SNP information rs1800858

Research and publications:

  8001158   Missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung disease.

  10090908   Double heterozygosity for a RET substitution interfering with splicing and an EDNRB missense mutation in Hirschsprung disease.

  10521317   Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.

  10528857   Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression.

  10922382   RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.

  11950855   Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma.

  15759212   Identifying candidate Hirschsprung disease-associated RET variants.

  16091499   Polymorphisms in the initiators of RET (rearranged during transfection) signaling pathway and susceptibility to sporadic medullary thyroid carcinoma.

  17267408   Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.

  18091754   Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10.

  18284634   RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series.

  19138047   Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.

  20123584   Polymorphisms of the RET gene in hirschsprung disease, anorectal malformation and intestinal pseudo-obstruction in Taiwan.

  20454948   Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.

  20532249   Haplotype analysis revealed a possible founder effect of the RET R114H mutation in Hirschsprung disease in a Chinese population.

  21349203   RET genetic variants and risk of Hirschsprung's disease in Southeast China: a haplotype-based analysis.

  22312249   Molecular basis of medullary thyroid carcinoma: the role of RET polymorphisms.

  23059849   Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form.

  23084198   Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.

  23527089   Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients.

  24897126   RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.

  26102504   KIT Mutation and Loss of 14q May Be Sufficient for the Development of Clinically Symptomatic Very Low-Risk GIST.

  29131865   Associations between RET tagSNPs and their haplotypes and susceptibility, clinical severity, and thyroid function in patients with differentiated thyroid cancer.

  30409984   Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.

  31644668   ASSOCIATION OF RS2435357 AND RS1800858 POLYMORPHISMS IN RET PROTO-ONCOGENE WITH HIRSCHSPRUNG DISEASE: SYSTEMATIC REVIEW AND META-ANALYSIS.

  34981673   Distribution of RET proto-oncogene variants in children with appendicitis.