Eline A. Nannenberg - Concepedia

Author

Eline A. Nannenberg

Amsterdam UMC Location University of Amsterdam

Also Known As

E A Nannenberg, E. A. Nannenberg, E. A. Nannenberg*, E. Nannenberg, E.A. Nannenberg, Eline A Nannenberg, Eline A. Nannenberg, Eline Nannenberg, Eline A. Nannenberg, Nannenberg, E. A.

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam University Medical Center Groningen University of Amsterdam University of Groningen Erasmus MC

About

Eline A. Nannenberg is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, cardiology, and cardiovascular disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	551
2	Public Health	1	1	56
3	Emergency Medicine	1	1	51
4	Molecular Genetics	1	1	61
5	Neurology	1	1	80

Eline A. Nannenberg

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Outcome in Phospholamban R14del Carriers Ingrid A.W. van Rijsingen, Paul A. van der Zwaag, Judith A. Groeneweg, Circulation Cardiovascular Genetics	2014	185
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics J. Peter van Tintelen, Robert M.W. Hofstra, Hilga Katerberg, American Heart Journal Outpatient ClinicsHeart FailureLmna MutationsCardiomyopathyCardiovascular Disease	2007	165
Gender-Specific Differences in Major Cardiac Events and Mortality in Lamin A/C Mutation Carriers Ingrid A.W. van Rijsingen, Eline A. Nannenberg, Eloisa Arbustini, European Journal of Heart Failure	2012	143
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome Najim Lahrouchi, Rafik Tadros, Lia Crotti, Circulation	2020	134
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death Roddy Walsh, Arnon Adler, Ahmad S. Amin, European Heart Journal	2021	126
Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Cardiovascular Research	2015	106
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls Roddy Walsh, Najim Lahrouchi, Florence Kyndt, Genetics in Medicine	2020	100
Recurrent and founder mutations in the Netherlands—Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy Paul A. van der Zwaag, Ingrid A.W. van Rijsingen, Roald Ruiter, Netherlands Heart Journal	2013	92
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsCognitive DisabilityGenetic Epidemiology	2016	80
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Imke Christiaans, Eline A. Nannenberg, Dennis Dooijes, Netherlands Heart Journal CardiomyopathyHeart FailureCardiovascular DiseaseGeneticsPathology	2010	78

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