Lista de obras - Yi-Ju Li - Dominio Público Uruguay

A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease

artículo científico publicado en 2007

A comparative analysis of the information content in long and short SAGE libraries

artículo científico publicado en 2006

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

artículo científico publicado en 2010

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity

artículo científico publicado en 2009

Age at onset in two common neurodegenerative diseases is genetically controlled

artículo científico publicado en 2002

An exploration of genetic association tests for disease risk and age at onset

artículo científico publicado en 2020

An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.

artículo científico publicado en 2012

An international collaborative family-based whole-genome linkage scan for high-grade myopia

artículo científico publicado en 2009

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

artículo científico publicado en 2004

Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.

artículo científico publicado en 2005

Articular hypermobility is a protective factor for hand osteoarthritis

scientific article published on 01 July 2004

Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease

artículo científico publicado en 2005

Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.

artículo científico publicado en 2013

Association test for X-linked QTL in family-based designs

artículo científico publicado en 2009

Baseline Pulse Pressure, Acute Kidney Injury, and Mortality After Noncardiac Surgery.

artículo científico publicado en 2016

Biomarkers associated with clinical phenotypes of hand osteoarthritis in a large multigenerational family: the CARRIAGE family study.

artículo científico publicado en 2008

Blood Pressure-Lowering Mechanisms of the DASH Dietary Pattern

artículo científico publicado en 2012

COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus

artículo científico publicado en 2009

Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia

artículo científico publicado en 2008

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

artículo científico publicado en 2010

Correlation of Virtual Reality Simulation and Dry Lab Robotic Technical Skills.

artículo científico publicado en 2017

Drawing inferences about the coancestry coefficient

artículo científico publicado en 2009

Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders

artículo científico publicado en 2013

Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

scientific article published on 20 December 2008

Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism

artículo científico publicado en 2005

Factors affecting success of thymus transplantation for complete DiGeorge anomaly

artículo científico publicado en 2008

Family-based association tests for rare variants with censored traits

artículo científico publicado en 2019

Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease

artículo científico publicado en 2006

Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving β-blockers

artículo científico publicado en 2016

Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort

artículo científico publicado en 2010

Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring

artículo científico publicado en 2006

Genetic screen of African Americans with Fuchs endothelial corneal dystrophy

artículo científico publicado en 2013

Genetic variants on chromosome 1q41 influence ocular axial length and high myopia

scientific journal article

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

artículo científico publicado en 2010

Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese

scientific journal article

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

artículo científico publicado en 2017

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

artículo científico publicado en 2009

Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery

artículo científico publicado en 2015

Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family

artículo científico publicado en 2013

Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family

artículo científico publicado en 2010

Genome-wide linkage scan in fuchs endothelial corneal dystrophy

artículo científico publicado en 2008

Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism

scientific journal article

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra

artículo científico publicado en 2005

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

artículo científico publicado en 2003

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease

artículo científico publicado en 2003

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease

artículo científico publicado en 2005

Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels

artículo científico publicado en 2008

Investigation of the PARK10 gene in Parkinson disease.

artículo científico publicado en 2007

Invited Commentary

artículo científico publicado en 2015

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

artículo científico publicado en 2012

Levels of Urinary Metabolites of Organophosphate Flame Retardants, TDCIPP, and TPHP, in Pregnant Women in Shanghai

scientific article published on 25 December 2016

Leveraging population information in family-based rare variant association analyses of quantitative traits.

artículo científico publicado en 2016

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

artículo científico publicado en 2005

Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly

artículo científico publicado en 2007

Maintenance and Representation of Mind Wandering during Resting-State fMRI

artículo científico publicado en 2017

Mast cell activation and arterial hypotension during proximal aortic repair requiring hypothermic circulatory arrest.

artículo científico publicado en 2016

Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations

artículo científico publicado en 2007

Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.

artículo científico publicado en 2009

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy

artículo científico publicado en 2014

Molecular clock and recombination in primate Mhc genes.

artículo científico publicado en 1999

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia

artículo científico publicado en 2013

Myocilin polymorphisms and high myopia in subjects of European origin

artículo científico publicado en 2009

NOS2A and the modulating effect of cigarette smoking in Parkinson's disease

artículo científico publicado en 2006

Paleo-demography of the Drosophila melanogaster subgroup: application of the maximum likelihood method.

artículo científico publicado en 1999

Paravertebral Block for Inguinal Herniorrhaphy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

artículo científico

Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family ⬇️

artículo científico publicado el 10 de agosto de 2011

Platelet Counts, Acute Kidney Injury, and Mortality after Coronary Artery Bypass Grafting Surgery

artículo científico publicado en 2015

Preterm Delivery and Low Birth Weight Among Neonates Conceived With Intracytoplasmic Sperm Injection Compared With Conventional In Vitro Fertilization.

artículo científico publicado en 2018

Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy

artículo científico publicado en 2011

Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases

artículo científico publicado en 2005

Serum proteomic panel validated for prediction of knee osteoarthritis progression

artículo científico publicado en 2024

The Role of Progesterone and a Novel Progesterone Receptor, Progesterone Receptor Membrane Component 1, in the Inflammatory Response of Fetal Membranes to Ureaplasma parvum Infection

artículo científico publicado en 2016

The neutral theory and natural selection in the HLA region.

artículo científico publicado en 1998

Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein

artículo científico publicado en 2008

X-APL: an improved family-based test of association in the presence of linkage for the X chromosome

artículo científico publicado en 2006

Lista de obras de Yi-Ju Li

A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease

A comparative analysis of the information content in long and short SAGE libraries

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity

Age at onset in two common neurodegenerative diseases is genetically controlled

An exploration of genetic association tests for disease risk and age at onset

An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.

An international collaborative family-based whole-genome linkage scan for high-grade myopia

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.

Articular hypermobility is a protective factor for hand osteoarthritis

Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease

Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.

Association test for X-linked QTL in family-based designs

Baseline Pulse Pressure, Acute Kidney Injury, and Mortality After Noncardiac Surgery.

Biomarkers associated with clinical phenotypes of hand osteoarthritis in a large multigenerational family: the CARRIAGE family study.

Blood Pressure-Lowering Mechanisms of the DASH Dietary Pattern

COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus

Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

Correlation of Virtual Reality Simulation and Dry Lab Robotic Technical Skills.

Drawing inferences about the coancestry coefficient

Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders

Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism

Factors affecting success of thymus transplantation for complete DiGeorge anomaly

Family-based association tests for rare variants with censored traits

Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease

Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving β-blockers

Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort

Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring

Genetic screen of African Americans with Fuchs endothelial corneal dystrophy

Genetic variants on chromosome 1q41 influence ocular axial length and high myopia

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery

Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family

Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family

Genome-wide linkage scan in fuchs endothelial corneal dystrophy

Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease

Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels

Investigation of the PARK10 gene in Parkinson disease.

Invited Commentary

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

Levels of Urinary Metabolites of Organophosphate Flame Retardants, TDCIPP, and TPHP, in Pregnant Women in Shanghai

Leveraging population information in family-based rare variant association analyses of quantitative traits.

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly

Maintenance and Representation of Mind Wandering during Resting-State fMRI

Mast cell activation and arterial hypotension during proximal aortic repair requiring hypothermic circulatory arrest.

Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations

Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy

Molecular clock and recombination in primate Mhc genes.

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia

Myocilin polymorphisms and high myopia in subjects of European origin

NOS2A and the modulating effect of cigarette smoking in Parkinson's disease

Paleo-demography of the Drosophila melanogaster subgroup: application of the maximum likelihood method.

Paravertebral Block for Inguinal Herniorrhaphy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family ⬇️

Platelet Counts, Acute Kidney Injury, and Mortality after Coronary Artery Bypass Grafting Surgery

Preterm Delivery and Low Birth Weight Among Neonates Conceived With Intracytoplasmic Sperm Injection Compared With Conventional In Vitro Fertilization.

Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy

Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases

Serum proteomic panel validated for prediction of knee osteoarthritis progression

The Role of Progesterone and a Novel Progesterone Receptor, Progesterone Receptor Membrane Component 1, in the Inflammatory Response of Fetal Membranes to Ureaplasma parvum Infection

The neutral theory and natural selection in the HLA region.

Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein

X-APL: an improved family-based test of association in the presence of linkage for the X chromosome