Bailey-Wilson JE - Search Results

1

A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability.

Marroni F, Pastrello C, Benatti P, Torrini M, Barana D, Cordisco EL, Viel A, Mareni C, Oliani C, Genuardi M, Bailey-Wilson JE, Ponz de Leon M, Presciuttini S. Marroni F, et al. Clin Genet. 2006 Mar;69(3):254-62. doi: 10.1111/j.1399-0004.2006.00577.x. Clin Genet. 2006. PMID: 16542391

2

Inferring relationships between pairs of individuals from locus heterozygosities.

Presciuttini S, Toni C, Tempestini E, Verdiani S, Casarino L, Spinetti I, De Stefano F, Domenici R, Bailey-Wilson JE. Presciuttini S, et al. BMC Genet. 2002 Nov 20;3:23. doi: 10.1186/1471-2156-3-23. Epub 2002 Nov 20. BMC Genet. 2002. PMID: 12441003 Free PMC article.

3

Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations.

Marroni F, Aretini P, D'Andrea E, Caligo MA, Cortesi L, Viel A, Ricevuto E, Montagna M, Cipollini G, Ferrari S, Santarosa M, Bisegna R, Bailey-Wilson JE, Bevilacqua G, Parmigiani G, Presciuttini S. Marroni F, et al. J Med Genet. 2004 Apr;41(4):278-85. doi: 10.1136/jmg.2003.013623. J Med Genet. 2004. PMID: 15060102 Free PMC article. No abstract available.

4

Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations.

Marroni F, Aretini P, D'Andrea E, Caligo MA, Cortesi L, Viel A, Ricevuto E, Montagna M, Cipollini G, Federico M, Santarosa M, Marchetti P, Bailey-Wilson JE, Bevilacqua G, Parmigiani G, Presciuttini S. Marroni F, et al. Eur J Hum Genet. 2004 Nov;12(11):899-906. doi: 10.1038/sj.ejhg.5201256. Eur J Hum Genet. 2004. PMID: 15340362 Free article.

5

Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages.

Marroni F, Toni C, Pennato B, Tsai YY, Duggal P, Bailey-Wilson JE, Presciuttini S. Marroni F, et al. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S77. doi: 10.1186/1471-2156-6-S1-S77. BMC Genet. 2005. PMID: 16451691 Free PMC article.

6

Population isolates in South Tyrol and their value for genetic dissection of complex diseases.

Marroni F, Pichler I, De Grandi A, Volpato CB, Vogl FD, Pinggera GK, Bailey-Wilson JE, Pramstaller PP. Marroni F, et al. Ann Hum Genet. 2006 Nov;70(Pt 6):812-21. doi: 10.1111/j.1469-1809.2006.00274.x. Ann Hum Genet. 2006. PMID: 17044856

7

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH Jr, Brant SR. Panhuysen CI, et al. Hum Genet. 2006 Aug;120(1):31-41. doi: 10.1007/s00439-006-0163-8. Epub 2006 May 30. Hum Genet. 2006. PMID: 16733713

8

Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data sets.

Cross JL, Iben J, Simpson CL, Thurm A, Swedo S, Tierney E, Bailey-Wilson JE, Biesecker LG, Porter FD, Wassif CA. Cross JL, et al. Clin Genet. 2015 Jun;87(6):570-5. doi: 10.1111/cge.12425. Epub 2014 Jun 6. Clin Genet. 2015. PMID: 24813812 Free PMC article.

9

Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance.

Pakkanen S, Baffoe-Bonnie AB, Matikainen MP, Koivisto PA, Tammela TL, Deshmukh S, Ou L, Bailey-Wilson JE, Schleutker J. Pakkanen S, et al. Hum Genet. 2007 Apr;121(2):257-67. doi: 10.1007/s00439-006-0310-2. Epub 2007 Jan 3. Hum Genet. 2007. PMID: 17203302 Free PMC article.

10

ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer.

Siltanen S, Syrjäkoski K, Fagerholm R, Ikonen T, Lipman P, Mallott J, Holli K, Tammela TL, Järvinen HJ, Mecklin JP, Aittomäki K, Blomqvist C, Bailey-Wilson JE, Nevanlinna H, Aaltonen LA, Schleutker J, Vahteristo P. Siltanen S, et al. Eur J Hum Genet. 2008 Aug;16(8):983-91. doi: 10.1038/ejhg.2008.43. Epub 2008 Mar 12. Eur J Hum Genet. 2008. PMID: 18337727 Free PMC article.

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