Calafell F - Search Results

1

Population genetics of a functional variant of the dopamine beta-hydroxylase gene (DBH).

Cubells JF, Kobayashi K, Nagatsu T, Kidd KK, Kidd JR, Calafell F, Kranzler HR, Ichinose H, Gelernter J. Cubells JF, et al. Among authors: calafell f. Am J Med Genet. 1997 Jul 25;74(4):374-9. doi: 10.1002/(sici)1096-8628(19970725)74:4<374::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9259372

2

Genealogy reconstruction from short tandem repeat genotypes in an Amazonian population.

Calafell F, Shuster A, Speed WC, Kidd JR, Black FL, Kidd KK. Calafell F, et al. Am J Phys Anthropol. 1999 Feb;108(2):137-46. doi: 10.1002/(SICI)1096-8644(199902)108:2<137::AID-AJPA1>3.0.CO;2-K. Am J Phys Anthropol. 1999. PMID: 9988377

3

Worldwide genetic analysis of the CFTR region.

Mateu E, Calafell F, Lao O, Bonné-Tamir B, Kidd JR, Pakstis A, Kidd KK, Bertranpetit J. Mateu E, et al. Among authors: calafell f. Am J Hum Genet. 2001 Jan;68(1):103-17. doi: 10.1086/316940. Epub 2000 Dec 4. Am J Hum Genet. 2001. PMID: 11104661 Free PMC article.

4

Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes.

Iyengar S, Calafell F, Kidd KK. Iyengar S, et al. Among authors: calafell f. Genet Epidemiol. 1997;14(6):809-14. doi: 10.1002/(SICI)1098-2272(1997)14:6<809::AID-GEPI41>3.0.CO;2-R. Genet Epidemiol. 1997. PMID: 9433582 Clinical Trial.

5

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

Tishkoff SA, Goldman A, Calafell F, Speed WC, Deinard AS, Bonne-Tamir B, Kidd JR, Pakstis AJ, Jenkins T, Kidd KK. Tishkoff SA, et al. Among authors: calafell f. Am J Hum Genet. 1998 Jun;62(6):1389-402. doi: 10.1086/301861. Am J Hum Genet. 1998. PMID: 9585589 Free PMC article.

6

Short tandem repeat polymorphism evolution in humans.

Calafell F, Shuster A, Speed WC, Kidd JR, Kidd KK. Calafell F, et al. Eur J Hum Genet. 1998 Jan;6(1):38-49. doi: 10.1038/sj.ejhg.5200151. Eur J Hum Genet. 1998. PMID: 9781013

7

Haplotype evolution and linkage disequilibrium: A simulation study.

Calafell F, Grigorenko EL, Chikanian AA, Kidd KK. Calafell F, et al. Hum Hered. 2001;51(1-2):85-96. doi: 10.1159/000022963. Hum Hered. 2001. PMID: 11096275

8

Allele frequencies in a worldwide survey of a CA repeat in the first intron of the CFTR gene.

Mateu E, Calafell F, Bonné-Tamir B, Kidd JR, Casals T, Kidd KK, Bertranpetit J. Mateu E, et al. Among authors: calafell f. Hum Hered. 1999 Jan;49(1):15-20. doi: 10.1159/000022834. Hum Hered. 1999. PMID: 9858852

9

Geographic patterns of mtDNA diversity in Europe.

Simoni L, Calafell F, Pettener D, Bertranpetit J, Barbujani G. Simoni L, et al. Among authors: calafell f. Am J Hum Genet. 2000 Jan;66(1):262-78. doi: 10.1086/302706. Am J Hum Genet. 2000. PMID: 10631156 Free PMC article.

10

The Mediterranean paradox for susceptibility factors in coronary heart disease extends to genetics.

Lao O, Dupanloup I, Barbujani G, Bertranpetit J, Calafell F. Lao O, et al. Among authors: calafell f. Ann Hum Genet. 2008 Jan;72(Pt 1):48-56. doi: 10.1111/j.1469-1809.2007.00387.x. Epub 2007 Aug 7. Ann Hum Genet. 2008. PMID: 17683517

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