Amsterdam Cardiovascular Sciences

Aho Ilgun

BEng

Affiliatie UvA Support Staff, Amsterdam Cardiovascular Sciences Support Staff, Medical Biology

Specialization

Focus of research

Latest publications

Erratum: Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms(Genet Med (2021)23(103-110)(s41436020009394)(10.1038/s41436-020-00939-4))
van Walree, E. S., Dombrowsky, G., Jansen, I. E., Umićević Mirkov, M., Zwart, R., Ilgun, A., Guo, D., Clur, S-A. B., Amin, A. S., Savage, J. E., van der Wal, A. C., Waisfisz, Q., Maugeri, A., Wilsdon, A., Bu'Lock, F. A., Hurles, M. E., Dittrich, S., Berger, F., Audain Martinez, E., Christoffels, V. M., & 6 othersHitz, M-P., Milewicz, D. M., Posthuma, D., Meijers-Heijboer, H., Postma, A. V. & Mathijssen, I. B., 1 Apr 2022, In: Genetics in medicine. 24, 4, p. 965 1 p.
Research output: Contribution to journal › Comment/Letter to the editor › Academic
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
KORA-Study Group, Tanck, M. W. T., Christoffels, V. M., Boogerd, C. J. & Postma, A. V., 21 Jan 2022, In: Circulation Research. 130, 2, p. 166-180 15 p.
Research output: Contribution to journal › Article › Academic › peer-review
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)
Škorić-Milosavljević, D., Lahrouchi, N., Bosada, F. M., Dombrowsky, G., Williams, S. G., Lesurf, R., Tjong, F. V. Y., Walsh, R., el Bouchikhi, I., Breckpot, J., Audain, E., Ilgun, A., Beekman, L., Ratbi, I., Strong, A., Muenke, M., Heide, S., Muir, A. M., Hababa, M., Cross, L., & 31 othersZhou, D., Pastinen, T., Hitz, M-P., Abdul-Khaliq, H., Berger, F., Dähnert, I., Dittrich, S., Uebing, A., German Competence Network for Congenital Heart Defects, Stiller, B., Zackai, E., Atmani, S., Ouldim, K., Adadi, N., Steindl, K., Rauch, A., Brook, D., Wilsdon, A., Kuipers, I., Blom, N. A., Mulder, B. J., Mefford, H. C., Keren, B., Joset, P., Kruszka, P., Thiffault, I., Lodder, E. M., Clur, S-A. B., Christoffels, V. M., Postma, A. V. & Bezzina, C. R., Oct 2021, In: Genetics in medicine. 23, 10, p. 2013 1 p.
Research output: Contribution to journal › Comment/Letter to the editor › Academic
All publications

Amsterdam Cardiovascular Sciences

Aho Ilgun

Specialization

Focus of research

Erratum: Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms(Genet Med (2021)23(103-110)(s41436020009394)(10.1038/s41436-020-00939-4))

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)