Evidence map›Paper›PMID 24569604›Full record

ArticleEuropean journal of human genetics : EJHG2014

Clinical utility gene card for: Williams-Beuren Syndrome [7q11.23].

Udo Koehler, Brigitte Pabst, Barbara Pober, Beth Kozel

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Udo KoehlerMGZ - Medizinisch Genetisches Zentrum, Munich, Germany.
Brigitte PabstInstitute for Human Genetics, Hannover Medical School, Hannover, Germany.
Barbara Pober1] Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA [2] Department of Medical Sciences, Frank H Netter School of Medicine, Quinnipiac University, North Haven, CT, USA.
Beth KozelDepartment of Pediatrics, Washington University School of Medicine, St Louis, MO, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic TestingChromosomes, Human, Pair 7Genetic LociHumansMuscle ProteinsMutationNADPH OxidasesNuclear ProteinsTrans-ActivatorsWilliams SyndromeGTF2IRD1 protein, humanMuscle ProteinsNADPH Oxidasesneutrophil cytosolic factor 1Nuclear ProteinsTrans-Activators

Identifiers

PMID24569604
PMCPMC4135419

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.