Author details

Full Name

Qunyuan Zhang

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
28215425	Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism.	J Pediatr	2017
28747753	Corrigendum: Protein-structure-guided discovery of functional mutations across 19 cancer types.	Nat Genet	2017
27294619	Protein-structure-guided discovery of functional mutations across 19 cancer types.	Nat Genet	2016
26935785	Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm, and Term Infants.	J Pediatr	2016
27060904	Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.	BMC Geriatrics	2016
26689913	Patterns and functional implications of rare germline variants across 12 cancer types.	Nat Commun	2015
25673413	Genetic studies of body mass index yield new insights for obesity biology.	Nature	2015
25797264	Vasohibin-1 suppresses colon cancer.	Oncotarget	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25704602	Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.	Am J Hum Genet	2015
25664523	Burden of disease variants in participants of the Long Life Family Study.	Aging (Albany NY)	2015
25904936	Associating rare genetic variants with human diseases.	Frontiers in Genetics	2015
25902833	Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study.	BMC Genet	2015
25568281	Selection of models for the analysis of risk-factor trees: leveraging biological knowledge to mine large sets of risk factors with application to microbiome data.	Bioinformatics	2015
25968569	CD4+ and CD8+ T cells have opposing roles in breast cancer progression and outcome.	Oncotarget	2015
25758594	Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index.	J Gerontol A Biol Sci Med Sci	2015
25044106	Estimating and testing pleiotropy of single genetic variant for two quantitative traits.	Genetic Epidemiology	2014
25553246	Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations.	BMJ Open Respir Res	2014
25282103	Defining the role of common variation in the genomic and biological architecture of adult human height.	Nat Genet	2014
23913930	Heritability of and mortality prediction with a longevity phenotype: the healthy aging index.	J Gerontol A Biol Sci Med Sci	2014
24448499	Integrated analysis of germline and somatic variants in ovarian cancer.	Nat Commun	2014
24371154	MSIsensor: microsatellite instability detection using paired tumor-normal sequence data.	Bioinformatics	2014
24497850	Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.	PLoS Genet	2014
25169066	Adjusting family relatedness in data-driven burden test of rare variants.	Genet Epidemiol	2014
24896187	Persistent gut microbiota immaturity in malnourished Bangladeshi children.	Nature	2014
24507775	Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.	Am J Hum Genet	2014
24507774	Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.	Am J Hum Genet	2014
23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Nat Genet	2013
23953852	Genome-wide association studies of maximum number of drinks.	Journal of Psychiatric Research	2013
24132290	Mutational landscape and significance across 12 major cancer types.	Nature	2013
23477746	The ERLIN1-CHUK-CWF19L1 gene cluster influences liver fat deposition and hepatic inflammation in the NHLBI Family Heart Study.	Atherosclerosis	2013
22072270	Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.	Journal of Neural Transmission	2012
22759861	MuSiC: identifying mutational significance in cancer genomes.	Genome Res	2012
22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Journal of Molecular Neuroscience	2012
22300766	VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.	Genome Res	2012
22336959	Rare PPARA variants and extreme response to fenofibrate in the Genetics of Lipid-Lowering Drugs and Diet Network Study.	Pharmacogenet Genomics	2012
22377092	ANAPC1 and SLCO3A1 are associated with nicotine dependence: meta-analysis of genome-wide association studies.		2012
22723548	Human regulatory T cells induce T-lymphocyte senescence.	Blood	2012
22715292	Atg16L1 deficiency confers protection from uropathogenic Escherichia coli infection in vivo.	Proceedings of the National Academy of Sciences of the United States of America	2012
22817890	The origin and evolution of mutations in acute myeloid leukemia.	Cell	2012
23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Am J Hum Genet	2012
23034170	Tumor-infiltrating Î³Î´ T lymphocytes predict clinical outcome in human breast cancer.	Journal of Immunology	2012
23166334	Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.	Pediatrics	2012
21651830	Parent-of-origin effects of FAS and PDLIM1 in attention-deficit/hyperactivity disorder.	Journal of Psychiatry and Neuroscience	2012
21688384	Genome-wide association analysis of age at onset in schizophrenia in a European-American sample.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2011
22373107	Distance-based phenotypic association analysis of DNA sequence data.	BMC Proceedings	2011
22373066	Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits.	BMC Proceedings	2011
21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Diabetes	2011
22144573	Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.	Circulation	2011
21703634	A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.	Journal of Psychiatric Research	2011