Evidence map›Paper›PMID 19319892›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2009

A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.

A J Jasinska, S Service, D Jawaheer, J DeYoung, M Levinson, Z Zhang, B Kremeyer, H Muller, I Aldana, J Garcia and 22 more

Abstract read
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

32 authors.

A J JasinskaCenter for Neurobehavioral Genetics, University of California, Los Angeles, California 90095, USA.
S Service
D Jawaheer
J DeYoung
M Levinson
Z Zhang
B Kremeyer
H Muller
I Aldana
J Garcia
G Restrepo
C Lopez
C Palacio
C Duque
M Parra
J Vega
D Ortiz
G Bedoya
C Mathews
P Davanzo
E Fournier
J Bejarano
M Ramirez
C Araya Ortiz
X Araya
J Molina
C Sabatti
V Reus
J Ospina
G Macaya
A Ruiz-Linares
N B Freimer

Funding

POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
GENETIC &EPIDEMIOLOGIC STUDIES OF BIPOLAR DISORDERR01MH049499 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FREIMER, NELSON B · 1992 to 2006
$2.9M
MOLECULAR AND POPULATION GENETICS OF BIPOLAR DISORDERK02MH001375 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FREIMER, NELSON B · 1996 to 2005
$675k
NIMH NIH HHS K02 MH 001375NIMH NIH HHS K02 MH001375NIMH NIH HHS R01 MH 049499NIMH NIH HHS R01 MH049499NLM NIH HHS T15 LM007033Wellcome TrustWellcome Trust 086052
6 · The paper itself

Abstract

We previously reported linkage of bipolar disorder to 5q33-q34 in families from two closely related population isolates, the Central Valley of Costa Rica (CVCR) and Antioquia, Colombia (CO). Here we present follow up results from fine-scale mapping in large CVCR and CO families segregating severe bipolar disorder, BP-I, and in 343 population trios/duos from CVCR and CO. Employing densely spaced SNPs to fine map the prior linkage peak region increases linkage evidence and clarifies the position of the putative BP-I locus. We performed two-point linkage analysis with 1134 SNPs in an approximately 9 Mb region between markers D5S410 and D5S422. Combining pedigrees from CVCR and CO yields a LOD score of 4.9 at SNP rs10035961. Two other SNPs (rs7721142 and rs1422795) within the same 94 kb region also displayed LOD scores greater than 4. This linkage peak coincides with our prior microsatellite results and suggests a narrowed BP-I susceptibility regions in these families. To investigate if the locus implicated in the familial form of BP-I also contributes to disease risk in the population, we followed up the family results with association analysis in duo and trio samples, obtaining signals within 2 Mb of the peak linkage signal in the pedigrees; rs12523547 and rs267015 (P = 0.00004 and 0.00016, respectively) in the CO sample and rs244960 in the CVCR sample and the combined sample, with P = 0.00032 and 0.00016, respectively. It remains unclear whether these association results reflect the same locus contributing to BP susceptibility within the extended pedigrees.

Indexed as

Genetic LinkagePedigreeAmerican Indian or Alaska NativeBipolar DisorderChromosomes, Human, Pair 5ColombiaCosta RicaFamilyFemaleGene FrequencyGenetic MarkersGenetic Predisposition to DiseaseHumansLatin AmericaLod ScoreMaleGenetic Markers

Identifiers

PMID19319892
PMCPMC4815924

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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.