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Fingerprint Dive into the research topics where Chiara Menin is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 4 Similar Profiles
Melanoma Medicine & Life Sciences
Human Herpesvirus 4 Medicine & Life Sciences
Mutation Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Ovarian Neoplasms Medicine & Life Sciences
B-Lymphocytes Medicine & Life Sciences
SCID Mice Medicine & Life Sciences
Breast Neoplasms Medicine & Life Sciences

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Research Output 1992 2019

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

Gu, F., Chen, T-H., Pfeiffer, R. M., Fargnoli, M. C., Calista, D., Ghiorzo, P., Peris, K., Puig, S., Menin, C., De Nicolo, A., Rodolfo, M., Pellegrini, C., Pastorino, L., Evangelou, E., Zhang, T., Hua, X., DellaValle, C. T., Timothy Bishop, D., MacGregor, S., Iles, M. I. & 10 others, Law, M. H., Cust, A., Brown, K. M., Stratigos, A. J., Nagore, E., Chanock, S., Shi, J., Consortium, MM-A., Consortium, M. & Landi, M. T., Feb 1 2019, In : Human Molecular Genetics. 27, 3, p. 4145-4156 12 p.

Research output: Contribution to journalArticle

Melanoma
Skin
Single Nucleotide Polymorphism
Area Under Curve
Odds Ratio

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Schlafly, A., Pfeiffer, R. M., Nagore, E., Puig, S., Calista, D., Ghiorzo, P., Menin, C., Fargnoli, M. C., Peris, K., Song, L., Zhang, T., Shi, J., Landi, M. T. & Sampson, J. N., Nov 1 2019, In : PLoS Genetics. 15, 11, p. e1008490

Research output: Contribution to journalArticle

Open Access
heritability
statistics
family structure
prioritization
melanoma

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Schlafly, A., Pfeiffer, R. M., Nagore, E., Puig, S., Calista, D., Ghiorzo, P., Menin, C., Fargnoli, M. C., Peris, K., Song, L., Zhang, T., Shi, J., Landi, M. T. & Sampson, J. N., Nov 1 2019, In : PLoS Genetics. 15, 11, p. 1-15 15 p., e1008490.

Research output: Contribution to journalArticle

heritability
statistics
family structure
prioritization
melanoma

Loss of BAP1 in Pheochromocytomas and Paragangliomas Seems Unrelated to Genetic Mutations

Maffeis, V., Cappellesso, R., Nicolè, L., Guzzardo, V., Menin, C., Elefanti, L., Schiavi, F., Guido, M. & Fassina, A., Dec 2019, In : Endocrine Pathology. 30, 4, p. 276-284 9 p.

Research output: Contribution to journalArticle

BRCA1 Protein
Paraganglioma
Pheochromocytoma
Mutation
Genes

MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

IMI Study Group, GEM Study Group & M-SKIP Study Group, May 1 2019, In : The Lancet Child and Adolescent Health. 3, 5, p. 332-342 11 p.

Research output: Contribution to journalArticle

Receptor, Melanocortin, Type 1
Melanoma
Genes
Odds Ratio
Serbia