Lista de obras - Shaoqi Rao - Dominio Público Uruguay

A fine map for maternal lineage analysis by mitochondrial hypervariable region in 12 Chinese goat breeds

artículo científico publicado en 2009

A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.

artículo científico publicado en 2010

A meta-analysis of the association between TNF-α -308G>A polymorphism and type 2 diabetes mellitus in Han Chinese population

artículo científico publicado en 2013

A novel evolution-based method for detecting gene-gene interactions

artículo científico publicado en 2011

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

artículo científico publicado en 2014

A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.

artículo científico publicado en 2006

A robust hybrid between genetic algorithm and support vector machine for extracting an optimal feature gene subset

artículo científico publicado en 2005

A systematic method for mapping multiple loci: an application to construct a genetic network for rheumatoid arthritis.

artículo científico publicado en 2007

AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3.

artículo científico publicado en 2006

Adaptation of the Audit of Diabetes-Dependent Quality of Life questionnaire to people with diabetes in China

artículo científico publicado en 2011

Ala499Val (C>T) and Lys939Gln (A>C) polymorphisms of the XPC gene: their correlation with the risk of primary gallbladder adenocarcinoma--a case-control study in China.

artículo científico publicado en 2010

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

artículo científico publicado en 2007

An ensemble method for gene discovery based on DNA microarray data

artículo científico publicado en 2004

Association Between Apolipoprotein B XbaI Polymorphism and Coronary Heart Disease in Han Chinese Population: A Meta-Analysis

artículo científico publicado en 2016

Association between apolipoprotein B EcoRI polymorphisms and coronary heart disease : A meta-analysis

artículo científico publicado en 2016

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

artículo científico publicado en 2007

Association between polymorphisms in SOD1 and noise-induced hearing loss in Chinese workers.

artículo científico publicado en 2010

Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans

scientific article published on 24 February 2013

Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based Case-Control Study

artículo científico publicado en 2015

Atorvastatin treatment of rats with ischemia-reperfusion injury improves adipose-derived mesenchymal stem cell migration and survival via the SDF-1α/CXCR-4 axis

artículo científico publicado en 2013

Behavioural development of school-aged children who live around a multi-metal sulphide mine in Guangdong province, China: a cross-sectional study

artículo científico publicado en 2009

Brief communication: Y-chromosome haplogroup analysis indicates that Chinese Tuvans share distinctive affinity with Siberian Tuvans.

artículo científico publicado en 2011

Constructing disease-specific gene networks using pair-wise relevance metric: application to colon cancer identifies interleukin 8, desmin and enolase 1 as the central elements

artículo científico publicado en 2008

DOSim: An R package for similarity between diseases based on Disease Ontology ⬇️

artículo científico publicado el 29 de junio de 2011

Disease embryo development network reveals the relationship between disease genes and embryo development genes

scientific article published on 03 August 2011

Efficacy of Atorvastatin combined with adipose-derived mesenchymal stem cell transplantation on cardiac function in rats with acute myocardial infarction

scientific article published on 06 October 2011

Efficacy of combined treatment with albendazole and baicalein against eosinophilic meningitis induced by Angiostrongylus cantonensis in mice

scientific article published on 29 June 2010

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

artículo científico publicado en 2007

Functional homogeneity in microRNA target heterogeneity--a new sight into human microRNomics

artículo científico publicado en 2010

Gene mining: a novel and powerful ensemble decision approach to hunting for disease genes using microarray expression profiling

artículo científico publicado en 2004

Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region

artículo científico publicado en 2009

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p

artículo científico publicado en 2004

Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs.

artículo científico publicado en 2014

Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data.

artículo científico publicado en 2016

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

artículo científico publicado en 2004

Identifying functional modules for coronary artery disease by a prior knowledge-based approach.

artículo científico

Knowledge-based analysis of genetic associations of rheumatoid arthritis to inform studies searching for pleiotropic genes: a literature review and network analysis

artículo científico publicado en 2015

Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study

artículo científico publicado en 2012

Laryngeal aerodynamic analysis in assisting with the diagnosis of muscle tension dysphonia

artículo científico publicado en 2011

Longitudinal data analysis in pedigree studies

artículo científico publicado en 2003

Miscues on the "lack of MEF2A mutations" in coronary artery disease

artículo científico publicado en 2005

Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation

artículo científico publicado en 2015

Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns ⬇️

artículo científico publicado el 17 de febrero de 2011

Pathway-based analysis of the hidden genetic heterogeneities in cancers

artículo científico publicado en 2014

Pathway-based analysis tools for complex diseases: a review

artículo científico publicado en 2014

Phenotype–Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the GJB2 Gene ⬇️

artículo científico publicado el 13 de abril de 2011

Plasma oxidized low-density lipoprotein is an independent risk factor in young patients with coronary artery disease

artículo científico publicado en 2011

Postoperative complications in patients with cochlear implants and impacts of nursing intervention.

artículo científico publicado en 2010

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

artículo científico publicado en 2004

Psychometric properties of the Chinese version of the Pediatric Quality of Life Inventory 4.0 generic core scales.

artículo científico publicado en 2010

Psychometric properties of the coronary heart disease scale of the quality-of-life instruments for chronic diseases (QLICD-CHD): an application to Cantonese patients.

artículo científico publicado en 2014

Rabies trend in China (1990-2007) and post-exposure prophylaxis in the Guangdong province.

artículo científico publicado en 2008

SDF-1α upregulation by atorvastatin in rats with acute myocardial infarction via nitric oxide production confers anti-inflammatory and anti-apoptotic effects.

artículo científico publicado en 2012

Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy

artículo científico publicado en 2010

Short-term outcomes of induction therapy with tacrolimus versus cyclophosphamide for active lupus nephritis: A multicenter randomized clinical trial

scientific article published on 21 December 2010

Strategies for genetic mapping of categorical traits

artículo científico publicado en 2000

To control false positives in gene-gene interaction analysis: two novel conditional entropy-based approaches

artículo científico publicado en 2013

Towards precise classification of cancers based on robust gene functional expression profiles

artículo científico publicado en 2005

Unravelling the hidden heterogeneities of diffuse large B-cell lymphoma based on coupled two-way clustering

artículo científico publicado en 2007

[Advances in development of gene-gene interaction analysis methods based on SNP data: a review].

artículo científico publicado en 2013

[Advances in genetics of restless legs syndrome]

artículo científico publicado en 2009

Lista de obras de Shaoqi Rao

A fine map for maternal lineage analysis by mitochondrial hypervariable region in 12 Chinese goat breeds

A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.

A meta-analysis of the association between TNF-α -308G>A polymorphism and type 2 diabetes mellitus in Han Chinese population

A novel evolution-based method for detecting gene-gene interactions

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.

A robust hybrid between genetic algorithm and support vector machine for extracting an optimal feature gene subset

A systematic method for mapping multiple loci: an application to construct a genetic network for rheumatoid arthritis.

AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3.

Adaptation of the Audit of Diabetes-Dependent Quality of Life questionnaire to people with diabetes in China

Ala499Val (C>T) and Lys939Gln (A>C) polymorphisms of the XPC gene: their correlation with the risk of primary gallbladder adenocarcinoma--a case-control study in China.

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

An ensemble method for gene discovery based on DNA microarray data

Association Between Apolipoprotein B XbaI Polymorphism and Coronary Heart Disease in Han Chinese Population: A Meta-Analysis

Association between apolipoprotein B EcoRI poly﻿mor﻿phisms and coronary heart disease : A meta-analysis

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

Association between polymorphisms in SOD1 and noise-induced hearing loss in Chinese workers.

Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans

Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based Case-Control Study

Atorvastatin treatment of rats with ischemia-reperfusion injury improves adipose-derived mesenchymal stem cell migration and survival via the SDF-1α/CXCR-4 axis

Behavioural development of school-aged children who live around a multi-metal sulphide mine in Guangdong province, China: a cross-sectional study

Brief communication: Y-chromosome haplogroup analysis indicates that Chinese Tuvans share distinctive affinity with Siberian Tuvans.

Constructing disease-specific gene networks using pair-wise relevance metric: application to colon cancer identifies interleukin 8, desmin and enolase 1 as the central elements

DOSim: An R package for similarity between diseases based on Disease Ontology ⬇️

Disease embryo development network reveals the relationship between disease genes and embryo development genes

Efficacy of Atorvastatin combined with adipose-derived mesenchymal stem cell transplantation on cardiac function in rats with acute myocardial infarction

Efficacy of combined treatment with albendazole and baicalein against eosinophilic meningitis induced by Angiostrongylus cantonensis in mice

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Functional homogeneity in microRNA target heterogeneity--a new sight into human microRNomics

Gene mining: a novel and powerful ensemble decision approach to hunting for disease genes using microarray expression profiling

Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p

Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs.

Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data.

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

Identifying functional modules for coronary artery disease by a prior knowledge-based approach.

Knowledge-based analysis of genetic associations of rheumatoid arthritis to inform studies searching for pleiotropic genes: a literature review and network analysis

Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study

Laryngeal aerodynamic analysis in assisting with the diagnosis of muscle tension dysphonia

Longitudinal data analysis in pedigree studies

Miscues on the "lack of MEF2A mutations" in coronary artery disease

Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation

Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns ⬇️

Pathway-based analysis of the hidden genetic heterogeneities in cancers

Pathway-based analysis tools for complex diseases: a review

Phenotype–Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the GJB2 Gene ⬇️

Plasma oxidized low-density lipoprotein is an independent risk factor in young patients with coronary artery disease

Postoperative complications in patients with cochlear implants and impacts of nursing intervention.

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

Psychometric properties of the Chinese version of the Pediatric Quality of Life Inventory 4.0 generic core scales.

Psychometric properties of the coronary heart disease scale of the quality-of-life instruments for chronic diseases (QLICD-CHD): an application to Cantonese patients.

Rabies trend in China (1990-2007) and post-exposure prophylaxis in the Guangdong province.

SDF-1α upregulation by atorvastatin in rats with acute myocardial infarction via nitric oxide production confers anti-inflammatory and anti-apoptotic effects.

Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy

Short-term outcomes of induction therapy with tacrolimus versus cyclophosphamide for active lupus nephritis: A multicenter randomized clinical trial

Strategies for genetic mapping of categorical traits

To control false positives in gene-gene interaction analysis: two novel conditional entropy-based approaches

Towards precise classification of cancers based on robust gene functional expression profiles

Unravelling the hidden heterogeneities of diffuse large B-cell lymphoma based on coupled two-way clustering

[Advances in development of gene-gene interaction analysis methods based on SNP data: a review].

[Advances in genetics of restless legs syndrome]

Association between apolipoprotein B EcoRI polymorphisms and coronary heart disease : A meta-analysis