G. Valle

Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder

S. Bortoluzzi, A. Coppe, G. Vazza, 2018, Molecular Neurobiology.

SAMHD1‐deficient fibroblasts from Aicardi‐Goutières Syndrome patients can escape senescence and accumulate mutations

S. Cagnin, E. Feltrin, V. Bianchi, 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Genomic instability: Crossing pathways at the origin of structural and numerical chromosome changes

D. Cimini, A. Natarajan, S. Pavanello, 2015, Environmental and molecular mutagenesis.

A specific microbiota signature is associated to various degrees of ulcerative colitis as assessed by a machine learning approach

E. Savarino, A. Ford, B. Simionati, 2022, Gut microbes.

Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder

S. Bortoluzzi, A. Coppe, G. Vazza, 2018, Molecular Neurobiology.

BVVL / FL : Features caused by SLC 52 A 3 mutations ; WDFY 4 and TNFSF 13 B may be 1 novel causative genes 2

A. Heshmati, J. Bras, E. Elahi, 2021 .

Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale

N. Elvassore, S. Zatti, E. Serena, 2020, PloS one.

Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families

R. Siebert, G. Avanzini, R. Michelucci, 2003, Epilepsia.

The LGI1/Epitempin gene encodes two protein isoforms differentially expressed in human brain

R. Michelucci, E. Calabria, L. Vitiello, 2006, Journal of neurochemistry.