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Journal Article
Ayub Q, Mezzavilla M, Pagani L, Haber M, Mohyuddin A, Khaliq S, Mehdi SQasim, Tyler-Smith C. The Kalash genetic isolate: ancient divergence, drift, and selection. Am J Hum Genet 2015;96(5):775-83.
Tisato V, Perri P, Rimondi E, Melloni E, Lamberti G, Milani D, Secchiero P, Zauli G. Kinetic Profiles of Inflammatory Mediators in the Conjunctival Sac Fluid of Patients upon Photorefractive Keratectomy. Mediators Inflamm 2015;2015:942948.
Zanella G, Tornese G, Mascheroni E, Faleschini E, Ventura A, Barbi E. A Klinefelter boy with congenital adrenal hyperplasia: too much or too little androgens?. Ital J Pediatr 2018;44(1):43.
Rocca MS, Pecile V, Cleva L, Speltra E, Selice R, Di Mambro A, Foresta C, Ferlin A. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype. Andrology 2016;4(2):328-34.
Celsi F, Piscianz E, Romano M, Crovella S. Knockdown of MVK does not lead to changes in NALP3 expression or activation. J Inflamm (Lond) 2015;12:7.

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