• 385 Citations
  • 10 h-Index
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Fingerprint Dive into the research topics where Monica Mencarelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Obesity Medicine & Life Sciences
Pro-Opiomelanocortin Medicine & Life Sciences
Mutation Medicine & Life Sciences
Receptor, Melanocortin, Type 3 Medicine & Life Sciences
Genes Medicine & Life Sciences
Subcutaneous Fat Medicine & Life Sciences
Melanocyte-Stimulating Hormones Medicine & Life Sciences
Leptin Medicine & Life Sciences

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Research Output 2003 2018

  • 385 Citations
  • 10 h-Index
  • 15 Article
17 Citations (Scopus)

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

Bonomi, M., Vezzoli, V., Krausz, C., Guizzardi, F., Vezzani, S., Simoni, M., Bassi, I., Duminuco, P., Di Iorgi, N., Giavoli, C., Pizzocaro, A., Russo, G., Moro, M., Fatti, L., Ferlin, A., Mazzanti, L., Zatelli, M. C., Cannavò, S., Isidori, A. M., Pincelli, A. I. & 31 others, Prodam, F., Mancini, A., Maghnie, M., Persani, L., Arosio, M., Balsamo, A., Beck-Peccoz, P., Bizzarri, C., Boschetti, M., Brunani, A., Brunelli, V., Cappa, M., Colombo, P., Corbetta, S., Corona, G., Di Iorgi, N., Fabbri, A., Ghezzi, M., Grosso, E., Grugni, G., Lania, A., Larizza, L., Lombardi, V., Mantovani, G., Mencarelli, M. A., Porcelli, P., Rossi, G., Sala, E., Spada, A., Weber, G. & on behalf of the Italian Network on Central Hypogonadism (NICe group), Jan 1 2018, In : European Journal of Endocrinology. 178, 1, p. 23-32 10 p.

Research output: Contribution to journalArticle

Kallmann Syndrome

Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma

Imperatore, V., Pinto, A. M., Gelli, E., Trevisson, E., Morbidoni, V., Frullanti, E., Hadjistilianou, T., De Francesco, S., Toti, P., Gusson, E., Roversi, G., Accogli, A., Capra, V., Mencarelli, M. A., Renieri, A. & Ariani, F., 2018, In : European Journal of Human Genetics. 26, 7, p. 1026-1037 12 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation

Pradotto, L., Mencarelli, M., Bigoni, M., Milesi, A., Di Blasio, A. & Mauro, A., Dec 15 2016, In : Journal of the Neurological Sciences. 371, p. 81-84 4 p.

Research output: Contribution to journalArticle

Cerebellar Ataxia
Missense Mutation
19 Citations (Scopus)

Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects

Cancello, R., Zulian, A., Gentilini, D., Mencarelli, M., Della Barba, A., Maffei, M., Vitti, P., Invitti, C., Liuzzi, A. & Di Blasio, A. M., Jun 2013, In : International Journal of Obesity. 37, 6, p. 867-873 7 p.

Research output: Contribution to journalArticle

Subcutaneous Fat
Body Mass Index
Weight Loss
Gene Expression
18 Citations (Scopus)
Missense Mutation
Protein Sorting Signals
Type 2 Diabetes Mellitus