Evidence map›Paper›PMID 9788970›Full record

ArticleThe Journal of clinical investigation1998

Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family.

C F Verge, P Vardi, S Babu, F Bao, H A Erlich, T Bugawan, D Tiosano, L Yu, G S Eisenbarth, P R Fain

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Genetic analysis of the LEW.1AR1-iddm rat: an animal model for spontaneous diabetes mellitus.Mammalian genome : official journal of the International Mammalian Genome Society · 2005
    Article
  8. Article
  9. Genetics of type 1 diabetes mellitus.Genes and immunity · 2002
    Review
  10. Article
  11. Article
  12. Article
  13. Multiple genes/multiple autoantigens role in type 1 diabetes.Clinical reviews in allergy & immunology · 2000
    Review
  14. 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.

C F VergeBarbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, Denver, Colorado 80262-0001, USA.
P Vardi
S Babu
F Bao
H A Erlich
T Bugawan
D Tiosano
L Yu
G S Eisenbarth
P R Fain

Funding

Multiple Autoantigens/Multiple Epitopes of Type 1DMR01DK032083 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 1986 to 2025
$6.9M
MULTIPLE AUTOANTIGENS OF PRETYPE I DMR37DK032083 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI EISENBARTH, GEORGE S · 1992 to 1999
–
NIDDK NIH HHS DK32083
6 · The paper itself

Abstract

Based on a genomic search for linkage, a locus contributing to type 1 diabetes in a large Bedouin Arab family (19 affected relatives) maps to the long arm of chromosome 10 (10q25; nonparametric linkage = 4.99; P = 0.00004). All affected relatives carry one or two high-risk HLA-DR3 haplotypes that are rarely found in other family members. One chromosome 10 haplotype, the B haplotype, was transmitted from a heterozygous parent to 13 of 13 affected offspring compared to 10 of 23 unaffected siblings. Recombination events occurring on this haplotype place the susceptibility locus in an 8-cM interval between markers D10S1750 and D10S1773. Two adjacent markers, D10S592 and D10S554, showed evidence of linkage disequilibrium with the disease locus. A 273-bp allele at D10S592 was transmitted to 8 of 10 affected offspring compared to 3 of 14 unaffected siblings, and a 151-bp allele at D10S554 was transmitted to 15 of 15 affected offspring compared with 10 of 24 unaffected siblings. D10S554 and D10S592 and the closest flanking markers are contained in a 1,240-kb yeast artificial chromosome, a region small enough to proceed with positional cloning.

Indexed as

ArabsChromosomes, Human, Pair 10Chromosome MappingDiabetes Mellitus, Type 1Genetic LinkageGenetic MarkersGenetic Predisposition to DiseaseHaplotypesHLA-DR3 AntigenHumansIsraelPedigreeWhite PeopleGenetic MarkersHLA-DR3 Antigen

Identifiers

PMID9788970
PMCPMC509007

What OpenQuestion holds

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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.