Menin C - Search Results

1

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.

Landi MT, Bishop DT, MacGregor S, Machiela MJ, Stratigos AJ, Ghiorzo P, Brossard M, Calista D, Choi J, Fargnoli MC, Zhang T, Rodolfo M, Trower AJ, Menin C, Martinez J, Hadjisavvas A, Song L, Stefanaki I, Scolyer R, Yang R, Goldstein AM, Potrony M, Kypreou KP, Pastorino L, Queirolo P, Pellegrini C, Cattaneo L, Zawistowski M, Gimenez-Xavier P, Rodriguez A, Elefanti L, Manoukian S, Rivoltini L, Smith BH, Loizidou MA, Del Regno L, Massi D, Mandala M, Khosrotehrani K, Akslen LA, Amos CI, Andresen PA, Avril MF, Azizi E, Soyer HP, Bataille V, Dalmasso B, Bowdler LM, Burdon KP, Chen WV, Codd V, Craig JE, Dębniak T, Falchi M, Fang S, Friedman E, Simi S, Galan P, Garcia-Casado Z, Gillanders EM, Gordon S, Green A, Gruis NA, Hansson J, Harland M, Harris J, Helsing P, Henders A, Hočevar M, Höiom V, Hunter D, Ingvar C, Kumar R, Lang J, Lathrop GM, Lee JE, Li X, Lubiński J, Mackie RM, Malt M, Malvehy J, McAloney K, Mohamdi H, Molven A, Moses EK, Neale RE, Novaković S, Nyholt DR, Olsson H, Orr N, Fritsche LG, Puig-Butille JA, Qureshi AA, Radford-Smith GL, Randerson-Moor J, Requena C, Rowe C, Samani NJ, Sanna M, Schadendorf D, Schulze HJ, Simms LA, Smithers M, Song F, Swerdlow AJ, van der S… See abstract for full author list ➔ Landi MT, et al. Among authors: menin c. Nat Genet. 2020 May;52(5):494-504. doi: 10.1038/s41588-020-0611-8. Epub 2020 Apr 27. Nat Genet. 2020. PMID: 32341527 Free PMC article.

2

Identification of BRCA1 and BRCA2 carriers by allele-specific gene expression (AGE) analysis.

Montagna M, Agata S, De Nicolo A, Menin C, Sordi G, Chieco-Bianchi L, D'Andrea E. Montagna M, et al. Among authors: menin c. Int J Cancer. 2002 Apr 10;98(5):732-6. doi: 10.1002/ijc.10273. Int J Cancer. 2002. PMID: 11920643 Free article.

3

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families.

Montagna M, Dalla Palma M, Menin C, Agata S, De Nicolo A, Chieco-Bianchi L, D'Andrea E. Montagna M, et al. Among authors: menin c. Hum Mol Genet. 2003 May 1;12(9):1055-61. doi: 10.1093/hmg/ddg120. Hum Mol Genet. 2003. PMID: 12700174

4

No evidence for linkage with melanoma in Italian melanoma-prone families.

Kerstann KF, Bradford PT, Steighner R, Calista D, Fargnoli MC, Peris K, Scaini MC, Menin C, Ghiorzo P, Bianchi-Scarra' G, Goldstein AM, Landi MT. Kerstann KF, et al. Among authors: menin c. Cancer Epidemiol Biomarkers Prev. 2008 Jul;17(7):1838-40. doi: 10.1158/1055-9965.EPI-08-0264. Cancer Epidemiol Biomarkers Prev. 2008. PMID: 18628440 Free PMC article. No abstract available.

5

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations.

Vignoli M, Scaini MC, Ghiorzo P, Sestini R, Bruno W, Menin C, Gensini F, Piazzini M, Testori A, Manoukian S, Orlando C, D'Andrea E, Bianchi-Scarrà G, Genuardi M. Vignoli M, et al. Among authors: menin c. Melanoma Res. 2008 Dec;18(6):431-7. doi: 10.1097/CMR.0b013e328319412f. Melanoma Res. 2008. PMID: 19011513

6

Clinical genetic testing for familial melanoma in Italy: a cooperative study.

Bruno W, Ghiorzo P, Battistuzzi L, Ascierto PA, Barile M, Gargiulo S, Gensini F, Gliori S, Guida M, Lombardo M, Manoukian S, Menin C, Nasti S, Origone P, Pasini B, Pastorino L, Peissel B, Pizzichetta MA, Queirolo P, Rodolfo M, Romanini A, Scaini MC, Testori A, Tibiletti MG, Turchetti D, Leachman SA, Bianchi Scarrà G; IMI, Italian Melanoma Intergroup. Bruno W, et al. Among authors: menin c. J Am Acad Dermatol. 2009 Nov;61(5):775-82. doi: 10.1016/j.jaad.2009.03.039. Epub 2009 Jun 4. J Am Acad Dermatol. 2009. PMID: 19500876

7

Dried blood spot sampling for detection of monoclonal immunoglobulin gene rearrangement.

Petrara MR, Elefanti L, Quaggio M, Zanchetta M, Scaini MC, Masalu N, De Rossi A, Menin C. Petrara MR, et al. Among authors: menin c. Leuk Res. 2013 Oct;37(10):1265-70. doi: 10.1016/j.leukres.2013.08.003. Epub 2013 Aug 13. Leuk Res. 2013. PMID: 23965169

8

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

Scaini MC, Minervini G, Elefanti L, Ghiorzo P, Pastorino L, Tognazzo S, Agata S, Quaggio M, Zullato D, Bianchi-Scarrà G, Montagna M, D'Andrea E, Menin C, Tosatto SC. Scaini MC, et al. Among authors: menin c. Hum Mutat. 2014 Jul;35(7):828-40. doi: 10.1002/humu.22550. Epub 2014 May 21. Hum Mutat. 2014. PMID: 24659262

9

Association of CDK4 germline and BRAF somatic mutations in a patient with multiple primary melanomas and BRAF inhibitor resistance.

Governa M, Caprarella E, Dalla Pozza E, Vigato E, Maritan M, Caputo GG, Zannoni M, Rosina P, Elefanti L, Stagni C, Menin C. Governa M, et al. Among authors: menin c. Melanoma Res. 2015 Oct;25(5):443-6. doi: 10.1097/CMR.0000000000000173. Melanoma Res. 2015. PMID: 26110554

10

The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma.

Andreotti V, Bisio A, Bressac-de Paillerets B, Harland M, Cabaret O, Newton-Bishop J, Pastorino L, Bruno W, Bertorelli R, De Sanctis V, Provenzani A, Menin C, Fronza G, Queirolo P, Spitale RC, Bianchi-Scarrà G, Inga A, Ghiorzo P. Andreotti V, et al. Among authors: menin c. Pigment Cell Melanoma Res. 2016 Mar;29(2):210-21. doi: 10.1111/pcmr.12444. Epub 2015 Dec 17. Pigment Cell Melanoma Res. 2016. PMID: 26581427

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