ArticleThe Journal of investigative dermatology2015
The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.
Article in The Journal of investigative dermatology, 2015. 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
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
15 citing papers in PubMed, 33 citations in OpenAlex.
- A Novel Homozygous 9385 bp Deletion in theInternational journal of molecular sciences · 2025Review
- Gene-edited cells: novel allogeneic gene/cell therapy for epidermolysis bullosa.Journal of applied genetics · 2024Review
- A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.European journal of human genetics : EJHG · 2023Article
- A novel frameshift mutation in theExperimental and therapeutic medicine · 2020Article
- FERMT1 promotes gastric cancer progression by activating the NF-κB pathway and predicts poor prognosis.Cancer biology & therapy · 2020Article
- Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa.The British journal of dermatology · 2020Article
- Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients.Orphanet journal of rare diseases · 2019Article
- Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes.European journal of human genetics : EJHG · 2017Article
- Structural basis of kindlin-mediated integrin recognition and activation.Proceedings of the National Academy of Sciences of the United States of America · 2017Article
- Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome.Annals of dermatology · 2016Article
- A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases.The Journal of investigative dermatology · 2015Article
- A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.Journal of Zhejiang University. Science. B · 2015Article
- Genetic Diagnosis of Kindler Syndrome, a Rare form of Genodermatosis in a Newborn with Identification of a Nonsense Mutation, c. 328C > T, in the FERMT1 Gene in the Indian Population.Indian journal of dermatologyArticle
- Blistering and Mottled Pigmentation in a Young Male.Indian dermatology online journalArticle
- Inherited epidermolysis bullosa: update on the clinical and genetic aspects.Anais brasileiros de dermatologiaReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors at 5 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What 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.