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Fingerprint Dive into the research topics where Valeria Novelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Frontotemporal Dementia Medicine & Life Sciences
Genome-Wide Association Study Medicine & Life Sciences
Mexiletine Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Gene Regulatory Networks Medicine & Life Sciences
Atrial Flutter Medicine & Life Sciences
Genes Medicine & Life Sciences
Erythrocyte Membrane Medicine & Life Sciences

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Research Output 2008 2019

  • 1090 Citations
  • 15 h-Index
  • 20 Article

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

International FTD-Genomics Consortium (IFGC) , Dec 1 2019, In : Scientific Reports. 9, 1, 10854.

Research output: Contribution to journalArticle

Open Access
Primary Progressive Aphasia
Gene Regulatory Networks
Semantics
Cell Death
RNA
1 Citation (Scopus)

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

International Frontotemporal Dementia Genomics Consortium, 2019, In : Nature Medicine. 25, 1, p. 152-164

Research output: Contribution to journalArticle

Gene Regulatory Networks
Dementia
Genes
MicroRNAs
Pharmaceutical Databases

CXCR4 involvement in neurodegenerative diseases

Bonham, L. W., Karch, C. M., Fan, C. C., Tan, C., Geier, E. G., Wang, Y., Wen, N., Broce, I. J., Li, Y., Barkovich, M. J., Ferrari, R., Hardy, J., Momeni, P., Höglinger, G., Müller, U., Hess, C. P., Sugrue, L. P., Dillon, W. P., Schellenberg, G. D., Miller, B. L. & 158 others, Andreassen, O. A., Dale, A. M., Barkovich, A. J., Yokoyama, J. S., Desikan, R. S., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Schofield, P. R., Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Haan, E., Hernández, I., Ruiz, A., Boada, M., Borroni, B., Padovani, A., Cruchaga, C., Cairns, N. J., Benussi, L., Binetti, G., Ghidoni, R., Forloni, G., Albani, D., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Clarimón, J., Lleó, A., Blesa, R., Waldö, M. L., Nilsson, K., Nilsson, C., MacKenzie, I. R. A., Hsiung, G-YR., Mann, D. M. A., Grafman, J., Morris, C. M., Attems, J., Griffiths, T. D., McKeith, I. G., Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Pastor, P., Razquin, C., Ortega-Cubero, S., Alonso, E., Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., George-Hyslop, P. S., Rossi, G., Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Mead, S., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., Van Der Zee, J., Cruts, M., Van Broeckhoven, C., Cappa, S. F., Leber, I., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Heutink, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Rademakers, R., Baker, M., Dickson, D. W., Graff-Radford, N. R., Petersen, R. C., Knopman, D., Josephs, K. A., Boeve, B. F., Parisi, J. E., Seeley, W. W., Karydas, A. M., Rosen, H., Van Swieten, J. C., Dopper, E. G. P., Seelaar, H., Pijnenburg, Y. A. L., Scheltens, P., Logroscino, G., Capozzo, R., Novelli, V., Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H-H., Graff, C., Pasquier, F., Rollin, A., Deramecourt, V., Lebouvier, T., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B. & International FTD-Genomics Consortium (IFGC) International Parkinson's Disease Genetics Consortium (IPDGC), I. G. O. A. P. IGAP., 2018, In : Translational Psychiatry. 8, 1

Research output: Contribution to journalArticle

Progressive Supranuclear Palsy
Neurodegenerative Diseases
Parkinson Disease
Frontotemporal Dementia
Brain
25 Citations (Scopus)

Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

International FTD-Genomics Consortium, Jan 1 2018, In : PLoS Medicine. 15, 1, e1002487.

Research output: Contribution to journalArticle

Frontotemporal Dementia
Genome-Wide Association Study
Immune System Diseases
HLA Antigens
Progressive Supranuclear Palsy
54 Citations (Scopus)

Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk

Mazzanti, A., Ng, K., Faragli, A., Maragna, R., Chiodaroli, E., Orphanou, N., Monteforte, N., Memmi, M., Gambelli, P., Novelli, V., Bloise, R., Moro, G., Tibollo, V., Morini, M., Bellazzi, R., Napolitano, C., Bagnardi, V. & Priori, S. G., Dec 13 2016, In : Journal of the American College of Cardiology. 68, 23, p. 2540-2550 11 p.

Research output: Contribution to journalArticle

Arrhythmogenic Right Ventricular Dysplasia
Cardiac Arrhythmias
Syncope
Ventricular Tachycardia
Exercise