Evidence map›Paper›PMID 1386495›Full record

ArticleAmerican journal of human genetics1992

A recombination event that redefines the Huntington disease region.

R G Snell, L M Thompson, D A Tagle, T L Holloway, G Barnes, H G Harley, L A Sandkuijl, M E MacDonald, F S Collins, J F Gusella

Abstract read
In one paragraph

Article in American journal of human genetics, 1992. 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. Defining the location of the Huntington disease gene.American journal of human genetics · 1993
    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

10 authors.

R G SnellDepartment of Medical Genetics, University of Wales College of Medicine, Cardiff, United Kingdom.
L M Thompson
D A Tagle
T L Holloway
G Barnes
H G Harley
L A Sandkuijl
M E MacDonald
F S Collins
J F Gusella

Funding

Wellcome Trust
6 · The paper itself

Abstract

We report both a recombination event that places the Huntington disease gene proximal to the marker D4S98 and an extended linkage-disequilibrium study that uses this marker and confirms the existence of disequilibrium between it and the HD locus. We also report the cloning of other sequences in the region around D4S98, including a new polymorphic marker R10 and conserved sequences that identify a gene in the region of interest.

Indexed as

Chromosomes, Human, Pair 4Recombination, GeneticFemaleGenetic MarkersGenotypeHumansHuntington DiseaseLinkage DisequilibriumMalePedigreePolymorphism, GeneticRestriction MappingGenetic Markers

Identifiers

PMID1386495
PMCPMC1682687

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.