ArticleGenetics in medicine : official journal of the American College of Medical Genetics2016
An electronic atlas of human malformation syndromes in diverse populations.
Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 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
29 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Williams-Beuren syndrome in diverse populations.American journal of medical genetics. Part A · 2018Pooled it
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- The DO-KB knowledgebase 2026 update: expanding programmatic and language access.Nucleic acids research · 2026Article
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- GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.Research square · 2024Article
- Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome.Scientific reports · 2024Article
- An interactive atlas of three-dimensional syndromic facial morphology.American journal of human genetics · 2024Article
- Privacy, bias and the clinical use of facial recognition technology: A survey of genetics professionals.American journal of medical genetics. Part C, Seminars in medical genetics · 2023Article
- Advancing Understanding of Inequities in Rare Disease Genomics.Clinical therapeutics · 2023Article
- Diagnosis and clinical presentation of two individuals with a rareBMJ case reports · 2022Article
- Scoping review and classification of deep learning in medical genetics.Genetics in medicine : official journal of the American College of Medical Genetics · 2022Article
- Neural network classifiers for images of genetic conditions with cutaneous manifestations.HGG advances · 2022Article
- The genetic determinants of oral diseases in Africa: The gaps should be filled.Frontiers in oral health · 2022Review
- Objective differential diagnosis of Noonan and Williams-Beuren syndromes in diverse populations using quantitative facial phenotyping.Molecular genetics & genomic medicine · 2021Article
- The influence of social determinants of health on the genetic diagnostic odyssey: who remains undiagnosed, why, and to what effect?Pediatric research · 2021Review
- Experiences with offering pro bono medical genetics services in the West Indies: Benefits to patients, physicians, and the community.American journal of medical genetics. Part C, Seminars in medical genetics · 2020Article
- Love in the time of COVID-19.American journal of medical genetics. Part A · 2020Article
- Turner syndrome in diverse populations.American journal of medical genetics. Part A · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
26938780What 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.