Evidence map›Paper›PMID 22105877›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2012

Genome-wide association studies for multiple diseases of the German Shepherd Dog.

Kate L Tsai, Rooksana E Noorai, Alison N Starr-Moss, Pascale Quignon, Caitlin J Rinz, Elaine A Ostrander, Jörg M Steiner, Keith E Murphy, Leigh Anne Clark

Open access · greenAbstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  5. Congenital Malformations in River Buffalo (Bubalus bubalis).Animals : an open access journal from MDPI · 2017
    Review
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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.

Kate L TsaiDepartment of Genetics and Biochemistry, College of Agriculture, Forestry and Life Sciences, Clemson University, Clemson, SC 29634, USA.
Rooksana E Noorai
Alison N Starr-Moss
Pascale Quignon
Caitlin J Rinz
Elaine A Ostrander
Jörg M Steiner
Keith E Murphy
Leigh Anne Clark
Clemson University · USCancer Genetics (United States) · USNational Human Genome Research Institute · USTexas A&M University · US

Funding

Comparative Mammalian GenomicsZIAHG200377 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI OSTRANDER, ELAINE · 2012 to 2025
$24.8M
Finding Genes for Human Prostate CancerZIAHG200325 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI OSTRANDER, ELAINE · 2009 to 2021
$17.7M
Intramural NIH HHS ZIA HG200325Intramural NIH HHS ZIA HG200377
6 · The paper itself

Abstract

The German Shepherd Dog (GSD) is a popular working and companion breed for which over 50 hereditary diseases have been documented. Herein, SNP profiles for 197 GSDs were generated using the Affymetrix v2 canine SNP array for a genome-wide association study to identify loci associated with four diseases: pituitary dwarfism, degenerative myelopathy (DM), congenital megaesophagus (ME), and pancreatic acinar atrophy (PAA). A locus on Chr 9 is strongly associated with pituitary dwarfism and is proximal to a plausible candidate gene, LHX3. Results for DM confirm a major locus encompassing SOD1, in which an associated point mutation was previously identified, but do not suggest modifier loci. Several SNPs on Chr 12 are associated with ME and a 4.7 Mb haplotype block is present in affected dogs. Analysis of additional ME cases for a SNP within the haplotype provides further support for this association. Results for PAA indicate more complex genetic underpinnings. Several regions on multiple chromosomes reach genome-wide significance. However, no major locus is apparent and only two associated haplotype blocks, on Chrs 7 and 12 are observed. These data suggest that PAA may be governed by multiple loci with small effects, or it may be a heterogeneous disorder.

Indexed as

AnimalsChromosome MappingDog DiseasesDogsDwarfism, PituitaryEsophageal AchalasiaGenetic Predisposition to DiseaseGenomeGenome-Wide Association StudyLIM-Homeodomain ProteinsPancreatic DiseasesPolymorphism, Single NucleotideSpinal Cord DiseasesSuperoxide DismutaseSuperoxide Dismutase-1Transcription FactorsLhx3 proteinLIM-Homeodomain ProteinsSuperoxide DismutaseSuperoxide Dismutase-1Transcription Factors

Identifiers

PMID22105877
PMCPMC3509149
OpenAlexW2016432254

What OpenQuestion holds

Textmetadata
LicenceTDM
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.