Evidence map›Paper›PMID 25928284›Full record

ArticleBMC medical genetics2014

Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result.

Linda Siggberg, Sirpa Ala-Mello, Tarja Linnankivi, Kristiina Avela, Ilari Scheinin, Kati Kristiansson, Päivi Lahermo, Marja Hietala, Liisa Metsähonkala, Esa Kuusinen and 3 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in BMC medical genetics, 2014. 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
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Linda SiggbergDepartment of Pathology, Haartman Institute, University of Helsinki, and Laboratory of Helsinki and Uusimaa University Hospital, Helsinki, Finland. linda.siggberg@helsinki.fi.
Sirpa Ala-MelloRinnekoti Foundation, Rehabilitation Home for Children, Espoo, Finland. sirpa.ala-mello@fimnet.fi.
Tarja LinnankiviDepartment of Pediatric Neurology, Helsinki University Central Hospital, Helsinki, Finland. tarja.linnankivi@hus.fi.
Kristiina AvelaDepartment of Medical Genetics, Väestöliitto, The Family Federation of Finland, Helsinki, Finland. kristiina.avela@vaestoliitto.fi.
Ilari ScheininDepartment of Pathology, Haartman Institute, University of Helsinki, and Laboratory of Helsinki and Uusimaa University Hospital, Helsinki, Finland. ilari.scheinin@helsinki.fi.
Kati KristianssonPublic Health Genomics Unit, Department of Chronic Disease Prevention, National Institute for Health and Welfare, Helsinki, Finland. kati.kristiansson@thl.fi.
Päivi LahermoInstitute for Molecular Medicine Finland FIMM, University Helsinki, Helsinki, Finland. paivi-lahermo@helsinki.fi.
Marja HietalaDepartment of Clinical Genetics, Turku University Hospital and Department of Medical Biochemistry and Genetics, University of Turku, Turku, Finland. marja.hietala@tyks.fi.
Liisa MetsähonkalaDepartment of Pediatric Neurology, Helsinki University Central Hospital, Helsinki, Finland. liisa.metsahonkala@hus.fi.
Esa KuusinenDepartment of Pediatrics, Satakunta Hospital District, Pori, Finland. esa.kuusinen@satshp.fi.
Maarit LaaksonenPopulation Health Unit, Department of Health, Functional Capacity and Welfare, National Institute for Health and Welfare, P.O. Box 21, 00014, Helsinki, Finland. maarit.laaksonen@thl.fi.
Janna SaarelaInstitute for Molecular Medicine Finland FIMM, University Helsinki, Helsinki, Finland. janna.saarela@helsinki.fi.
Sakari KnuutilaDepartment of Pathology, Haartman Institute, University of Helsinki, and Laboratory of Helsinki and Uusimaa University Hospital, Helsinki, Finland. sakari.knuutila@helsinki.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID25928284
PMCPMC4429685

What OpenQuestion holds

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Registered trials

None linked

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.