Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases

Identification of Non-HLA Genes Associated with Celiac Disease and Country-Specific Differences in a Large, International Pediatric Cohort

(2016) Ashok Sharma et al.   PLoS One

Genes involved in muscle contractility and nutrient signaling pathways within celiac disease risk loci show differential mRNA expression

(2015) Caroline Montén et al.   BMC Medical Genetics

Peroxisome proliferator-activated receptors and their ligands: nutritional and clinical implications - a review

(2014) Bogna Grygiel-Górniak   Nutrition Journal

Defective Expression of Scavenger Receptors in Celiac Disease Mucosa

(2014) Maria Laura Cupi et al.   PLoS One

Genome-Wide Association Study of Celiac Disease in North America Confirms FRMD4B as New Celiac Locus

(2014) Chad Garner et al.   PLoS One

Association of renin-angiotensin system genes polymorphism with progression of diabetic nephropathy in patients with type 1 diabetes mellitus

(2014) Vesna Ilic et al.   Vojnosanitetski Pregled

PPARs Integrate the Mammalian Clock and Energy Metabolism

(2014) Lihong Chen et al.   PPAR Research

Protein kinase C delta is a substrate of tissue transglutaminase and a novel autoantigen in coeliac disease

(2013) Greg Byrne et al.   CLINICAL IMMUNOLOGY

Patients With Celiac Disease Have a Lower Prevalence of Non–Insulin-Dependent Diabetes Mellitus and Metabolic Syndrome

(2013) Toufic A. Kabbani et al.   GASTROENTEROLOGY

A Possible Mechanism behind Autoimmune Disorders Discovered By Genome-Wide Linkage and Association Analysis in Celiac Disease

(2013) Malin Östensson et al.   PLoS One

The origin of circulating CD36 in type 2 diabetes

(2013) M J Alkhatatbeh et al.   Nutrition & Diabetes

Reevaluation of the association of seven candidate genes with blood pressure and hypertension: a replication study and meta-analysis with a larger sample size

(2012) Fumihiko Takeuchi et al.   HYPERTENSION RESEARCH

Severe Spruelike Enteropathy Associated With Olmesartan

(2012) Alberto Rubio-Tapia et al.   MAYO CLINIC PROCEEDINGS

Influence of Renin-Angiotensin System Gene Polymorphisms on the Risk of ST-Segment-Elevation Myocardial Infarction and Association with Coronary Artery Disease Risk Factors

(2012) Anna Konopka et al.   Molecular Diagnosis & Therapy

Celiac disease: moving from genetic associations to causal variants

(2011) B Hrdlickova et al.   CLINICAL GENETICS

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

(2011) Gosia Trynka et al.   NATURE GENETICS

Detection of Celiac Disease and Lymphocytic Enteropathy by Parallel Serology and Histopathology in a Population-Based Study

(2010) Marjorie M. Walker et al.   GASTROENTEROLOGY

Soluble CD36 (sCD36) Clusters with Markers of Insulin Resistance, and High sCD36 Is Associated with Increased Type 2 Diabetes Risk

(2010) A. Handberg et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

(2010) K Wang et al.   MOLECULAR PSYCHIATRY

Multiple common variants for celiac disease influencing immune gene expression

(2010) Patrick C A Dubois et al.   NATURE GENETICS

Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development

(2009) X. Feng et al.   BLOOD

Increased Prevalence and Mortality in Undiagnosed Celiac Disease

(2009) Alberto Rubio–Tapia et al.   GASTROENTEROLOGY

Lysosomal accumulation of gliadin p31-43 peptide induces oxidative stress and tissue transglutaminase-mediated PPAR  downregulation in intestinal epithelial cells and coeliac mucosa

(2009) A. Luciani et al.   GUT

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

(2009) J. E. Landers et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Axon guidance and synaptic maintenance: preclinical markers for neurodegenerative disease and therapeutics

(2009) Ling Lin et al.   TRENDS IN NEUROSCIENCES

Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations

(2008) T. Ohtsuki et al.   NEUROSCIENCE LETTERS

PPARs and Female Reproduction: Evidence from Genetically Manipulated Mice

(2008) Jichun Yang et al.   PPAR Research