Evidence map›Paper›PMID 11572994›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population.

L A McInnes, S K Service, V I Reus, G Barnes, O Charlat, S Jawahar, S Lewitzky, Q Yang, Q Duong, M Spesny and 25 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. 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
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Modeling mania in preclinical settings: A comprehensive review.Progress in neuro-psychopharmacology & biological psychiatry · 2016
    Review
  4. Article
  5. Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2015
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Genetics of bipolar disorder.Dialogues in clinical neuroscience · 2008
    Review
  11. Article
  12. Article
  13. Article
  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

35 authors at 1 institution in 1 country.

L A McInnesNeurogenetics Laboratory, Center for Neurobiology and Psychiatry, and Department of Psychiatry, University of California, San Francisco, CA 94143, USA.
S K Service
V I Reus
G Barnes
O Charlat
S Jawahar
S Lewitzky
Q Yang
Q Duong
M Spesny
C Araya
X Araya
A Gallegos
L Meza
J Molina
R Ramirez
R Mendez
S Silva
E Fournier
S L Batki
C A Mathews
T Neylan
C E Glatt
M A Escamilla
D Luo
P Gajiwala
T Song
S Crook
J B Nguyen
E Roche
J M Meyer
P Leon
L A Sandkuijl
N B Freimer
H Chen
Universidad de Costa Rica · CR

Funding

GENETIC &EPIDEMIOLOGIC STUDIES OF BIPOLAR DISORDERR01MH049499 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FREIMER, NELSON B · 1992 to 2006
$2.9M
GENETIC INVESTIGATION OF MOOD DISORDERSK01MH001748 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MCINNES, LYNNE ALISON · 1999 to 2003
$653k
MOLECULAR GENETICS OF X-LINKED BIPOLAR DISORDERK21MH000916 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FREIMER, NELSON B · 1991 to 1995
–
INVESTIGATING COSTA RICAN FAMILIES FOR BIPOLAR DISORDERR03MH048695 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FREIMER, NELSON B · 1992 to 1993
–
NIMH NIH HHS MH00916NIMH NIH HHS MH01748NIMH NIH HHS MH47563NIMH NIH HHS MH48695NIMH NIH HHS MH49499NIMH NIH HHS R01 MH049499
6 · The paper itself

Abstract

We have searched for genes predisposing to bipolar disorder (BP) by studying individuals with the most extreme form of the affected phenotype, BP-I, ascertained from the genetically isolated population of the Central Valley of Costa Rica (CVCR). The results of a previous linkage analysis on two extended CVCR BP-I pedigrees, CR001 and CR004, and of linkage disequilibrium (LD) analyses of a CVCR population sample of BP-I patients implicated a candidate region on 18p11.3. We further investigated this region by creating a physical map and developing 4 new microsatellite and 26 single-nucleotide polymorphism markers for typing in the pedigree and population samples. We report the results of fine-scale association analyses in the population sample, as well as evaluation of haplotypes in pedigree CR001. Our results suggest a candidate region containing six genes but also highlight the complexities of LD mapping of common disorders.

Indexed as

Chromosome MappingChromosomes, Human, Pair 18AllelesBipolar DisorderCosta RicaFemaleGenetic MarkersGenetic Predisposition to DiseaseHumansMaleMicrosatellite RepeatsMood DisordersPedigreeGenetic Markers

Identifiers

PMID11572994
PMCPMC58756
OpenAlexW2122617238

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.