AM Goldstein, SN Stacey, JH Olafsson, GF … - British Medical Journal, 2008 - jmg.bmj.com Results: We identified a novel germline variant, G89D, that was strongly
associated with increased melanoma risk and appeared to be an Icelandic founder
mutation. The G89D variant was present in about 2% of Icelandic invasive ... Cited by 3 - Related articles - BL Direct - All 8 versions
JA Newton Bishop, NA Gruis - Seminars in Oncology, 2007 - Elsevier A significantly increased susceptibility to melanoma may manifest as a family
history of melanoma (plus or minus pancreatic cancer), the development of
multiple primary tumors, or melanoma in the context of numerous and ... Cited by 4 - Related articles - All 21 versions
[CITATION] the Lund Melanoma Study Group, the Melanoma Genetics Consortium (GenoMEL). High risk …
SV Tavtigian, MS Greenblatt, DE Goldgar, P … - Human mutation, 2008 - ncbi.nlm.nih.gov Assessing pathogenicity: overview of results from the IARC Unclassified Genetic
Variants Working Group. ... Tavtigian SV, Greenblatt MS, Goldgar DE, Boffetta
P; IARC Unclassified Genetic Variants Working Group. Cited by 3 - Related articles - All 2 versions
TM Becker, AL Ayub, RF Kefford, GJ Mann, H … - International Journal of Cancer, 2005 - interscience.wiley.com Melanoma-associated germline mutations affecting the tumor suppressor and
cyclin-dependent kinase (CDK) inhibitor, CDKN2A/p16INK4a, have been identified
in over 100 melanoma-prone families worldwide. To predict the melanoma risk ... Cited by 3 - Related articles - BL Direct - All 4 versions
[CITATION] Five novel somatic CDKN2/p16 mutations identified in melanoma, glioma and carcinoma of …
TA Young, BL Burgess, NP Rao, MB Gorin, … - Mol Vis, 2007 - molvis.org Results: FISH yielded chromosome 3 status in 38 of 59 (64%) eyes, while
high-density SNP mapping array yielded chromosome 3 status in 43 of 59 (73%)
eyes. Monosomy 3 was detected by FISH in 15 of 38 (39%) cases, and ... Cited by 4 - Related articles - Cached - All 3 versions
