Recent advances in the molecular understanding of glioblastoma

por Bleeker, Fonnet E., Molenaar, Remco J., Leenstra, Sieger
Publicado 2012

Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?

por Douma, Kirsten F. L., Bleeker, Fonnet E., Medendorp, Niki M., Croes, Emmelyn A. J., Smets, Ellen M. A.
Publicado 2018

Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome

por Geurts‐Giele, Willemina R., Rosenberg, Efraim H., van Rens, Anja, van Leerdam, Monique E., Dinjens, Winand N., Bleeker, Fonnet E.
Publicado 2019

Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation

por de Jong, Vincent M. T., Pruntel, Roelof, Steenbruggen, Tessa G., Bleeker, Fonnet E., Nederlof, Petra, Hogervorst, Frans B. L., linn, Sabine C.
Publicado 2022

Absence of AKT1 Mutations in Glioblastoma

por Bleeker, Fonnet E., Lamba, Simona, Zanon, Carlo, van Tilborg, Angela A., Leenstra, Sieger, Troost, Dirk, Hulsebos, Theo, Vandertop, W. Peter, Bardelli, Alberto
Publicado 2009

Mutational Profile of GNAQ (Q209) in Human Tumors

por Lamba, Simona, Felicioni, Lara, Buttitta, Fiamma, Bleeker, Fonnet E., Malatesta, Sara, Corbo, Vincenzo, Scarpa, Aldo, Rodolfo, Monica, Knowles, Margaret, Frattini, Milo, Marchetti, Antonio, Bardelli, Alberto
Publicado 2009

The prognostic IDH1(R132) mutation is associated with reduced NADP(+)-dependent IDH activity in glioblastoma

por Bleeker, Fonnet E., Atai, Nadia A., Lamba, Simona, Jonker, Ard, Rijkeboer, Denise, Bosch, Klazien S., Tigchelaar, Wikky, Troost, Dirk, Vandertop, W. Peter, Bardelli, Alberto, Van Noorden, Cornelis J. F.
Publicado 2010

Mutational profiling of kinases in glioblastoma

por Bleeker, Fonnet E, Lamba, Simona, Zanon, Carlo, Molenaar, Remco J, Hulsebos, Theo JM, Troost, Dirk, van Tilborg, Angela A, Vandertop, W Peter, Leenstra, Sieger, van Noorden, Cornelis JF, Bardelli, Alberto
Publicado 2014

CLINICAL AND BIOLOGICAL IMPLICATIONS OF ANCESTRAL AND NON-ANCESTRAL IDH1 AND IDH2 MUTATIONS IN MYELOID NEOPLASMS

por Molenaar, Remco J., Thota, Swapna, Nagata, Yasunobu, Patel, Bhumika, Clemente, Michael, Hirsh, Cassandra, Viny, Aaron D., Hosano, Naoko, Bleeker, Fonnet E., Meggendorfer, Manja, Alpermann, Tamara, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, van Noorden, Cornelis J.F., Radivoyevitch, Tomas, Caraway, Hetty, Makishima, Hideki, Miyano, Satoru, Sekeres, Mikkael A., Ogawa, Seishi, Haferlach, Torsten, Maciejewski, Jaroslaw P.
Publicado 2015

Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines

por Chau, Cindy, van Doorn, Remco, van Poppelen, Natasha M., van der Stoep, Nienke, Mensenkamp, Arjen R., Sijmons, Rolf H., van Paassen, Barbara W., van den Ouweland, Ans M. W., Naus, Nicole C., van der Hout, Annemieke H., Potjer, Thomas P., Bleeker, Fonnet E., Wevers, Marijke R., van Hest, Liselotte P., Jongmans, Marjolijn C. J., Marinkovic, Marina, Bleeker, Jaco C., Jager, Martine J., Luyten, Gregorius P. M., Nielsen, Maartje
Publicado 2019

Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study

por Postema, Floor A. M., Hopman, Saskia M. J., de Borgie, Corianne A. J. M., Aalfs, Cora M., Anninga, Jakob K., Berger, Lieke P. V., Bleeker, Fonnet E., Dommering, Charlotte J., van Eijkelenburg, Natasha K. A., Hammond, Peter, van den Heuvel-Eibrink, Marry M., Hol, Janna A., Kors, Wijnanda A., Letteboer, Tom G. W., Loeffen, Jan L. C. M., Meijer, Lisethe, Olderode-Berends, Maran J. W., Wagner, Anja, Hennekam, Raoul C., Merks, Johannes H. M.
Publicado 2021

Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre s...

por Postema, Floor A M, Hopman, Saskia M J, de Borgie, Corianne A J M, Hammond, Peter, Hennekam, Raoul C, Merks, Johannes H M, Aalfs, Cora M, Anninga, Jakob K, Berger, Lieke PV, Bleeker, Fonnet E, de Bont, Eveline SJM, de Borgie, Corianne AJM, Dommering, Charlotte J, van Eijkelenburg, Natasha KA, Hammond, Peter, Hennekam, Raoul C, van den Heuvel-Eibrink, Marry M, Hopman, Saskia MJ, Jongmans, Marjolijn CJ, Kors, Wijnanda A, Letteboer, Tom GW, Loeffen, Jan LCM, Merks, Johannes HM, Olderode-Berends, Maran JW, Postema, Floor AM, Wagner, Anja
Publicado 2017