Evidence map›Paper›PMID 7783171›Full record

ArticleJournal of medical genetics1995

Haplotype analysis in autosomal dominant polycystic kidney disease.

S E Pound, S Thomas, A Snarey, A M Macnicol, M L Watson, P M Pignatelli, A M Frischauf, P C Harris, A F Wright

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of medical genetics, 1995. 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, top 92% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 4 institutions in 2 countries.

S E PoundMRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
S Thomas
A Snarey
A M Macnicol
M L Watson
P M Pignatelli
A M Frischauf
P C Harris
A F Wright
Western General Hospital · GBCancer Research UK · GBHypertension Institute · USUniversity of Edinburgh · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Haplotype analysis was performed in 35 autosomal dominant polycystic kidney disease (ADPKD) families typed with 13 markers close to the PKD1 locus. The identification of recombinants close to the PKD1 gene on chromosome 16p indicates that PKD1 lies between CMM65 distally and 26-6 proximally. In addition, three unlinked (PKD2) families and two families with potential new mutation were identified.

Indexed as

AdultAgedChromosomes, Human, Pair 16FemaleGenetic LinkageGenetic MarkersHaplotypesHumansMaleMiddle AgedMutationPolycystic Kidney, Autosomal DominantProteinsTRPP Cation ChannelsGenetic MarkersProteinsTRPP Cation Channels

Identifiers

PMID7783171
PMCPMC1050319
OpenAlexW1998653205

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.