Works by Deden


Results: 246
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    Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.

    Published in:
    2020
    By:
    • Deden, Chantal;
    • Neveling, Kornelia;
    • Zafeiropopoulou, Dimitra;
    • Gilissen, Christian;
    • Pfundt, Rolph;
    • Rinne, Tuula;
    • Leeuw, Nicole;
    • Faas, Brigitte;
    • Gardeitchik, Thatjana;
    • Sallevelt, Suzanne C. E. H.;
    • Paulussen, Aimee;
    • Stevens, Servi J. C.;
    • Sikkel, Esther;
    • Elting, Mariet W.;
    • Maarle, Merel C.;
    • Diderich, Karin E. M.;
    • Corsten‐Janssen, Nicole;
    • Lichtenbelt, Klaske D.;
    • Lachmeijer, Guus;
    • Vissers, Lisenka E. L. M.
    Publication type:
    journal article
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    Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands.

    Published in:
    European Journal of Pediatrics, 2023, v. 182, n. 6, p. 2683, doi. 10.1007/s00431-023-04909-1
    By:
    • Olde Keizer, Richelle A. C. M.;
    • Marouane, Abderrahim;
    • Kerstjens-Frederikse, Wilhelmina S.;
    • Deden, A. Chantal;
    • Lichtenbelt, Klaske D.;
    • Jonckers, Tinneke;
    • Vervoorn, Marieke;
    • Vreeburg, Maaike;
    • Henneman, Lidewij;
    • de Vries, Linda S.;
    • Sinke, Richard J.;
    • Pfundt, Rolph;
    • Stevens, Servi J. C.;
    • Andriessen, Peter;
    • van Lingen, Richard A.;
    • Nelen, Marcel;
    • Scheffer, Hans;
    • Stemkens, Daphne;
    • Oosterwijk, Cor;
    • van Amstel, Hans Kristian Ploos
    Publication type:
    Article
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    Inspirations in Planning: Edited by John Forester.

    Published in:
    Planning Theory & Practice, 2025, v. 26, n. 1, p. 109, doi. 10.1080/14649357.2025.2474336
    By:
    • Forester, John;
    • Balakrishnan, Sai;
    • Frimpong Boamah, Emmanuel;
    • Fullilove, Mindy Thompson;
    • Hoch, Charles;
    • Hou, Jeffrey;
    • Lim, Theodore;
    • Matthews, Senchel;
    • Mouat, Clare;
    • Purcell, Mark;
    • Rukmana, Deden;
    • Umemoto, Karen;
    • Yiftachel, Oren
    Publication type:
    Article
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    Lessons learned from rapid exome sequencing for 575 critically ill patients across the broad spectrum of rare disease.

    Published in:
    Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2023.1304520
    By:
    • Marouane, Abderrahim;
    • Neveling, Kornelia;
    • Deden, A. Chantal;
    • van den Heuvel, Simone;
    • Zafeiropoulou, Dimitra;
    • Castelein, Steven;
    • van de Veerdonk, Frank;
    • Koolen, David A.;
    • Simons, Annet;
    • Rodenburg, Richard;
    • Westra, Dineke;
    • Mensenkamp, Arjen R.;
    • de Leeuw, Nicole;
    • Ligtenberg, Marjolijn;
    • Matthijsse, Rene;
    • Pfundt, Rolph;
    • Kamsteeg, Erik Jan;
    • Brunner, Han G.;
    • Gilissen, Christian;
    • Feenstra, Ilse
    Publication type:
    Article
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