Pasquale Striano, MD, PhD

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Zara FedericoInstitute G. Gaslini, University of GenoaEmail verificata su gaslini.org
Carlo MinettiUniversity of Genova and G.Gaslini Institute, GenovaEmail verificata su unige.it
roberto micheluccidirettore neurologia irccs istituto delle scienze neurologiche di bolognaEmail verificata su ausl.bo.it
Alessandro OrsiniSezione Neurologia Pediatrica, U.O Pediatria, Azienda Ospedaliera Universitaria PisanaEmail verificata su uslnordovest.toscana.it
Edoardo FerlazzoRicercatore in Neurologia, Università di Catanzaro, ItaliaEmail verificata su unicz.it
Antonio GambardellaUniversità degli Studi "Magna Graecia" CatanzaroEmail verificata su unicz.it
Renzo GuerriniProfessore di Neuropsichiatria Infantile, Università di FirenzeEmail verificata su meyer.it
Michele IacominoInstitute G. Gaslini, GenovaEmail verificata su virgilio.it
Emilio RussoUniversity Magna Grecia of CatanzaroEmail verificata su unicz.it
Francesca BisulliIRCCS Istituto delle Scienze Neurologiche di Bologna (ISNB)Email verificata su unibo.it
Mariasavina SeverinoIRCCS Istituto Giannina GasliniEmail verificata su gaslini.org
Alberto SpaliceProfessore Associato Pediatria La sapienza università RomaEmail verificata su uniroma1.it
Berge MinassianProfessor, Pediatrics, University of Toronto, Sr. Scientist, Genetics and Genome Biology, Sick KidsEmail verificata su sickkids.ca
Ganna BalaguraUniversità degli Studi di GenovaEmail verificata su edu.unige.it
Raffaele FalsaperlaUOC Pediatria, Neonatologia e TINEmail verificata su ao-ve.it
Diego PeroniUniversita' di FerraraEmail verificata su unife.it
Valeria CapraIstituto Giannina GasliniEmail verificata su gaslini.org
Francesco BrigoInnovation, Research and Teaching Service - Bolzano/Bozen, ItalyEmail verificata su sabes.it
Alice BonuccelliAzienda Ospedaliera Universitaria PisanaEmail verificata su ao-pisa.toscana.it
Angelo LabateFull Professor of Neurology, University of MessinaEmail verificata su unime.it

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Pasquale Striano, MD, PhD

Pediatric neurologist, IRCCS 'G. Gaslini'; Professor of Paediatrics, University of Genova

Email verificata su gaslini.org

Neurology Paediatrics Epilepsy Genetics Treatment


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1454	2018
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ... New England Journal of Medicine 359 (16), 1685-1699, 2008	857	2008
Mapping the human genetic architecture of COVID-19 W leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai Masahiro 2, ... Nature 600 (7889), 472-477, 2021	805	2021
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders M Wolff, KM Johannesen, UBS Hedrich, S Masnada, G Rubboli, ... Brain 140 (5), 1316-1336, 2017	559	2017
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ... The American Journal of Human Genetics 95 (4), 360-370, 2014	461	2014
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study CD Whelan, A Altmann, JA Botía, N Jahanshad, DP Hibar, J Absil, ... Brain 141 (2), 391-408, 2018	456	2018
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations E Parrini, A Ramazzotti, WB Dobyns, D Mei, F Moro, P Veggiotti, C Marini, ... Brain 129 (7), 1892-1906, 2006	382	2006
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy H Stamberger, M Nikanorova, MH Willemsen, P Accorsi, M Angriman, ... Neurology 86 (10), 954-962, 2016	331	2016
The phenotypic spectrum of SCN8A encephalopathy J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ... Neurology 84 (5), 480-489, 2015	304	2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy S Syrbe, UBS Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ... Nature genetics 47 (4), 393-399, 2015	297	2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export A Legati, D Giovannini, G Nicolas, U López-Sánchez, B Quintáns, ... Nature genetics 47 (6), 579-581, 2015	287	2015
Posterior reversible encephalopathy syndrome in intensive care medicine G Servillo, F Bifulco, E De Robertis, O Piazza, P Striano, F Tortora, ... Intensive care medicine 33, 230-236, 2007	286	2007
De novo variants in neurodevelopmental disorders with epilepsy HO Heyne, T Singh, H Stamberger, R Abou Jamra, H Caglayan, D Craiu, ... Nature genetics 50 (7), 1048-1053, 2018	284	2018
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome A Suls, JA Jaehn, A Kecskés, Y Weber, S Weckhuysen, DC Craiu, ... The American Journal of Human Genetics 93 (5), 967-975, 2013	263	2013
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019	261	2019
Posterior reversible encephalopathy syndrome: the endothelial hypotheses A Marra, M Vargas, P Striano, L Del Guercio, P Buonanno, G Servillo Medical hypotheses 82 (5), 619-622, 2014	258	2014
De novo mutations in HCN1 cause early infantile epileptic encephalopathy C Nava, C Dalle, A Rastetter, P Striano, CGF De Kovel, R Nabbout, ... Nature genetics 46 (6), 640-645, 2014	253	2014
Extending the KCNQ2 encephalopathy spectrum: Clinical and neuroimaging findings in 17 patients S Weckhuysen, V Ivanovic, R Hendrickx, R Van Coster, H Hjalgrim, ... Neurology 81 (19), 1697-1703, 2013	243	2013
Infantile spasms syndrome, West syndrome and related phenotypes: what we know in 2013 P Pavone, P Striano, R Falsaperla, L Pavone, M Ruggieri Brain and development 36 (9), 739-751, 2014	241	2014
Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic-atonic seizures GL Carvill, JM McMahon, A Schneider, M Zemel, CT Myers, J Saykally, ... The American Journal of Human Genetics 96 (5), 808-815, 2015	229	2015

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