Literature DB >> 12734544

Spatial patterns of cystic fibrosis mutation spectra in European populations.

Oscar Lao1, Aida M Andrés, Eva Mateu, Jaume Bertranpetit, Francesc Calafell.   

Abstract

Cystic fibrosis (CF) is the most frequent severe recessive disorder in European populations. We have analyzed its mutation frequency spectrum in 94 European, North African and SW Asian populations taken from the literature. Most major mutations as well as the incidence of CF mutations showed clinals patterns as demonstrated by autocorrelogram analysis. More importantly, measures of mutation diversity did also show clinal patterns, with mutation spectra being more diverse in southern than in northern Europe. This increased diversity would imply roughly a three-fold long-term effective population size in southern than in northern Europe. Distances were computed among populations based on their CF mutation frequencies and compared with distances based on other genic regions. CF-based distances correlated with mtDNA but not with Y-chromosome-based distances, which may be a consequence of the relatively homogeneous CF mutation frequencies in European populations.

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Year:  2003        PMID: 12734544     DOI: 10.1038/sj.ejhg.5200970

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  16 in total

1.  Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation.

Authors:  S Ogino; R B Wilson; W W Grody
Journal:  J Med Genet       Date:  2004-05       Impact factor: 6.318

2.  Linkage disequilibrium patterns and tagSNP transferability among European populations.

Authors:  Jakob C Mueller; Elin Lõhmussaar; Reedik Mägi; Maido Remm; Thomas Bettecken; Peter Lichtner; Saskia Biskup; Thomas Illig; Arne Pfeufer; Jan Luedemann; Stefan Schreiber; Peter Pramstaller; Irene Pichler; Giovanni Romeo; Anthony Gaddi; Alessandra Testa; Heinz-Erich Wichmann; Andres Metspalu; Thomas Meitinger
Journal:  Am J Hum Genet       Date:  2005-01-06       Impact factor: 11.025

3.  Human F7 sequence is split into three deep clades that are related to FVII plasma levels.

Authors:  Maria Sabater-Lleal; José Manuel Soria; Jaume Bertranpetit; Laura Almasy; John Blangero; Jordi Fontcuberta; Francesc Calafell
Journal:  Hum Genet       Date:  2005-11-16       Impact factor: 4.132

4.  Atlas of human diseases influenced by genetic variants with extreme allele frequency differences.

Authors:  Arvis Sulovari; Yolanda H Chen; James J Hudziak; Dawei Li
Journal:  Hum Genet       Date:  2016-10-03       Impact factor: 4.132

Review 5.  Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Authors:  C Castellani; H Cuppens; M Macek; J J Cassiman; E Kerem; P Durie; E Tullis; B M Assael; C Bombieri; A Brown; T Casals; M Claustres; G R Cutting; E Dequeker; J Dodge; I Doull; P Farrell; C Ferec; E Girodon; M Johannesson; B Kerem; M Knowles; A Munck; P F Pignatti; D Radojkovic; P Rizzotti; M Schwarz; M Stuhrmann; M Tzetis; J Zielenski; J S Elborn
Journal:  J Cyst Fibros       Date:  2008-05       Impact factor: 5.482

6.  Detecting Common CFTR Mutations by Reverse Dot Blot Hybridization Method in Cystic Fibrosis First Report from Northern Iran.

Authors:  Mohammad-Reza Esmaeili Dooki; Haleh Akhavan-Niaki; Ali Ghabeli Juibary
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

7.  Biophysical characterisation of calumenin as a charged F508del-CFTR folding modulator.

Authors:  Rashmi Tripathi; Nathalie Benz; Bridget Culleton; Pascal Trouvé; Claude Férec
Journal:  PLoS One       Date:  2014-08-13       Impact factor: 3.240

Review 8.  Cystic Fibrosis from Laboratory to Bedside: The Role of A20 in NF-κB-Mediated Inflammation.

Authors:  Aidan Bannon; Shu-Dong Zhang; Bettina C Schock; Madeleine Ennis
Journal:  Med Princ Pract       Date:  2015-04-25       Impact factor: 1.927

9.  Cystic fibrosis prevalence among a group of high-risk children in the main referral children hospital in Iran.

Authors:  Mohammad Reza Modaresi; Jamal Faghinia; Mohsen Reisi; Majid Keivanfar; Shiva Navaie; Javad Seyyedi; Faride Baharzade
Journal:  J Educ Health Promot       Date:  2017-06-05

10.  Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation.

Authors:  Nika Petrova; Natalia Balinova; Andrey Marakhonov; Tatyana Vasilyeva; Nataliya Kashirskaya; Varvara Galkina; Evgeniy Ginter; Sergey Kutsev; Rena Zinchenko
Journal:  Front Genet       Date:  2021-06-16       Impact factor: 4.599

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