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Integrating predicted transcriptome from multiple tissues improves association detection

PLoS genetics, 2019-01, Vol.15 (1), p.e1007889-e1007889

2019

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Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies

The lancet respiratory medicine, 2019-06, Vol.7 (6), p.509-522

2019

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Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues

PLoS genetics, 2016-11, Vol.12 (11), p.e1006423

2016

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Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

PLoS genetics, 2010-04, Vol.6 (4), p.e1000888-e1000888

2010

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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

Nature genetics, 2018-07, Vol.50 (7), p.956-967

2018

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A gene-based association method for mapping traits using reference transcriptome data

Nature genetics, 2015-09, Vol.47 (9), p.1091-1098

2015

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Association Tests for Rare Variants

Annual review of genomics and human genetics, 2016-08, Vol.17 (1), p.117-130

Nicolae, Dan L

2016

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Hemofiltration with the Seraph® 100 Microbind® Affinity filter decreases SARS-CoV-2 nucleocapsid protein in critically ill COVID-19 patients

Critical care (London, England), 2021-06, Vol.25 (1), p.1-190, Article 190

2021

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Effects of Eccentric-Oriented Strength Training on Return to Sport Criteria in Late-Stage Anterior Cruciate Ligament (ACL)-Reconstructed Professional Team Sport Players

Medicina (Kaunas, Lithuania), 2023-06, Vol.59 (6), p.1111

2023

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Prior sample size extensions for assessing prior impact and prior‐likelihood discordance

Journal of the Royal Statistical Society. Series B, Statistical methodology, 2021-07, Vol.83 (3), p.413-437

2021

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Complicated idiopathic portal and mesenteric venous thrombosis: A case report

Acta Marisiensis - Seria Medica, 2023-06, Vol.69 (2), p.138-140

Bele, Dan Nicolae

2023

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Recent Developments in Metallic Nanomaterials for Cancer Therapy, Diagnosing and Imaging Applications

Pharmaceutics, 2022-02, Vol.14 (2), p.435

2022

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An Updated Overview of Cyclodextrin-Based Drug Delivery Systems for Cancer Therapy

Pharmaceutics, 2022-08, Vol.14 (8), p.1748

2022

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A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle

Journal of allergy and clinical immunology, 2018-09, Vol.142 (3), p.749-764.e3

2018

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Multidrug resistance in Helicobacter pylori infection

Frontiers in microbiology, 2023-02, Vol.14, p.1128497-1128497

2023

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

Journal of allergy and clinical immunology, 2012-10, Vol.130 (4), p.861-868.e7

2012

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SCAN: SNP and copy number annotation

Bioinformatics, 2010-01, Vol.26 (2), p.259-262

2010

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On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic Privacy

American journal of human genetics, 2012-04, Vol.90 (4), p.591-598

2012

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Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways

American journal of respiratory and critical care medicine, 2016-02, Vol.193 (4), p.376-385

2016

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Rhinovirus Wheezing Illness and Genetic Risk of Childhood-Onset Asthma

The New England journal of medicine, 2013-04, Vol.368 (15), p.1398-1407

2013

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Post-thyroidectomy Hypocalcemia - Risk Factors and Management

Chirurgia (Bucharest, Romania : 1990), 2019-09, Vol.114 (5), p.564-570

2019

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Clinical Applications of Artificial Intelligence-An Updated Overview

Journal of clinical medicine, 2022-04, Vol.11 (8), p.2265

2022

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Nature genetics, 2007-05, Vol.39 (5), p.596-604

2007

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An Up-to-Date Review of Natural Nanoparticles for Cancer Management

Pharmaceutics, 2021-12, Vol.14 (1), p.18

2021

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Rare non-coding variants are associated with plasma lipid traits in a founder population

Scientific reports, 2017-11, Vol.7 (1), p.16415-13, Article 16415

2017

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Integrating predicted transcriptome from multiple tissues improves association detection

Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies

Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

A gene-based association method for mapping traits using reference transcriptome data

Association Tests for Rare Variants

Hemofiltration with the Seraph® 100 Microbind® Affinity filter decreases SARS-CoV-2 nucleocapsid protein in critically ill COVID-19 patients

Effects of Eccentric-Oriented Strength Training on Return to Sport Criteria in Late-Stage Anterior Cruciate Ligament (ACL)-Reconstructed Professional Team Sport Players

Prior sample size extensions for assessing prior impact and prior‐likelihood discordance

Complicated idiopathic portal and mesenteric venous thrombosis: A case report

Recent Developments in Metallic Nanomaterials for Cancer Therapy, Diagnosing and Imaging Applications

An Updated Overview of Cyclodextrin-Based Drug Delivery Systems for Cancer Therapy

A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle

Multidrug resistance in Helicobacter pylori infection

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

SCAN: SNP and copy number annotation

On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic Privacy

Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways

Rhinovirus Wheezing Illness and Genetic Risk of Childhood-Onset Asthma

Post-thyroidectomy Hypocalcemia - Risk Factors and Management

Clinical Applications of Artificial Intelligence-An Updated Overview

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

An Up-to-Date Review of Natural Nanoparticles for Cancer Management

Rare non-coding variants are associated with plasma lipid traits in a founder population

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