Evidence map›Paper›PMID 27900855›Full record

ArticlePigment cell & melanoma research2017

A new type of syndromic albinism associated with mutations in AP3D1.

Lluis Montoliu, Michael S Marks

Open access · bronzeAbstract readNewsComment
In one paragraph

Article in Pigment cell & melanoma research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

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

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Lluis Montoliu
Michael S Marks
Children's Hospital of Philadelphia · USInstituto de Salud Carlos III · ES

Funding

Hermansky Pudlak Syndrome &melanosome formationR01EY015625 · NEI · UNIVERSITY OF PENNSYLVANIA · PI Michael S Marks · 2004 to 2026
$9.2M
Melanosome BiogenesisR01AR048155 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MARKS, MICHAEL S · 2002 to 2017
$4.2M
NEI NIH HHS R01 EY015625NIAMS NIH HHS R01 AR048155
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AlbinismMutationAdaptor Protein Complex 3Adaptor Protein Complex delta SubunitsAlbinism, OculocutaneousHumansSyndromeAdaptor Protein Complex 3Adaptor Protein Complex delta SubunitsAP3D1 protein, human

Identifiers

PMID27900855
PMCPMC5555751
OpenAlexW2533367163

What OpenQuestion holds

Textmetadata
LicenceTDM
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.