ArticleAmerican journal of human genetics2002
The ABCA4 gene in autosomal recessive cone-rod dystrophies.
Article in American journal of human genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
22 citing papers in PubMed, 41 citations in OpenAlex.
- Review
- Review
- Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations.Investigative ophthalmology & visual science · 2022Article
- Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies.Scientific reports · 2020Article
- Genetic spectrum of retinal dystrophies in Tunisia.Scientific reports · 2020Article
- The Rapid-Onset Chorioretinopathy Phenotype of ABCA4 Disease.Ophthalmology · 2018Article
- Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases.Meta gene · 2016Article
- Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy.European journal of human genetics : EJHG · 2015Article
- Structures and biogenetic analysis of lipofuscin bis-retinoids.Journal of Zhejiang University. Science. B · 2013Review
- Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genes.PloS one · 2013Article
- A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.BMC medical genetics · 2011Article
- Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical characterizations.Investigative ophthalmology & visual science · 2010Article
- Identification of genetic variation and haplotype structure of the canine ABCA4 gene for retinal disease association studies.Molecular genetics and genomics : MGG · 2010Article
- Outcome of ABCA4 microarray screening in routine clinical practice.Molecular vision · 2009Article
- Peripapillary retinal nerve fiber layer thinning in patients with autosomal recessive cone-rod dystrophy.American journal of ophthalmology · 2009Article
- Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice.American journal of human genetics · 2009Article
- Host genetic and epigenetic factors in toxoplasmosis.Memorias do Instituto Oswaldo Cruz · 2009Article
- ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.European journal of human genetics : EJHG · 2008Article
- Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis.PloS one · 2008Article
- Cone rod dystrophies.Orphanet journal of rare diseases · 2007Review
Corrections and comments
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Authors and funding
11 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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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.