Hogg D - Search Results

1

Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.

Loo JC, Paterson AD, Hao A, Shennan M, Peretz H, Sidi Y, Hogg D, Yakobson E. Loo JC, et al. Among authors: hogg d. J Med Genet. 2005 May;42(5):e30. doi: 10.1136/jmg.2004.027300. J Med Genet. 2005. PMID: 15863662 Free PMC article. No abstract available.

2

MELPREDICT: a logistic regression model to estimate CDKN2A carrier probability.

Niendorf KB, Goggins W, Yang G, Tsai KY, Shennan M, Bell DW, Sober AJ, Hogg D, Tsao H. Niendorf KB, et al. Among authors: hogg d. J Med Genet. 2006 Jun;43(6):501-6. doi: 10.1136/jmg.2005.032441. Epub 2005 Sep 16. J Med Genet. 2006. PMID: 16169933 Free PMC article.

3

Lack of germline CDK6 mutations in familial melanoma.

Shennan MG, Badin AC, Walsh S, Summers A, From L, McKenzie M, Goldstein AM, Tucker MA, Hogg D, Lassam N. Shennan MG, et al. Among authors: hogg d. Oncogene. 2000 Mar 30;19(14):1849-52. doi: 10.1038/sj.onc.1203507. Oncogene. 2000. PMID: 10777219

4

Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families.

Yakobson E, Shemesh P, Azizi E, Winkler E, Lassam N, Hogg D, Brookes S, Peters G, Lotem M, Zlotogorski A, Landau M, Safro M, Shafir R, Friedman E, Peretz H. Yakobson E, et al. Among authors: hogg d. Eur J Hum Genet. 2000 Aug;8(8):590-6. doi: 10.1038/sj.ejhg.5200505. Eur J Hum Genet. 2000. PMID: 10951521

5

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.

Goldstein AM, Liu L, Shennan MG, Hogg D, Tucker MA, Struewing JP. Goldstein AM, et al. Among authors: hogg d. Br J Cancer. 2001 Aug 17;85(4):527-30. doi: 10.1054/bjoc.2001.1944. Br J Cancer. 2001. PMID: 11506491 Free PMC article.

6

Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma.

Sabbaghian N, Kyle R, Hao A, Hogg D, Tischkowitz M. Sabbaghian N, et al. Among authors: hogg d. Fam Cancer. 2011 Jun;10(2):315-7. doi: 10.1007/s10689-010-9405-y. Fam Cancer. 2011. PMID: 21153565

7

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma.

Liu L, Dilworth D, Gao L, Monzon J, Summers A, Lassam N, Hogg D. Liu L, et al. Among authors: hogg d. Nat Genet. 1999 Jan;21(1):128-32. doi: 10.1038/5082. Nat Genet. 1999. PMID: 9916806

8

Genetic susceptibility in familial melanoma from northeastern Italy.

Landi MT, Goldstein AM, Tsang S, Munroe D, Modi W, Ter-Minassian M, Steighner R, Dean M, Metheny N, Staats B, Agatep R, Hogg D, Calista D. Landi MT, et al. Among authors: hogg d. J Med Genet. 2004 Jul;41(7):557-66. doi: 10.1136/jmg.2003.016907. J Med Genet. 2004. PMID: 15235029 Free PMC article. No abstract available.

9

Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF.

Liu L, Goldstein AM, Tucker MA, Brill H, Gruis NA, Hogg D, Lassam NJ. Liu L, et al. Among authors: hogg d. Genes Chromosomes Cancer. 1997 May;19(1):52-4. Genes Chromosomes Cancer. 1997. PMID: 9135995

10

Patients with both pancreatic adenocarcinoma and melanoma may harbor germline CDKN2A mutations.

Lal G, Liu L, Hogg D, Lassam NJ, Redston MS, Gallinger S. Lal G, et al. Among authors: hogg d. Genes Chromosomes Cancer. 2000 Apr;27(4):358-61. Genes Chromosomes Cancer. 2000. PMID: 10719365

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