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Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography chromosome recombination frequency and selection

Articolo
Data di Pubblicazione:
2000
Citazione:
Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography chromosome recombination frequency and selection / Zavattari, P; Deidda, E; Whalen, M; Lampis, R; Mulargia, A; Loddo, M; Eaves, I; Mastio, G; Todd, Ja; Cucca, Francesco. - In: HUMAN MOLECULAR GENETICS. - ISSN 0964-6906. - 9:20(2000), pp. 2947-2957. [10.1093/hmg/9.20.2947]
Abstract:
Linkage disequilibrium (LD) mapping of disease genes is complicated by population- and chromosome-region-specific factors. We have analysed demographic factors by contrasting intermarker LD results obtained in a large cosmopolitan population (UK), a targe genetic isolate (Sardinia) and a subisolate (village of Gavoi) for two regions of the X chromosome. A dramatic increase of LD was found in the subisolate. Demographic history of populations therefore influences LD. Chromosome-region-specific effects, namely the pattern and frequency of homologous recombination, were next delineated by the analysis of chromosome 6p21, including the HLA region. Patterns of global LD in this region were very similar in the UK and Sardinian populations despite their entirely distinct demographies, and correlate well with the pattern of recombinations. Nevertheless, haplotypes extend across recombination hot spots indicative of selection of certain haplotypes, Subisolate aside, chromosome-region-specific differences in LD patterns appear to be more important than the differences in intermarker LD between distinct populations.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Zavattari, P; Deidda, E; Whalen, M; Lampis, R; Mulargia, A; Loddo, M; Eaves, I; Mastio, G; Todd, Ja; Cucca, Francesco
Autori di Ateneo:
CUCCA Francesco
Link alla scheda completa:
https://iris.uniss.it/handle/11388/60103
Pubblicato in:
HUMAN MOLECULAR GENETICS
Journal
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