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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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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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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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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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SCAN: SNP and copy number annotation

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

2010

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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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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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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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Noninvasive analysis of the sputum transcriptome discriminates clinical phenotypes of asthma

American journal of respiratory and critical care medicine, 2015-05, Vol.191 (10), p.1116-1125

2015

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Genome-wide association study of recalcitrant atopic dermatitis in Korean children

Journal of allergy and clinical immunology, 2015-09, Vol.136 (3), p.678-684.e4

2015

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Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx

American journal of human genetics, 2016-04, Vol.98 (4), p.697-708

2016

Volltextzugriff (PDF)

Testing Untyped Alleles (TUNA)-applications to genome-wide association studies

Genetic epidemiology, 2006-12, Vol.30 (8), p.718-727

Nicolae, Dan L.

2006

Volltextzugriff (PDF)

Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications

American journal of human genetics, 2011-12, Vol.89 (6), p.701-712

2011

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Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions

PloS one, 2018-09, Vol.13 (9), p.e0203906-e0203906

2018

Volltextzugriff (PDF)

Ethnic Differences and Functional Analysis of MET Mutations in Lung Cancer

Clinical cancer research, 2009-09, Vol.15 (18), p.5714-5723

2009

Volltextzugriff (PDF)

PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population

PLoS computational biology, 2015-03, Vol.11 (3), p.e1004139-e1004139

2015

Volltextzugriff (PDF)

Association Tests for Rare Variants

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

Nicolae, Dan L

2016

Volltextzugriff (PDF)

Recombination rates in admixed individuals identified by ancestry-based inference

Nature genetics, 2011-09, Vol.43 (9), p.847-853

2011

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Genome-wide association study of lung function phenotypes in a founder population

Journal of allergy and clinical immunology, 2014-01, Vol.133 (1), p.248-255.e10

2014

Volltextzugriff (PDF)

Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Genome medicine, 2021-10, Vol.13 (1), p.157-22, Article 157

2021

Volltextzugriff (PDF)

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

Human molecular genetics, 2011-04, Vol.20 (7), p.1285-1289

2011

Volltextzugriff (PDF)

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

PLoS genetics, 2011-02, Vol.7 (2), p.e1001292-e1001292

2011

Volltextzugriff (PDF)

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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

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

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

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

SCAN: SNP and copy number annotation

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

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

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

Noninvasive analysis of the sputum transcriptome discriminates clinical phenotypes of asthma

Genome-wide association study of recalcitrant atopic dermatitis in Korean children

Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx

Testing Untyped Alleles (TUNA)-applications to genome-wide association studies

Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications

Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions

Ethnic Differences and Functional Analysis of MET Mutations in Lung Cancer

PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population

Association Tests for Rare Variants

Recombination rates in admixed individuals identified by ancestry-based inference

Genome-wide association study of lung function phenotypes in a founder population

Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

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