Evidence map›Paper›PMID 15180241›Full record

ReviewAdvances in experimental medicine and biology2003

Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP.

Stephen P Daiger, Lori S Sullivan, Sara J Bowne, Avril Kennan, Peter Humphries, David G Birch, John R Heckenlively, RP1 Consortium

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

8 authors.

Stephen P DaigerHuman Genetics Center, Dept. of Ophthalmology, The Univ. of Texas, Houston, TX, USA. stephen.p.daiger@uth.tmc.edu
Lori S Sullivan
Sara J Bowne
Avril Kennan
Peter Humphries
David G Birch
John R Heckenlively
RP1 Consortium

Funding

DNA LINKAGE STUDIES OF DEGENERATIVE RETINAL DISEASESR01EY007142 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DAIGER, STEPHEN P · 1989 to 2017
$4.1M
RETINAL PATHOPHYSIOLOGY OF INFANTS AND ADULTSR01EY005235 · NEI · RETINA FOUNDATION OF THE SOUTHWEST · PI BIRCH, DAVID G · 1985 to 2005
$1.6M
Identifying the RP10 gene causing retinitis pigmentosaR01EY014170 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DAIGER, STEPHEN P · 2002 to 2004
$881k
NEI NIH HHS EY05235NEI NIH HHS EY07142NEI NIH HHS EY14170NEI NIH HHS R01 EY005235NEI NIH HHS R01 EY007142NEI NIH HHS R01 EY014170
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genes, DominantAmino Acid SequenceChromosome MappingCloning, MolecularEye ProteinsGenetic LinkageGenetic TestingHumansIMP DehydrogenaseMicrotubule-Associated ProteinsMolecular Sequence DataMutationPedigreeRetinitis PigmentosaEye ProteinsIMP DehydrogenaseIMPDH1 protein, humanMicrotubule-Associated ProteinsRP1 protein, human

Identifiers

PMID15180241
PMCPMC2583078

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.