Yongyong Shi mainly focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Haplotype and Case-control study. His research in Genetics intersects with topics in Psychosis and Schizophrenia. His Genome-wide association study research incorporates themes from Odds ratio, Susceptibility locus, Han chinese, Pharmacogenetics and Genetic architecture.
His biological study spans a wide range of topics, including Internal medicine, Genetic variation and Polymorphism. Yongyong Shi has researched Haplotype in several fields, including Genetic linkage and Computational biology. Yongyong Shi works mostly in the field of Linkage disequilibrium, limiting it down to topics relating to Tag SNP and, in certain cases, Association mapping, as a part of the same area of interest.
His primary scientific interests are in Genetics, Single-nucleotide polymorphism, Genome-wide association study, Genetic association and Haplotype. His Genetics study frequently draws connections to other fields, such as Psychosis. He has included themes like Major depressive disorder, Schizophrenia and Internal medicine, Case-control study in his Single-nucleotide polymorphism study.
His studies in Genome-wide association study integrate themes in fields like Oncology, Han chinese, Expression quantitative trait loci, Locus and Heritability. His Genetic association study incorporates themes from Bioinformatics, Schizophrenia, Genotyping, Cohort and Candidate gene. The Haplotype study combines topics in areas such as Genetic linkage, Genetic variation and Allele frequency.
His scientific interests lie mostly in Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Allele. His Genome-wide association study study integrates concerns from other disciplines, such as Expression quantitative trait loci, Gout, Disease and Heritability. His study in Gene, Locus, Genotype, Linkage disequilibrium and Nonsynonymous substitution falls within the category of Genetics.
His studies deal with areas such as Schizophrenia, Genotyping and Chinese population as well as Genetic association. His work carried out in the field of Single-nucleotide polymorphism brings together such families of science as Bipolar disorder, Internal medicine, Case-control study and Oncology. His work investigates the relationship between Allele and topics such as Schizophrenia that intersect with problems in Genetic variants and Genome.
His primary areas of investigation include Genome-wide association study, Case-control study, Single-nucleotide polymorphism, Genetics and Genetic association. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Expression quantitative trait loci and Disease. His Case-control study research is multidisciplinary, incorporating perspectives in Evolutionary biology, Polygenic risk score and Lifetime risk.
His study involves Cervical cancer, SNP, Glutamate receptor signaling pathway and Gene expression, a branch of Genetics. His research combines Linkage disequilibrium and Genetic association. His Linkage disequilibrium study necessitates a more in-depth grasp of Haplotype.
SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci.
Yong Yong Shi;Lin He.
Cell Research (2005)
The sequence and de novo assembly of the giant panda genome
Ruiqiang Li;Wei Fan;Geng Tian;Hongmei Zhu.
Identification of loci associated with schizophrenia by genome-wide association and follow-up
Michael C. O'Donovan;Nicholas Craddock;Nadine Norton;Hywel Williams.
Nature Genetics (2008)
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Zi-Jiang Chen;Han Zhao;Lin He;Lin He;Lin He;Yuhua Shi.
Nature Genetics (2011)
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Yongyong Shi;Han Zhao;Yuhua Shi;Yunxia Cao.
Nature Genetics (2012)
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Zhibin Hu;Chen Wu;Yongyong Shi;Huan Guo.
Nature Genetics (2011)
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.
Zhiqiang Li;Jianhua Chen;Hao Yu;Hao Yu;Hao Yu;Lin He.
Nature Genetics (2017)
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Xiangfeng Lu;Laiyuan Wang;Laiyuan Wang;Shufeng Chen;Lin He.
web science (2012)
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
Christopher I. Amos;Joe Dennis;Zhaoming Wang;Jinyoung Byun.
Cancer Epidemiology, Biomarkers & Prevention (2017)
Comparative genetic architectures of schizophrenia in East Asian and European populations
Max Lam;Chia-Yen Chen;Zhiqiang Li;Alicia R. Martin;Alicia R. Martin.
Nature Genetics (2019)
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