Amedeo Bianchi - Concepedia

Author

Amedeo Bianchi

Also Known As

A Bianchi, A. BIANCHI, A. Bianchi, A.M. Bianchi, Amedeo Bianchi, Antonietta Coppola, Antonio Gambardella, Bianchi, A, G. Beretta, Vincenzo Belcastro

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Ospedale San Donato Istituto Giannina Gaslini Ente Ospedaliero Ospedali Galliera Azienda Ospedaliera Carlo Poma Fondazione IRCCS Istituto Neurologico Carlo Besta

About

Amedeo Bianchi is an author at Ospedale San Donato specializing in medicine, neurogenetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	457
2	Social Sciences	7	7	182
3	Public Health	2	2	58
4	Education	1	1	40
5	Epidemiology	1	1	21

Amedeo Bianchi

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Spectrum of<i>SCN1A</i>mutations in severe myoclonic epilepsy of infancy Rima Nabbout, Elena Di Gennaro, Bernardo Dalla Bernardina, Neurology	2003	245
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert, Human Molecular Genetics	2012	149
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance Federico Zara, Nicola Specchio, Pasquale Striano, Epilepsia	2013	122
PRRT2 Mutations are the major cause of benign familial infantile seizures Julian Schubert, Roberta Paravidino, Felicitas Becker, Human Mutation	2012	104
Progressive myoclonic epilepsies Silvana Franceschetti, Roberto Michelucci, Laura Canafoglia, Neurology	2014	102
Benign Familial Infantile Convulsions: Mapping of a Novel Locus on Chromosome 2q24 and Evidence for Genetic Heterogeneity Michela Malacarne, Elena Di Gennaro, Francesca Madia, The American Journal of Human Genetics Down SyndromeChromosome 2Q24Mendelian DisorderGenetic DisorderGenetics	2001	73
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy Ida Manna, Antonio Gambardella, Amedeo Bianchi, Epilepsia Scn1a PolymorphismGenetic EpidemiologyHuman PolymorphismPharmacotherapySocial Sciences	2011	54
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity. Elena Di Gennaro, Pierangelo Veggiotti, Michele Malacarne, PubMed	2003	54
Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with<i>SCN1A</i>Mutations Maria Margherita Mancardi, Pasquale Striano, Elena Di Gennaro, Epilepsia	2006	54
Mutational Analysis of <i>EFHC1</i> Gene in Italian Families with Juvenile Myoclonic Epilepsy Ferdinanda Annesi, Antonio Gambardella, Roberto Michelucci, Epilepsia	2007	52

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