Zobrazeno 1 - 10
of 358
pro vyhledávání: '"A. Gnazzo"'
We propose an extremely versatile approach to address a large family of matrix nearness problems, possibly with additional linear constraints. Our method is based on splitting a matrix nearness problem into two nested optimization problems, of which
Externí odkaz:
http://arxiv.org/abs/2407.03957
Backward errors for multiple eigenpairs in structured and unstructured nonlinear eigenvalue problems
Autor:
Gnazzo, Miryam, Robol, Leonardo
Given a nonlinear matrix-valued function $F(\lambda)$ and approximate eigenpairs $(\lambda_i, v_i)$, we discuss how to determine the smallest perturbation $\delta F$ such that $[F + \delta F](\lambda_i) v_i = 0$; we call the distance between the $F$
Externí odkaz:
http://arxiv.org/abs/2405.06327
Autor:
Lisa Asta, Arianna Ricciardello, Francesca Cucinotta, Laura Turriziani, Maria Boncoddo, Fabiana Bellomo, Jessica Angelini, Martina Gnazzo, Giulia Scandolo, Giulia Pisanò, Francesco Pelagatti, Fethia Chehbani, Michela Camia, Antonio M. Persico
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-24 (2024)
Abstract Background Phelan-McDermid syndrome (PMS) is caused by monoallelic loss or inactivation at the SHANK3 gene, located in human chr 22q13.33, and is often associated with Autism Spectrum Disorder (ASD). Objectives To assess the clinical and dev
Externí odkaz:
https://doaj.org/article/8b092706895e4762b4e869959cc80894
Autor:
Gnazzo, Miryam, Guglielmi, Nicola
Given a matrix-valued function $\mathcal{F}(\lambda)=\sum_{i=1}^d f_i(\lambda) A_i$, with complex matrices $A_i$ and $f_i(\lambda)$ entire functions for $i=1,\ldots,d$, we discuss a method for the numerical approximation of the distance to singularit
Externí odkaz:
http://arxiv.org/abs/2309.01220
Autor:
Gnazzo, Miryam, Guglielmi, Nicola
Consider a matrix polynomial $P \left( \lambda \right)= A_0 + \lambda A_1 + \ldots + \lambda^d A_d$, with $A_0,\ldots, A_d$ complex (or real) matrices with a certain structure. In this paper we discuss an iterative method to numerically approximate t
Externí odkaz:
http://arxiv.org/abs/2301.06335
Autor:
Valentina Baldini, Martina Gnazzo, Giada Rapelli, Mattia Marchi, Luca Pingani, Silvia Ferrari, Diana De Ronchi, Giorgia Varallo, Fabrizio Starace, Christian Franceschini, Alessandro Musetti, Michele Poletti, Giovanni Ostuzzi, Fabio Pizza, Gian Maria Galeazzi, Giuseppe Plazzi
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
IntroductionAdolescents’ health and well-being are seriously threatened by suicidal behaviors, which have become a severe social issue worldwide. Suicide is one of the leading causes of mortality for adolescents in low and middle-income countries,
Externí odkaz:
https://doaj.org/article/04662eb4c25a4b23bf17f128b41202c2
Autor:
Gnazzo, Maria1 (AUTHOR) maria.gnazzo@opbg.net, Parlapiano, Giovanni2 (AUTHOR) giovanni.parlapiano@opbg.net, Di Lorenzo, Francesca2 (AUTHOR) francesca1.dilorenzo@opbg.net, Perrino, Daniele1 (AUTHOR) daniele.perrino@opbg.net, Genovese, Silvia1 (AUTHOR) silvia.genovese@opbg.net, Lanari, Valentina1 (AUTHOR) valentina.lanari@opbg.net, Righi, Daniela3 (AUTHOR) daniela.righi@opbg.net, Calì, Federica3 (AUTHOR) federica1.cali@opbg.net, Silvetti, Massimo Stefano3 (AUTHOR) mstefano.silvetti@opbg.net, Falcone, Elena4 (AUTHOR) biogenetsrl@gmail.com, Bauleo, Alessia4 (AUTHOR) info@biogenet.it, Drago, Fabrizio3,5 (AUTHOR) fabrizio.drago@opbg.net, Novelli, Antonio1 (AUTHOR) antonio.novelli@opbg.net, Baban, Anwar2,5 (AUTHOR) anwar.baban@opbg.net
Publikováno v:
Biomolecules (2218-273X). Nov2024, Vol. 14 Issue 11, p1450. 16p.
Autor:
Kara Goodkey, Anita Wischmeijer, Laurence Perrin, Adrianne E. S. Watson, Leenah Qureshi, Duccio Maria Cordelli, Francesco Toni, Maria Gnazzo, Francesco Benedicenti, Monique Elmaleh-Bergès, Karen J. Low, Anastassia Voronova
Publikováno v:
BMC Medicine, Vol 22, Iss 1, Pp 1-24 (2024)
Abstract ANKRD11 (ankyrin repeat domain 11) is a chromatin regulator and the only gene associated with KBG syndrome, a rare neurodevelopmental disorder. We have previously shown that Ankrd11 regulates murine embryonic cortical neurogenesis. Here, we
Externí odkaz:
https://doaj.org/article/e5bd30dce1194973adab02f96ce05861
Autor:
Meyers, Allison M., Gnazzo, Federico G., Barrera, Eddy D., Nabatian, Tikva, Chan, Larry, Beeler, Jeff A.
Publikováno v:
In Neuroscience 17 December 2024 563:43-50
Autor:
Maria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, Daniele Perrino, Silvia Genovese, Valentina Lanari, Daniela Righi, Federica Calì, Massimo Stefano Silvetti, Elena Falcone, Alessia Bauleo, Fabrizio Drago, Antonio Novelli, Anwar Baban
Publikováno v:
Biomolecules, Vol 14, Iss 11, p 1450 (2024)
Inherited cardiac channelopathies are major causes of sudden cardiac death (SCD) in young people. Genetic testing is focused on the identification of single-nucleotide variants (SNVs) by Next-Generation Sequencing (NGS). However, genetically elusive
Externí odkaz:
https://doaj.org/article/b3bd4e44dfc84444b67c1e1bd3874d3b