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Christa M. de Geus

Maastricht University

7H-index
15Paper Count
353Citation Count
Published Papers 7
Publication Date
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8
err2022-10-01
err16
errOAAI
errDingemans, Alexander J. M.; Truijen, Kim M. G.; van de Ven, Sam; Bernier, Raphael; Bongers, Ernie M. H. F.; Bouman, Arjan; de Graaff-Herder, Laura; Eichler, Evan E.; Gerkes, Erica H.; De Geus, Christa M.; van Hagen, Johanna M.; Jansen, Philip R.; Kerkhof, Jennifer; Kievit, Anneke J. A.; Kleefstra, Tjitske; Maas, Saskia M.; de Man, Stella A.; McConkey, Haley; Patterson, Wesley G.; Dobson, Amy T.; Prijoles, Eloise J.; Sadikovic, Bekim; Relator, Raissa; Stevenson, Roger E.; Stumpel, Connie T. R. M.; Heijligers, Malou; Stuurman, Kyra E.; Lohner, Katharina; Zeidler, Shimriet; Lee, Jennifer A.; Lindy, Amanda; Zou, Fanggeng; Tedder, Matthew L.; Vissers, Lisenka E. L. M.; de Vries, Bert B. A.
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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
err2021-06-01
err45
errOAAI
errRots, Dmitrijs; Chater-Diehl, Eric; Dingemans, Alexander J. M.; Goodman, Sarah J.; Siu, Michelle T.; Cytrynbaum, Cheryl; Choufani, Sanaa; Hoang, Ny; Walker, Susan; Awamleh, Zain; Charkow, Joshua; Meyn, Stephen; Pfundt, Rolph; Rinne, Tuula; Gardeitchik, Thatjana; de Vries, Bert B. A.; Deden, A. Chantal; Leenders, Erika; Kwint, Michael; Stumpel, Constance T. R. M.; Stevens, Servi J. C.; Vermeulen, Jeroen R.; van Harssel, Jeske V. T.; Bosch, Danielle G. M.; van Gassen, Koen L., I; van Binsbergen, Ellen; de Geus, Christa M.; Brackel, Hein; Hempel, Maja; Lessel, Davor; Denecke, Jonas; Slavotinek, Anne; Strober, Jonathan; Crunk, Amy; Folk, Leandra; Wentzensen, Ingrid M.; Yang, Hui; Zou, Fanggeng; Millan, Francisca; Person, Richard; Xie, Yili; Liu, Shuxi; Ousager, Lilian B.; Larsen, Martin; Schultz-Rogers, Laura; Morava, Eva; Klee, Eric W.; Berry, Ian R.; Campbell, Jennifer; Lindstrom, Kristin; Pruniski, Brianna; Neumeyer, Ann M.; Radley, Jessica A.; Phornphutkul, Chanika; Schmidt, Berkley; Wilson, William G.; Ounap, Katrin; Reinson, Karit; Pajusalu, Sander; van Haeringen, Arie; Ruivenkamp, Claudia; Cuperus, Roos; Santos-Simarro, Fernando; Palomares-Bralo, Maria; Pacio-Miguez, Marta; Ritter, Alyssa; Bhoj, Elizabeth; Tonne, Elin; Tveten, Kristian; Cappuccio, Gerarda; Brunetti-Pierri, Nicola; Rowe, Leah; Bunn, Jason; Saenz, Margarita; Platzer, Konrad; Mertens, Mareike; Caluseriu, Oana; Nowaczyk, Malgorzata J. M.; Cohn, Ronald D.; Kannu, Peter; Alkhunaizi, Ebba; Chitayat, David; Scherer, Stephen W.; Brunner, Han G.; Vissers, Lisenka E. L. M.; Kleefstra, Tjitske; Koolen, David A.; Weksberg, Rosanna
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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns
err2021-02-01
err41
errOAAI
errStamberger, Hannah; Hammer, Trine B.; Gardella, Elena; Vlaskamp, Danique R. M.; Bertelsen, Birgitte; Mandelstam, Simone; de Lange, Iris; Zhang, Jing; Myers, Candace T.; Fenger, Christina; Afawi, Zaid; Fuerte, Edith P. Almanza; Andrade, Danielle M.; Balcik, Yunus; Ben Zeev, Bruria; Bennett, Mark F.; Berkovic, Samuel F.; Isidor, Bertrand; Bouman, Arjan; Brilstra, Eva; Busk, Oyvind L.; Cairns, Anita; Caumes, Roseline; Chatron, Nicolas; Dale, Russell C.; de Geus, Christa; Edery, Patrick; Gill, Deepak; Granild-Jensen, Jacob Bie; Gunderson, Lauren; Gunning, Boudewijn; Heimer, Gali; Helle, Johan R.; Hildebrand, Michael S.; Hollingsworth, Georgie; Kharytonov, Volodymyr; Klee, Eric W.; Koeleman, Bobby P. C.; Koolen, David A.; Korff, Christian; Kury, Sebastien; Lesca, Gaetan; Lev, Dorit; Leventer, Richard J.; Mackay, Mark T.; Macke, Erica L.; McEntagart, Meriel; Mohammad, Shekeeb S.; Monin, Pauline; Montomoli, Martino; Morava, Eva; Moutton, Sebastien; Muir, Alison M.; Parrini, Elena; Procopis, Peter; Ranza, Emmanuelle; Reed, Laura; Reif, Philipp S.; Rosenow, Felix; Rossi, Massimiliano; Sadleir, Lynette G.; Sadoway, Tara; Schelhaas, Helenius J.; Schneider, Amy L.; Shah, Krati; Shalev, Ruth; Sisodiya, Sanjay M.; Smol, Thomas; Stumpel, Connie T. R. M.; Stuurman, Kyra; Symonds, Joseph D.; Mau-Them, Frederic Tran; Verbeek, Nienke; Verhoeven, Judith S.; Wallace, Geoffrey; Yosovich, Keren; Zarate, Yuri A.; Zerem, Ayelet; Zuberi, Sameer M.; Guerrini, Renzo; Mefford, Heather C.; Patel, Chirag; Zhang, Yue-Hua; Moller, Rikke S.; Scheffer, Ingrid E.
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Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service
err2019-05-21
err37
PREAI
errWestra, Dineke; Schouten, Meyke, I; Stunnenberg, Bas C.; Kusters, Benno; Saris, Christiaan G. J.; Erasmus, Corrie E.; van Engelen, Baziel G.; Bulk, Saskia; Verschuuren-Bemelmans, Corien C.; Gerkes, E. H.; de Geus, Christa; van Der Zwaag, P. A.; Chan, Sophelia; Chung, Brian; Barge-Schaapveld, Daniela Q. C. M.; Kriek, Marjolein; Sznajer, Yves; Van Spaendonck-Zwarts, Karin; van Der Kooi, Anneke J.; Krause, Amanda; Schonewolf-Greulich, Bitten; De Die-Smulders, Christine; Sallevelt, Suzanne C. E. H.; Krapels, Ingrid P. C.; Rasmussen, Magnhild; Maystadt, Isabelle; Kievit, Anneke J. A.; Witting, Nanna; Pennings, Maartje; Meijer, Rowdy; Gillissen, Christian; Kamsteeg, Erik-Jan; Voermans, Nicol C.
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GRIN2A-related disorders: genotype and functional consequence predict phenotype
errBRAIN
IF11.7
err2018-12-12
err153
errOAAI
errStrehlow, Vincent; Heyne, Henrike O.; Vlaskamp, Danique R. M.; Marwick, Katie F. M.; Rudolf, Gabrielle; De Bellescize, Julitta; Biskup, Saskia; Brilstra, Eva H.; Brouwer, Oebele F.; Callenbach, Petra M. C.; Hentschel, Julia; Hirsch, Edouard; Kind, Peter C.; Mignot, Cyril; Platzer, Konrad; Rump, Patrick; Skehel, Paul A.; Wyllie, David J. A.; Hardingham, Giles E.; van Ravenswaaij-Arts, Conny M. A.; Lesca, Gaetan; Lemke, Johannes R.; Arzimanoglou, Alexis; Augustijn, Paul B.; Van Bogaert, Patrick; Bourry, Helene; Burfeind, Peter; Chu, Yoyo; Chung, Brian; Doummar, Diane; Edery, Patrick; Fattal-Valevski, Aviva; Fradin, Melanie; Gerard, Marion; de Geus, Christa; Gunning, Boudewijn; Hasaerts, Danielle; Helbig, Ingo; Helbig, Katherine L.; Jamra, Rami; Lyver, Melanie Jennesson; Wassink-Ruiter, Jolien S. Klein; Koolen, David A.; Lederer, Damien; Lunsing, Roelineke J.; Mathot, Mikael; Maurey, Helene; Menascu, Shay; Michel, Anne; Mirzaa, Ghayda; Mitter, Diana; Muhle, Hiltrud; Moller, Rikke S.; Nava, Caroline; O'Brien, Margaret; van Pinxteren-Nagler, Evelyn; van Riesen, Anne; Rougeot, Christelle; Sanlaville, Damien; Schieving, Jolanda H.; Syrbe, Steffen; Veenstra-Knol, Hermine E.; Verbeek, Nienke; Ville, Dorothee; Vos, Yvonne J.; Vrielynck, Pascal; Wagner, Sabrina; Weckhuysen, Sarah; Willemsen, Marjolein H.
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Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control Study
err2018-09-20
err8
errOAAI
errde Geus, C. M.; Bergman, J. E. H.; van Ravenswaaij-Arts, C. M. A.; Meiners, L. C.
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The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands
err2016-12-21
err100
errOAAI
errSeco, Celia Zazo; Wesdorp, Mieke; Feenstra, Ilse; Pfundt, Rolph; Hehir-Kwa, Jayne Y.; Lelieveld, Stefan H.; Castelein, Steven; Gilissen, Christian; de Wijs, Ilse J.; Admiraal, Ronald J. C.; Pennings, Ronald J. E.; Kunst, Henricus P. M.; van de Kamp, Jiddeke M.; Tamminga, Saskia; Houweling, Arjan C.; Plomp, Astrid S.; Maas, Saskia M.; Gans, Pia A. M. de Koning; Kant, Sarina G.; de Geus, Christa M.; Frints, Suzanna G. M.; Vanhoutte, Els K.; van Dooren, Marieke F.; van den Boogaard, Marie-Jose H.; Scheffer, Hans; Nelen, Marcel; Kremer, Hannie; Hoefsloot, Lies; Schraders, Margit; Yntema, Helger G.
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