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HLA diversity in the 1000 genomes dataset

PloS one, 2014-07, Vol.9 (7), p.e97282-e97282

2014

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Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant

PloS one, 2008-10, Vol.3 (10), p.e3391-e3391

2008

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Prostaglandins and calprotectin are genetically and functionally linked to the Inflammatory Bowel Diseases

PLoS genetics, 2022-09, Vol.18 (9), p.e1010189-e1010189

2022

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Defining the role of the MHC in autoimmunity: a review and pooled analysis

PLoS genetics, 2008-04, Vol.4 (4), p.e1000024-e1000024

2008

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IL23R (Interleukin 23 Receptor) Variants Protective against Inflammatory Bowel Diseases (IBD) Display Loss of Function due to Impaired Protein Stability and Intracellular Trafficking

The Journal of biological chemistry, 2016-04, Vol.291 (16), p.8673-8685

2016

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A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease

PLoS genetics, 2011-01, Vol.7 (1), p.e1001283-e1001283

2011

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Relationship between proximal Crohn's disease location and disease behavior and surgery: a cross-sectional study of the IBD Genetics Consortium

The American journal of gastroenterology, 2013-01, Vol.108 (1), p.106-112

2013

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Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation

Immunity (Cambridge, Mass.), 2015-10, Vol.43 (4), p.715-726

2015

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A transcriptome-based approach to identify functional modules within and across primary human immune cells

PloS one, 2020-05, Vol.15 (5), p.e0233543-e0233543

2020

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Common variants in the NLRP3 region contribute to Crohn's disease susceptibility

Nature genetics, 2009-01, Vol.41 (1), p.71-76

2009

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Investigating the Crime Scene-Molecular Signatures in Inflammatory Bowel Disease

International journal of molecular sciences, 2023-07, Vol.24 (13), p.11217

2023

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Human induced pluripotent stem cells (hiPSCs) derived cells reflect tissue specificity found in patients with Leigh syndrome French Canadian variant (LSFC)

Frontiers in genetics, 2024, Vol.15, p.1375467-1375467

2024

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Paths to understanding the genetic basis of autoimmune disease

Nature, 2005-06, Vol.435 (7042), p.584-589

2005

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High-resolution haplotype structure in the human genome

Nature genetics, 2001-10, Vol.29 (2), p.229-232

2001

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Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles

Human molecular genetics, 2019-06, Vol.28 (12), p.2078-2092

2019

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A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh Syndrome

Cell reports (Cambridge), 2015-11, Vol.13 (5), p.981-989

2015

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Inflammatory bowel disease patient perceptions of diagnostic and monitoring tests and procedures

BMC gastroenterology, 2019-02, Vol.19 (1), p.30-30, Article 30

2019

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The dichotomous pattern of IL-12r and IL-23R expression elucidates the role of IL-12 and IL-23 in inflammation

PloS one, 2014-02, Vol.9 (2), p.e89092-e89092

2014

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Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Nature communications, 2023-04, Vol.14 (1), p.2256-2256, Article 2256

2023

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Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus

Nature genetics, 2008-01, Vol.40 (1), p.83-89

2008

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Molecular Genetics of Inflammatory Bowel Disease

2nd ed. 2019, 2019

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Identification of a Gene Causing Human Cytochrome c Oxidase Deficiency by Integrative Genomics

Proceedings of the National Academy of Sciences - PNAS, 2003-01, Vol.100 (2), p.605-610

2003

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Crohn disease: A current perspective on genetics, autophagy and immunity

Autophagy, 2011-04, Vol.7 (4), p.355-374

2011

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HLA diversity in the 1000 genomes dataset

Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant

Prostaglandins and calprotectin are genetically and functionally linked to the Inflammatory Bowel Diseases

Defining the role of the MHC in autoimmunity: a review and pooled analysis

IL23R (Interleukin 23 Receptor) Variants Protective against Inflammatory Bowel Diseases (IBD) Display Loss of Function due to Impaired Protein Stability and Intracellular Trafficking

A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease

Relationship between proximal Crohn's disease location and disease behavior and surgery: a cross-sectional study of the IBD Genetics Consortium

Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation

A transcriptome-based approach to identify functional modules within and across primary human immune cells

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

Common variants in the NLRP3 region contribute to Crohn's disease susceptibility

Investigating the Crime Scene-Molecular Signatures in Inflammatory Bowel Disease

Human induced pluripotent stem cells (hiPSCs) derived cells reflect tissue specificity found in patients with Leigh syndrome French Canadian variant (LSFC)

Paths to understanding the genetic basis of autoimmune disease

High-resolution haplotype structure in the human genome

Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC

A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh Syndrome

Inflammatory bowel disease patient perceptions of diagnostic and monitoring tests and procedures

The dichotomous pattern of IL-12r and IL-23R expression elucidates the role of IL-12 and IL-23 in inflammation

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus

Molecular Genetics of Inflammatory Bowel Disease

Identification of a Gene Causing Human Cytochrome c Oxidase Deficiency by Integrative Genomics

Crohn disease: A current perspective on genetics, autophagy and immunity

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