M. Bonis

Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome.

M. D'Esposito, M. R. Matarazzo, F. D. Ragione, 2009, The international journal of biochemistry & cell biology.

Risk Factors for Gestational Diseases

F. Petraglia, M. Torricelli, M. D. Bonis, 2012 .

Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variant

G. Scambia, E. Capoluongo, G. Zannoni, 2018, Familial Cancer.

High Resolution Melting Analysis is Very Useful to Identify Breast Cancer Type 1 Susceptibility Protein (BRCA1) c.4964_4982del19 (rs80359876) Founder Calabrian Pathogenic Variant on Peripheral Blood and Buccal Swab DNA

F. Mignone, E. Capoluongo, P. Concolino, 2017, Molecular Diagnosis & Therapy.

Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications.

M. D'Esposito, R. Hansen, M. Strazzullo, 2006, Human molecular genetics.

BDNF Val66Met polymorphism and brain volumes in multiple sclerosis

A. Tessitore, G. Tedeschi, B. Alfano, 2011, Neurological Sciences.

Stress and Pregnancy: CRF as Biochemical Marker

F. Petraglia, Irene Zerbetto, S. Luisi, 2008 .