Evidence map›Paper›PMID 27110297›Full record

ArticleClinical epigenetics2016

Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.

Silvia Russo, Luciano Calzari, Alessandro Mussa, Ester Mainini, Matteo Cassina, Stefania Di Candia, Maurizio Clementi, Sara Guzzetti, Silvia Tabano, Monica Miozzo and 13 more

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

Article in Clinical epigenetics, 2016. 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

23 authors.

Silvia Russo *Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
Luciano Calzari *Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
Alessandro MussaDepartment of Pediatric and Public Health Sciences, University of Turin, Torino, Italy.
Ester MaininiHuman Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
Matteo CassinaClinical Genetics Unit, Department of Women's and Children's Health, University of Padua, Padova, Italy.
Stefania Di CandiaDepartment of Pediatrics, San Raffaele Scientific Institute, Milano, Italy.
Maurizio ClementiClinical Genetics Unit, Department of Women's and Children's Health, University of Padua, Padova, Italy.
Sara GuzzettiHuman Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
Silvia TabanoDivision of Pathology - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Department of Pathophysiology and Transplantation, University of Milan, Milano, Italy.
Monica MiozzoDivision of Pathology - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Department of Pathophysiology and Transplantation, University of Milan, Milano, Italy.
Silvia SirchiaDepartment of Health Sciences, University of Milan, Milano, Italy.
Palma FinelliHuman Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
Paolo PronteraMedical Genetics Unit, Department of Surgical and Biomedical Sciences, University of Perugia, Hospital "S. M. della Misericordia", Perugia, Italy.
Silvia MaitzClinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, Monza, Italy.
Giovanni SorgeDepartment of Pediatrics and Medical Sciences, AO "Policlinico Vittorio Emanuele", Catania, Italy.
Annalisa CalcagnoPediatric Endocrine Unit, Department of Pediatrics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
Mohamad MaghniePediatric Endocrine Unit, Department of Pediatrics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
Maria Teresa DiviziaDepartment of Medical Genetics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
Daniela MelisClinical Pediatric Genetics, Department of Pediatrics, University "Federico II", Napoli, Italy.
Emanuela ManfrediniMedical Genetics Unit, Department of Laboratory Medicine, Niguarda Ca' Granda Hospital, Milano, Italy.
Giovanni Battista FerreroDepartment of Pediatric and Public Health Sciences, University of Turin, Torino, Italy.
Vanna PecileInstitute for Maternal and Child Health, Foundation IRCCS Burlo Garofolo Institute, Trieste, Italy.
Lidia LarizzaHuman Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID27110297
PMCPMC4840904

What OpenQuestion holds

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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.