Lista de obras - Yongyong Shi - Dominio Público Uruguay

A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1.

artículo científico publicado en 2011

A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12

scientific journal article

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

artículo científico publicado en 2013

A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility.

artículo científico publicado en 2014

A novel variant associated with HDL-C levels by modifying DAGLB expression levels: An annotation-based genome-wide association study

artículo científico publicado en 2018

A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn).

artículo científico publicado en 2009

A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population

artículo científico publicado en 2008

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

artículo científico publicado en 2008

Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population

artículo científico publicado en 2012

CTLA-4 confers a risk of recurrent schizophrenia, major depressive disorder and bipolar disorder in the Chinese Han population ⬇️

artículo científico publicado el 30 de octubre de 2010

Common SNPs and haplotypes in DGKH are associated with bipolar disorder and schizophrenia in the Chinese Han population

artículo científico publicado en 2010

Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma

artículo científico publicado en 2015

Common variants in ZMIZ1 and near NGF confer risk for primary dysmenorrhoea

artículo científico publicado en 2017

Common variants in major histocompatibility complex region and TCF4 gene are significantly associated with schizophrenia in Han Chinese

artículo científico publicado en 2010

Common variants in the BCL9 gene conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

artículo científico publicado en 2011

Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection

artículo científico publicado en 2014

Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

artículo científico publicado en 2020

DNA origami-based shape IDs for single-molecule nanomechanical genotyping

artículo científico publicado en 2017

Effect of aerobic exercise and diet on liver fat in pre-diabetic patients with non-alcoholic-fatty-liver-disease: A randomized controlled trial

artículo científico publicado en 2017

Erratum: The sequence and de novo assembly of the giant panda genome

artículo científico publicado en 2010

Exome Array Analysis Identifies Variants in SPOCD1 and BTN3A2 That Affect Risk for Gastric Cancer

artículo científico publicado en 2017

Fine-mapping of ZDHHC2 identifies risk variants for schizophrenia in the Han Chinese population

artículo científico publicado en 2020

GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers

scientific journal article

Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population

artículo científico publicado en 2004

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

artículo científico publicado en 2014

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

artículo científico publicado en 2017

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese

artículo científico publicado en 2015

Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

artículo científico publicado en 2017

Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese.

artículo científico publicado en 2015

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome

scientific journal article

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3 ⬇️

artículo científico publicado el 12 de diciembre de 2010

Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese

scientific article published in Nature Communications

Genome-wide two-locus interaction analysis identifies multiple epistatic SNP pairs that confer risk of prostate cancer: A cross-population study.

artículo científico publicado en 2017

Gold nanoparticles for high-throughput genotyping of long-range haplotypes.

artículo científico publicado en 2011

ITIH family genes confer risk to schizophrenia and major depressive disorder in the Han Chinese population

artículo científico publicado en 2014

Identification of loci associated with schizophrenia by genome-wide association and follow-up

artículo científico publicado en 2008

Identification of recurrent USP48 and BRAF mutations in Cushing's disease

artículo científico publicado en 2018

Loci with genome-wide associations with schizophrenia in the Han Chinese population

artículo científico publicado en 2015

Mapping of hepatic expression quantitative trait loci (eQTLs) in a Han Chinese population.

artículo científico publicado en 2014

New loci associated with chronic hepatitis B virus infection in Han Chinese

artículo científico publicado en 2013

No Association of the YWHAE Gene with Schizophrenia, Major Depressive Disorder or Bipolar Disorder in the Han Chinese Population ⬇️

artículo científico publicado el 24 de diciembre de 2010

Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy.

artículo científico publicado en 2015

Polymorphisms of renin-angiotensin-aldosterone system gene in chinese han patients with nonfamilial atrial fibrillation

artículo científico publicado en 2015

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

artículo científico publicado en 2005

SHEsisEpi, a GPU-enhanced genome-wide SNP-SNP interaction scanning algorithm, efficiently reveals the risk genetic epistasis in bipolar disorder

artículo científico publicado en 2010

SHEsisPCA: a GPU-based software to correct for population stratification that efficiently accelerates the process for handling genome-wide datasets

artículo científico publicado en 2015

SHEsisPlus, a toolset for genetic studies on polyploid species.

artículo científico publicado en 2016

Structural Comparison and Drug Screening of Spike Proteins of Ten SARS-CoV-2 Variants

artículo científico publicado en 2022

The Endothelial Nitric Oxide Synthase Gene Is Associated with Coronary Artery Disease: A Meta-Analysis ⬇️

artículo científico publicado el 22 de septiembre de 2010

The MDGA1 gene confers risk to schizophrenia and bipolar disorder ⬇️

artículo científico publicado el 13 de diciembre de 2010

The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

artículo científico publicado en 2016

The genome-wide mutational landscape of pituitary adenomas.

scientific article published on 27 September 2016

The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies

scientific article published on 27 August 2019

The sequence and de novo assembly of the giant panda genome

artículo científico publicado en 2010

Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

artículo científico publicado en 2020

[Current status of studies on genome-wide gene-gene interactions]

scientific article published on 01 August 2011

eRFSVM: a hybrid classifier to predict enhancers-integrating random forests with support vector machines

artículo científico publicado en 2016

Lista de obras de Yongyong Shi

A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1.

A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility.

A novel variant associated with HDL-C levels by modifying DAGLB expression levels: An annotation-based genome-wide association study

A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn).

A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population

CTLA-4 confers a risk of recurrent schizophrenia, major depressive disorder and bipolar disorder in the Chinese Han population ⬇️

Common SNPs and haplotypes in DGKH are associated with bipolar disorder and schizophrenia in the Chinese Han population

Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma

Common variants in ZMIZ1 and near NGF confer risk for primary dysmenorrhoea

Common variants in major histocompatibility complex region and TCF4 gene are significantly associated with schizophrenia in Han Chinese

Common variants in the BCL9 gene conferring risk of schizophrenia

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection

Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

DNA origami-based shape IDs for single-molecule nanomechanical genotyping

Effect of aerobic exercise and diet on liver fat in pre-diabetic patients with non-alcoholic-fatty-liver-disease: A randomized controlled trial

Erratum: The sequence and de novo assembly of the giant panda genome

Exome Array Analysis Identifies Variants in SPOCD1 and BTN3A2 That Affect Risk for Gastric Cancer

Fine-mapping of ZDHHC2 identifies risk variants for schizophrenia in the Han Chinese population

GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers

Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese

Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese.

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3 ⬇️

Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese

Genome-wide two-locus interaction analysis identifies multiple epistatic SNP pairs that confer risk of prostate cancer: A cross-population study.

Gold nanoparticles for high-throughput genotyping of long-range haplotypes.

ITIH family genes confer risk to schizophrenia and major depressive disorder in the Han Chinese population

Identification of loci associated with schizophrenia by genome-wide association and follow-up

Identification of recurrent USP48 and BRAF mutations in Cushing's disease

Loci with genome-wide associations with schizophrenia in the Han Chinese population

Mapping of hepatic expression quantitative trait loci (eQTLs) in a Han Chinese population.

New loci associated with chronic hepatitis B virus infection in Han Chinese

No Association of the YWHAE Gene with Schizophrenia, Major Depressive Disorder or Bipolar Disorder in the Han Chinese Population ⬇️

Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy.

Polymorphisms of renin-angiotensin-aldosterone system gene in chinese han patients with nonfamilial atrial fibrillation

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

SHEsisEpi, a GPU-enhanced genome-wide SNP-SNP interaction scanning algorithm, efficiently reveals the risk genetic epistasis in bipolar disorder

SHEsisPCA: a GPU-based software to correct for population stratification that efficiently accelerates the process for handling genome-wide datasets

SHEsisPlus, a toolset for genetic studies on polyploid species.

Structural Comparison and Drug Screening of Spike Proteins of Ten SARS-CoV-2 Variants

The Endothelial Nitric Oxide Synthase Gene Is Associated with Coronary Artery Disease: A Meta-Analysis ⬇️

The MDGA1 gene confers risk to schizophrenia and bipolar disorder ⬇️

The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

The genome-wide mutational landscape of pituitary adenomas.

The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies

The sequence and de novo assembly of the giant panda genome

Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

[Current status of studies on genome-wide gene-gene interactions]

eRFSVM: a hybrid classifier to predict enhancers-integrating random forests with support vector machines