E.A. Nannenberg publications

2021

• Walsh Roddy, Lahrouchi Najim, Tadros Rafik, Kyndt Florence, Glinge Charlotte, Postema Pieter G., Amin Ahmad S., Nannenberg Eline A., Ware James S., Whiffin Nicola, Mazzarotto Francesco, Škorić-Milosavljević Doris, Krijger Christian, Arbelo Elena, Babuty Dominique, Barajas-Martinez Hector, Beckmann Britt M., Bézieau Stéphane, Bos J. Martijn, Breckpot Jeroen, Campuzano Oscar, Castelletti Silvia, Celen Candan, Clauss Sebastian, Corveleyn Anniek, Crotti Lia, Dagradi Federica, de Asmundis Carlo, Denjoy Isabelle, Dittmann Sven, Ellinor Patrick T., Ortuño Cristina Gil, Giustetto Carla, Gourraud Jean-Baptiste, Hazeki Daisuke, Horie Minoru, Ishikawa Taisuke, Itoh Hideki, Kaneko Yoshiaki, Kanters J. rgen K., Kimoto Hiroki, Kotta Maria-Christina, Krapels Ingrid P. C., Kurabayashi Masahiko, Lazarte Julieta, Leenhardt Antoine, Loeys Bart L., Robyns Tomas, Barc Julien, Bezzina Connie R. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls Genetics in medicine 2021;23 (1):47-58 [PubMed]

2020

• Adler Arnon, Novelli Valeria, Amin Ahmad S., Abiusi Emanuela, Care Melanie, Nannenberg Eline A., Feilotter Harriet, Amenta Simona, Mazza Daniela, Bikker Hennie, Sturm Amy C., Garcia John, Ackerman Michael J., Hershberger Raymond E., Perez Marco V., Zareba Wojciech, Ware James S., Wilde Arthur A. M., Gollob Michael H. An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome Circulation 2020;141 (6):418-428 [PubMed]
• Wilde A. A. M., Nannenberg E., van der Werf C. Cardiogenetics, 25 years a growing subspecialism Netherlands heart journal 2020;28:39-43 [PubMed]
• Wijeyeratne Yanushi D., Tanck Michael W., Mizusawa Yuka, Batchvarov Velislav, Barc Julien, Crotti Lia, Bos J. Martijn, Tester David J., Muir Alison, Veltmann Christian, Ohno Seiko, Page Stephen P., Galvin Joseph, Tadros Rafik, Muggenthaler Martina, Raju Hariharan, Denjoy Isabelle, Schott Jean-Jacques, Gourraud Jean-Baptiste, Skoric-Milosavljevic Doris, Nannenberg Eline A., Redon Richard, Papadakis Michael, Kyndt Florence, Dagradi Federica, Castelletti Silvia, Torchio Margherita, Meitinger Thomas, Lichtner Peter, Ishikawa Taisuke, Wilde Arthur A. M., Takahashi Kazuhiro, Sharma Sanjay, Roden Dan M., Borggrefe Martin M., McKeown Pascal P., Shimizu Wataru, Horie Minoru, Makita Naomasa, Aiba Takeshi, Ackerman Michael J., Schwartz Peter J., Probst Vincent, Bezzina Connie R., Behr Elijah R. Scn5a mutation type and a genetic risk score associate variably with brugada syndrome phenotype in scn5a families Circulation. Genomic and precision medicine 2020:599-608 [PubMed]
• Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G., Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L., Mazzanti Andrea, Beckmann Britt M., Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D., Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A., Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M. Ben, Weeke Peter E., Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J., Bos J. Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G., Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A., Veldink Jan H., van den Berg Leonard H., Al-Chalabi Ammar, Shaw Christopher E., Shaw Pamela J., Morrison Karen E., Andersen Peter M., Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C., Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J. Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D., Antzelevitch Charles, Roden Dan M., Saenen Johan, Borggrefe Martin, Odening Katja E., Ellinor Patrick T., Tfelt-Hansen Jacob, Skinner Jonathan R., van den Berg Maarten P., Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R., Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G., Guicheney Pascale, Tan Hanno L., Newton-Cheh Christopher, Ackerman Michael J., Schwartz Peter J., Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A., Tanck Michael W. T., Bezzina Connie R. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome Circulation 2020;142 (4):324-338 [PubMed]

2019

• Cheung Christopher C., Lieve Krystien V., Roston Thomas M., van der Ree Martijn H., Deyell Marc W., Andrade Jason G., Laksman Zachary W., Nannenberg Eline A., Tadros Rafik, Pang Benjamin, Rutberg Julie, Green Martin S., Conacher Susan, Seifer Colette M., Roberts Jason D., Steinberg Christian, Sanatani Shubhayan, Wilde Arthur A., Krahn Andrew D. Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia JACC. Clinical electrophysiology 2019;5 (3):387-394 [PubMed]

2018

• Rivaud Mathilde R., Jansen John A., Postema Pieter G., Nannenberg Eline A., Mizusawa Yuka, van der Nagel Roel, Wolswinkel Rianne, van der Made Ingeborg, Marchal Gerard A., Rajamani Sridharan, Belardinelli Luiz, van Tintelen J. Peter, Tanck Michael W. T., van DerWal Allard C., de Bakker Jacques M. T., van Rijen Harold V., Creemers Esther E., Wilde Arthur A. M., van den Berg Maarten P., van Veen Toon A. B., Bezzina Connie R., Remme Carol Ann A common co-morbiditymodulates disease expression and treatment efficacy in inherited cardiac sodiumchannelopathy European heart journal 2018;39 (31):2898-2907 [PubMed]
• Nannenberg Eline A., van Rijsingen Ingrid A. W., van der Zwaag Paul A., van den Berg Maarten P., van Tintelen J. Peter, Tanck Michael W. T., Ackerman Michael J., Wilde Arthur A. M., Christiaans Imke Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases Circulation. Genomic and precision medicine 2018;11 (10):e001797 [PubMed]

2017

• Tadros Rafik, Nannenberg Eline A., Lieve Krystien V. , Skoric-Milosavljevic Doris, Lahrouchi Najim, Lekanne Dit Deprez Ronald H., Vendrik Jeroen, Reckman Yolan J. , Postema Pieter G., Amin Ahmad S., Bezzina Connie R. , Wilde Arthur A. M., Tan Hanno L. Yield and pitfalls of ajmaline testing in the evaluation of unexplained cardiac arrest and sudden unexplained death: Single centre experience of 482 families. Journal of the American College of Cardiology Clinical Electrophysiology 2017;3 (12):1400-1408 [PubMed]

2016

• ten Sande Judith N., Postema Pieter G., Boekholdt S. Matthijs, Tan Hanno L., van der Heijden Jeroen F., de Groot Natasja M. S., Volders Paul G. A., Zeppenfeld Katja, Boersma Lucas V. A., Nannenberg Eline A., Christiaans Imke, Wilde Arthur A. M. Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus Heart rhythm 2016;13 (4):905-912 [PubMed]
• Lodder Elisabeth M., de Nittis Pasquelena, Koopman Charlotte D., Wiszniewski Wojciech, Moura de Souza Carolina Fischinger, Lahrouchi Najim, Guex Nicolas, Napolioni Valerio, Tessadori Federico, Beekman Leander, Nannenberg Eline A., Boualla Lamiae, Blom Nico A., de Graaff Wim, Kamermans Maarten, Cocciadiferro Dario, Malerba Natascia, Mandriani Barbara, Akdemir Zeynep Hande Coban, Fish Richard J., Eldomery Mohammad K., Ratbi Ilham, Wilde Arthur A. M., de Boer Teun, Simonds William F., Neerman-Arbez Marguerite, Sutton V. Reid, Kok Fernando, Lupski James R., Reymond Alexandre, Bezzina Connie R., Bakkers Jeroen, Merla Giuseppe GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability American journal of human genetics 2016;99 (3):704-710 [PubMed]
• Hulsebos Theo J. M., Kenter Susan, Baas Frank, Nannenberg Eline A., Bleeker Fonnet E., van Minkelen Rick, van den Ouweland Ans M. W., Wesseling Pieter, Flucke Uta 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 & cancer 2016;55 (4):350-354 [PubMed]

2015

• Behr Elijah R., Savio-Galimberti Eleonora, Barc Julien, Holst Anders G., Petropoulou Evmorfia, Prins Bram P., Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A., Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J., Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M., Bezzina Connie R., Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, Jamshidi Yalda Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study Cardiovascular research 2015;106 (3):520-529 [PubMed]

2014

• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J.E., Michels M., Postema P. G., Majoor-Krakauer D., Van Den Wijngaard A., Mannens M. M.A.M., Van Tintelen J. P., Van Langen I. M., Wilde A. A.M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlandsin: Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu von Loghum; 2014. p. 37-42, ISBN 9036807042; 9789036807043
• Nannenberg Eline Alberdina Mortality in inherited cardiac diseases: Directing care in affected families 2014. 176p. ISBN 9789462593886. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Sijbrands E. J. G.; Co-supervisor: Christiaans I.)
• van Rijsingen Ingrid A. W., van der Zwaag Paul A., Groeneweg Judith A., Nannenberg Eline A., Jongbloed Jan D. H., Zwinderman Aeilko H., Pinto Yigal M., Dit Deprez Ronald H. Lekanne, Post Jan G., Tan Hanno L., de Boer Rudolf A., Hauer Richard N. W., Christiaans Imke, van den Berg Maarten P., van Tintelen J. Peter, Wilde Arthur A. M. Outcome in phospholamban R14del carriers: results of a large multicentre cohort study Circulation. Cardiovascular genetics 2014;7 (4):455-465 [PubMed]

2013

• van Rijsingen Ingrid A. W., Nannenberg Eline A., Arbustini Eloisa, Elliott Perry M., Mogensen Jens, Hermans-van Ast Johanna F., van der Kooi Anneke J., van Tintelen J. Peter, van den Berg Maarten P., Grasso Maurizia, Serio Alessandra, Jenkins Sharon, Rowland Camilla, Richard Pascale, Wilde Arthur A. M., Perrot Andreas, Pankuweit Sabine, Zwinderman Aeilko H., Charron Philippe, Christiaans Imke, Pinto Yigal M. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers European journal of heart failure 2013;15 (4):376-384 [PubMed]
• van der Zwaag P. A., van Rijsingen I. A. W., de Ruiter R., Nannenberg E. A., Groeneweg J. A., Post J. G., Hauer R. N. W., van Gelder I. C., van den Berg M. P., van der Harst P., Wilde A. A. M., van Tintelen J. P. Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy Netherlands heart journal 2013;21 (6):286-293 [PubMed]

2012

• Nannenberg Eline A., Sijbrands Eric J. G., Dijksman Lea M., Alders Marielle, van Tintelen J. Peter, Birnie Martijn, van Langen Irene M., Wilde Arthur A. M. Mortality of Inherited Arrhythmia Syndromes Insight Into Their Natural History Circulation. Cardiovascular genetics 2012;5 (2):183-189 [PubMed]

2011

• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2011;19 (Suppl. S):32-37
• Nannenberg Eline A., Michels Michelle, Christiaans Imke, Majoor-Krakauer Danielle, Hoedemaekers Yvonne M., van Tintelen J. Peter, Lombardi M. Paola, ten Cate Folkert J., Schinkel Arend F. L., Tijssen Jan G. P., van Langen Irene M., Wilde Arthur A. M., Sijbrands Eric J. G. Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history Journal of the American College of Cardiology 2011;58 (23):2406-2414 [PubMed]

2010

• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2010;18 (5):248-254 [PubMed]

2009

• Postema P. G., van den Berg M., van Tintelen J. P., van den Heuvel F., Grundeken M., Hofman N., van der Roest W. P., Nannenberg E. A., Krapels I. P. C., Bezzina C. R., Wilde A. Founder mutations in the Netherlands SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide Netherlands heart journal 2009;17 (11):422-428 [PubMed]

2007

• Nannenberg E. A., Wilde A. A. M., van Langen I. M. Een familie met een aantal malen plotselinge hartdoodin: N. J. Leschot, D. L. Willems, editors. Probleemgeoriënteerd denken in de genetica in klinisch en ethisch perspectief. Utrecht: De Tijdstroom; 2007. p. 267-276, ISBN 9789058981073
• Hofman N., Postema P. G., van Langen I. M., Nannenberg E. A., Alders M., Jongbloed R., Smeets H. J. M., Wilde A. A. M. Genetische identificatie van patiënten en families met lange-QT-syndroom: grote regionale verschillen in de resultaten van 10 jaar Nederlands tijdschrift voor geneeskunde 2007;151 (11):644-648 [PubMed]
• van Tintelen J. Peter, Hofstra Robert M. W., Katerberg Hilga, Rossenbacker Tom, Wiesfeld Ans C. P., Sarvaas Gideon J. du Marchie, Wilde Arthur A. M., van Langen Irene M., Nannenberg Eline A., van der Kooi Anneke J., Kraak Marian, van Gelder Isabelle C., van Veldhuisen Dirk Jan, Vos Yvonne, van den Berg Maarten P. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics American heart journal 2007;154 (6):1130 1130-9-1139 [PubMed]
• Nannenberg Eline A., Wilde Arthur A. M. Syncope bij patiënt met een familieanamnese voor plotselinge dood.in: G. K. Hovingh, G. A. Somsen, editors. Probleemgeoriënteerd denken in de cardiologie. Utrecht: De Tijdstroom; 2007. p. 109-122, ISBN 9789058981080

2005

• Nannenberg Eline A., Bijlmer Rob, van Geel Bjorn M., Hennekam Raoul C. M. Neonatal paroxysmal trismus and camptodactyly: The Crisponi syndrome American journal of medical genetics. Part A 2005;133A (1):90-92 [PubMed]

2004

• Kuijpers Taco W., Nannenberg Eline, Alders Marielle, Bredius Robbert, Hennekam Raoul C. M. Congenital aplastic anemia caused by mutations in the SBDS gene: A rare presentation of Shwachman-Diamond syndrome Pediatrics 2004;114 (3):E387-E391 [PubMed]