Drs. E.A. Nannenberg publications

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Publications Drs. E.A. Nannenberg

Position
Other
Main activities
Patient care, Research
Specialisation
Clinical Geneticist
Focus of research

Inherited Cardiovascular Diseases

2018

  • Nannenberg EA, van Rijsingen IAW, van der Zwaag PA, van den Berg MP, van Tintelen JP, Tanck MWT, Ackerman MJ, Wilde AAM, Christiaans I, Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases. CIRC-GENOM PRECIS ME 2018;11 (10):UNSP e001797 [PubMed]
  • Rivaud MR, Jansen JA, Postema PG, Nannenberg EA, Mizusawa Y, van der Nagel R, Wolswinkel R, van der Made I, Marchal GA, Rajamani S, Belardinelli L, van Tintelen JP, Tanck MWT, van der Wal AC, de Bakker JMT, van Rijen HV, Creemers EE, Wilde AAM, van den Berg MP, van Veen TAB, Bezzina CR, Remme CA, A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy. EUR HEART J 2018;39 (31):2898-2907 [PubMed]

2017

  • Tadros R, Nannenberg EA, Lieve KV, Škorić-Milosavljević D, Lahrouchi N, Lekanne Deprez RH, Vendrik J, Reckman YJ, Postema PG, Amin AS, Bezzina CR, Wilde AAM, Tan HL, Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families. JACC CLIN ELECTROPHYSIOL 2017;3 (12):1400-1408 [PubMed]

2016

  • Hulsebos TJM, Kenter S, Baas F, Nannenberg EA, Bleeker FE, van Minkelen R, van den Ouweland AMW, Wesseling P, Flucke U, Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cells. GENE CHROMOSOME CANC 2016;55 (4):350-354 [PubMed]
  • Lodder EM, de Nittis P, Koopman CD, Wiszniewski W, Moura de Souza CF, Lahrouchi N, Guex N, Napolioni V, Tessadori F, Beekman L, Nannenberg EA, Boualla L, Blom NA, de Graaff W, Kamermans M , Cocciadiferro D, Malerba N, Mandriani B, Akdemir ZHC, Fish RJ, Eldomery MK, Ratbi I, Wilde AAM, de Boer T, Simonds WF, Neerman-Arbez M, Sutton VR, Kok F, Lupski JR, Reymond A, Bezzina CR, Bakkers J, Merla G, GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. AM J HUM GENET 2016;99 (3):704-710 [PubMed]
  • ten Sande JN , Postema PG, Boekholdt SM, Tan HL, van der Heijden JF, de Groot NMS, Volders PGA, Zeppenfeld K, Boersma LVA, Nannenberg EA, Christiaans I, Wilde AAM, Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus. HEART RHYTHM 2016;13 (4):905-912 [PubMed]

2015

  • Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, Ackerman MJ, Haunso S, Leenhardt A, Kääb S, Probst V, Redon R, Sharma S, Wilde A, Tfelt-Hansen J, Schwartz P, Roden DM, Bezzina CR, Olesen M, Darbar D, Guicheney P, Crotti L, Jamshidi Y, Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. CARDIOVASC RES 2015;106 (3):520-529 [PubMed]

2014

  • Nannenberg EA. Mortality in inherited cardiac diseases: Directing care in affected families. S.l.: s.n.; 2014. 176p. ISBN 9789462593886 [UvA Dissertations Online] Proefschrift Universiteit van Amsterdam. (Promotor(s): Wilde AAM, Sijbrands EJG; copromotor(s): Christiaans I)
  • van Rijsingen IAW, van der Zwaag PA, Groeneweg JA, Nannenberg EA, Jongbloed JDH, Zwinderman AH, Pinto YM, Dit Deprez RHL, Post JG, Tan HL, de Boer RA, Hauer RNW, Christiaans I, van den Berg MP, van Tintelen JP, Wilde AAM, Outcome in phospholamban R14del carriers: results of a large multicentre cohort study. CIRC-CARDIOVASC GENE 2014;7 (4):455-465 [PubMed]

2013

  • van der Zwaag PA, van Rijsingen IAW, de Ruiter R, Nannenberg EA, Groeneweg JA, Post JG, Hauer RNW, van Gelder IC, van den Berg MP, van der Harst P, Wilde AAM, van Tintelen JP, Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy. NETH HEART J 2013;21 (6):286-293 [PubMed]
  • van Rijsingen IAW, Nannenberg EA, Arbustini E, Elliott PM, Mogensen J, Hermans-van Ast JF, van der Kooi AJ, van Tintelen JP, van den Berg MP, Grasso M, Serio A, Jenkins S, Rowland C, Richard P, Wilde AAM, Perrot A, Pankuweit S, Zwinderman AH, Charron P, Christiaans I, Pinto YM, Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. EUR J HEART FAIL 2013;15 (4):376-384 [PubMed]

2012

  • Nannenberg EA, Sijbrands EJG, Dijksman LM, Alders M, van Tintelen JP, Birnie M, van Langen IM, Wilde AAM, Mortality of Inherited Arrhythmia Syndromes Insight Into Their Natural History. CIRC-CARDIOVASC GENE 2012;5 (2):183-189 [PubMed]

2011

  • Christiaans I, Nannenberg EA, Dooijes D, Jongbloed RJE, Michels M, Postema PG, Majoor-Krakauer D, van den Wijngaard A, Mannens MMAM, van Tintelen JP, van Langen IM, Wilde AAM, Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. NETH HEART J 2011;19 (Suppl. S):32-37
  • Nannenberg EA, Michels M, Christiaans I, Majoor-Krakauer D, Hoedemaekers YM, van Tintelen JP, Lombardi MP, ten Cate FJ, Schinkel AFL, Tijssen JGP, van Langen IM, Wilde AAM, Sijbrands EJG, Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history. J AM COLL CARDIOL 2011;58 (23):2406-2414 [PubMed]

2010

  • Christiaans I, Nannenberg EA, Dooijes D, Jongbloed RJE, Michels M, Postema PG, Majoor-Krakauer D, van den Wijngaard A, Mannens MMAM, van Tintelen JP, van Langen IM, Wilde AAM, Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. NETH HEART J 2010;18 (5):248-254 [PubMed]

2009

  • Postema PG, van den Berg M, van Tintelen JP, van den Heuvel F, Grundeken M, Hofman N, van der Roest WP, Nannenberg EA, Krapels IPC, Bezzina CR, 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. NETH HEART J 2009;17 (11):422-428 [PubMed]

2007

  • Hofman N, Postema PG, van Langen IM, Nannenberg EA, Alders M, Jongbloed R, Smeets HJM, Wilde AAM, Genetische identificatie van patiënten en families met lange-QT-syndroom: grote regionale verschillen in de resultaten van 10 jaar. NED TIJDSCHR GENEESKD 2007;151 (11):644-648 [PubMed]
  • Nannenberg EA, Wilde AAM. Syncope bij patiënt met een familieanamnese voor plotselinge dood. in: Hovingh GK, Somsen GA, editors. Probleemgeoriënteerd denken in de cardiologie. Utrecht: de Tijdstroom; 2007., p. 109-122
  • Nannenberg EA, Wilde AAM, van Langen IM. Een familie met een aantal malen plotselinge hartdood in: Leschot NJ, Willems DL, editors. Probleemgeoriënteerd denken in de genetica in klinisch en ethisch perspectief. Utrecht: De Tijdstroom; 2007., p. 267-276
  • van Tintelen JP, Hofstra RMW, Katerberg H, Rossenbacker T, Wiesfeld ACP, Sarvaas GJDM, Wilde AAM, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP, High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. AM HEART J 2007;154 (6):1130 1130-9-1139 [PubMed]

2005

  • Nannenberg EA, Bijlmer R, van Geel BM, Hennekam RCM, Neonatal paroxysmal trismus and camptodactyly: The Crisponi syndrome. AM J MED GENET A 2005;133A (1):90-92 [PubMed]

2004

  • Kuijpers TW, Nannenberg E, Alders M, Bredius R, Hennekam RCM, Congenital aplastic anemia caused by mutations in the SBDS gene: A rare presentation of Shwachman-Diamond syndrome. PEDIATRICS 2004;114 (3):E387-E391 [PubMed]