Entries of Dhaenens, Claire-Marie on the publication server

Runhart, Esmee H., Khan, Mubeen, Cornelis, Stéphanie S., Roosing, Susanne, Del Pozo-Valero, Marta, Lamey, Tina M., Liskova, Petra , Roberts, Lisa , Stöhr, Heidi, Klaver, Caroline C. W., Hoyng, Carel B., Cremers, Frans P. M., Dhaenens, Claire-Marie, AlTabishi, Alaa, Ayuso, Carmen, Banfi, Sandro, Ben-Yosef, Tamar, van den Born, L. Ingeborgh, Fakin, Ana, Farrar, G. Jane, Ferraz Sallum, Juliana Maria, Fujinami, Kaoru, Gorin, Michael B., Hlavata, Lucia, Kamakari, Smaragda, Kousal, Bohdan, MacDonald, Ian M., McLaren, Terri L., Matynia, Anna, Oldak, Monika, Podhajcer, Osvaldo L., Ramesar, Raj, De Roach, John N., Sharon, Dror, Simonelli, Francesca, Testa, Francesco, Thompson, Jennifer A., Tracewska, Anna M., Vincent, Andrea L. and Weber, Bernhard H. F. (2020) Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease. JAMA Ophthalmology 138 (10), p. 1035. Fulltext not available.

Sangermano, Riccardo , Garanto, Alejandro , Khan, Mubeen, Runhart, Esmee H., Bauwens, Miriam, Bax, Nathalie M., van den Born, L. Ingeborgh, Khan, Muhammad Imran, Cornelis, Stéphanie S., Verheij, Joke B. G. M., Pott, Jan-Willem R., Thiadens, Alberta A. H. J., Klaver, Caroline C. W., Puech, Bernard, Meunier, Isabelle, Naessens, Sarah, Arno, Gavin, Fakin, Ana, Carss, Keren J., Raymond, F. Lucy, Webster, Andrew R., Dhaenens, Claire-Marie, Stöhr, Heidi, Grassmann, Felix , Weber, Bernhard H. F., Hoyng, Carel B., De Baere, Elfride, Albert, Silvia , Collin, Rob W. J. and Cremers, Frans P. M. (2019) Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides. Genetics in Medicine 21 (8), pp. 1751-1760. Fulltext not available.