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WWP1 germline variants are associated with normocephalic autism spectrum disorder.
Novelli G, Novelli A, Borgiani P, Cocciadiferro D, Biancolella M, Agolini E, Pietrosanto M, Casalone R, Helmer-Citterich M, Giardina E, Jain SK, Wei W, Eng C, Pandolfi PP. Novelli G, et al. Cell Death Dis. 2020 Jul 23;11(7):529. doi: 10.1038/s41419-020-2681-z. Cell Death Dis. 2020. PMID: 32699206 Free PMC article. No abstract available.
Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome.
Mango R, Luchetti A, Sangiuolo R, Ferradini V, Briglia N, Giardina E, Ferrè F, Helmer Citterich M, Romeo F, Novelli G, Sangiuolo F. Mango R, et al. Circ J. 2016;80(4):938-49. doi: 10.1253/circj.CJ-15-0685. Epub 2016 Mar 9. Circ J. 2016. PMID: 26960954 Free article.
BEAM web server: a tool for structural RNA motif discovery.
Pietrosanto M, Adinolfi M, Casula R, Ausiello G, Ferrè F, Helmer-Citterich M. Pietrosanto M, et al. Bioinformatics. 2018 Mar 15;34(6):1058-1060. doi: 10.1093/bioinformatics/btx704. Bioinformatics. 2018. PMID: 29095974 Free PMC article.
Modeling cancer drug response through drug-specific informative genes.
Parca L, Pepe G, Pietrosanto M, Galvan G, Galli L, Palmeri A, Sciandrone M, Ferrè F, Ausiello G, Helmer-Citterich M. Parca L, et al. Sci Rep. 2019 Oct 23;9(1):15222. doi: 10.1038/s41598-019-50720-0. Sci Rep. 2019. PMID: 31645597 Free PMC article.
132 results