Evidence map›Paper›PMID 16894393›Full record

ArticleMolecular psychiatry2006

Genetic and clinical analysis of a large Dutch Gilles de la Tourette family.

A J M H Verkerk, D C Cath, H C van der Linde, J Both, P Heutink, G Breedveld, Y S Aulchenko, B A Oostra

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Lack of Association ofNeuropsychiatric disease and treatment · 2022
    Article
  4. Genes · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Genetic susceptibility and neurotransmitters in Tourette syndrome.International review of neurobiology · 2013
    Review
  13. Article
  14. Review
  15. Review
  16. The genetics of Tourette syndrome.Nature reviews. Neurology · 2012
    Review
  17. The genetics of Tourette disorder.Current opinion in genetics & development · 2011
    Review
  18. Review
  19. Article
  20. 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.

A J M H VerkerkDepartment of Bioinformatics, Erasmus Medical Center, Rotterdam, The Netherlands. j.verkerk@erasmusmc.nl
D C Cath
H C van der Linde
J Both
P Heutink
G Breedveld
Y S Aulchenko
B A Oostra

Funding

A GENETIC LINKAGE STUDY OF GTSR01NS040024 · NINDS · TOURETTE SYNDROME ASSOCIATION, INC · PI PAULS, DAVID L · 2000 to 2004
$9.5M
A Genetic Linkage Study of GTSU01NS040024 · NINDS · TOURETTE ASSOCIATION OF AMERICA, INC. · PI SCHARF, JEREMIAH M · 2007 to 2012
$8.0M
NINDS NIH HHS NS-40024-01
6 · The paper itself

Abstract

Gilles de la Tourette syndrome is a complex neuropsychiatric disorder, which becomes evident in childhood between the ages of 2 and 15 years. Tourette syndrome is defined by the occurrence of a large range and variable number of unwanted repetitive simple or complex motor and vocal tics that start in childhood and follow a waxing and waning course. A major gene for this syndrome has not yet been identified, probably owing to both genetic and phenotypic heterogeneity of this disease. This article describes the clinical evaluation of patients and family members in a large Dutch Gilles de la Tourette Syndrome pedigree and the decisions encountered with respect to phenotyping. The importance of an accurate definition of the Tourette phenotype is discussed, which is highly important for reliable genetic linkage and association studies. Subsequent linkage analysis resulted in three linkage peaks on different chromosomes 3q, 9q, and 13q. Multipoint analysis resulted in a single linkage peak with logarithm of odds score 2.55 with marker D3S1311 on chromosome 3q.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChromosomes, Human, Pair 3FemaleGenetic Predisposition to DiseaseHumansLod ScoreMaleMembrane ProteinsMiddle AgedNerve Tissue ProteinsPedigreePhenotypeMembrane ProteinsNerve Tissue ProteinsSLITRK1 protein, human

Identifiers

PMID16894393

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.