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Panminerva Medica|July 3, 2018
Preimplantation genetic testing in assisted reproductive technologyValeria Romanelli, Maurizio Poli, Antonio Capalbo
Magnetic Resonance in Chemistry : MRC|July 11, 2008
A preliminary study of soft cheese degradation in different packaging conditions by 1H-NMRRaffaele Lamanna, Ilario Piscioneri, Valeria Romanelli, et al.
Journal of the American Chemical Society|February 11, 2005
Reactivity of secondary metal-alkyls in catalytic propene polymerization: how dormant are "dormant chains"?Vincenzo Busico, Roberta Cipullo, Valeria Romanelli, et al.
American Journal of Medical Genetics. Part A|December 1, 2012
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creasesPiranit Nik Kantaputra, Rekwan Sittiwangkul, Nuntigar Sonsuwan, et al.
Frontiers in Endocrinology|April 4, 2019
Past, Present, and Future Strategies for Enhanced Assessment of Embryo's Genome and Reproductive Competence in Women of Advanced Reproductive AgeMaurizio Poli, Laura Girardi, Marco Fabiani, et al.
Journal of Assisted Reproduction and Genetics|July 18, 2016
Implementing PGD/PGD-A in IVF clinics: considerations for the best laboratory approach and managementAntonio Capalbo, Valeria Romanelli, Danilo Cimadomo, et al.
Fertility and Sterility|October 15, 2018
Diagnostic efficacy of blastocoel fluid and spent media as sources of DNA for preimplantation genetic testing in standard clinical conditionsAntonio Capalbo, Valeria Romanelli, Cristina Patassini, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2012
Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locusGustavo Perez-Nanclares, Valeria Romanelli, Sonia Mayo, et al.
Epigenetics|March 5, 2014
Variable maternal methylation overlapping the nc886/vtRNA2-1 locus is locked between hypermethylated repeats and is frequently altered in cancerValeria Romanelli, Kazuhiko Nakabayashi, Miguel Vizoso, et al.
Human Mutation|January 22, 2013
Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromesFranck Court, Alex Martin-Trujillo, Valeria Romanelli, et al.
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