Evidence map›Paper›PMID 24516651›Full record

ArticlePloS one2014

Combined genetic and high-throughput strategies for molecular diagnosis of inherited retinal dystrophies.

Marta de Castro-Miró, Esther Pomares, Laura Lorés-Motta, Raul Tonda, Joaquín Dopazo, Gemma Marfany, Roser Gonzàlez-Duarte

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from 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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 36 citations in OpenAlex.

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  6. Novel compound heterozygous variants in theFrontiers in cell and developmental biology · 2023
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  7. Genes · 2022
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  9. Structural modeling, mutation analysis, andComputational and structural biotechnology journal · 2020
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Marta de Castro-MiróDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain ; Institut de Biomedicina (IBUB), Universitat de Barcelona, Barcelona, Spain.
Esther PomaresDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain.
Laura Lorés-MottaDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Raul TondaCentre Nacional d'Anàlisi Genòmica, PCB, Barcelona, Spain.
Joaquín DopazoDepartment of Computational Genomics, Centro de Investigación Príncipe Felipe, Valencia, Spain ; BIER, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Valencia, Spain.
Gemma MarfanyDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain ; Institut de Biomedicina (IBUB), Universitat de Barcelona, Barcelona, Spain.
Roser Gonzàlez-DuarteDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain ; Institut de Biomedicina (IBUB), Universitat de Barcelona, Barcelona, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESUniversitat de Barcelona · ESCentro Nacional de Análisis Genómico · ESInstituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most diagnostic laboratories are confronted with the increasing demand for molecular diagnosis from patients and families and the ever-increasing genetic heterogeneity of visual disorders. Concerning Retinal Dystrophies (RD), almost 200 causative genes have been reported to date, and most families carry private mutations. We aimed to approach RD genetic diagnosis using all the available genetic information to prioritize candidates for mutational screening, and then restrict the number of cases to be analyzed by massive sequencing. We constructed and optimized a comprehensive cosegregation RD-chip based on SNP genotyping and haplotype analysis. The RD-chip allows to genotype 768 selected SNPs (closely linked to 100 RD causative genes) in a single cost-, time-effective step. Full diagnosis was attained in 17/36 Spanish pedigrees, yielding 12 new and 12 previously reported mutations in 9 RD genes. The most frequently mutated genes were USH2A and CRB1. Notably, RD3-up to now only associated to Leber Congenital Amaurosis- was identified as causative of Retinitis Pigmentosa. The main assets of the RD-chip are: i) the robustness of the genetic information that underscores the most probable candidates, ii) the invaluable clues in cases of shared haplotypes, which are indicative of a common founder effect, and iii) the detection of extended haplotypes over closely mapping genes, which substantiates cosegregation, although the assumptions in which the genetic analysis is based could exceptionally lead astray. The combination of the genetic approach with whole exome sequencing (WES) greatly increases the diagnosis efficiency, and revealed novel mutations in USH2A and GUCY2D. Overall, the RD-chip diagnosis efficiency ranges from 16% in dominant, to 80% in consanguineous recessive pedigrees, with an average of 47%, well within the upper range of massive sequencing approaches, highlighting the validity of this time- and cost-effective approach whilst high-throughput methodologies become amenable for routine diagnosis in medium sized labs.

Indexed as

DNA Mutational AnalysisFemaleGenetic TestingGenotypeHaplotypesHumansMaleMolecular Diagnostic TechniquesMutationPedigreePolymorphism, Single NucleotideRetinal DystrophiesSpain

Identifiers

PMID24516651
PMCPMC3917917
OpenAlexW2081660551

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.