Author details

Full Name

Tasha E Fingerlin

Affiliation

ORCID

Career Start Year

1999

Papers

143

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37221924	Identification of influential rare variants in aggregate testing using random forest importance measures.	Ann Hum Genet	2023
36094461	Incidence and Progression of Fibrotic Lung Disease in an At-Risk Cohort.	American Journal of Respiratory and Critical Care Medicine	2023
37978501	Spatially distinct molecular patterns of gene expression in idiopathic pulmonary fibrosis.		2023
37790375	Breathing zone pollutant levels are associated with asthma exacerbations in high-risk children.		2023
37620507	Quantifying the spatial clustering characteristics of radiographic emphysema explains variability in pulmonary function.		2023
38054751	Genome and Transcriptome-Wide Association Study of Fibrotic Sarcoidosis in European Americans.		2023
37865580	Genetic predisposition to sarcoidosis.		2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36602845	Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.	Am J Respir Crit Care Med	2023
37523715	A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities.	Am J Respir Crit Care Med	2023
37546732	Association study of human leukocyte antigen (HLA) variants and idiopathic pulmonary fibrosis.	medRxiv	2023
34535537	HLA-DPB1 E69 genotype and exposure in beryllium sensitisation and disease.	Occupational and Environmental Medicine	2022
35397561	Clinical phenotyping in sarcoidosis using cluster analysis.	Respir Res	2022
35972918	Multiomic Signatures of Chronic Beryllium Disease Bronchoalveolar Lavage Cells Relate to T-Cell Function and Innate Immunity.	American Journal of Respiratory Cell and Molecular Biology	2022
35511761	Blood mRNA biomarkers distinguish variable systemic and sputum inflammation at treatment initiation of inhaled antibiotics in cystic fibrosis: A prospective non-randomized trial.	PLoS ONE	2022
35830265	Evolution of the Gain-of-Function Promoter Variant.	American Journal of Respiratory and Critical Care Medicine	2022
35643435	A comparison of methods for multiple degree of freedom testing in repeated measures RNA-sequencing experiments.	BMC Medical Research Methodology	2022
35816432	Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of <i>MUC5B</i> and <i>DSP</i> in Idiopathic Pulmonary Fibrosis.	Am J Respir Crit Care Med	2022
35932543	Occupational and environmental exposures in the Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis (GRADS) study.	Respiratory Medicine	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35724268	Changes in the Coexpression of Innate Immunity Genes During Persistent Islet Autoimmunity Are Associated With Progression of Islet Autoimmunity: Diabetes Autoimmunity Study in the Young (DAISY).		2022
35274026	Cluster activation mapping with application to computed tomography scans of the lung.	Journal of Medical Imaging	2022
35034774	Refractory neutrophilic asthma and ciliary genes.	J Allergy Clin Immunol	2022
34399367	Genomic biomarkers in chronic beryllium disease and sarcoidosis.	Respiratory Medicine	2021
33567433	Identification of Influential Variants in Significant Aggregate Rare Variant Tests.	Hum Hered	2021
34038697	Molecular Signatures of Idiopathic Pulmonary Fibrosis.	American Journal of Respiratory Cell and Molecular Biology	2021
33863802	Phospholipid Levels at Seroconversion Are Associated With Resolution of Persistent Islet Autoimmunity: The Diabetes Autoimmunity Study in the Young.	Diabetes	2021
33276252	Association of inhaled and systemic corticosteroid use with Coronavirus Disease 2019 (COVID-19) test positivity in patients with chronic pulmonary diseases.	Respiratory Medicine	2021
32859148	MCMSeq: Bayesian hierarchical modeling of clustered and repeated measures RNA sequencing experiments.	BMC Bioinformatics	2020
32111940	Longitudinal DNA methylation differences precede type 1 diabetes.	Scientific Reports	2020
31710517	Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.	Am J Respir Crit Care Med	2020
32764642	Novel protein pathways in development and progression of pulmonary sarcoidosis.	Sci Rep	2020
31196947	Radiomic measures from chest high-resolution computed tomography associated with lung function in sarcoidosis.	European Respiratory Journal	2019
31581212	eQTL mapping of rare variant associations using RNA-seq data: An evaluation of approaches.	PLoS ONE	2019
31558622	variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis.	Thorax	2019
31750077	Using a spatial point process framework to characterize lung computed tomography scans.	Spatial Statistics	2019
32721961	Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification.	Human Heredity	2019
30141971	DNA Methylation Changes in Lung Immune Cells Are Associated with Granulomatous Lung Disease.	American Journal of Respiratory Cell and Molecular Biology	2019
31034279	Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis.	Am J Respir Crit Care Med	2019
31219225	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	Obesity (Silver Spring)	2019
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
30345907	MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease.	N Engl J Med	2018
29461653	Epigenetic marks of in utero exposure to gestational diabetes and childhood adiposity outcomes: the EPOCHÂ study.	Diabetic Medicine	2018
29636099	Correction to: Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome.	Genome Biol	2018
29279374	Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.	Proc Natl Acad Sci U S A	2018
27900789	A general approach to testing for pleiotropy with rare and common variants.	Genetic Epidemiology	2017
28775099	Alternative pre-mRNA splicing of Toll-like receptor signaling components in peripheral blood mononuclear cells from patients with ARDS.	Am J Physiol Lung Cell Mol Physiol	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28421818	Cell Origin Dictates Programming of Resident versus Recruited Macrophages during Acute Lung Injury.	Am J Respir Cell Mol Biol	2017