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A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci

Nature genetics, 2017-10, Vol.49 (10), p.1511-1516

2017

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Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus

PLoS genetics, 2011-10, Vol.7 (10), p.e1002341-e1002341

2011

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Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade

Nature communications, 2021-06, Vol.12 (1), p.3355-12, Article 3355

2021

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Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration

Science translational medicine, 2017-06, Vol.9 (395)

2017

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Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration

Proceedings of the National Academy of Sciences - PNAS, 2018-12, Vol.115 (50), p.E11701-E11710

2018

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A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death

Nature medicine, 2014-12, Vol.20 (12), p.1452-1457

2014

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Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (22), p.12288-12294

2020

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Identifying and mitigating batch effects in whole genome sequencing data

BMC bioinformatics, 2017-07, Vol.18 (1), p.351-351, Article 351

2017

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Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration

Cell reports (Cambridge), 2020-01, Vol.30 (4), p.1246-1259.e6

2020

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Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study

The lancet respiratory medicine, 2018-08, Vol.6 (8), p.603-614

2018

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A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk

Scientific reports, 2022-04, Vol.12 (1), p.5574-5574, Article 5574

2022

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Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease

PLoS genetics, 2018-11, Vol.14 (11), p.e1007427-e1007427

2018

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GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies

Bioinformatics, 2012-12, Vol.28 (24), p.3329-3331

2012

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Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of ERAP2 transcripts under balancing selection

Genome research, 2018-12, Vol.28 (12), p.1812

2018

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Genetic ablation of Gpnmb does not alter synuclein-related pathology

Neurobiology of disease, 2021-11, Vol.159, p.105494-105494, Article 105494

2021

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geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation

Bioinformatics (Oxford, England), 2017-02, Vol.33 (4), p.599-600

2017

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Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials

Scientific reports, 2023-08, Vol.13 (1), p.14313-14313, Article 14313

2023

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Quality control and quality assurance in genotypic data for genome-wide association studies

Genetic epidemiology, 2010-09, Vol.34 (6), p.591-602

2010

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Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India

BMC medical genetics, 2018-02, Vol.19 (1), p.22-22, Article 22

2018

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Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy

Genome medicine, 2023-06, Vol.15 (1), p.45-45, Article 45

2023

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Automating resequencing-based detection of insertion-deletion polymorphisms

Nature genetics, 2006-12, Vol.38 (12), p.1457-1462

2006

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Estimating coverage and power for genetic association studies using near-complete variation data

Nature genetics, 2008-07, Vol.40 (7), p.841-843

2008

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A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains

Journal of Alzheimer's disease, 2017-01, Vol.56 (3), p.1037

2017

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Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration

Cell reports (Cambridge), 2023-03, Vol.42 (3), p.112298-112298, Article 112298

2023

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Comprehensive identification and characterization of diallelic insertion–deletion polymorphisms in 330 human candidate genes

Human molecular genetics, 2005-01, Vol.14 (1), p.59-69

2005

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A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci

Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus

Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade

Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration

Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration

A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death

Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer

Identifying and mitigating batch effects in whole genome sequencing data

Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration

Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study

A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk

Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease

GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies

Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of ERAP2 transcripts under balancing selection

Genetic ablation of Gpnmb does not alter synuclein-related pathology

geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation

Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials

Quality control and quality assurance in genotypic data for genome-wide association studies

Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India

Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy

Automating resequencing-based detection of insertion-deletion polymorphisms

Estimating coverage and power for genetic association studies using near-complete variation data

A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains

Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration

Comprehensive identification and characterization of diallelic insertion–deletion polymorphisms in 330 human candidate genes

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