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BMC Bioinformatics|February 26, 2014
CorrelaGenes: a new tool for the interpretation of the human transcriptomePaolo Cremaschi, Sergio Rovida, Lucia Sacchi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2007
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposisFrancesca Cattaneo, Sara Molatore, Markos Mihalatos, et al.
Plos One|January 24, 2008
Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease?Flavio Rizzolio, Silvia Bione, Cinzia Sala, et al.
Plos One|July 8, 2015
Chronic Replication Problems Impact Cell Morphology and Adhesion of DNA Ligase I Defective CellsPaolo Cremaschi, Matteo Oliverio, Valentina Leva, et al.
Haematologica|July 8, 2008
Variation of hemoglobin levels in normal Italian populations from genetic isolatesCinzia Sala, Marina Ciullo, Carmela Lanzara, et al.
Human Reproduction (Oxford, England)|April 14, 2009
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failureTanguy Corre, Julia Schuettler, Silvia Bione, et al.
Human Reproduction (Oxford, England)|February 25, 2006
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literatureFlavio Rizzolio, Silvia Bione, Cinzia Sala, et al.
Human Mutation|March 6, 2009
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive proteinRaffaella Rossetti, Elisa Di Pasquale, Anna Marozzi, et al.
BMC Genetics|November 11, 2015
Characterization of the biological processes shaping the genetic structure of the Italian populationSilvia Parolo, Antonella Lisa, Davide Gentilini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2021
Reduced levels of prostaglandin I2 synthase: a distinctive feature of the cancer-free trichothiodystrophyAnita Lombardi, Lavinia Arseni, Roberta Carriero, et al.
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