Eline A. Nannenberg

2.2k total citations
21 papers, 890 citations indexed

About

Eline A. Nannenberg is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Eline A. Nannenberg has authored 21 papers receiving a total of 890 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cardiology and Cardiovascular Medicine, 6 papers in Molecular Biology and 2 papers in Epidemiology. Recurrent topics in Eline A. Nannenberg's work include Cardiac electrophysiology and arrhythmias (12 papers), Cardiomyopathy and Myosin Studies (10 papers) and Cardiac pacing and defibrillation studies (7 papers). Eline A. Nannenberg is often cited by papers focused on Cardiac electrophysiology and arrhythmias (12 papers), Cardiomyopathy and Myosin Studies (10 papers) and Cardiac pacing and defibrillation studies (7 papers). Eline A. Nannenberg collaborates with scholars based in Netherlands, Canada and United States. Eline A. Nannenberg's co-authors include Arthur A.M. Wilde, J. Peter van Tintelen, Maarten P. van den Berg, Irene M. van Langen, Ahmad S. Amin, Imke Christiaans, Melanie Care, Ingrid A.W. van Rijsingen, Wojciech Zaręba and John Garcia and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PEDIATRICS.

In The Last Decade

Eline A. Nannenberg

21 papers receiving 880 citations

Peers

Eline A. Nannenberg

CCM

GENET

EPIDE

IMMUN

Javad Jabbari Denmark

Xiao Zhu United States

C. Ledeuil France

Paul A. van der Zwaag Netherlands

Katherine Neas New Zealand

Laura Andreasen Denmark

Karen McGuire United Kingdom

Jean Cavanaugh United States

Mariel Alders Netherlands

H. Haase Germany

Javad Jabbari Denmark

Eline A. Nannenberg

492 ×0.7

CCM

464 ×1.1

49 ×0.7

GENET

17 ×0.5

EPIDE

11 ×0.3

IMMUN

Citations per year, relative to Eline A. Nannenberg Eline A. Nannenberg (= 1×) peers Javad Jabbari

Countries citing papers authored by Eline A. Nannenberg

Since Specialization

Citations

This map shows the geographic impact of Eline A. Nannenberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Eline A. Nannenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eline A. Nannenberg more than expected).

Fields of papers citing papers by Eline A. Nannenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eline A. Nannenberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Eline A. Nannenberg. The network helps show where Eline A. Nannenberg may publish in the future.

Co-authorship network of co-authors of Eline A. Nannenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Eline A. Nannenberg. A scholar is included among the top collaborators of Eline A. Nannenberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eline A. Nannenberg. Eline A. Nannenberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Walsh, Roddy, Arnon Adler, Ahmad S. Amin, et al.. (2021). Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death. European Heart Journal. 43(15). 1500–1510. 71 indexed citations

Bruyndonckx, Luc, Marianna Bugiani, Bart Straver, et al.. (2021). Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case. American Journal of Medical Genetics Part A. 185(8). 2464–2470. 17 indexed citations

Wilde, Arthur A.M., Eline A. Nannenberg, & Christian van der Werf. (2020). Cardiogenetics, 25 years a growing subspecialism. Netherlands Heart Journal. 28(S1). 39–43. 8 indexed citations

Adler, Arnon, Valeria Novelli, Ahmad S. Amin, et al.. (2020). An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome. Circulation. 141(6). 418–428. 204 indexed citations

Cheung, Christopher C., Krystien V.V. Lieve, Thomas M. Roston, et al.. (2018). Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia. JACC. Clinical electrophysiology. 5(3). 387–394. 16 indexed citations

Nannenberg, Eline A., Ingrid A.W. van Rijsingen, Paul A. van der Zwaag, et al.. (2018). Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases. Circulation Genomic and Precision Medicine. 11(10). e001797–e001797. 7 indexed citations

Tadros, Rafik, Eline A. Nannenberg, Krystien V.V. Lieve, et al.. (2017). Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death. JACC. Clinical electrophysiology. 3(12). 1400–1408. 30 indexed citations

Hulsebos, Theo J.M., Susan Kenter, Frank Baas, et al.. (2016). Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cells. Genes Chromosomes and Cancer. 55(4). 350–354. 8 indexed citations

Postema, Pieter G., S. Matthijs Boekholdt, Hanno L. Tan, et al.. (2015). Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus. Heart Rhythm. 13(4). 905–912. 32 indexed citations

10.

Rijsingen, Ingrid A.W. van, Paul A. van der Zwaag, Judith A. Groeneweg, et al.. (2014). Outcome in Phospholamban R14del Carriers. Circulation Cardiovascular Genetics. 7(4). 455–465. 113 indexed citations

11.

Zwaag, Paul A. van der, Ingrid A.W. van Rijsingen, Eline A. Nannenberg, et al.. (2013). Mortality and risk factors for malignant ventricular arrhythmias in carriers of the phospholamban R14del mutation. European Heart Journal. 34(suppl 1). P2287–P2287. 1 indexed citations

12.

Zwaag, Paul A. van der, Ingrid A.W. van Rijsingen, Eline A. Nannenberg, et al.. (2013). Recurrent and founder mutations in the Netherlands—Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy. Netherlands Heart Journal. 21(6). 286–293. 67 indexed citations

13.

Nannenberg, Eline A., Eric J.G. Sijbrands, Lea M. Dijksman, et al.. (2012). Mortality of Inherited Arrhythmia Syndromes. Circulation Cardiovascular Genetics. 5(2). 183–189. 29 indexed citations

14.

Nannenberg, Eline A., Michelle Michels, Imke Christiaans, et al.. (2011). Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 58(23). 2406–2414. 16 indexed citations

15.

Hofman, Nynke, R. J. E. Jongbloed, Pieter G. Postema, et al.. (2010). Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome. Netherlands Heart Journal. 19(1). 10–16. 5 indexed citations

16.

Postema, Pieter G., Maarten P. van den Berg, J. Peter van Tintelen, et al.. (2009). Founder mutations in the Netherlands. Netherlands Heart Journal. 17(11). 422–428. 40 indexed citations

17.

Postema, Pieter G., Irene M. van Langen, Eline A. Nannenberg, et al.. (2007). Genetische identificatie van patiënten en families met lange-QT-syndroom: Grote regionale verschillen in de resultaten van 10 jaar. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 151(11). 644–648. 3 indexed citations

18.

Tintelen, J. Peter van, Robert M.W. Hofstra, Hilga Katerberg, et al.. (2007). High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. American Heart Journal. 154(6). 1130–1139. 120 indexed citations

19.

Nannenberg, Eline A., R. P. G. M. Bijlmer, Björn M. van Geel, & Raoul C. M. Hennekam. (2005). Neonatal paroxysmal trismus and camptodactyly: The Crisponi syndrome. American Journal of Medical Genetics Part A. 133A(1). 90–92. 24 indexed citations

20.

Kuijpers, Taco W., Eline A. Nannenberg, Mariëlle Alders, Robbert G. M. Bredius, & Raoul C. M. Hennekam. (2004). Congenital Aplastic Anemia Caused by Mutations in the SBDS Gene: A Rare Presentation of Shwachman-Diamond Syndrome. PEDIATRICS. 114(3). e387–e391. 26 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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