Evidence map›Paper›PMID 17273929›Full record

ArticleNeurochemical research2007

Mapping of QTLs for oral alcohol self-administration in B6.C and B6.I quasi-congenic RQI strains.

Csaba Vadasz, Mariko Saito, Beatrix M Gyetvai, Melinda Oros, Istvan Szakall, Krisztina M Kovacs, Vidudala V T S Prasad, Grant Morahan, Reka Toth

Open access · greenAbstract read
In one paragraph

Article in Neurochemical research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Pleiotropic Effects ofBiomolecules · 2025
    Review
  2. Article
  3. Article
  4. A Spontaneous Mutation inFrontiers in pharmacology · 2017
    Article
  5. Article
  6. Article
  7. Quantitative trait loci for sensitivity to ethanol intoxication in a C57BL/6J×129S1/SvImJ inbred mouse cross.Mammalian genome : official journal of the International Mammalian Genome Society · 2012
    Article
  8. The influence of sex and estrous cycle on QTL for emotionality and ethanol consumption.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    Article
  9. Article
  10. Review
  11. A method for mapping intralocus interactions influencing excessive alcohol drinking.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  12. Article
  13. 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

9 authors at 4 institutions in 2 countries.

Csaba VadaszLaboratory of Neurobehavioral Genetics, Nathan S. Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY 10962, USA. vadasz@nki.rfmh.org
Mariko Saito
Beatrix M Gyetvai
Melinda Oros
Istvan Szakall
Krisztina M Kovacs
Vidudala V T S Prasad
Grant Morahan
Reka Toth
Nathan Kline Institute for Psychiatric Research · USColumbia University Irving Medical Center · USHarry Perkins Institute of Medical Research · AUNew York University · US

Funding

MAPPING OF ALCOHOL PREFERENCE GENES IN RQI STRAINSR01AA011031 · NIAAA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI VADASZ, CSABA · 1996 to 2002
$599k
NIAAA NIH HHS AA11031NIAAA NIH HHS R01 AA011031
6 · The paper itself

Abstract

One strategy to identify neurochemical pathways of addiction is to map the relevant genes. In the present study we used 43 B6.C and 35 B6.I inbred RQI mouse strains, carrying <3% donor genome on C57BL/6ByJ background, for gene mapping. The strains were phenotyped for consumption of alcohol (12% v/v) in a two-bottle-choice paradigm, and genotyped for 396 microsatellite markers. The current mapping study extends our earlier experiment scanning five mouse chromosomes (Vadasz et al. (2000) Scanning of five chromosomes for alcohol consumption loci. Alcohol 22:25-34) to a whole-genome study, and discusses the differences and limitations. Data were analyzed with composite interval (CIM) and multiple interval (MIM) QTL mapping methods. CIM of B6.C strains detected significant QTLs on chrs. 6 and 12. A suggestive, but not significant, locus was detected in the B6.I strains on chr. 12. The best MIM model for B6.C strains confirmed one QTL on chr. 6 and one QTL on chr. 12, while the MIM model for the B6.I strains confirmed the suggestive locus on chr. 12. Some of the QTLs for alcohol consumption are new, while others confirm previously reported QTLs for alcohol preference, and alcohol acceptance.

Indexed as

Chromosome MappingQuantitative Trait LociSelf AdministrationAlcohol DrinkingAnimalsEthanolGenetic VariationMaleMiceMice, CongenicMice, Inbred StrainsPhenotypeEthanol

Identifiers

PMID17273929
PMCPMC2595145
OpenAlexW2083506069

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.