Author

Annukka M. Lahtinen

Observed names: ANNUKKA M. LAHTINEN, Annukka Lahtinen, Annukka M Lahtinen, Lahtinen, Annukka M.

Institutions: University of Helsinki, University of Pavia, Stellenbosch University, Helsinki University Hospital, German Centre for Cardiovascular Research, IRCCS Istituto Auxologico Italiano, University of Milano-Bicocca

Observed institutions: Broad Institute, University of Bern, University Medical Center Groningen, University of Helsinki, Inserm, University of Groningen, University of Pavia, Stellenbosch University, Helsinki University Hospital, Finnish Institute for Health and Welfare, Massachusetts General Hospital, Tampere University Hospital, German Centre for Cardiovascular Research, Institute for Molecular Medicine Finland, IRCCS Istituto Auxologico Italiano, Fondation pour l’innovation en Cadiométabolisme et Nutrition, University of Tampere, Université Pierre-et-Marie-Curie, University of Milano-Bicocca

OpenAlex ID: A5111510481

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

2014 · Dan E Arking, DCCT/EDIC, et al. · Nature Genetics · 321

Cell Model of Catecholaminergic Polymorphic Ventricular Tachycardia Reveals Early and Delayed Afterdepolarizations

2012 · Kirsi Kujala, Jere Paavola, et al. · PLoS ONE · 141

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Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models

2015 · Kirsi Penttinen, Heikki Swan, et al. · PLoS ONE · 111

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Intravenous Epinephrine Infusion Test in Diagnosis of Catecholaminergic Polymorphic Ventricular Tachycardia

2011 · ANNUKKA MARJAMAA, ANITA HIIPPALA, et al. · Journal of Cardiovascular Electrophysiology · 84

Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

2013 · Sabine Duchatelet, Lia Crotti, et al. · Circulation Cardiovascular Genetics · 71

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

2009 · Annukka Marjamaa, Päivi Laitinen-Forsblom, et al. · BMC Medical Genetics · 66

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Gain-of-Function Mutation of the SCN5A Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias

2014 · Heikki Swan, Mohamed Yassine Amarouch, et al. · Circulation Cardiovascular Genetics · 61

Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy

2011 · Annukka M. Lahtinen, Eero Lehtonen, et al. · Heart Rhythm · 55

Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study

2011 · Peter A. Noseworthy, Aki S. Havulinna, et al. · Circulation Cardiovascular Genetics · 54

Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general population

2014 · Annukka M. Lahtinen, Aki S. Havulinna, et al. · Atherosclerosis · 53

KCNE1D85N polymorphism — a sex-specific modifier in type 1 long QT syndrome?

2011 · Annukka M Lahtinen, Annukka Marjamaa, et al. · BMC Medical Genetics · 47

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Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study

2012 · Annukka M. Lahtinen, Peter A. Noseworthy, et al. · PLoS ONE · 45

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Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy

2007 · Annukka M. Lahtinen, Annukka Lehtonen, et al. · International Journal of Cardiology · 44

Follow-Up of 316 Molecularly Defined Pediatric Long-QT Syndrome Patients

2015 · Mikael Koponen, Annukka Marjamaa, et al. · Circulation Arrhythmia and Electrophysiology · 29

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Genetic Modifiers for the Long-QT Syndrome

2016 · Lia Crotti, Annukka M. Lahtinen, et al. · Circulation Cardiovascular Genetics · 26

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Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population

2013 · Annukka M. Lahtinen, Aki S. Havulinna, et al. · Annals of Medicine · 22

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Correction: Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models

2015 · Kirsi Penttinen, Heikki Swan, et al. · PLoS ONE · 16

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Response by Crotti et al to Letter Regarding Article, “Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?”

2016 · Lia Crotti, Annukka M. Lahtinen, et al. · Circulation Cardiovascular Genetics · 9

Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain‐of‐Function Mutation in the Nav1.5 Sodium Channel

2015 · Mohamed Y. Amarouch, Heikki Swan, et al. · Annals of Noninvasive Electrocardiology · 6

Lamin A/C Mutation Affecting Primarily the Right Side of the Heart

2013 · Laura Ollila, Johanna Kuusisto, et al. · Cardiogenetics · 4

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Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland

2007 · Maija Kaartinen, Tiina Heliö, et al. · Annals of Medicine · 4

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0265: A novel SCN5A mutation associated with exercise-induced polymorphic ventricular arrhythmias resembling CPVT

2014 · Mohamed Yassine Amarouch, Jaakko Leinonen, et al. · Archives of Cardiovascular Diseases Supplements · 1

0012 : Antiarrhythmic action of flecainide in polymorphic ventricular arrhythmias caused by a gain-of-function mutation in the Nav1.5 sodium channel

2016 · Mohamed Yassine Amarouch, Jaakko Leinonen, et al. · Archives of Cardiovascular Diseases Supplements

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Genetic Variants Predisposing to Cardiac Arrhythmia Disorders and Sudden Cardiac Death

2012 · Annukka M. Lahtinen · Työväentutkimus Vuosikirja

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Works count: 28

Citation count: 1,270

H-index: 16

I10-index: 17