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Chiara Menin

1992 …2020

Research output per year

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Research Output

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

AMFS Investigators, MelaNostrum Consortium, GenoMEL Consortium, Q-MEGA and QTWIN Investigators, ATHENS Melanoma Study Group, 23andMe, The SDH Study Group, IBD Investigators & Essen-Heidelberg Investigators, Jan 1 2020, (Accepted/In press) In : Nature Genetics.

Research output: Contribution to journal › Article

    • 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 journal › Article

    • 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 journal › Article

    Open Access

    • 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 journal › Article

    • 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 journal › Article