Capon F - Search Results

1

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24.

Everett KV, Capon F, Georgoula C, Chioza BA, Reece A, Jaswon M, Pierro A, Puri P, Gardiner RM, Chung EM. Everett KV, et al. Among authors: capon f. Eur J Hum Genet. 2008 Sep;16(9):1151-4. doi: 10.1038/ejhg.2008.86. Epub 2008 May 14. Eur J Hum Genet. 2008. PMID: 18478043

2

Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.

Everett KV, Chioza BA, Georgoula C, Reece A, Capon F, Parker KA, Cord-Udy C, McKeigue P, Mitton S, Pierro A, Puri P, Mitchison HM, Chung EM, Gardiner RM. Everett KV, et al. Among authors: capon f. Am J Hum Genet. 2008 Mar;82(3):756-62. doi: 10.1016/j.ajhg.2007.12.023. Epub 2008 Feb 28. Am J Hum Genet. 2008. PMID: 18308288 Free PMC article.

3

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16p12-p13 and evidence for genetic heterogeneity.

Capon F, Reece A, Ravindrarajah R, Chung E. Capon F, et al. Am J Hum Genet. 2006 Aug;79(2):378-82. doi: 10.1086/505952. Epub 2006 Jun 7. Am J Hum Genet. 2006. PMID: 16826529 Free PMC article.

4

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.

Mangino M, Flex E, Capon F, Sangiuolo F, Carraro E, Gualandi F, Mazzoli M, Martini A, Novelli G, Dallapiccola B. Mangino M, et al. Among authors: capon f. Eur J Hum Genet. 2001 Sep;9(9):667-71. doi: 10.1038/sj.ejhg.5200707. Eur J Hum Genet. 2001. PMID: 11571554

5

Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.

Sangiuolo F, Bruscia E, Capon F, Servidei S, Dallapiccola B, Novelli G. Sangiuolo F, et al. Among authors: capon f. Eur J Hum Genet. 2000 Oct;8(10):809-12. doi: 10.1038/sj.ejhg.5200547. Eur J Hum Genet. 2000. PMID: 11039585

6

Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11.

Salehi LB, Mangino M, De Serio S, De Cicco D, Capon F, Semprini S, Pizzuti A, Novelli G, Dallapiccola B. Salehi LB, et al. Among authors: capon f. Hum Genet. 2002 Oct;111(4-5):401-4. doi: 10.1007/s00439-002-0785-4. Epub 2002 Aug 21. Hum Genet. 2002. PMID: 12384783

7

Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis.

Capon F, Di Meglio P, Szaub J, Prescott NJ, Dunster C, Baumber L, Timms K, Gutin A, Abkevic V, Burden AD, Lanchbury J, Barker JN, Trembath RC, Nestle FO. Capon F, et al. Hum Genet. 2007 Sep;122(2):201-6. doi: 10.1007/s00439-007-0397-0. Epub 2007 Jun 22. Hum Genet. 2007. PMID: 17587057

8

Mapping a dominant form of multinodular goiter to chromosome Xp22.

Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G. Capon F, et al. Am J Hum Genet. 2000 Oct;67(4):1004-7. doi: 10.1086/303095. Epub 2000 Sep 11. Am J Hum Genet. 2000. PMID: 10986044 Free PMC article.

9

Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene.

Capon F, Bijlmakers MJ, Wolf N, Quaranta M, Huffmeier U, Allen M, Timms K, Abkevich V, Gutin A, Smith R, Warren RB, Young HS, Worthington J, Burden AD, Griffiths CE, Hayday A, Nestle FO, Reis A, Lanchbury J, Barker JN, Trembath RC. Capon F, et al. Hum Mol Genet. 2008 Jul 1;17(13):1938-45. doi: 10.1093/hmg/ddn091. Epub 2008 Mar 25. Hum Mol Genet. 2008. PMID: 18364390 Free PMC article.

10

Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22.

Mangino M, Sanchez O, Torrente I, De Luca A, Capon F, Novelli G, Dallapiccola B. Mangino M, et al. Among authors: capon f. Am J Hum Genet. 1999 Aug;65(2):441-7. doi: 10.1086/302505. Am J Hum Genet. 1999. PMID: 10417287 Free PMC article.

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