Y. Meng

发表

The Genotype-Tissue Expression (GTEx) project

Ellen T. Gelfand, Bryan M. Gillard, Karna L. Robinson, 2013, Nature Genetics.

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

Jun S. Liu, Ellen T. Gelfand, Ayellet V. Segrè, 2015, Science.

Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks

Qiong Yang, Anita L DeStefano, Kathryn L Lunetta, 2007, BMC proceedings.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Xiaofeng Zhu, Olufunmilayo I. Olopade, Alex P. Reiner, 2013, Nature Genetics.

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Manuel A. R. Ferreira, S. Gabriel, M. Daly, 2008, Nature Genetics.

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

K. Lunetta, R. Green, You-Qiang Song, 2007, Nature Genetics.

Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Ellen T. Gelfand, Ayellet V. Segrè, Casandra A. Trowbridge, 2016, Scientific Reports.

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

Yusuke Nakamura, Yukinori Okada, David Couper, 2011, PLoS genetics.

Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts

Wei Chen, Luigi Ferrucci, Yun Li, 2012, Circulation. Cardiovascular genetics.

Restoration of copper metabolism and rescue of hepatic abnormalities in LEC rats, an animal model of Wilson disease, by expression of human ATP7B gene.

Y. Meng, T. Okamura, T. Sugiyama, 2004, Biochimica et biophysica acta.

Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript

Y. Meng, Jiuyong Xie, Shangzhi Huang, 2015, Genes & Nutrition.

A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness

J. Hirschhorn, Y. Meng, S. Vedantam, 2020, The Journal of clinical endocrinology and metabolism.

Replication and fine mapping of asthma-associated loci in individuals of African ancestry

Cameron D. Palmer, J. Hirschhorn, A. Price, 2013, Human Genetics.

Correlation between CYP2C19 gene polymorphism and clinical efficacy of clopidogrel in patients with coronary artery heart disease

Y. Meng, Y. Gong, Xiangxi Wang, 2020 .

Coding sequence, genomic organization and expression of a folate binding protein gene in the rat.

Y. Meng, S. Rothenberg, E. Sadasivan, 2000, Gene.

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.

M. Nalls, A. Singleton, A. Reiner, 2013, Human molecular genetics.

Three novel homozygous mutations in the GNPTG gene that cause mucolipidosis type III gamma.

Y. Meng, Wei-min Zhang, Shuang Liu, 2014, Gene.

Association studies between the plasmin genes and late-onset Alzheimer's disease

Y. Meng, R. Mayeux, L. Farrer, 2007, Neurobiology of Aging.

[An analysis of mutations causing Gaucher disease in Chinese population].

Y. Meng, N. Tang, Wei-min Zhang, 2009, Zhonghua yi xue za zhi.

Mucopolysaccharidosis IVA mutations in Chinese patients: 16 novel mutations

Y. Meng, Z. Wang, Shangzhi Huang, 2010, Journal of Human Genetics.

Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Andrew B. Nobel, Fred A. Wright, Ivan Rusyn, 2015, Scientific Reports.

Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.

Cameron D. Palmer, M. Nalls, C. Rotimi, 2011, Human molecular genetics.

Analysis of the glucocerebrosidase gene in Parkinson's disease

P. S. St George-Hyslop, Y. Meng, A. Lang, 2005, Movement disorders : official journal of the Movement Disorder Society.

Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.

E. Demerath, J. Hirschhorn, Y. Meng, 2011, American journal of human genetics.

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.

Toshiko Tanaka, M. Nalls, A. Singleton, 2016, Human molecular genetics.

Genome-Wide Association Studies of the PR Interval in African Americans

Kathleen F. Kerr, Jared W. Magnani, Susan Redline, 2011, PLoS genetics.

Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans

Kathleen F. Kerr, Cameron D. Palmer, Toshiko Tanaka, 2012, Circulation. Cardiovascular genetics.

A novel mutation at the JK locus causing Jknull phenotype in a Chinese family

Y. Meng, Baoxue Yang, Dan Zhao, 2005, Science in China Series C: Life Sciences.

Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease

P. S. St George-Hyslop, Y. Meng, R. Mayeux, 2008, Neurogenetics.

Mucopolysaccharidosis I mutations in Chinese patients: identification of 27 novel mutations and 6 cases involving prenatal diagnosis

Y. Meng, W. Zhang, Wei-min Zhang, 2012, Clinical genetics.

[Postnatal and prenatal diagnosis of mucopolysaccharidosis type III (Sanfilippo syndrome)].

Y. Meng, Wei-min Zhang, Hui-ping Shi, 2008, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.

Scott M. Williams, Yu-Han H. Hsu, Nicholette D. Palmer, 2021, American journal of human genetics.

IL-6 gene promoter polymorphisms and risk of coronary artery disease in a Chinese population.

Y. Meng, B. Du, Y. Li, 2014, Genetics and molecular research : GMR.

Association between SORL1 and Alzheimer's disease in a genome-wide study

P. S. St George-Hyslop, Y. Meng, R. Mayeux, 2007, Neuroreport.

Gene-Centric Analysis of Serum Cotinine Levels in African and European American Populations

Robert J. Goodloe, Cameron D. Palmer, M. Pletcher, 2012, Neuropsychopharmacology.

Association of polymorphisms in the Angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community.

Rivka Inzelberg, Y. Meng, L. Farrer, 2006, American journal of human genetics.

Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript

Y. Meng, Jiuyong Xie, Shangzhi Huang, 2015, Genes & Nutrition.

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

Cameron D. Palmer, A. Reiner, J. Pankow, 2014, Human Genetics.

Identification of novel mutations of PKD1 gene in Chinese patients with autosomal dominant polycystic kidney disease by targeted next-generation sequencing.

Y. Meng, Shangzhi Huang, Mingrong Zhang, 2014, Clinica chimica acta; international journal of clinical chemistry.

Performance of random forest when SNPs are in linkage disequilibrium

Yi Yu, Lindsay A. Farrer, L. Adrienne Cupples, 2009, BMC Bioinformatics.

Genetic Variability of Smoking Persistence in African Americans

Robert J. Goodloe, D. Levy, S. Redline, 2011, Cancer Prevention Research.

Phenotypic and genetic characterization of the Atp7a(Mo-Tohm) mottled mouse: a new murine model of Menkes disease.

Y. Meng, T. Okamura, N. Kasai, 2006, Genomics.

A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmus

Y. Meng, Z. Wang, Shangzhi Huang, 2009, Molecular vision.

Association of PS1 1/2, ACE I/D, and LRP C/T polymorphisms with Alzheimer's disease in the Chinese population: a meta-analysis of case-control studies.

Y. Meng, L. Yang, Y.-J. Wang, 2015, Genetics and molecular research : GMR.

Human pituitary homeobox-3 gene in congenital cataract in a Chinese family.

Y. Meng, N. Dong, X. Ye, 2015, International journal of clinical and experimental medicine.

Replication and fine mapping of asthma-associated loci in individuals of African ancestry

J. Hirschhorn, A. Price, Taylor R. Young, 2013, Human Genetics.

[Clinical manifestations and mutation study in 16 Chinese patients with Fabry disease].

Y. Meng, Wei-min Zhang, M. Wei, 2010, Zhonghua yi xue za zhi.

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.

A preliminary investigation of amino acid and acylcarnitine levels in neonates from the Tibet autonomous

Y. Meng, Tao Jiang, Yaping Tian, 2022, Frontiers in Genetics.

Y. Meng, R. Mayeux, L. Farrer, 2022 .

[Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome].

Y. Meng, Wei-Chen Wang, Hui-ping Shi, 2011, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Mutation analysis of the PAH gene in patients with phenylketonuria in Gansu province].

Y. Meng, Z. Wang, Yousheng Yan, 2009, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[The power of linkage analysis on PAH gene in prenatal gene diagnosis is improved with three additional short tandem repeat markers].

Y. Meng, Hui Guo, F. Yao, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

S. Gabriel, M. Daly, D. Collier, 2008, Nature Genetics.

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

Cameron D. Palmer, A. Reiner, J. Pankow, 2014, Human Genetics.

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.

Kathleen F. Kerr, M. Nalls, A. Singleton, 2016, Human Molecular Genetics.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Gary K. Chen, Scott M. Williams, Nicholette D. Palmer, 2013, Nature Genetics.