Evidence map›Paper›PMID 15494893›Full record

ArticleAmerican journal of human genetics2004

A second-generation genomic screen for multiple sclerosis.

S J Kenealy, M-C Babron, Y Bradford, N Schnetz-Boutaud, J L Haines, J B Rimmler, S Schmidt, M A Pericak-Vance, L F Barcellos, R R Lincoln and 11 more

Abstract read
In one paragraph

Article in American journal of human genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
–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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Meta-analysis of genome-wide linkage studies across autoimmune diseases.European journal of human genetics : EJHG · 2009
    Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. The genetic aspects of multiple sclerosis.Annals of Indian Academy of Neurology · 2009
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. A high-density screen for linkage in multiple sclerosis.American journal of human genetics · 2005
    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

21 authors.

S J KenealyCenter for Human Genetics Research, Vanderbilt University Medical Center, Nashville, TN 37232-0700, USA.
M-C Babron
Y Bradford
N Schnetz-Boutaud
J L Haines
J B Rimmler
S Schmidt
M A Pericak-Vance
L F Barcellos
R R Lincoln
J R Oksenberg
S L Hauser
M Clanet
D Brassat
G Edan
J Yaouanq
G Semana
I Cournu-Rebeix
O Lyon-Caen
B Fontaine
American-French Multiple Sclerosis Genetics Group

Funding

The Genetic Epemiology of Multiple SclerosisR01NS032830 · NINDS · VANDERBILT UNIVERSITY · PI HAINES, JONATHAN L · 1995 to 2010
$8.9M
GENE LINKAGE STUDY OF MULTIPLE SCLEROSIS SIBLING PAIRSR01NS026799 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HAUSER, STEPHEN L, OKSENBERG, JORGE R. · 1989 to 2018
$6.8M
NINDS NIH HHS NS26799NINDS NIH HHS NS32830NINDS NIH HHS R01 NS026799NINDS NIH HHS R01 NS032830
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a debilitating neuroimmunological and neurodegenerative disorder. Despite substantial evidence for polygenic inheritance of the disease, the major histocompatibility complex is the only region that clearly and consistently demonstrates linkage and association in MS studies. The goal of this study was to identify additional chromosomal regions that harbor susceptibility genes for MS. With a panel of 390 microsatellite markers genotyped in 245 U.S. and French multiplex families (456 affected relative pairs), this is the largest genomic screen for MS conducted to date. Four regions met both of our primary criteria for further interest (heterogeneity LOD [HLOD] and Z scores >2.0): 1q (HLOD=2.17; Z=3.38), 6p (HLOD=4.21; Z=2.26), 9q (HLOD; Z=2.71), and 16p (HLOD=2.64; Z=2.05). Two additional regions met only the Z score criterion: 3q (Z=2.39) and 5q (Z=2.17). Further examination of the data by country (United States vs. France) identified one additional region demonstrating suggestive linkage in the U.S. subset (18p [HLOD=2.39]) and two additional regions generating suggestive linkage in the French subset (1p [HLOD=2.08] and 22q [HLOD=2.06]). Examination of the data by human leukocyte antigen (HLA)-DR2 stratification identified four additional regions demonstrating suggestive linkage: 2q (HLOD=3.09 in the U.S. DR2- families), 6q (HLOD=3.10 in the French DR2- families), 13q (HLOD=2.32 in all DR2+ families and HLOD=2.17 in the U.S. DR2+ families), and 16q (HLOD=2.32 in all DR2+ families and HLOD=2.13 in the U.S. DR2+ families). These data suggest several regions that warrant further investigation in the search for MS susceptibility genes.

Indexed as

Chromosome MappingGenome, HumanChromosomes, Human, Pair 13Chromosomes, Human, Pair 16Chromosomes, Human, Pair 2Chromosomes, Human, Pair 6FranceGene FrequencyGenetic TestingHLA-DR2 AntigenHumansLod ScoreMicrosatellite RepeatsModels, GeneticMultiple SclerosisUnited StatesHLA-DR2 Antigen

Identifiers

PMID15494893
PMCPMC1182142

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.