ArticleAmerican journal of human genetics1996
The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.
Article in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
What it found
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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.
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Who cites it
15 citing papers in PubMed.
- Lynch Syndrome: An Update of Underlying Molecular Mechanisms, Phenotypes and Methods to Classify Variants of Uncertain Significance.Biomedicines · 2026Review
- [Recurrent eyelid tumors with different dignities].Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft · 2019Article
- Parotid Sebaceous Carcinoma in Patient with Muir Torre Syndrome, Caused by MSH2 Mutation.Head and neck pathology · 2016Review
- Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions.The Journal of investigative dermatology · 2015Article
- Synchronous gastric and sebaceous cancers, a rare manifestation of MLH1-related Muir-Torre syndrome.International journal of clinical and experimental pathology · 2014Article
- [Muir-Torre syndrome with previously undescribed frameshift mutation in the MSH2 gene].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2013Article
- Simultaneous Muir-Torre and Turcot's syndrome: A case report and review of the literature.Surgical neurology international · 2013Article
- Identifying Muir-Torre syndrome in a patient with glioblastoma multiforme.Neuro-oncology · 2009Article
- Endometrial cancer as a familial tumor: pathology and molecular carcinogenesis (review).Current genomics · 2009Article
- Molecular epidemiological and mutational analysis of DNA mismatch repair (MMR) genes in endometrial cancer patients with HNPCC-associated familial predisposition to cancer.Cancer science · 2008Article
- Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutation.Familial cancer · 2008Article
- An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.Familial cancer · 2007Article
- Genetics of skin appendage neoplasms and related syndromes.Journal of medical genetics · 2005Review
- Genetic susceptibility to non-polyposis colorectal cancer.Journal of medical genetics · 1999Review
- Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.American journal of human genetics · 1998Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
8751876PMC1914892What OpenQuestion holds
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.