Laura Licchetta - Concepedia

Author

Laura Licchetta

Also Known As

Barbara Mostacci, Calwing Liao, Gaetano Cantalupo, L. Licchetta, Laura Licchetta, Laura Licchetta, MD, Licchetta, Laura, Norman Delanty, Paolo Tinuper, Valentina Imperatore

182

Publications

5.3K

Citations

H-Index

Concepts

All Affiliations

University of Bologna Istituti di Ricovero e Cura a Carattere Scientifico Istituto delle Scienze Neurologiche di Bologna IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola Institute of Neurological Sciences

About

Laura Licchetta is an author at University of Bologna specializing in medicine, neuroscience, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	24	2.1K
2	Social Sciences	11	12	844
3	Public Health	3	3	103
4	Health Sciences	2	2	60
5	Behavioral Sciences	1	1	10

Laura Licchetta

Publications

Citations

H-Index

Page 1

	Year	Citations
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy Sarah E. Heron, Katherine R. Smith, Melanie Bahlo, Nature Genetics ChannelopathiesMissense MutationsHyperpolarization (Biology)NeurophysiologyGenetics	2012	405
Mutations in DEPDC5 cause familial focal epilepsy with variable foci Leanne M. Dibbens, Boukje de Vries, Simona Donatello, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsNeurogeneticsVariable Foci	2013	358
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens, Nature Genetics GeneticsNeuroscienceCentral Nervous SystemMedicinePotassium Homeostasis	2014	311
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298
The landscape of epilepsy-related GATOR1 variants Sara Baldassari, Fabienne Picard, Nienke E. Verbeek, Genetics in Medicine	2018	236
Mutations in the mammalian target of rapamycin pathway regulators <i>NPRL2</i> and <i>NPRL3</i> cause focal epilepsy Michael G. Ricos, Bree Hodgson, Tommaso Pippucci, Annals of Neurology	2015	229
Mutations in mammalian target of rapamycin regulator <i>DEPDC5</i> cause focal epilepsy with brain malformations Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan, Annals of Neurology GeneticsDepdc5 MutationsDisease Gene IdentificationSynaptic SignalingDepdc5-associated Malformations	2014	218
Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug‐refractory epilepsy Maria Paola Canevini, Giovambattista De Sarro, Carlo Andrea Galimberti, Epilepsia	2010	188
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 Rahel T. Florian, Florian Kraft, Elsa Leitão, Nature Communications	2019	161
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 Mark Corbett, Thessa Kroes, Liana Veneziano, Nature Communications	2019	154

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