Roberto Insolia - Concepedia

Author

Roberto Insolia

University of Pavia

Also Known As

Alice Ghidoni, Hamilton, Robert M, Insolia, Roberto, Lia Crotti, M Grasso, R Insolia, R. Insolia, Roberto Insolia

Publications

Citations

H-Index

Concepts

All Affiliations

University of Pavia Istituti di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo Fondazione University of Cape Town Stellenbosch University

About

Roberto Insolia is an author at University of Pavia specializing in medicine, genetics, and epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	86
2	Natural Sciences	1	1	42
3	Public Health	1	1	44
4	Epidemiology	1	1	44
5	Molecular Biology	1	1	42

Roberto Insolia

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Prevalence of the Congenital Long-QT Syndrome Peter J. Schwartz, Marco Stramba‐Badiale, Lia Crotti, Circulation	2009	1K
Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome Marianne Arnestad, Lia Crotti, Torleiv O. Rognum, Circulation	2007	524
<i>NOS1AP</i> Is a Genetic Modifier of the Long-QT Syndrome Lia Crotti, Maria Cristina Monti, Roberto Insolia, Circulation	2009	265
<i>KCNH2</i> -K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome Lia Crotti, Andrew L. Lundquist, Roberto Insolia, Circulation	2005	239
Cardiac Sodium Channel Dysfunction in Sudden Infant Death Syndrome Dao Wen Wang, Reshma R. Desai, Lia Crotti, Circulation	2007	184
Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death Lia Crotti, David J. Tester, Wendy White, JAMA	2013	171
The Common Long-QT Syndrome Mutation KCNQ1/A341V Causes Unusually Severe Clinical Manifestations in Patients With Different Ethnic Backgrounds Lia Crotti, Carla Spazzolini, Peter J. Schwartz, Circulation	2007	171
Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant Lia Crotti, Dan Hu, Héctor Barajas-Martínez, Heart Rhythm Deadly LinkCardiomyopathyHeart FailureCommon Genetic VariantCardiovascular Disease	2012	44
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome Lia Crotti, Marzena Anna Lewandowska, Peter J. Schwartz, Heart Rhythm Transcriptional RegulationGenetic DisorderNatural SciencesGeneticsMolecular Biology	2008	42
Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: Implications for the clinical management of LQT3 patients Laura Calvillo, Carla Spazzolini, Eleonora Lo Vullo, Heart Rhythm	2013	33

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