Lista de obras - William S Bush - Dominio Público Uruguay

<i>TNFRSF1B</i> Gene Variants and Related Soluble TNFR2 Levels Impact Resilience in Alzheimer's Disease

artículo científico publicado en 2021

A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction.

artículo científico publicado en 2007

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data

artículo científico publicado en 2012

A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.

artículo científico publicado en 2011

A small number of candidate gene SNPs reveal continental ancestry in African Americans.

artículo científico publicado en 2013

Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank ⬇️

artículo científico publicado en 2014

Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction

artículo científico publicado en 2008

Analysis of Heritability Using Genome-Wide Data

artículo científico publicado en 2016

Antibody-specific detection of caveolin-1 in subapical compartments of MDCK cells.

artículo científico publicado en 2006

Antiepileptic activity of preferential inhibitors of persistent sodium current

artículo científico publicado en 2014

Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?

artículo científico publicado en 2016

Association Rule Discovery Has the Ability to Model Complex Genetic Effects

artículo científico publicado en 2007

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

artículo científico publicado en 2016

Associations between KCNJ6 (GIRK2) gene polymorphisms and pain-related phenotypes.

artículo científico publicado en 2013

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Automated extraction of clinical traits of multiple sclerosis in electronic medical records

artículo científico publicado en 2013

Automated quantification of pancreatic β-cell mass.

artículo científico publicado en 2014

Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies.

artículo científico publicado en 2009

Bioinformatics challenges in genome-wide association studies (GWAS).

artículo científico publicado en 2014

Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines

artículo científico publicado en 2019

Catechol-O-methyltransferase polymorphism Val158Met is associated with distal neuropathic pain in HIV-associated sensory neuropathy

scientific article published on 01 August 2019

Cerebrospinal Fluid Ceruloplasmin, Haptoglobin, and Vascular Endothelial Growth Factor Are Associated with Neurocognitive Impairment in Adults with HIV Infection

scientific article published on 12 September 2018

Cerebrospinal fluid (CSF) biomarkers of iron status are associated with CSF viral load, antiretroviral therapy, and demographic factors in HIV-infected adults

artículo científico publicado en 2017

Chapter 11: Genome-Wide Association Studies ⬇️

artículo científico publicado el 27 de diciembre de 2012

Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project

artículo científico publicado en 2013

Comprehensive Analysis of Constraint on the Spatial Distribution of Missense Variants in Human Protein Structures

artículo científico publicado en 2018

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

artículo científico publicado en 2019

Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins

artículo científico publicado en 2014

Cystic fibrosis-related diabetes is caused by islet loss and inflammation

artículo científico publicado en 2018

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

artículo científico publicado en 2015

Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky

artículo científico publicado en 2007

European Mitochondrial DNA Haplogroups are Associated with Cerebrospinal Fluid Biomarkers of Inflammation in HIV Infection

scientific article published on September 2016

Evidence for extensive pleiotropy among pharmacogenes

scientific article published on June 2016

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come

artículo científico publicado en 2010

Exploring epistasis in candidate genes for rheumatoid arthritis

artículo científico publicado en 2007

Extracting Country-of-Origin from Electronic Health Records for Gene- Environment Studies as Part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) Study

artículo científico publicado en 2017

Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants

article

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

artículo científico publicado en 2016

Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital

artículo científico publicado en 2020

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease

scientific article published on 01 August 2018

GSK3β Interactions with Amyloid Genes: An Autopsy Verification and Extension

artículo científico publicado en 2015

Gene expression in cell lines from propionic acidemia patients, carrier parents, and controls.

artículo científico publicado en 2015

Genetic Programming Neural Networks: A Powerful Bioinformatics Tool for Human Genetics

artículo científico publicado en 2007

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

artículo científico publicado en 2018

Genetic analysis of biological pathway data through genomic randomization

artículo científico publicado en 2011

Genetic and clinical risk prediction model for postoperative atrial fibrillation.

artículo científico publicado en 2015

Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

scientific article published on 01 August 2020

Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias

artículo científico publicado en 2009

Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study

artículo científico publicado en 2017

Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population

artículo científico publicado en 2017

Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome

artículo científico publicado en 2014

Germline Genetic Variants and Lung Cancer Survival in African Americans

artículo científico publicado en 2017

Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies

artículo científico publicado en 2020

Human islet preparations distributed for research exhibit a variety of insulin-secretory profiles.

artículo científico publicado en 2015

ICD-9 tobacco use codes are effective identifiers of smoking status

artículo científico publicado en 2013

INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH.

artículo científico publicado en 2018

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

artículo científico publicado en 2018

In Silico Functional Annotation of Genomic Variation.

artículo científico publicado en 2016

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex

artículo científico publicado en 2011

Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies

artículo científico publicado en 2014

Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study

artículo científico publicado en 2016

Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests

artículo científico publicado en 2013

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

artículo científico publicado en 2017

Local ancestry transitions modify snp-trait associations

artículo científico publicado en 2018

Mitochondrial DNA Haplogroups and Neurocognitive Impairment During HIV Infection

artículo científico publicado en 2015

Modeling transcriptional regulation using gene regulatory networks based on multi-omics data sources

artículo científico publicado en 2021

Nuclear-Mitochondrial interactions influence susceptibility to HIV-associated neurocognitive impairment

scientific article published on 17 July 2018

Packaging Biocomputing Software to Maximize Distribution and Reuse

artículo científico publicado en 2020

Phenotyping Adverse Drug Reactions: Statin-Related Myotoxicity

artículo científico

Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study

artículo científico publicado en 2015

Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia

artículo científico publicado en 2014

Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia

artículo científico publicado en 2013

Predicting Incident Coronary Heart Disease Many Markers at a Time

artículo científico publicado en 2016

Protein-altering germline mutations implicate novel genes related to lung cancer development

scientific article published on 11 May 2020

Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data

artículo científico publicado en 2013

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

article

RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways

artículo científico publicado en 2019

Racial Disparities in Lung Cancer Survival: The Contribution of Stage, Treatment, and Ancestry

artículo científico publicado en 2018

Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists.

artículo científico publicado en 2013

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record

artículo científico publicado en 2017

Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.

artículo científico publicado en 2014

SecureMA: protecting participant privacy in genetic association meta-analysis

artículo científico publicado en 2014

Sex differences in the genetic predictors of Alzheimer's pathology

scientific article published on 01 September 2019

Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau

scientific article published on 01 August 2018

Sex-Specific Parental Effects on Offspring Lipid Levels

artículo científico publicado en 2015

Sex-specific genetic predictors of Alzheimer's disease biomarkers

artículo científico publicado en 2018

Somatic T-cell Receptor Diversity in a Chronic Kidney Disease PatientPopulation Linked to Electronic Health Records.

artículo científico publicado en 2018

The MafA transcription factor becomes essential to islet β-cells soon after birth.

artículo científico publicado en 2014

The phenotypic legacy of admixture between modern humans and Neandertals

artículo científico publicado en 2016

Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia.

artículo científico publicado en 2018

Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.

artículo científico publicado en 2015

Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.

artículo científico publicado en 2017

Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci

artículo científico publicado en 2017

Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS

artículo científico publicado en 2018

Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry.

artículo científico publicado en 2017

Unravelling the human genome-phenome relationship using phenome-wide association studies.

artículo científico publicado en 2016

Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients

artículo científico publicado en 2014

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.

artículo científico publicado en 2018

Willingness to Participate in a National Precision Medicine Cohort: Attitudes of Chronic Kidney Disease Patients at a Cleveland Public Hospital

artículo científico publicado en 2018

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

artículo científico publicado en 2016

eMERGEing progress in genomics-the first seven years

artículo científico publicado en 2014

Lista de obras de William S Bush

<i>TNFRSF1B</i> Gene Variants and Related Soluble TNFR2 Levels Impact Resilience in Alzheimer's Disease

A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction.

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data

A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.

A small number of candidate gene SNPs reveal continental ancestry in African Americans.

Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank ⬇️

Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction

Analysis of Heritability Using Genome-Wide Data

Antibody-specific detection of caveolin-1 in subapical compartments of MDCK cells.

Antiepileptic activity of preferential inhibitors of persistent sodium current

Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?

Association Rule Discovery Has the Ability to Model Complex Genetic Effects

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

Associations between KCNJ6 (GIRK2) gene polymorphisms and pain-related phenotypes.

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Automated extraction of clinical traits of multiple sclerosis in electronic medical records

Automated quantification of pancreatic β-cell mass.

Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies.

Bioinformatics challenges in genome-wide association studies (GWAS).

Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines

Catechol-O-methyltransferase polymorphism Val158Met is associated with distal neuropathic pain in HIV-associated sensory neuropathy

Cerebrospinal Fluid Ceruloplasmin, Haptoglobin, and Vascular Endothelial Growth Factor Are Associated with Neurocognitive Impairment in Adults with HIV Infection

Cerebrospinal fluid (CSF) biomarkers of iron status are associated with CSF viral load, antiretroviral therapy, and demographic factors in HIV-infected adults

Chapter 11: Genome-Wide Association Studies ⬇️

Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project

Comprehensive Analysis of Constraint on the Spatial Distribution of Missense Variants in Human Protein Structures

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins

Cystic fibrosis-related diabetes is caused by islet loss and inflammation

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky

European Mitochondrial DNA Haplogroups are Associated with Cerebrospinal Fluid Biomarkers of Inflammation in HIV Infection

Evidence for extensive pleiotropy among pharmacogenes

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come

Exploring epistasis in candidate genes for rheumatoid arthritis

Extracting Country-of-Origin from Electronic Health Records for Gene- Environment Studies as Part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) Study

Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease

GSK3β Interactions with Amyloid Genes: An Autopsy Verification and Extension

Gene expression in cell lines from propionic acidemia patients, carrier parents, and controls.

Genetic Programming Neural Networks: A Powerful Bioinformatics Tool for Human Genetics

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

Genetic analysis of biological pathway data through genomic randomization

Genetic and clinical risk prediction model for postoperative atrial fibrillation.

Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias

Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study

Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population

Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome

Germline Genetic Variants and Lung Cancer Survival in African Americans

Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies

Human islet preparations distributed for research exhibit a variety of insulin-secretory profiles.

ICD-9 tobacco use codes are effective identifiers of smoking status

INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH.

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

In Silico Functional Annotation of Genomic Variation.

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex

Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies

Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study

Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

Local ancestry transitions modify snp-trait associations

Mitochondrial DNA Haplogroups and Neurocognitive Impairment During HIV Infection

Modeling transcriptional regulation using gene regulatory networks based on multi-omics data sources

Nuclear-Mitochondrial interactions influence susceptibility to HIV-associated neurocognitive impairment

Packaging Biocomputing Software to Maximize Distribution and Reuse

Phenotyping Adverse Drug Reactions: Statin-Related Myotoxicity

Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study

Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia

Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia

Predicting Incident Coronary Heart Disease Many Markers at a Time

Protein-altering germline mutations implicate novel genes related to lung cancer development

Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways