Diego García-Giustiniani

Author

Universidade da Coruña ORCID

Also Known As

D Garcia-Giustiniani, Diego A. García-Giustiniani, Diego Garcia-Giustiniani, Diego García-Giustiniani

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Universidade da Coruña Instituto de Investigación Biomédica de A Coruña University College London Complexo Hospitalario Universitario A Coruña Hospital Universitario Virgen de la Arrixaca

About

Diego García-Giustiniani is an author at Universidade da Coruña specializing in cardiology, cardiovascular genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	528
2	Molecular Genetics	2	2	497
3	Public Health	1	1	13
4	Biostatistics	1	1	13
5	Epidemiology	1	1	13

Diego García-Giustiniani

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Atlas of the clinical genetics of human dilated cardiomyopathy Jan Haas, Karen Frese, Barbara Peil, European Heart Journal	2014	556
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies Martín Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, Journal of the American College of Cardiology CardiomyopathyHeart FailureGeneticsArrhythmogenic CardiomyopathiesPathology	2016	458
Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia Francisco Bermúdez-Jiménez, Víctor Carriel, Andreas Brodehl, Circulation	2017	98
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy Juan Pablo Ochoa, María Sabater‐Molina, José Manuel García‐Pinilla, Journal of the American College of Cardiology	2018	96
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain Diego García-Giustiniani, Michael Arad, Martín Ortiz-Genga, Heart	2015	68
Mutations in <i>TRIM63</i> cause an autosomal-recessive form of hypertrophic cardiomyopathy Joel Salazar‐Mendiguchía, Juan Pablo Ochoa, Julián Palomino-Doza, Heart	2020	49
Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy Carmen Suay‐Corredera, María Rosaria Pricolo, Elías Herrero‐Galán, Journal of Biological Chemistry Cardiac MuscleCardiomyopathyMolecular PhysiologyGeneticsProtein Haploinsufficiency Drivers	2021	39
Verification of Underlying Genetic Cause in a Cohort of Russian Patients with Familial Hypercholesterolemia Using Targeted Next Generation Sequencing Diego García-Giustiniani, Lorenzo Monserrat Journal of Cardiovascular Development and Disease	2020	20
The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals Joel Salazar‐Mendiguchía, Roberto Barriales‐Villa, Luís R. Lopes, European Journal of Medical Genetics Cardiac MuscleCardiomyopathyHeterozygous IndividualsMolecular PhysiologyLate-onset Hypertrophic Cardiomyopathy	2020	18
The Interpretation of Genetic Tests in Inherited Cardiovascular Diseases Lorenzo Monserrat, Andrea Mazzanti, Martín Ortiz‐Genga, Cardiogenetics Genetic TestingHeart FailureGeneticsGenetic EpidemiologyCongenital Heart Anomaly	2011	13

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