Fransiska Malfait

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 9

Top Venues

Human mutation

medRxiv : the preprint server for health sciences

American journal of medical genetics. Part C, Seminars in medical genetics

Genetics in medicine : official journal of the American College of Medical Genetics

Ghent University Hospital

Ghent University (PHD)

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

Affiliation History

Ghent University Hospital Sep 01 2009

Belgium

Researcher- Associate Professor :: Center for Medical Genetics

Education History

Ghent University Oct 01 1993 - Jul 01 2000

Belgium

PHD

Publications

Marlies Colman, Delfien Syx, Inge De Wandele, Lies Rombaut, Deborah Wille, Zoë Malfait, Mira Meeus, Anne-Marie Malfait, Jessica Van Oosterwijck, Fransiska Malfait
Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation. medRxiv : the preprint server for health sciences (2023)
Marlies Colman, Delfien Syx, Inge De Wandele, Lies Rombaut, Deborah Wille, Zoë Malfait, Mira Meeus, Anne-Marie Malfait, Jessica Van Oosterwijck, Fransiska Malfait
Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation. medRxiv : the preprint server for health sciences (2023)
Tibbe Dhooge, Tim Van Damme, Delfien Syx, Laura Muiño Mosquera, Sheela Nampoothiri, Anil Radhakrishnan, Pelin Özlem Şimsek Kiper, Gülen Eda Utine, Maryse Bonduelle, Isabelle Migeotte, Osama Essawi, Serdar Ceylaner, Adila Al Kindy, Brad Tinkle, Sofie Symoens, Fransiska Malfait
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome. Human mutation 42 (6) (2021)
Tibbe Dhooge, Delfien Syx, Trinh Hermanns-Lê, Ingrid Hausser, Geert Mortier, Jonathan Zonana, Sofie Symoens, Peter H Byers, Fransiska Malfait
Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen. Genetics in medicine : official journal of the American College of Medical Genetics 23 (12) (2021)
Rosaria Talarico, Silvia Aguilera, Alexander Tobias, Zahir Amoura, Ana M Antunes, Laurent Arnaud, Tadej Avcin, Lorenzo Beretta, Stefano Bombardieri, Gerd R Burmester, Sara Cannizzo, Lorenzo Cavagna, Benjamin Chaigne, Alain Cornet, Nathalie Costedoat-Chalumeau, Andrea Doria, Alessandro Ferraris, Rebecca Fischer-Betz, João E Fonseca, Charissa Frank, Andrea Gaglioti, Ilaria Galetti, Jürgen Grunert, Vera Guimarães, Eric Hachulla, Frederic Houssiau, Luca Iaccarino, Thomas Krieg, Marteen Limper, Fransiska Malfait, Xavier Mariette, Diana Marinello, Thierry Martin, Lisa Matthews, Marco Matucci-Cerinic, Alain Meyer, Carlomaurizio Montecucco, Luc Mouthon, Ulf Müller-Ladner, Simona Rednic, Vasco C Romão, Matthias Schneider, Vanessa Smith, Alberto Sulli, Farah Tamirou, Domenica Taruscio, Anna V Taulaigo, Enrique Terol, Angela Tincani, Simone Ticciati, Giuseppe Turchetti, P Martin van Hagen, Jacob M van Laar, Ana Vieira, Jeska K de Vries-Bouwstra, Maurizio Cutolo, Marta Mosca
The impact of COVID-19 on rare and complex connective tissue diseases: the experience of ERN ReCONNET. Nature reviews. Rheumatology 17 (3) (2021)
Marlies Colman, Delfien Syx, Inge De Wandele, Tibbe Dhooge, Sofie Symoens, Fransiska Malfait
Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers-Danlos syndrome. Human mutation 42 (10) (2021)
Fransiska Malfait, Marlies Colman, Robin Vroman, Inge De Wandele, Lies Rombaut, Rachel E Miller, Anne-Marie Malfait, Delfien Syx
Pain in the Ehlers-Danlos syndromes: Mechanisms, models, and challenges. American journal of medical genetics. Part C, Seminars in medical genetics 187 (4) (2021)
Juan Li, Marco Ritelli, Cindy S Ma, Geetha Rao, Tanwir Habib, Emilie Corvilain, Salim Bougarn, Sophie Cypowyj, Lucie Grodecká, Romain Levy, Vivien Béziat, Lei Shang, Kathryn J Payne, Danielle T Avery, Mélanie Migaud, Soraya Boucherit, Sabri Boughorbel, Andrea Guennoun, Maya Chrabieh, Franck Rapaport, Benedetta Bigio, Yuval Itan, Bertrand Boisson, Valérie Cormier-Daire, Delfien Syx, Fransiska Malfait, Nicoletta Zoppi, Laurent Abel, Tomas Freiberger, Harry C Dietz, Nico Marr, Stuart G Tangye, Marina Colombi, Jean Laurent Casanova, Anne Puel
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β. Science immunology 4 (41) (2020)
Angela F Brady, Serwet Demirdas, Sylvie Fournel-Gigleux, Neeti Ghali, Cecilia Giunta, Ines Kapferer-Seebacher, Tomoki Kosho, Roberto Mendoza-Londono, Michael F Pope, Marianne Rohrbach, Tim Van Damme, Anthony Vandersteen, Caroline van Mourik, Nicol Voermans, Johannes Zschocke, Fransiska Malfait
The Ehlers-Danlos syndromes, rare types. American journal of medical genetics. Part C, Seminars in medical genetics 175 (1) (2017)

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Publication Activity (10 Years)

Top Topics

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Fransiska Malfait