Valeria Novelli

Valeria Novelli

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Valeria Novelli

Valeria Novelli

Publications by authors named "Valeria Novelli"

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Pleiotropic Phenotypes Associated With PKP2 Variants.

Front Cardiovasc Med 2018 18;5:184. Epub 2018 Dec 18.

Leon H. Charney Division of Cardiology, NYU School of Medicine, New York, NY, United States.

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https://www.frontiersin.org/article/10.3389/fcvm.2018.00184/
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http://dx.doi.org/10.3389/fcvm.2018.00184DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305316PMC
December 2018

Editorial: Current Challenges in Cardiovascular Molecular Diagnostics.

Front Cardiovasc Med 2017 1;4:54. Epub 2017 Sep 1.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, United States.

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http://dx.doi.org/10.3389/fcvm.2017.00054DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585151PMC
September 2017

Challenges in Molecular Diagnostics of Channelopathies in the Next-Generation Sequencing Era: Less Is More?

Front Cardiovasc Med 2016 12;3:29. Epub 2016 Sep 12.

Molecular Cardiology, IRCCS Fondazione Salvatore Maugeri , Pavia , Italy.

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http://dx.doi.org/10.3389/fcvm.2016.00029DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018689PMC
September 2016

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3.

J Am Coll Cardiol 2016 Mar;67(9):1053-8

Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, Pavia, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2015.12.033DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773513PMC
March 2016

Genetic modulators of the phenotype in the long QT syndrome: state of the art and clinical impact.

Curr Opin Genet Dev 2015 Aug 2;33:17-24. Epub 2015 Aug 2.

Department of Molecular Medicine University of Pavia, Pavia, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.gde.2015.06.009DOI Listing
August 2015

Frontotemporal dementia and its subtypes: a genome-wide association study.

Authors:
Raffaele Ferrari Dena G Hernandez Michael A Nalls Jonathan D Rohrer Adaikalavan Ramasamy John B J Kwok Carol Dobson-Stone William S Brooks Peter R Schofield Glenda M Halliday John R Hodges Olivier Piguet Lauren Bartley Elizabeth Thompson Eric Haan Isabel Hernández Agustín Ruiz Mercè Boada Barbara Borroni Alessandro Padovani Carlos Cruchaga Nigel J Cairns Luisa Benussi Giuliano Binetti Roberta Ghidoni Gianluigi Forloni Daniela Galimberti Chiara Fenoglio Maria Serpente Elio Scarpini Jordi Clarimón Alberto Lleó Rafael Blesa Maria Landqvist Waldö Karin Nilsson Christer Nilsson Ian R A Mackenzie Ging-Yuek R Hsiung David M A Mann Jordan Grafman Christopher M Morris Johannes Attems Timothy D Griffiths Ian G McKeith Alan J Thomas P Pietrini Edward D Huey Eric M Wassermann Atik Baborie Evelyn Jaros Michael C Tierney Pau Pastor Cristina Razquin Sara Ortega-Cubero Elena Alonso Robert Perneczky Janine Diehl-Schmid Panagiotis Alexopoulos Alexander Kurz Innocenzo Rainero Elisa Rubino Lorenzo Pinessi Ekaterina Rogaeva Peter St George-Hyslop Giacomina Rossi Fabrizio Tagliavini Giorgio Giaccone James B Rowe Johannes C M Schlachetzki James Uphill John Collinge Simon Mead Adrian Danek Vivianna M Van Deerlin Murray Grossman John Q Trojanowski Julie van der Zee William Deschamps Tim Van Langenhove Marc Cruts Christine Van Broeckhoven Stefano F Cappa Isabelle Le Ber Didier Hannequin Véronique Golfier Martine Vercelletto Alexis Brice Benedetta Nacmias Sandro Sorbi Silvia Bagnoli Irene Piaceri Jørgen E Nielsen Lena E Hjermind Matthias Riemenschneider Manuel Mayhaus Bernd Ibach Gilles Gasparoni Sabrina Pichler Wei Gu Martin N Rossor Nick C Fox Jason D Warren Maria Grazia Spillantini Huw R Morris Patrizia Rizzu Peter Heutink Julie S Snowden Sara Rollinson Anna Richardson Alexander Gerhard Amalia C Bruni Raffaele Maletta Francesca Frangipane Chiara Cupidi Livia Bernardi Maria Anfossi Maura Gallo Maria Elena Conidi Nicoletta Smirne Rosa Rademakers Matt Baker Dennis W Dickson Neill R Graff-Radford Ronald C Petersen David Knopman Keith A Josephs Bradley F Boeve Joseph E Parisi William W Seeley Bruce L Miller Anna M Karydas Howard Rosen John C van Swieten Elise G P Dopper Harro Seelaar Yolande A L Pijnenburg Philip Scheltens Giancarlo Logroscino Rosa Capozzo Valeria Novelli Annibale A Puca Massimo Franceschi Alfredo Postiglione Graziella Milan Paolo Sorrentino Mark Kristiansen Huei-Hsin Chiang Caroline Graff Florence Pasquier Adeline Rollin Vincent Deramecourt Florence Lebert Dimitrios Kapogiannis Luigi Ferrucci Stuart Pickering-Brown Andrew B Singleton John Hardy Parastoo Momeni

Lancet Neurol 2014 Jul;13(7):686-99

Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Science Center, Lubbock, Texas, USA.

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http://dx.doi.org/10.1016/S1474-4422(14)70065-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112126PMC
July 2014

Novel insight into the natural history of short QT syndrome.

J Am Coll Cardiol 2014 Apr 28;63(13):1300-1308. Epub 2013 Nov 28.

Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, Pavia, Italy; Cardiovascular Genetics Program, Leon H. Charney Division of Cardiology, New York University School of Medicine, New York, New York; Department of Molecular Medicine, University of Pavia, Pavia, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2013.09.078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988978PMC
April 2014

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.

Circulation 2014 Mar 18;129(10):1092-103. Epub 2013 Dec 18.

Leon H. Charney Division of Cardiology (M.C., X.L., M.Z., E.A.-P., A.P., H.C.G., S.P., M.D.), and Cardiovascular Genetics Program (M.C., S.P.), NYU School of Medicine, New York, NY; Molecular Cardiology, Maugeri Foundation, Pavia, Italy (V.N., C.N., S.P.); Del E. Webb Center for Neuroscience, Aging & Stem Cell Research, Sanford-Burnham Medical Research Institute, La Jolla, CA (C.K., T.T., H.-S.V.C.); Department of Bioscience and Biotechnology, Sejong University, Seoul, Korea (C.K.); Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (D.P.J.); and Department of Pharmacology, NYU School of Medicine, New York, NY (E.R.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.113.003077DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3954430PMC
March 2014

Association of the FOXO3A locus with extreme longevity in a southern Italian centenarian study.

Rejuvenation Res 2009 Apr;12(2):95-104

Unit of Genetics and Cardiovascular Research Institute, Istituto Ricovero Cura Carattere Scientifico Multimedica, Sesto S. Giovanni, Italy.

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http://dx.doi.org/10.1089/rej.2008.0827DOI Listing
April 2009

Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients.

Hum Mutat 2008 Oct;29(10):1237-46

Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy.

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http://dx.doi.org/10.1002/humu.20792DOI Listing
October 2008

Lack of replication of genetic associations with human longevity.

Biogerontology 2008 Apr 23;9(2):85-92. Epub 2007 Nov 23.

Genetic Department, IRCCS Multimedica, via Milanese 300, Sesto S. Giovanni (Milan), 20099, Italy.

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http://dx.doi.org/10.1007/s10522-007-9116-4DOI Listing
April 2008