Cargando…

Evaluation of European coeliac disease risk variants in a north Indian population

Studies in European populations have contributed to a better understanding of the genetics of complex diseases, for example, in coeliac disease (CeD), studies of over 23 000 European samples have reported association to the HLA locus and another 39 loci. However, these associations have not been eva...

Descripción completa

Detalles Bibliográficos
Autores principales:	Senapati, Sabyasachi, Gutierrez-Achury, Javier, Sood, Ajit, Midha, Vandana, Szperl, Agata, Romanos, Jihane, Zhernakova, Alexandra, Franke, Lude, Alonso, Santos, Thelma, B K, Wijmenga, Cisca, Trynka, Gosia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2015
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666579/ https://www.ncbi.nlm.nih.gov/pubmed/25052311 http://dx.doi.org/10.1038/ejhg.2014.137

Ejemplares similares

Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants
por: Romanos, Jihane, et al.
Publicado: (2014)

Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease
por: Gutierrez-Achury, Javier, et al.
Publicado: (2015)

An Investigation of Genome-Wide Studies Reported Susceptibility Loci for Ulcerative Colitis Shows Limited Replication in North Indians
por: Juyal, Garima, et al.
Publicado: (2011)

Association study identified biologically relevant receptor genes with synergistic functions in celiac disease
por: Banerjee, Pratibha, et al.
Publicado: (2019)

Shared and unique common genetic determinants between pediatric and adult celiac disease
por: Senapati, Sabyasachi, et al.
Publicado: (2016)

Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant
por: Almeida, Rodrigo, et al.
Publicado: (2014)

Low hygiene and exposure to infections may be associated with increased risk for ulcerative colitis in a North Indian population
por: Sood, Ajit, et al.
Publicado: (2014)

Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity
por: Gutierrez-Achury, Javier, et al.
Publicado: (2015)

Complex nature of SNP genotype effects on gene expression in primary human leucocytes
por: Heap, Graham A, et al.
Publicado: (2009)

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci
por: Coleman, Ciara, et al.
Publicado: (2016)

The influence of a short-term gluten-free diet on the human gut microbiome
por: Bonder, Marc Jan, et al.
Publicado: (2016)

No Evidence in a Large UK Collection for Celiac Disease Risk Variants Reported by a Spanish Study
por: Hunt, Karen A., et al.
Publicado: (2008)

The MHC locus and genetic susceptibility to autoimmune and infectious diseases
por: Matzaraki, Vasiliki, et al.
Publicado: (2017)

Ciliary Genes Are Down-Regulated in Bronchial Tissue of Primary Ciliary Dyskinesia Patients
por: Geremek, Maciej, et al.
Publicado: (2014)

Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms
por: Monsuur, Alienke J., et al.
Publicado: (2008)

Correction: Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms
por: Monsuur, Alienke J., et al.
Publicado: (2009)

Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes
por: Lopera Maya, Esteban A., et al.
Publicado: (2020)

Relationship between gut microbiota and circulating metabolites in population-based cohorts
por: Vojinovic, Dina, et al.
Publicado: (2019)

A giant spider nevus in a patient of hepatitis C-related liver cirrhosis: A rare presentation
por: Sood, Ajit, et al.
Publicado: (2015)

Potential Celiac Patients: A Model of Celiac Disease Pathogenesis
por: Sperandeo, Maria Pia, et al.
Publicado: (2011)

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
por: Trynka, Gosia, et al.
Publicado: (2011)

Exclusive enteral nutrition for induction of remission in anti-tumor necrosis factor refractory adult Crohn’s disease: the Indian experience
por: Sood, Ajit, et al.
Publicado: (2020)

Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression
por: Kumar, Vinod, et al.
Publicado: (2013)

Studying the gut virome in the metagenomic era: challenges and perspectives
por: Garmaeva, Sanzhima, et al.
Publicado: (2019)

Adult celiac disease: delayed onset or delayed diagnosis?
por: Sood, Ajit, et al.
Publicado: (2014)

A simple phenotypic classification for celiac disease
por: Sood, Ajit, et al.
Publicado: (2018)

Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome
por: Zhernakova, Daria V., et al.
Publicado: (2018)

Genetic, parental and lifestyle factors influence telomere length
por: Andreu-Sánchez, Sergio, et al.
Publicado: (2022)

Functional studies of GWAS variants are gaining momentum
por: Lichou, Florence, et al.
Publicado: (2020)

Effects of Non-HLA Gene Polymorphisms on Development of Islet Autoimmunity and Type 1 Diabetes in a Population With High-Risk HLA-DR,DQ Genotypes
por: Steck, Andrea K., et al.
Publicado: (2012)

Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity
por: Hrdlickova, Barbara, et al.
Publicado: (2014)

From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
por: Cano-Gamez, Eddie, et al.
Publicado: (2020)

Impact of Corona Virus Disease-19 (COVID-19) pandemic on gastrointestinal disorders
por: Baryah, Amol Nanak Singh, et al.
Publicado: (2020)

Endoscopy for assessment of mucosal healing in ulcerative colitis: time bound or response guided?
por: Sood, Ajit, et al.
Publicado: (2022)

Coeliac disease hidden by cryptogenic hypertransaminasaemia in children: a case report
por: El Hasbaoui, Brahim, et al.
Publicado: (2022)

Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels
por: Deelen, Patrick, et al.
Publicado: (2015)

HCC surveillance results in earlier HCC detection: results from an Indian cohort
por: Kohli, Anita, et al.
Publicado: (2014)

Limited Evidence for Parent-of-Origin Effects in Inflammatory Bowel Disease Associated Loci
por: Fransen, Karin, et al.
Publicado: (2012)

Association of endoscopic and histological remission with clinical course in patients of ulcerative colitis
por: Narang, Vikram, et al.
Publicado: (2018)

Variants in Neuropeptide Y Receptor 1 and 5 Are Associated with Nutrient-Specific Food Intake and Are Under Recent Selection in Europeans
por: Elbers, Clara C., et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_tcdmn02brhm9gje878ongct5gj