Specialization
Clinical Geneticist
Focus of research
Inherited Cardiovascular Diseases
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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
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Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case
Bruyndonckx, L., Vogelzang, J. L., Bugiani, M., 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 › Review article › Academic › peer-review
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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Walsh, R., Lahrouchi, N., Tadros, R., Kyndt, F., Glinge, C., Postema, P. G., Amin, A. S., Nannenberg, E. A., Ware, J. S., Whiffin, N., Mazzarotto, F., Škorić-Milosavljević, D., Krijger, C., Arbelo, E., Babuty, D., Barajas-Martinez, H., Beckmann, B. M., Bézieau, S., Bos, J. M. & Breckpot, J. & 31 others, , Jan 2021, In: Genetics in medicine. 23, 1, p. 47-58 12 p.Research output: Contribution to journal › Article › Academic › peer-review
- All publications