Candy Kumps

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Gene Expression

Top Venues

Clinical genetics

European journal of human genetics : EJHG

International neurourology journal

This page only lists publications with an associated author ORCID identifier.

Publications

Candy Kumps, Erika D'haenens, Jennifer Kerkhof, Haley McConkey, Marielle Alders, Bekim Sadikovic, Olivier M Vanakker
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome. European journal of human genetics : EJHG (2023)
Maria Bejerholm Christensen, Amanda M Levy, Nazanin A Mohammadi, Marcello Niceta, Rauan Kaiyrzhanov, Maria Lisa Dentici, Chadi Al Alam, Viola Alesi, Valérie Benoit, Kailash P Bhatia, Tatjana Bierhals, Christian Malte Boßelmann, Julien Buratti, Bert Callewaert, Berten Ceulemans, Perrine Charles, Matthias De Wachter, Mohammadreza Dehghani, Erika D'haenens, Martine Doco-Fenzy, Michaela Geßner, Cyrielle Gobert, Ulviyya Guliyeva, Tobias B Haack, Trine B Hammer, Tilman Heinrich, Maja Hempel, Theresia Herget, Ute Hoffmann, Judit Horvath, Henry Houlden, Boris Keren, Christina Kresge, Candy Kumps, Damien Lederer, Alban Lermine, Francesca Magrinelli, Reza Maroofian, Mohammad Yahya Vahidi Mehrjardi, Mahdiyeh Moudi, Amelie J Müller, Anna J Oostra, Beth A Pletcher, David Ros-Pardo, Shanika R Samarasekera, Tartaglia Marco, Kristof Van Schil, Julie Vogt, Evangeline Wassmer, Juliane Winkelmann, Maha Saad Zaki, Michael Zech, Holger Lerche, Francesca Clementina Radio, Paulino Gómez-Puertas, Rikke Steensjerre Moller, Zeynep Tümer
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Clinical genetics 102 (2) (2022)
Diego Lopergolo, Flavia Privitera, Giuseppe Castello, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Anna Maria Pinto, Francesca Ariani, Aurora Currò, Vittoria Lamacchia, Roberto Canitano, Elisabetta Vaghi, Alessandra Ferrarini, Gerardo Mejia Baltodano, Damien Lederer, Lionel Van Maldergem, Mercedes Serrano, Mercè Pineda, Maria Del Carmen Fons-Estupina, Hilde Van Esch, Jeroen Breckpot, Candy Kumps, Bert Callewaert, Sabrina Mueller, Gian Paolo Ramelli, Judith Armstrong, Alessandra Renieri, Francesca Mari
IQSEC2 disorder: A new disease entity or a Rett spectrum continuum? Clinical genetics 99 (3) (2021)
Candy Kumps, Erika D'haenens, Sarah Vergult, Jasmine Leus, Rudy van Coster, Anna Jansen, Koen Devriendt, Anna Oostra, Olivier M Vanakker
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clinical genetics 99 (3) (2021)
Laurens Weynants, François Hervé, Veerle H Decalf, Candy Kumps, Ronny Pieters, Bart de Troyer, Karel Everaert
Clean Intermittent Self-Catheterization as a Treatment Modality for Urinary Retention: Perceptions of Urologists. International neurourology journal 21 (3) (2017)