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Giornale Italiano Di Cardiologia (2006)|December 22, 2012
[Clinical conditions associated with abnormal QT interval: clinical implications]Lia Crotti, Cinzia Dossena, Elisa Mastantuono, et al.
Gene|January 7, 2022
There is more to it than just congenital heart defects - The phenotypic spectrum of TAB2-related syndromeDominik S Westphal, Elisa Mastantuono, Heide Seidel, et al.
JIMD Reports|June 21, 2018
A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic EncephalopathyArcangela Iuso, Bader Alhaddad, Corina Weigel, et al.
Circulation. Cardiovascular Genetics|August 18, 2016
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?Lia Crotti, Annukka M Lahtinen, Carla Spazzolini, et al.
Iscience|January 6, 2022
Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndromeAnna B Meier, Sarala Raj Murthi, Hilansi Rawat, et al.
European Heart Journal|December 31, 2015
The genetics underlying acquired long QT syndrome: impact for genetic screeningHideki Itoh, Lia Crotti, Takeshi Aiba, et al.
Circulation. Cardiovascular Genetics|March 11, 2017
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular CardiomyopathyBongani M Mayosi, Maryam Fish, Gasnat Shaboodien, et al.
The EMBO Journal|May 17, 2018
Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identityTatjana Dorn, Jessica Kornherr, Elvira I Parrotta, et al.
The Journal of Clinical Investigation|November 17, 2020
Congenital heart disease risk loci identified by genome-wide association study in European patientsHarald Lahm, Meiwen Jia, Martina Dreßen, et al.
Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.
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