Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia
Author:
Funder
Indonesian Ministry of Research, Technology and Higher Education and Fulbright
Publisher
Elsevier BV
Subject
Surgery
Reference18 articles.
1. Hirschsprung disease;Chakravarti,2001
2. Hirschsprung disease, associated syndromes and genetics: a review;Amiel;J Med Genet,2008
3. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease;Garcia-Barcelo;Proc Natl Acad Sci U S A,2009
4. Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability;Emison;Am J Hum Genet,2010
5. Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease;Gunadi;J Pediatr Surg,2014
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1. Aberrant SOX10 and RET expressions in patients with Hirschsprung disease;BMC Pediatrics;2024-03-16
2. The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease;Frontiers in Cell and Developmental Biology;2023-07-07
3. Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease;Journal of Pediatric Surgery;2023-04
4. Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease;Scientific Reports;2022-11-28
5. The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease;BMC Pediatrics;2022-04-20
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