Evidence map›Paper›PMID 28626639›Full record

ArticleMolecular genetics and metabolism reports2017

A non-mosaic

Simran Madan, Wei Liu, James T Lu, V Reid Sutton, Bryant Toth, Priscilla Joe, John R Waterson, Richard A Gibbs, Ignatia B Van den Veyver, Edward J Lammer and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Focal Dermal Hypoplasia in Males: A Systematic Review.Dermatology practical & conceptual · 2026
    Review
  3. Article
  4. Article
  5. 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

12 authors at 2 institutions in 1 country.

Simran MadanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Wei LiuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
James T LuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
V Reid SuttonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Bryant TothChildren's Hospital & Research Center, Oakland, CA, USA.
Priscilla JoeChildren's Hospital & Research Center, Oakland, CA, USA.
John R WatersonChildren's Hospital & Research Center, Oakland, CA, USA.
Richard A GibbsDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Ignatia B Van den VeyverDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Edward J LammerChildren's Hospital & Research Center, Oakland, CA, USA.
Philippe M CampeauDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Brendan H LeeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Baylor College of Medicine · USHoward Hughes Medical Institute · US

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI WESTBROOK, THOMAS · 1988 to 2013
$29.4M
THE SKELETAL DYSPLASIASP01HD022657 · NICHD · CEDARS-SINAI MEDICAL CENTER · PI COHN, DANIEL H · 1987 to 2011
$17.0M
Project 3: Collagen post-translational modification and cross-linking in OIP01HD070394 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI LEE, BRENDAN · 2011 to 2020
$13.4M
HIGH THROUGHPUT SEQUENCING OF AUTISM SPECTRUM DISORDER (ASD) ENDOPHENOTYPESF30MH098571 · NIMH · BAYLOR COLLEGE OF MEDICINE · PI LU, JAMES T · 2012 to 2014
$119k
NHGRI NIH HHS U54 HG003273NICHD NIH HHS P01 HD022657NICHD NIH HHS P01 HD070394NICHD NIH HHS P30 HD024064NIMH NIH HHS F30 MH098571
6 · The paper itself

Abstract

Mutations in the

Indexed as

Focal dermal hypoplasiaGoltz syndromeMicro-opthalmiaNon-mosaicPORCN

Identifiers

PMID28626639
PMCPMC5466597
OpenAlexW2624469680

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.