome haplotype and mitochondrial DNA in the Bouyei people in China.

Li Jin, Wei Huang, B. Wen, 2004, Chinese Medical Journal.

[CHEK2 c.1100delC may not contribute to genetic background of hereditary breast cancer from Shanghai of China].

Z. Shao, G. Di, Wei Huang, 2006, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Origins and migrations of Bouyei people in China--insights from Y chromosome and mitochondrion].

Li Jin, Wei Huang, B. Wen, 2002, Yi chuan xue bao = Acta genetica Sinica.

α-ADDUCIN GENE AND ESSENTIAL HYPERTENSION IN CHINA

Li Jin, Wei Huang, Ding-liang Zhu, 2001 .

[Association of angiotensin I converting enzyme 2 gene polymorphism with essential hypertension in Chinese].

Wei Huang, Kui Zhang, Yi Zhang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Identification of type 2 diabetes loci in 433,540 East Asian individuals

Y. J. Kim, M. McCarthy, A. Morris, 2020, Nature.

Chromosome 2p14 Is Linked to Susceptibility to Leprosy

Jianjun Liu, Hong Liu, Yongxiang Yu, 2012, PloS one.

Mutation M157R of keratin 9 in a Chinese family with epidermolytic palmoplantar keratoderma

Wei Huang, Zhi-zhong Zheng, Z. Niu, 2008, International journal of dermatology.

Reassessment of microarray expression data of porokeratosis by quantitative real‐time polymerase chain reaction

Wei Huang, Zhi-zhong Zheng, M. Crosby, 2010, Journal of cutaneous pathology.

A functional variant in the transcriptional regulatory region of gene LOC344967 cosegregates with disease phenotype in familial nasopharyngeal carcinoma.

H. Qin, W. Jia, Wei Huang, 2006, Cancer research.

Evidence for a novel psoriasis susceptibility locus at 9q33-9q34 in Chinese Hans.

Wei Li, Liangdan Sun, Xuejun Zhang, 2007, The Journal of investigative dermatology.

Integration of genetic signature and TNM staging system for predicting the relapse of locally advanced colorectal cancer

Ying Ding, Wei Huang, Haifeng Wang, 2010, International Journal of Colorectal Disease.

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Michael S. Reidy, Tanya M. Teslovich, Anne W. Ndungu, 2023, Diabetologia.

Protein kinase C/zeta (PRKCZ) gene is associated with type 2 diabetes in Han population of North China and analysis of its haplotypes.

Yan Shen, Zhu Chen, Y. Meng, 2003, World journal of gastroenterology.

Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

Yoonjung Yoonie Joo, Cassandra N. Spracklen, Y. J. Kim, 2023, medRxiv.

Confirmation of susceptibility gene loci on chromosome 1 in northern China Han families with type 2 diabetes.

Yan Shen, Zhijian Yao, Zhu Chen, 2001, Chinese medical journal.

Analysis of genome‐wide association study‐linked loci in Parkinson's disease of Mainland China

Ying Wang, Jianfang Ma, Wei Huang, 2013, Movement disorders : official journal of the Movement Disorder Society.

[A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].

D. Hu, Wei Huang, Zong-hou Shen, 2005, [Zhonghua yan ke za zhi] Chinese journal of ophthalmology.

genomesDrosophilaAdaptive genic evolution in the

R. Hudson, Zhu Chen, M. Hubisz, 2007 .

Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.

Wei Huang, Shu Zheng, Su-zhan Zhang, 2004, Chinese Medical Journal.

Bmc Medical Genetics

Wei Huang, Yi Wang, Yan Dong, 2022 .

A saturated map of common genetic variants associated with human height

Aaron F. McDaid, M. P. Concas, Cassandra N. Spracklen, 2022, Nature.

The prevalence of BRCA1 and BRCA2 mutations in eastern Chinese women with breast cancer

Z. Shao, Jiong Wu, Wei Huang, 2006, Journal of Cancer Research and Clinical Oncology.

Compound heterozygosity for an apolipoprotein A1 gene promoter mutation and a structural nonsense mutation with apolipoprotein A1 deficiency.

Wei Huang, J. Sasaki, K. Arakawa, 1999, Arteriosclerosis, thrombosis, and vascular biology.

A functional polymorphism affecting the APOA5 gene expression is causally associated with plasma triglyceride levels conferring coronary atherosclerosis risk in Han Chinese Population.

Yi Wang, Ying Wang, Wei Huang, 2014, Biochimica et Biophysica Acta.

An ankylosing spondylitis risk variant alters osteoclast differentiation.

Wei Huang, Jiucun Wang, Li Jin, 2022, Rheumatology.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2022, American journal of human genetics.

Gene expression profiling of porokeratosis

Wei Huang, Haifeng Wang, Zhi-zhong Zheng, 2008, Journal of cutaneous pathology.

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

Stephen C. J. Parker, Tanya M. Teslovich, Anne W. Ndungu, 2020 .

Single nucleotide polymorphisms in promoter of angiotensin II type 1 receptor gene associated with essential hypertension and coronary heart disease in Chinese population.

Yayun Shen, Wei Huang, Huang Wei, 2003, Acta pharmacologica Sinica.

Single nucleotide polymorphisms in CAPN10 gene of Chinese people and its correlation with type 2 diabetes mellitus in Han people of northern China.

Wei Huang, Jin Zuo, Yan Shen, 2002, Biomedical and environmental sciences : BES.

The localization of type 2 diabetes susceptibility gene loci in northern Chinese Han families

M. Xiong, Li Jin, Zhu Chen, 2000 .

An SNP of the ZBTB38 gene is associated with idiopathic short stature in the Chinese Han population

Wei Wang, X. Chu, Ying Wang, 2013, Clinical endocrinology.