Lista de obras - Keyue Ding - Dominio Público Uruguay

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

artículo científico publicado en 2013

A genome-wide association study of red blood cell traits using the electronic medical record.

artículo científico publicado en 2010

Association between genetic variation of CACNA1H and childhood absence epilepsy

artículo científico publicado en 2003

Comparative and evolutionary pharmacogenetics of ABCB1: complex signatures of positive selection on coding and regulatory regions.

artículo científico publicado en 2007

Comparison of error correction algorithms for Ion Torrent PGM data: application to hepatitis B virus

artículo científico

Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate

artículo científico publicado en 2011

DNA and RNA Sequencing Recapitulated Aberrant Tumor Metabolism in Liver Cancer Cell Lines

artículo científico publicado en 2021

Deep phenotyping and whole-exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders

artículo científico publicado en 2022

Esophageal cancer in Chinese population: no polymorphism in codon 149 of P21(Waf1/Cip1) cyclin dependent kinase gene

artículo científico publicado en 2002

Evidence for positive selection in the C-terminal domain of the cholesterol metabolism gene PCSK9 based on phylogenetic analysis in 14 primate species

artículo científico publicado en 2007

Evolutionary genetics of coronary heart disease.

artículo científico publicado en 2009

Gene expression profiling of peripheral blood mononuclear cells in the setting of peripheral arterial disease.

artículo científico publicado en 2012

Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits

artículo científico publicado en 2012

Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study

artículo científico publicado en 2013

Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record

artículo científico publicado en 2011

Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease

artículo científico publicado en 2011

LDA—a java-based linkage disequilibrium analyzer ⬇️

artículo científico publicado el 1 de noviembre de 2003

Leveraging a Multi-Omics Strategy for Prioritizing Personalized Candidate Mutation-Driver Genes: A Proof-of-Concept Study.

artículo científico publicado en 2015

Mechanisms of disease: The genetic basis of coronary heart disease.

artículo científico publicado en 2007

Methods for the selection of tagging SNPs: a comparison of tagging efficiency and performance

artículo científico publicado en 2006

Molecular evolution of 5' flanking regions of 87 candidate genes for atherosclerotic cardiovascular disease.

artículo científico publicado en 2006

Molecular population genetics of PCSK9: a signature of recent positive selection.

artículo científico publicado en 2008

Mutation screening of BMP4, BMP7, HOXA4 and HOXB6 genes in Chinese patients with hypospadias

scientific article published on 27 September 2006

Patterns of population differentiation of candidate genes for cardiovascular disease

artículo científico publicado en 2007

Relationship between mitochondrial DNA mutations and clinical characteristics in human lung cancer

artículo científico publicado en 2007

The effect of haplotype-block definitions on inference of haplotype-block structure and htSNPs selection.

artículo científico publicado en 2004

Transcriptome sequencing identified hub genes for hepatocellular carcinoma by weighted-gene co-expression analysis.

artículo científico publicado en 2016

Using natural language processing to extract clinically useful information from Chinese electronic medical records

scientific article published on 07 January 2019

Validation of a multi-omics strategy for prioritizing personalized candidate driver genes

artículo científico publicado en 2016

htSNPer1.0: software for haplotype block partition and htSNPs selection.

artículo científico publicado en 2005

p53 polymorphism and p21WAF1/CIP1 haplotype in the intestinal gastric cancer and the precancerous lesions.

artículo científico publicado en 2004

Lista de obras de Keyue Ding

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

A genome-wide association study of red blood cell traits using the electronic medical record.

Association between genetic variation of CACNA1H and childhood absence epilepsy

Comparative and evolutionary pharmacogenetics of ABCB1: complex signatures of positive selection on coding and regulatory regions.

Comparison of error correction algorithms for Ion Torrent PGM data: application to hepatitis B virus

Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate

DNA and RNA Sequencing Recapitulated Aberrant Tumor Metabolism in Liver Cancer Cell Lines

Deep phenotyping and whole-exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders

Esophageal cancer in Chinese population: no polymorphism in codon 149 of P21(Waf1/Cip1) cyclin dependent kinase gene

Evidence for positive selection in the C-terminal domain of the cholesterol metabolism gene PCSK9 based on phylogenetic analysis in 14 primate species

Evolutionary genetics of coronary heart disease.

Gene expression profiling of peripheral blood mononuclear cells in the setting of peripheral arterial disease.

Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits

Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study

Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record

Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease

LDA—a java-based linkage disequilibrium analyzer ⬇️

Leveraging a Multi-Omics Strategy for Prioritizing Personalized Candidate Mutation-Driver Genes: A Proof-of-Concept Study.

Mechanisms of disease: The genetic basis of coronary heart disease.

Methods for the selection of tagging SNPs: a comparison of tagging efficiency and performance

Molecular evolution of 5' flanking regions of 87 candidate genes for atherosclerotic cardiovascular disease.

Molecular population genetics of PCSK9: a signature of recent positive selection.

Mutation screening of BMP4, BMP7, HOXA4 and HOXB6 genes in Chinese patients with hypospadias

Patterns of population differentiation of candidate genes for cardiovascular disease

Relationship between mitochondrial DNA mutations and clinical characteristics in human lung cancer

The effect of haplotype-block definitions on inference of haplotype-block structure and htSNPs selection.

Transcriptome sequencing identified hub genes for hepatocellular carcinoma by weighted-gene co-expression analysis.

Using natural language processing to extract clinically useful information from Chinese electronic medical records

Validation of a multi-omics strategy for prioritizing personalized candidate driver genes

htSNPer1.0: software for haplotype block partition and htSNPs selection.

p53 polymorphism and p21WAF1/CIP1 haplotype in the intestinal gastric cancer and the precancerous lesions.