Talin Haritunians

Comprehensive Association Analyses of Extraintestinal Manifestations in Inflammatory Bowel Disease

Eleven Grand Challenges for Inflammatory Bowel Disease Genetics and Genomics

Ancestral Diversity in Pharmacogenomics Affects Treatment for Hispanic/Latine Populations With Inflammatory Bowel Disease

Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn’s disease and leads to impaired CFB cleavage and phagocytosis

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

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Inflamed Ulcerative Colitis Regions Associated With MRGPRX2-Mediated Mast Cell Degranulation and Cell Activation Modules, Defining a New Therapeutic Target

Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease

Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

Serum Analyte Profiles Associated With Crohn’s Disease and Disease Location

Altered Intestinal ACE2 Levels Are Associated With Inflammation, Severe Disease, and Response to Anti-Cytokine Therapy in Inflammatory Bowel Disease

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Fine-mapping inflammatory bowel disease loci to single-variant resolution

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn’s Disease and Human Gut Microbiome Composition

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF

A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

Increased Prevalence of Inflammatory Bowel Disease in Patients with Mutations in Genes Encoding the Receptor Subunits for TGFβ

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans

Ocular Manifestations in Inflammatory Bowel Disease Are Associated with Other Extra-intestinal Manifestations, Gender, and Genes Implicated in Other Immune-related Traits

Reprograming of gut microbiome energy metabolism by the <i>FUT2</i> Crohn’s disease risk polymorphism

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

Immunochip Analysis Identification of 6 Additional Susceptibility Loci for Crohnʼs Disease in Koreans

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium