Year |
Citation |
Score |
2021 |
Tinarelli F, Ivanova E, Colombi I, Barini E, Balzani E, Garcia CG, Gasparini L, Chiappalone M, Kelsey G, Tucci V. Cell-cell coupling and DNA methylation abnormal phenotypes in the after-hours mice. Epigenetics & Chromatin. 14: 1. PMID 33407878 DOI: 10.1186/s13072-020-00373-5 |
0.717 |
|
2017 |
Maggi S, Balzani E, Lassi G, Garcia-Garcia C, Plano A, Espinoza S, Mus L, Tinarelli F, Nolan PM, Gainetdinov RR, Balci F, Nieus T, Tucci V. The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis. Scientific Reports. 7: 17765. PMID 29259298 DOI: 10.1038/S41598-017-18130-2 |
0.696 |
|
2017 |
Barini E, Miccoli A, Tinarelli F, Mulholand K, Kadri H, Khanim F, Stojanovski L, Read KD, Burness K, Blow JJ, Mehellou Y, Muqit M. The Anthelmintic Drug Niclosamide and its Analogues Activate the Parkinson's Disease Associated Protein Kinase PINK1. Chembiochem : a European Journal of Chemical Biology. PMID 29226533 DOI: 10.1002/Cbic.201700500 |
0.709 |
|
2017 |
Banks G, Lassi G, Hoerder-Suabedissen A, Tinarelli F, Simon MM, Wilcox A, Lau P, Lawson TN, Johnson S, Rutman A, Sweeting M, Chesham JE, Barnard AR, Horner N, Westerberg H, et al. A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies. Molecular Psychiatry. PMID 28373692 DOI: 10.1038/Mp.2017.54 |
0.79 |
|
2016 |
Colombi I, Tinarelli F, Pasquale V, Tucci V, Chiappalone M. Corrigendum: A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep. Frontiers in Neuroscience. 10: 409. PMID 27610075 DOI: 10.3389/Fnins.2016.00409 |
0.651 |
|
2016 |
Colombi I, Tinarelli F, Pasquale V, Tucci V, Chiappalone M. A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep. Frontiers in Neuroscience. 10: 315. PMID 27458335 DOI: 10.3389/Fnins.2016.00315 |
0.652 |
|
2016 |
Lassi G, Priano L, Maggi S, Garcia-Garcia C, Balzani E, El-Assawy N, Pagani M, Tinarelli F, Giardino D, Mauro A, Peters J, Gozzi A, Grugni G, Tucci V. Deletion of the Snor D116/S no RD116 alters sleep in mice and patients with Prader-Willi syndrome Sleep. 39: 637-644. DOI: 10.5665/sleep.5542 |
0.725 |
|
2015 |
Lassi G, Priano L, Maggi S, Garcia-Garcia C, Balzani E, El-Assawy N, Pagani M, Tinarelli F, Giardino D, Mauro A, Peters J, Gozzi A, Grugni G, Tucci V. Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome. Sleep. PMID 26446116 DOI: 10.5665/Sleep.5542 |
0.715 |
|
2014 |
Tucci V, Kleefstra T, Hardy A, Heise I, Maggi S, Willemsen MH, Hilton H, Esapa C, Simon M, Buenavista MT, McGuffin LJ, Vizor L, Dodero L, Tsaftaris S, Romero R, ... ... Tinarelli F, et al. Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features. The Journal of Clinical Investigation. 124: 1468-82. PMID 24614104 DOI: 10.1172/Jci70372 |
0.661 |
|
2014 |
Tinarelli F, Garcia-Garcia C, Nicassio F, Tucci V. Parent-of-origin genetic background affects the transcriptional levels of circadian and neuronal plasticity genes following sleep loss. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 369: 20120471. PMID 24446504 DOI: 10.1098/Rstb.2012.0471 |
0.822 |
|
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