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STS pathogenic variants in a Dutch patient cohort clinically suspected for X-linked ichthyosis show genetic heterogeneity

Nagtzaam, Ivo F., van Leersum, Frank S., Kouwenberg, Laurie C.M., Blok, Marinus J., Vreeburg, Maaike, Steijlen, Peter M., Gostyński, Antoni, van Geel, Michel
Veröffentlicht in: British Journal of Dermatology ; volume 187, issue 5, page 820-822 ; ISSN 1365-2133 0007-0963;
2022

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Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients

Wieme, Greet, Kral, Jan, Rosseel, Toon, Zemankova, Petra, Parton, Bram, Vocka, Michal, Van Heetvelde, Mattias, Kleiblova, Petra, Blaumeiser, Bettina, Soukupova, Jana, van den Ende, Jenneke, Nehasil, Petr, Tejpar, Sabine, Borecka, Marianna, Garcia, Encarna B. Gomez, Blok, Marinus J., Safarikova, Marketa, Kalousova, Marta, Geboes, Karen, De Putter, Robin, Poppe, Bruce, De Leeneer, Kim, Kleibl, Zdenek, Janatova, Marketa, Claes, Kathleen B.M.
2021

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Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing data

Fokkema, Ivo F. A. C., van der Velde, Kasper J., Slofstra, Mariska K., Ruivenkamp, Claudia A. L., Vogel, Maartje J., Pfundt, Rolph, Blok, Marinus J., Lekanne Deprez, Ronald H., Waisfisz, Quinten, Abbott, Kristin M., Sinke, Richard J., Rahman, Rubayte, Nijman, Isaäc J., de Koning, Bart, Thijs, Gert, Wieskamp, Nienke, Moritz, Ruben J. G., Charbon, Bart, Saris, Jasper J., den Dunnen, Johan T., Laros, Jeroen F. J., Swertz, Morris A., van Gijn, Marielle E.
Veröffentlicht in: Fokkema , I F A C , van der Velde , K J , Slofstra , M K , Ruivenkamp , C A L , Vogel , M J , Pfundt , R , Blok , M J , Lekanne Deprez , R H , Waisfisz , Q , Abbott , K M , Sinke , R J , Rahman , R , Nijman , I J , de Koning , B , Thijs , G , Wieskamp , N , Moritz , R J G , Charbon , B , Saris , J J , den Dunnen , J T , Laros , J F J , Swertz , M A & van Gijn , M E 2019 , ' Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing data ' , Human Mutation , vol. 40 , no. 12 , pp. 2230-2238 . https://doi.org/10.1002/humu.23896;
2019