Lista de obras -

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A common MUC5B promoter polymorphism and pulmonary fibrosis.

artículo científico publicado en 2011

A general approach to testing for pleiotropy with rare and common variants

artículo científico publicado en 2016

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14

artículo científico publicado en 2004

A likelihood model that accounts for censoring due to fetal loss can accurately test the effects of maternal and fetal genotype on the probability of miscarriage

artículo científico publicado en 2008

Adaptation of Mycobacterium tuberculosis to Impaired Host Immunity in HIV-Infected Patients

artículo científico publicado en 2016

Alternative Pre-mRNA Splicing of Toll-Like Receptor Signaling Components in Peripheral Blood Mononuclear Cells from ARDS Patients

artículo científico publicado en 2017

An epidemiologic simulation model of the spread and control of highly pathogenic avian influenza (H5N1) among commercial and backyard poultry flocks in South Carolina, United States.

artículo científico publicado en 2013

Analysis of single nucleotide polymorphisms identifies major type 1A diabetes locus telomeric of the major histocompatibility complex

artículo científico publicado en 2007

Application of 'Omics' and Systems Biology to Sarcoidosis Research

artículo científico publicado en 2017

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

artículo científico publicado en 2017

Association between gestational diabetes mellitus exposure and childhood adiposity is not substantially explained by offspring genetic risk of obesity.

artículo científico publicado en 2017

Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis

artículo científico publicado en 2013

Association between vitamin D metabolism gene polymorphisms and risk of islet autoimmunity and progression to type 1 diabetes: the diabetes autoimmunity study in the young (DAISY).

scientific article published on 26 August 2013

Association methods in human genetics

artículo científico publicado en 2007

Association of 25-hydroxyvitamin D with blood pressure in predominantly 25-hydroxyvitamin D deficient Hispanic and African Americans

artículo científico publicado en 2009

Association of HLA class II genes with clinical hyporesponsiveness to trivalent inactivated influenza vaccine in children

artículo científico publicado en 2012

Association of inhaled and systemic corticosteroid use with Coronavirus Disease 2019 (COVID-19) test positivity in patients with chronic pulmonary diseases

artículo científico publicado en 2020

Association of the 5'-upstream regulatory region of the alpha7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophrenia

artículo científico publicado en 2009

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses

article

Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado.

artículo científico publicado en 2007

Beryllium-induced lung disease exhibits expression profiles similar to sarcoidosis

artículo científico publicado en 2016

Blood Transcriptional Biomarkers for Active Tuberculosis among Patients in the United States: a Case-Control Study with Systematic Cross-Classifier Evaluation

artículo científico publicado en 2015

Brief Report: Prevalence of Self-injurious Behaviors among Children with Autism Spectrum Disorder-A Population-Based Study

artículo científico publicado en 2016

CALCULATING AVERAGE POWER FOR THE BENJAMINI-HOCHBERG PROCEDURE.

artículo científico publicado en 2009

CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism

scientific article published on 13 January 2016

CT scan findings of probable usual interstitial pneumonitis have a high predictive value for histologic usual interstitial pneumonitis

artículo científico publicado en 2015

Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study

artículo científico publicado en 2009

Cell Origin Dictates Programming of Resident versus Recruited Macrophages during Acute Lung Injury

artículo científico publicado en 2017

Challenges and opportunities in genome-wide environmental interaction (GWEI) studies

artículo científico publicado en 2012

Chronic beryllium disease, HLA-DPB1, and the DP peptide binding groove

abstract published in 2011

Chronic beryllium disease, HLA-DPB1, and the DP peptide binding groove

artículo científico publicado en 2012

Clinical tool for disease phenotyping in granulomatous lung disease

artículo científico publicado en 2017

Complex segregation analysis of obsessive-compulsive disorder in families with pediatric probands

artículo científico publicado en 2005

Correction to: Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome.

artículo científico publicado en 2018

DNA Methylation Changes in Lung Immune Cells Are Associated with Granulomatous Lung Disease

artículo científico publicado en 2019

DUF1220-domain copy number implicated in human brain-size pathology and evolution

artículo científico publicado en 2012

Desmoplakin Variants Are Associated with Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2015

Dissecting childhood asthma with nasal transcriptomics distinguishes subphenotypes of disease

artículo científico publicado en 2014

Distribution of orofacial clefts and frequent occurrence of an unusual cleft variant in the Rift Valley of Kenya

scientific article published on 01 July 2007

Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome

artículo científico publicado en 2017

Epigenetic marks of in utero exposure to gestational diabetes and childhood adiposity outcomes: the EPOCH study.

artículo científico publicado en 2018

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Erythrocyte membrane docosapentaenoic acid levels are associated with islet autoimmunity: the Diabetes Autoimmunity Study in the Young ⬇️

artículo científico publicado en 2013

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

artículo científico publicado en 2017

Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans

artículo científico publicado en 2007

Expanded genetic landscape of chronic obstructive pulmonary disease reveals heterogeneous cell type and phenotype associations

scholarly article published 26 June 2018

Exploring differences in adiposity in two U.S. Hispanic populations of Mexican origin using social, behavioral, physiologic and genetic markers: the IRAS Family Study

artículo científico publicado en 2012

Exposure to prenatal smoking and early-life body composition: the healthy start study

artículo científico publicado en 2014

Expression of cilium-associated genes defines novel molecular subtypes of idiopathic pulmonary fibrosis

artículo científico publicado en 2013

Genetic Evaluation and Testing of Patients and Families with Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2016

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

artículo científico publicado en 2014

Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans

artículo científico publicado en 2008

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

artículo científico publicado en 2019

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

artículo científico publicado en 2017

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.

artículo científico publicado en 2017

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes

artículo científico publicado en 2004

Genetics of Sarcoidosis

artículo científico publicado en 2015

Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci

artículo científico publicado en 2017

Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium

scientific article published on 20 June 2019

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

scientific article published on 01 March 2020

Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study

artículo científico publicado en 2009

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

scientific journal article

Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study

artículo científico publicado en 2010

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

artículo científico publicado en 2016

Height growth velocity, islet autoimmunity and type 1 diabetes development: the Diabetes Autoimmunity Study in the Young

artículo científico publicado en 2009

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

artículo científico publicado en 2002

Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways

artículo científico publicado en 2016

Impact of glycemic control on heart rate variability in youth with type 1 diabetes: the SEARCH CVD study

artículo científico publicado en 2013

Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium

artículo científico publicado en 2016

Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

artículo científico publicado en 2004

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans

artículo científico publicado en 2014

Investigation of the vitamin D receptor gene (VDR) and its interaction with protein tyrosine phosphatase, non-receptor type 2 gene (PTPN2) on risk of islet autoimmunity and type 1 diabetes: the Diabetes Autoimmunity Study in the Young (DAISY).

artículo científico publicado en 2012

Levels of free fatty acids (FFA) are associated with insulin resistance but do not explain the relationship between adiposity and insulin resistance in Hispanic Americans: the IRAS Family Study

artículo científico publicado en 2012

Longitudinal DNA methylation differences precede type 1 diabetes

scientific article published on 28 February 2020

MCMSeq: Bayesian hierarchical modeling of clustered and repeated measures RNA sequencing experiments

artículo científico publicado en 2020

MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

artículo científico publicado en 2018

MUC5B and Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2015

MUC5B promoter polymorphism and interstitial lung abnormalities

artículo científico publicado en 2013

MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis

artículo científico publicado en 2019

Multiple genes in the 15q13-q14 chromosomal region are associated with schizophrenia

artículo científico publicado en 2012

Observed Home Dampness and Mold Are Associated with Sustained Spikes in Personal Exposure to Particulate Matter Less than 10 μm in Diameter in Exacerbation-Prone Children with Asthma.

artículo científico publicado en 2018

Omega-3 fatty acids are associated with a lower prevalence of autoantibodies in shared epitope-positive subjects at risk for rheumatoid arthritis

scientific article published on 17 May 2016

Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis

scientific article published on 01 December 2019

Physical activity in pregnancy and neonatal body composition: the Healthy Start study

artículo científico publicado en 2014

Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2017

Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification

artículo científico publicado en 2020

Quantity and timing of maternal prenatal smoking on neonatal body composition: the Healthy Start study

artículo científico publicado en 2014

Rare variants in RTEL1 are associated with familial interstitial pneumonia

artículo científico publicado en 2015

Reduced heart rate variability among youth with type 1 diabetes: the SEARCH CVD study

artículo científico publicado en 2012

Reduced heart rate variability is associated with increased arterial stiffness in youth with type 1 diabetes: the SEARCH CVD study

artículo científico publicado en 2013

Relationship between gene expression and lung function in Idiopathic Interstitial Pneumonias

artículo científico publicado en 2015

Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2019

Risk of chronic beryllium disease by HLA-DPB1 E69 genotype and beryllium exposure in nuclear workers

artículo científico publicado en 2011

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Statistical Approaches to Combine Genetic Association Data

artículo científico publicado en 2013

TGF-beta 1 variants in chronic beryllium disease and sarcoidosis

artículo científico publicado en 2007

TNF polymorphism and bronchoalveolar lavage cell TNF-alpha levels in chronic beryllium disease and beryllium sensitization.

artículo científico publicado en 2007

Testing gene-environment interactions in family-based association studies using trait-based ascertained samples

artículo científico publicado en 2013

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

artículo científico publicado en 2000

The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries.

artículo científico publicado en 2015

The PPARgamma Pro12Ala polymorphism is not associated with body mass index or waist circumference among Hispanics from Colorado.

artículo científico publicado en 2007

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado.

artículo científico publicado en 2007

The pulmonary fibrosis-associated MUC5B promoter polymorphism does not influence the development of interstitial pneumonia in systemic sclerosis

artículo científico publicado en 2012

The relationship between HLA-DPB1, HLA-DRB1 and CBD/BeS ⬇️

abstract published in 2014

The α7 nicotinic acetylcholine receptor and the acute stress response: Maternal genotype determines offspring phenotype ⬇️

artículo científico publicado el 10 de noviembre de 2010

Transcriptional Adaptation of Drug-tolerant Mycobacterium tuberculosis During Treatment of Human Tuberculosis

artículo científico publicado en 2015

Using a spatial point process framework to characterize lung computed tomography scans

scientific article published on 31 December 2018

Using sex-averaged genetic maps in multipoint linkage analysis when identity-by-descent status is incompletely known.

artículo científico publicado en 2006

Variant in the 3' region of the IkappaBalpha gene associated with insulin resistance in Hispanic Americans: The IRAS Family Study

artículo científico publicado en 2009

Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort

artículo científico publicado en 2002

eQTL mapping of rare variant associations using RNA-seq data: An evaluation of approaches

scientific article published on 03 October 2019

Radiomic measures from chest high-resolution computed tomography associated with lung function in sarcoidosis

artículo científico publicado el 29 de agosto de 2019

Lista de obras de

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

A common MUC5B promoter polymorphism and pulmonary fibrosis.

A general approach to testing for pleiotropy with rare and common variants

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14

A likelihood model that accounts for censoring due to fetal loss can accurately test the effects of maternal and fetal genotype on the probability of miscarriage

Adaptation of Mycobacterium tuberculosis to Impaired Host Immunity in HIV-Infected Patients

Alternative Pre-mRNA Splicing of Toll-Like Receptor Signaling Components in Peripheral Blood Mononuclear Cells from ARDS Patients

An epidemiologic simulation model of the spread and control of highly pathogenic avian influenza (H5N1) among commercial and backyard poultry flocks in South Carolina, United States.

Analysis of single nucleotide polymorphisms identifies major type 1A diabetes locus telomeric of the major histocompatibility complex

Application of 'Omics' and Systems Biology to Sarcoidosis Research

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

Association between gestational diabetes mellitus exposure and childhood adiposity is not substantially explained by offspring genetic risk of obesity.

Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis

Association between vitamin D metabolism gene polymorphisms and risk of islet autoimmunity and progression to type 1 diabetes: the diabetes autoimmunity study in the young (DAISY).

Association methods in human genetics

Association of 25-hydroxyvitamin D with blood pressure in predominantly 25-hydroxyvitamin D deficient Hispanic and African Americans

Association of HLA class II genes with clinical hyporesponsiveness to trivalent inactivated influenza vaccine in children

Association of inhaled and systemic corticosteroid use with Coronavirus Disease 2019 (COVID-19) test positivity in patients with chronic pulmonary diseases

Association of the 5'-upstream regulatory region of the alpha7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophrenia

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses

Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado.

Beryllium-induced lung disease exhibits expression profiles similar to sarcoidosis

Blood Transcriptional Biomarkers for Active Tuberculosis among Patients in the United States: a Case-Control Study with Systematic Cross-Classifier Evaluation

Brief Report: Prevalence of Self-injurious Behaviors among Children with Autism Spectrum Disorder-A Population-Based Study

CALCULATING AVERAGE POWER FOR THE BENJAMINI-HOCHBERG PROCEDURE.

CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism

CT scan findings of probable usual interstitial pneumonitis have a high predictive value for histologic usual interstitial pneumonitis

Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study

Cell Origin Dictates Programming of Resident versus Recruited Macrophages during Acute Lung Injury

Challenges and opportunities in genome-wide environmental interaction (GWEI) studies

Chronic beryllium disease, HLA-DPB1, and the DP peptide binding groove

Chronic beryllium disease, HLA-DPB1, and the DP peptide binding groove

Clinical tool for disease phenotyping in granulomatous lung disease

Complex segregation analysis of obsessive-compulsive disorder in families with pediatric probands

Correction to: Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome.

DNA Methylation Changes in Lung Immune Cells Are Associated with Granulomatous Lung Disease

DUF1220-domain copy number implicated in human brain-size pathology and evolution

Desmoplakin Variants Are Associated with Idiopathic Pulmonary Fibrosis

Dissecting childhood asthma with nasal transcriptomics distinguishes subphenotypes of disease

Distribution of orofacial clefts and frequent occurrence of an unusual cleft variant in the Rift Valley of Kenya

Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome

Epigenetic marks of in utero exposure to gestational diabetes and childhood adiposity outcomes: the EPOCH study.

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Erythrocyte membrane docosapentaenoic acid levels are associated with islet autoimmunity: the Diabetes Autoimmunity Study in the Young ⬇️

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans

Expanded genetic landscape of chronic obstructive pulmonary disease reveals heterogeneous cell type and phenotype associations

Exploring differences in adiposity in two U.S. Hispanic populations of Mexican origin using social, behavioral, physiologic and genetic markers: the IRAS Family Study

Exposure to prenatal smoking and early-life body composition: the healthy start study

Expression of cilium-associated genes defines novel molecular subtypes of idiopathic pulmonary fibrosis

Genetic Evaluation and Testing of Patients and Families with Idiopathic Pulmonary Fibrosis

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes

Genetics of Sarcoidosis

Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci

Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

Height growth velocity, islet autoimmunity and type 1 diabetes development: the Diabetes Autoimmunity Study in the Young

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways

Impact of glycemic control on heart rate variability in youth with type 1 diabetes: the SEARCH CVD study

Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium

Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans

Investigation of the vitamin D receptor gene (VDR) and its interaction with protein tyrosine phosphatase, non-receptor type 2 gene (PTPN2) on risk of islet autoimmunity and type 1 diabetes: the Diabetes Autoimmunity Study in the Young (DAISY).

Levels of free fatty acids (FFA) are associated with insulin resistance but do not explain the relationship between adiposity and insulin resistance in Hispanic Americans: the IRAS Family Study

Longitudinal DNA methylation differences precede type 1 diabetes

MCMSeq: Bayesian hierarchical modeling of clustered and repeated measures RNA sequencing experiments

MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease