Renato Borgatti - Concepedia

Author

Renato Borgatti

Also Known As

Aglaia Vignoli, Borgatti Renato, Borgatti, Renato, E Tronick, Elisa Baroffio, Jean-Louis Mandel, Lane, Erlend, MOM-COPE Study Group, Nitsch, Lucio, R Borgatti

493

Publications

9.7K

Citations

H-Index

252

Concepts

All Affiliations

IRCCS Eugenio Medea University of Pavia Istituti di Ricovero e Cura a Carattere Scientifico University of Milan University of Insubria

About

Renato Borgatti is an author at IRCCS Eugenio Medea specializing in medicine, social sciences, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	16	20	897
2	Health Sciences	9	9	424
3	Language Studies	4	4	123
4	Arts	1	1	20
5	Engineering	1	1	44

Renato Borgatti

148

Publications

7.9K

Citations

H-Index

Page 1

	Year	Citations
Disorders of cognitive and affective development in cerebellar malformations Alessandro Tavano, Roberto Grasso, Chiara Gagliardi, Brain NeuropsychologyDevelopmental Cognitive NeuroscienceBrain DevelopmentNeurological DisorderCorticobasal Degeneration	2007	374
Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome María Clara Bonaglia, Roberto Giorda, Renato Borgatti, The American Journal of Human Genetics Gene Deletion DataDeletion SyndromeSignal TransductionGenetic DisorderGenetics	2001	323
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome María Clara Bonaglia, Roberto Giorda, Silvana Beri, PLoS Genetics	2011	223
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment Nicola Brunetti‐Pierri, Alex R. Paciorkowski, Roberto Ciccone, European Journal of Human Genetics Developmental BiologyMendelian DisorderSevere Speech ImpairmentGenetic DisorderGenetics	2010	187
Level of NICU Quality of Developmental Care and Neurobehavioral Performance in Very Preterm Infants Rosario Montirosso, Alberto Del Prete, Roberto Bellù, PEDIATRICS	2012	174
Agenesis of the Corpus Callosum: Clinical and Genetic Study in 63 Young Patients Maria Francesca Bedeschi, María Clara Bonaglia, Rita Grasso, Pediatric Neurology NeurologyCorpus CallosumGenetic StudyMedicineYoung Patients	2006	170
Characterization of mutations in the genedoublecortin in patients with double cortex syndrome Joseph G. Gleeson, Sharon Minnerath, Jeremy W. Fox, Annals of Neurology	1999	166
Is everybody always my friend? Perception of approachability in Williams syndrome Elisa Frigerio, D. M. Burt, Chiara Gagliardi, Neuropsychologia Cognitive SciencePersonality PsychologySocial PsychologyPsychologyWilliams Syndrome	2005	161
Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment Marilisa M. Guerreiro, E. Andermann, Renzo Guerrini, Annals of Neurology Familial Perisylvian PolymicrogyriaCorticobasal DegenerationGeneticsMendelian DisorderX-linked Inheritance	2000	159
The Development of Dynamic Facial Expression Recognition at Different Intensities in 4- to 18-Year-Olds Rosario Montirosso, Milena Peverelli, Elisa Frigerio, Social Development Affective VariableEmpathyAffective NeuroscienceDifferent IntensitiesEducation	2009	157

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