A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31.

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.

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.

Who cites it

30 citing papers in PubMed.

1. Organization, functions, and mechanisms of the BBSome in development, ciliopathies, and beyond.eLife · 2023
   Review
2. Genetics behind Cerebral Disease with Ocular Comorbidity: Finding Parallels between the Brain and Eye Molecular Pathology.International journal of molecular sciences · 2022
   Review
3. A mutation in IFT43 causes non-syndromic recessive retinal degeneration.Human molecular genetics · 2017
   Article
4. Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.Molecular vision · 2017
   Article
5. Genetics of Obesity.Indian journal of clinical biochemistry : IJCB · 2016
   Review
6. Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21).Human molecular genetics · 2016
   Article
7. Functional modelling of a novel mutation in BBS5.Cilia · 2014
   Article
8. The genetics of human obesity.Annals of the New York Academy of Sciences · 2013
   Review
9. Genetic control of ATGL-mediated lipolysis modulates adipose triglyceride stores in leptin-deficient mice.Journal of lipid research · 2012
   Article
10. A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.BMC medical genetics · 2011
    Article
11. Genetics of childhood obesity.Journal of obesity · 2011
    Article
12. Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals.Human genetics · 2011
    Article
13. Global survey of protein expression during gonadal sex determination in mice.Molecular & cellular proteomics : MCP · 2009
    Article
14. Genetics of obesity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2006
    Review
15. Chromosome 2 locus Nidd5 has a potent effect on adiposity in the TSOD mouse.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
16. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
17. Major quantitative trait locus on chromosome 2 for glucose tolerance in diabetic SMXA-5 mouse established from non-diabetic SM/J and A/J strains.Diabetologia · 2006
    Article
18. Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene.American journal of human genetics · 2005
    Article
19. Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study.American journal of medical genetics. Part A · 2005
    Article
20. Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet-Biedl syndrome 1 critical interval.Human genetics · 2005
    Article

Corrections and comments

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Authors and funding

7 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

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