ArticleAmerican journal of human genetics1999
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
Article in American journal of human genetics, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
24 citing papers in PubMed, 1 synthesis or guideline pooled it.
- RET polymorphisms and sporadic medullary thyroid carcinoma in a Portuguese population.Endocrine · 2005Pooled it
- DNA damage and repair: underlying mechanisms leading to microcephaly.Frontiers in cell and developmental biology · 2023Review
- Distribution of RET proto-oncogene variants in children with appendicitis.Molecular genetics & genomic medicine · 2022Article
- Multiple endocrine neoplasias type 2B and RET proto-oncogene.Italian journal of pediatrics · 2012Review
- RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2.Journal of endocrinological investigation · 2011Article
- Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.BMC medical genetics · 2011Article
- Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.American journal of human genetics · 2010Article
- Genetic basis of Hirschsprung's disease.Pediatric surgery international · 2009Review
- Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.Proceedings of the National Academy of Sciences of the United States of America · 2009Article
- RET polymorphisms and the risk of Hirschsprung's disease in a Chinese population.Journal of human genetics · 2008Article
- Single nucleotide polymorphisms in the RET gene and their correlations with Hirschsprung disease phenotype.Journal of applied genetics · 2006Article
- Low RET mutation frequency and polymorphism analysis of the RET and EDNRB genes in patients with Hirschsprung disease in Taiwan.Journal of human genetics · 2005Article
- Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.Human genetics · 2004Article
- A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.American journal of human genetics · 2003Article
- Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.Annals of surgery · 2002Article
- Association of RET codon 691 polymorphism in radiation-induced human thyroid tumours with C-cell hyperplasia in peritumoural tissue.British journal of cancer · 2002Article
- Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma.Journal of medical genetics · 2002Article
- The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis.Molecular and cellular biology · 2001Article
- Article
- Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis.Journal of medical genetics · 2000Review
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.