Evidence map›Paper›PMID 23890820›Full record

ArticleCell2013

Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat.

Santosh S Atanur, Ana Garcia Diaz, Klio Maratou, Allison Sarkis, Maxime Rotival, Laurence Game, Michael R Tschannen, Pamela J Kaisaki, Georg W Otto, Man Chun John Ma and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 3 pooled it
15.8field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 3 syntheses or guidelines pooled it, 171 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Article
  5. Review
  6. Article
  7. Article
  8. Establishing the hybrid rat diversity program: a resource for dissecting complex traits.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. A Genetically Heterogeneous Rat Model with Divergent Mitochondrial Genomes.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Coding variants in mouse and rat model organisms: mousepost and ratpost.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Article
  19. Article
  20. Cpxm2 as a novel candidate for cardiac hypertrophy and failure in hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article

47 more citing papers are in PubMed but not listed here.

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

32 authors at 12 institutions in 6 countries.

Santosh S AtanurPhysiological Genomic and Medicine Group, MRC Clinical Sciences Centre, Imperial College London, London W12 0NN, UK.
Ana Garcia Diaz
Klio Maratou
Allison Sarkis
Maxime Rotival
Laurence Game
Michael R Tschannen
Pamela J Kaisaki
Georg W Otto
Man Chun John Ma
Thomas M Keane
Oliver Hummel
Kathrin Saar
Wei Chen
Victor Guryev
Kathirvel Gopalakrishnan
Michael R Garrett
Bina Joe
Lorena Citterio
Giuseppe Bianchi
Martin McBride
Anna Dominiczak
David J Adams
Tadao Serikawa
Paul Flicek
Edwin Cuppen
Norbert Hubner
Enrico Petretto
Dominique Gauguier
Anne Kwitek
Howard Jacob
Timothy J Aitman
Imperial College London · GBMax Delbrück Center · DECentre for Human Genetics · GBMedical College of Wisconsin · USUniversity Medical Center Utrecht · NLUniversity of Glasgow · GBUniversity of Iowa · USUniversity of Toledo · USWellcome Sanger Institute · GBEuropean Bioinformatics Institute · GBKyoto University · JPUniversity of Mississippi Medical Center · US

Funding

Genetics of HypertensionR01HL020176 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI JOE, BINA · 1985 to 2017
$8.1M
Physiological Genomics of Hypertensive Renal DiseaseR01HL069321 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI LAZAR, JOZEF · 2001 to 2017
$5.6M
Genetics of Renal End Organ Damage in HypertensionR01HL094446 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI GARRETT, MICHAEL R · 2009 to 2013
$1.8M
Dissecting the genetics of the Metabolic Syndrome on Chromosome 17 of the LH ratR01HL089895 · NHLBI · UNIVERSITY OF IOWA · PI KWITEK, ANNE E. · 2008 to 2012
$1.7M
Identification of a metabolic syndrome transcriptome signature in the LH ratR21DK089417 · NIDDK · UNIVERSITY OF IOWA · PI KWITEK, ANNE E., XING, YI · 2010 to 2011
$411k
British Heart Foundation RE/08/002Cancer Research UK 13031Medical Research Council G0800024Medical Research Council MC_U120061454Medical Research Council MC_U120097112NHLBI NIH HHS HL094446NHLBI NIH HHS R01 HL020176NHLBI NIH HHS R01 HL069321NHLBI NIH HHS R01 HL089895NHLBI NIH HHS R01 HL094446Wellcome TrustWellcome Trust 075491/Z/04
6 · The paper itself

Abstract

Large numbers of inbred laboratory rat strains have been developed for a range of complex disease phenotypes. To gain insights into the evolutionary pressures underlying selection for these phenotypes, we sequenced the genomes of 27 rat strains, including 11 models of hypertension, diabetes, and insulin resistance, along with their respective control strains. Altogether, we identified more than 13 million single-nucleotide variants, indels, and structural variants across these rat strains. Analysis of strain-specific selective sweeps and gene clusters implicated genes and pathways involved in cation transport, angiotensin production, and regulators of oxidative stress in the development of cardiovascular disease phenotypes in rats. Many of the rat loci that we identified overlap with previously mapped loci for related traits in humans, indicating the presence of shared pathways underlying these phenotypes in rats and humans. These data represent a step change in resources available for evolutionary analysis of complex traits in disease models.

Indexed as

AnimalsDisease Models, AnimalGenomePhenotypePhylogenyPolymorphism, Single NucleotideRatsRats, Inbred Strains

Identifiers

PMID23890820
PMCPMC3732391
OpenAlexW2168798091

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.