ArticleGenes2023
Mutational Spectrum, Ocular and Olfactory Phenotypes of
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes and 5 more
Open access · goldAbstract read
In one paragraphArticle in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% of its field
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed, 0 citations in OpenAlex.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
15 authors at 6 institutions in 2 countries.
Sara GeadaOphthalmology Unit, Centro Hospitalar e Universitário de Coimbra (CHUC), 3000-075 Coimbra, Portugal.ORCID 0000-0002-6851-6201 Francisco Teixeira-MarquesDepartment of Otorhinolaryngology, Centro Hospitalar do Tâmega e Sousa (CHTS), 4560-162 Penafiel, Portugal.ORCID 0000-0002-3621-2203 Bruno TeixeiraOphthalmology Unit, Centro Hospitalar e Universitário de Coimbra (CHUC), 3000-075 Coimbra, Portugal.
Ana Luísa CarvalhoMedical Genetics Unit, Centro Hospitalar e Universitário de Coimbra, 3000-602 Coimbra, Portugal.
Nuno LousanDepartment of Otorhinolaryngology, Centro Hospitalar do Tâmega e Sousa (CHTS), 4560-162 Penafiel, Portugal.
Jorge SaraivaMedical Genetics Unit, Centro Hospitalar e Universitário de Coimbra, 3000-602 Coimbra, Portugal.
Joaquim MurtaOphthalmology Unit, Centro Hospitalar e Universitário de Coimbra (CHUC), 3000-075 Coimbra, Portugal.
Rufino SilvaOphthalmology Unit, Centro Hospitalar e Universitário de Coimbra (CHUC), 3000-075 Coimbra, Portugal.ORCID 0000-0001-8676-0833 Xavier ZanlonghiEye Department, Rennes University Hospital, 35 033 Rennes, France.
Sabine Defoort-DhellemmesDepartment of Visual Exploration and Neuro-Ophthalmology, Robert Salengro Hospital, 59 037 Lille, France.
Vasily SmirnovDepartment of Visual Exploration and Neuro-Ophthalmology, Robert Salengro Hospital, 59 037 Lille, France.ORCID 0000-0003-4172-514X Claire-Marie DhaenensUniversity of Lille, INSERM, CHU Lille, U1172-LilNCog-Lille Neuroscience & Cognition, 59 000 Lille, France.ORCID 0000-0003-4719-4124 Catherine BlanchetReference Centre for Inherited Sensory Diseases, Montpellier University Hospital, 34 295 Montpellier, France.
João Pedro MarquesOphthalmology Unit, Centro Hospitalar e Universitário de Coimbra (CHUC), 3000-075 Coimbra, Portugal.ORCID 0000-0002-1014-0483 Hospitais da Universidade de Coimbra · PTCentro Hospitalar do Tâmega e Sousa · PTHôpital Roger Salengro · FRInserm · FRCentre Hospitalier Universitaire de Rennes · FRUniversité de Montpellier · FR
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
Olfaction DisordersRetinitis PigmentosaCross-Sectional StudiesCyclic Nucleotide-Gated Cation ChannelsHumansHypopituitarismMutationPhenotypeCNGB1 protein, humanCyclic Nucleotide-Gated Cation ChannelsCNGB1inherited retinal diseaseolfactory dysfunctionretinitis pigmentosarod-cone degeneration
Identifiers
PMID37107588
PMCPMC10137467
OpenAlexW4361274789
What OpenQuestion holds
Textmetadata
LicenceCC BY
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