Personal profile
Research interests
Inherited Cardiovascular Diseases
Specialisation
Clinical Geneticist
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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SDG 3 Good Health and Well-being
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Dive into the research topics where Eline Nannenberg is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Walsh, R., Adler, A., Amin, A. S., Abiusi, E., Care, M., Bikker, H., Amenta, S., Feilotter, H., Nannenberg, E. A., Mazzarotto, F., Trevisan, V., Garcia, J., Hershberger, R. E., Perez, M. V., Sturm, A. C., Ware, J. S., Zareba, W., Novelli, V., Wilde, A. A. M. & Gollob, M. H., 14 Apr 2022, In: European heart journal. 43, 15, p. 1500-1510 11 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile52 Downloads (Pure) -
Verklarende Mechanismen
Clur, S. A. B. B., Engelberts, A., Liebrechts-Akkerman, G. & Nannenberg, E. A., 2022, Wiegendood Kennis en Praktijk: Een uitgave van de Vereniging Ouders van Wiegedoodkinderen en de Expertisegroep Wiegendood van de Nederlandse Vereniging voor Kindergeneeskunde.Research output: Chapter in Book/Report/Conference proceeding › Chapter › Professional
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Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case: A heterozygous and a homozygous case
Bruyndonckx, L., Vogelzang, J. L., Bugiani, M., Straver, B., Kuipers, I. M., Onland, W., Nannenberg, E. A., Clur, S.-A. & & van der Crabben, S. N., Aug 2021, In: American journal of medical genetics. Part A. 185, 8, p. 2464-2470 7 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile26 Downloads (Pure) -
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Nantes Referral Center for inherited cardiac arrhythmia, Jan 2021, In: Genetics in medicine. 23, 1, p. 47-58 12 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome
Adler, A., Novelli, V., Amin, A. S., Abiusi, E., Care, M., Nannenberg, E. A., Feilotter, H., Amenta, S., Mazza, D., Bikker, H., Sturm, A. C., Garcia, J., Ackerman, M. J., Hershberger, R. E., Perez, M. V., Zareba, W., Ware, J. S., Wilde, A. A. M. & Gollob, M. H., 2020, In: Circulation. 141, 6, p. 418-428 11 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile87 Downloads (Pure)