Lista de obras -

116 Genome-Wide Association Studies of Asthma Indicate Opposite Immunopathogenesis Direction From Autoimmune Diseases.

artículo científico publicado en 2012

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

artículo científico publicado en 2017

APOL1 Kidney-Risk Variants Induce Mitochondrial Fission

artículo científico publicado en 2020

APOL1 Renal-Risk Variants Induce Mitochondrial Dysfunction

artículo científico publicado en 2016

Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study

artículo científico publicado en 2017

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study

artículo científico publicado en 2017

Association between genetic polymorphisms in the prostate-specific antigen gene promoter and serum prostate-specific antigen levels.

artículo científico publicado en 2003

Associations between hOGG1 sequence variants and prostate cancer susceptibility

artículo científico publicado en 2002

Attenuating hypoxia driven malignant behavior in glioblastoma with a novel hypoxia-inducible factor 2 alpha inhibitor

scientific article published on 16 September 2020

Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.

artículo científico publicado en 2016

Common estrogen receptor polymorphism augments effects of hormone replacement therapy on E-selectin but not C-reactive protein

artículo científico publicado en 2002

Common sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

artículo científico publicado en 2003

Density functional solvation model based on CM2 atomic charges

article

Effect of rare variants in ADRB2 on risk of severe exacerbations and symptom control during longacting β agonist treatment in a multiethnic asthma population: a genetic study

artículo científico publicado en 2014

Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

artículo científico publicado en 2014

Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease

artículo científico publicado en 2002

Evaluation of DLC1 as a prostate cancer susceptibility gene: mutation screen and association study.

artículo científico publicado en 2003

Expression of asthma susceptibility genes in bronchial epithelial cells and bronchial alveolar lavage in the Severe Asthma Research Program (SARP) cohort

artículo científico publicado en 2016

FAM13A, A Fatty Acid Oxidation Switch in Mitochondria. Friend or Foe in Chronic Obstructive Pulmonary Disease Pathogenesis?

artículo científico publicado en 2017

Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases

artículo científico publicado en 2012

Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients

artículo científico publicado en 2013

Genome-wide association study of lung function and clinical implication in heavy smokers

Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk

artículo científico publicado en 2014

Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans

artículo científico publicado en 2016

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

artículo científico publicado en 2002

Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk

artículo científico publicado en 2002

IL4R alpha mutations are associated with asthma exacerbations and mast cell/IgE expression

artículo científico publicado en 2006

Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease

artículo científico publicado en 2005

Importance of hedgehog interacting protein and other lung function genes in asthma

artículo científico publicado en 2011

Improved methods for semiempirical solvation models

article

Joint effect of HSD3B1 and HSD3B2 genes is associated with hereditary and sporadic prostate cancer susceptibility

scientific article published on 01 March 2002

Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study ⬇️

artículo científico publicado el 5 de agosto de 2010

Mutational Landscapes of Smoking-Related Cancers in Caucasians and African Americans: Precision Oncology Perspectives at Wake Forest Baptist Comprehensive Cancer Center

artículo científico publicado en 2017

Mutational analysis of PINX1 in hereditary prostate cancer.

artículo científico publicado en 2004

Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster

scientific article published on 01 August 2003

Pairwise solute descreening of solute charges from a dielectric medium

Phenotype of asthmatics with increased airway S-nitrosoglutathione reductase activity

artículo científico publicado en 2014

Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk

scientific article published on 23 January 2002

Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk

artículo científico publicado en 2003

Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression

artículo científico publicado en 2015

Sequence variants in the human 25-hydroxyvitamin D3 1-alpha-hydroxylase (CYP27B1) gene are not associated with prostate cancer risk

artículo científico publicado en 2002

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk

artículo científico publicado en 2002

The C11orf30-LRRC32 region is associated with total serum IgE levels in asthmatic patients

artículo científico publicado en 2011

The Effects of Rare SERPINA1 Variants on Lung Function and Emphysema in SPIROMICS

scientific article published on 01 March 2020

The IL6R variation Asp(358)Ala is a potential modifier of lung function in subjects with asthma

artículo científico publicado en 2012

Tissue-Specific and Genetic Regulation of Insulin Sensitivity-Associated Transcripts in African Americans.

artículo científico publicado en 2016

Variability of Serum Soluble Intercellular Adhesion Molecule-1 Measurements Attributable to a Common Polymorphism

artículo científico publicado en 2004

Lista de obras de

116 Genome-Wide Association Studies of Asthma Indicate Opposite Immunopathogenesis Direction From Autoimmune Diseases.

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

APOL1 Kidney-Risk Variants Induce Mitochondrial Fission

APOL1 Renal-Risk Variants Induce Mitochondrial Dysfunction

Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study

Association between genetic polymorphisms in the prostate-specific antigen gene promoter and serum prostate-specific antigen levels.

Associations between hOGG1 sequence variants and prostate cancer susceptibility

Attenuating hypoxia driven malignant behavior in glioblastoma with a novel hypoxia-inducible factor 2 alpha inhibitor

Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.

Common estrogen receptor polymorphism augments effects of hormone replacement therapy on E-selectin but not C-reactive protein

Common sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Density functional solvation model based on CM2 atomic charges

Effect of rare variants in ADRB2 on risk of severe exacerbations and symptom control during longacting β agonist treatment in a multiethnic asthma population: a genetic study

Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease

Evaluation of DLC1 as a prostate cancer susceptibility gene: mutation screen and association study.

Expression of asthma susceptibility genes in bronchial epithelial cells and bronchial alveolar lavage in the Severe Asthma Research Program (SARP) cohort

FAM13A, A Fatty Acid Oxidation Switch in Mitochondria. Friend or Foe in Chronic Obstructive Pulmonary Disease Pathogenesis?

Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases

Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients

Genome-wide association study of lung function and clinical implication in heavy smokers

Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk

Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk

IL4R alpha mutations are associated with asthma exacerbations and mast cell/IgE expression

Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease

Importance of hedgehog interacting protein and other lung function genes in asthma

Improved methods for semiempirical solvation models

Joint effect of HSD3B1 and HSD3B2 genes is associated with hereditary and sporadic prostate cancer susceptibility

Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study ⬇️

Mutational Landscapes of Smoking-Related Cancers in Caucasians and African Americans: Precision Oncology Perspectives at Wake Forest Baptist Comprehensive Cancer Center

Mutational analysis of PINX1 in hereditary prostate cancer.

Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster

Pairwise solute descreening of solute charges from a dielectric medium

Phenotype of asthmatics with increased airway S-nitrosoglutathione reductase activity

Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk

Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk

Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression

Sequence variants in the human 25-hydroxyvitamin D3 1-alpha-hydroxylase (CYP27B1) gene are not associated with prostate cancer risk

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk

The C11orf30-LRRC32 region is associated with total serum IgE levels in asthmatic patients

The Effects of Rare SERPINA1 Variants on Lung Function and Emphysema in SPIROMICS

The IL6R variation Asp(358)Ala is a potential modifier of lung function in subjects with asthma

Tissue-Specific and Genetic Regulation of Insulin Sensitivity-Associated Transcripts in African Americans.

Variability of Serum Soluble Intercellular Adhesion Molecule-1 Measurements Attributable to a Common Polymorphism