Research output per year
Research output per year
Fingerprint
Dive into the research topics where Daphne Heijsman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Research output
- 12 Article
-
FLNC missense variants in familial noncompaction cardiomyopathy
Waning, J., Hoedemaekers, Y., te Rijdt, W., IJpma, A., Heijsman, D., Caliskan, K., Hoendermis, E., Willems, T., van den Wijngaard, A., Suurmeijer, A., van Slegtenhorst, M., Jongbloed, J., Majoor - Krakauer, D. & van der Zwaag, P., 2019, In: Cardiogenetics. 9, 1, p. 9-13 5 p., 8181.Research output: Contribution to journal › Article › Professional › peer-review
Open AccessFile15 Downloads (Pure) -
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics
Vandervore, L., Schot, R., Kasteleijn, E., Oegema, R., Stouffs, K., Gheldof, A., Grochowska, M., Sterre, M., Unen, L., Wilke, M., Elfferich, P., van der Spek, P., Heijsman, D., Grandone, A., Demmers, J., Dekkers, D., Slotman, J., Kremers, G.-J., Schaaf, G. & Masius, R. & 12 others, , 2019, In: Brain. 142, p. 867-884 18 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile23 Citations (Scopus)26 Downloads (Pure) -
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
Quadri, M., Mandemakers, W., Grochowska, M., Masius, R., Geut, H., Fabrizio, E., Breedveld, G., Kuipers, D., Minneboo, M., Vergouw, L., Carreras Mascaro, A., Yonova, E., Simons, E., Zhao, T., Di Fonzo, A., Chang, H., Parchi, P., Melis, M., Guedes, L. & Criscuolo, C. & 37 others, , 2018, In: Lancet Neurology. 17, 7, p. 597-608 12 p.Research output: Contribution to journal › Article › Academic › peer-review
98 Citations (Scopus) -
Human mutations in integrator complex subunits link transcriptome integrity to brain development
Oegema, R., Baillat, D., Schot, R., Unen, L., Brooks, A., Kheradmand Kia, S., Hoogeboom, J., Xia, Z., Li, W., Cesaroni, M., Lequin, M., van Slegtenhorst, M., Dobyns, W., Coo, I., Verheijen, F., Kremer, A., van der Spek, P., Heijsman, D., Wagner, E. & Fornerod, M. W. J. & 1 others, , 2017, In: PLoS Genetics (online). 13, 5, e1006809.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile77 Citations (Scopus)14 Downloads (Pure) -
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TOR CH syndrome
Meuwissen, M., Schot, R., Buta, S., Oudesluijs, G., Tinschert, S., Speer, S., Li, Z., Unen, L., Heijsman, D., Goldmann, T., Lequin, M., Kros, J. M., Stam, W., Hermann, M., Willemsen, R., Brouwer, R., van Ijcken, W., Martin-Fernandez, M., Coo, I. & Dudink, J. & 8 others, , 2016, In: Journal of Experimental Medicine. 213, 7, p. 1163-1174 12 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile219 Citations (Scopus)17 Downloads (Pure)