Literature DB >> 9057345

Seventeenth-century European origins of hereditary diseases in the Saguenay population (Quebec, Canada).

E Heyer1, M Tremblay, B Desjardins.   

Abstract

For over three decades much research has been devoted to the identification of founders who could have been the first carriers of different deleterious genes in the French Canadian population. In some cases this research led to an investigation of the European origins of these founders. Using up-to-date data on genealogical records of 673 probands (6 hereditary diseases) and 99 control group individuals born in the Saguenay region (Quebec, Canada), we show that it is difficult to identify a precise region where a deleterious gene could have originated. By taking several key factors into consideration (founders' genetic contribution, level of commonness, sex, birth year), we found many possible candidates for each disease, leading to various regions of origin in France (Aunis, Maine, Normandie, Orléanais, Perche, and other provinces) or outside France (British Isles, other European countries). Our results also showed notable differences between the origins of male and female founders. Furthermore, all founders common to at least 95% of the probands of a given disease were also common to 95% of the probands of at least one other disease; among these founders 29 were common to 95% or more of the probands of each group (including the control group).

Entities:  

Mesh:

Year:  1997        PMID: 9057345

Source DB:  PubMed          Journal:  Hum Biol        ISSN: 0018-7143            Impact factor:   0.553


  13 in total

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5.  New estimates of intergenerational time intervals for the calculation of age and origins of mutations.

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8.  Social transmission of reproductive behavior increases frequency of inherited disorders in a young-expanding population.

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Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-08       Impact factor: 11.205

9.  Impact of inbreeding on fertility in a pre-industrial population.

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10.  Assessment of the impact of an exercise program on the physical and functional capacity in patients with autosomal recessive spastic ataxia of Charlevoix-Saguenay: An exploratory study.

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Journal:  Intractable Rare Dis Res       Date:  2018-08
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