Duffy D - Search Results

1

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

Jeske YW, So A, Kelemen L, Sukor N, Willys C, Bulmer B, Gordon RD, Duffy D, Stowasser M. Jeske YW, et al. Among authors: duffy d. Clin Exp Pharmacol Physiol. 2008 Apr;35(4):380-5. doi: 10.1111/j.1440-1681.2008.04882.x. Clin Exp Pharmacol Physiol. 2008. PMID: 18307725

2

Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.

Sukor N, Mulatero P, Gordon RD, So A, Duffy D, Bertello C, Kelemen L, Jeske Y, Veglio F, Stowasser M. Sukor N, et al. Among authors: duffy d. J Hypertens. 2008 Aug;26(8):1577-82. doi: 10.1097/HJH.0b013e3283028352. J Hypertens. 2008. PMID: 18622235

3

No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II.

So A, Jeske YW, Gordon RD, Duffy D, Kelemen L, Stowasser M. So A, et al. Among authors: duffy d. Clin Endocrinol (Oxf). 2006 Dec;65(6):829-31. doi: 10.1111/j.1365-2265.2006.02674.x. Clin Endocrinol (Oxf). 2006. PMID: 17121540 No abstract available.

4

BRAF polymorphisms and the risk of ovarian cancer of low malignant potential.

Kelemen L, James M, Spurdle A, Campbell I, Chang-Claude J, Peel D, Anton-Culver H, Berchuck A, Schildkraut J, Whittemore A, McGurie V, DiCioccio RA, Duffy D, Chenevix-Trench G. Kelemen L, et al. Among authors: duffy d. Gynecol Oncol. 2005 Jun;97(3):807-12. doi: 10.1016/j.ygyno.2005.03.007. Gynecol Oncol. 2005. PMID: 15904951

5

No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Spurdle AB, Deans AJ, Duffy D, Goldgar DE, Chen X, Beesley J; kConFaB; Easton DF, Antoniou AC, Peock S, Cook M; EMBRACE Study Collaborators; Nathanson KL, Domchek SM, MacArthur GA, Chenevix-Trench G. Spurdle AB, et al. Among authors: duffy d. Breast Cancer Res Treat. 2009 May;115(2):307-13. doi: 10.1007/s10549-008-0083-5. Epub 2008 Jun 10. Breast Cancer Res Treat. 2009. PMID: 18543099

6

Calculation of IBD probabilities with dense SNP or sequence data.

Keith JM, McRae A, Duffy D, Mengersen K, Visscher PM. Keith JM, et al. Among authors: duffy d. Genet Epidemiol. 2008 Sep;32(6):513-9. doi: 10.1002/gepi.20324. Genet Epidemiol. 2008. PMID: 18357613

7

Linkage and association analysis of radiation damage repair genes XRCC3 and XRCC5 with nevus density in adolescent twins.

Zhu G, Duffy DL, Turner DR, Ewen KR, Montgomery GW, Martin NG. Zhu G, et al. Twin Res. 2003 Aug;6(4):315-21. doi: 10.1375/136905203322296683. Twin Res. 2003. PMID: 14511439

8

The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits.

Visscher PM, Duffy DL. Visscher PM, et al. Genet Epidemiol. 2006 Jan;30(1):30-6. doi: 10.1002/gepi.20124. Genet Epidemiol. 2006. PMID: 16355405

9

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

Zhu G, Evans DM, Duffy DL, Montgomery GW, Medland SE, Gillespie NA, Ewen KR, Jewell M, Liew YW, Hayward NK, Sturm RA, Trent JM, Martin NG. Zhu G, et al. Twin Res. 2004 Apr;7(2):197-210. doi: 10.1375/136905204323016186. Twin Res. 2004. PMID: 15169604 Free article.

10

Linkage confirms canine pkd1 orthologue as a candidate for bull terrier polycystic kidney disease.

O'Leary CA, Duffy D, Biros I, Corley S. O'Leary CA, et al. Among authors: duffy d. Anim Genet. 2009 Aug;40(4):543-6. doi: 10.1111/j.1365-2052.2009.01863.x. Epub 2009 Apr 3. Anim Genet. 2009. PMID: 19397527

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