Tim Van Damme

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 9

Top Topics

Intellectual Disability

Heat Shock Protein

Top Venues

European journal of human genetics : EJHG

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

Publications

Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG 32 (9) (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Tim Van Damme, Marlies Colman, Delfien Syx, Fransiska Malfait
The Ehlers-Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism. Genes 13 (2) (2022)
Mahnaz Nikpour, Fredrik Noborn, Jonas Nilsson, Tim Van Damme, Olivier Kaye, Delfien Syx, Fransiska Malfait, Göran Larson
Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6-deficient spondylodysplastic Ehlers-Danlos syndrome. JIMD reports 63 (5) (2022)
Tim Van Damme, Nic Veys, Marijn M Speeckaert, Sigurd E Delanghe
Shunt Nephritis: A Case of Mistaken Identity. Acta clinica Belgica (2022)
Delfien Syx, Yoshihiro Ishikawa, Jan M Gebauer, Sergei P Boudko, Brecht Guillemyn, Tim Van Damme, Sanne D'hondt, Sofie Symoens, Sheela Nampoothiri, Douglas B Gould, Ulrich Baumann, Hans Peter Bächinger, Fransiska Malfait
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta. PLoS genetics 17 (2) (2021)
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)
Tim Van Damme, Alain Colige, Delfien Syx, Cecilia Giunta, Uschi Lindert, Marianne Rohrbach, Omid Aryani, Yasemin Alanay, Pelin Özlem Simsek-Kiper, Hester Y Kroes, Koen Devriendt, Marc Thiry, Sofie Symoens, Anne De Paepe, Fransiska Malfait
Expanding the clinical and mutational spectrum of the Ehlers-Danlos syndrome, dermatosparaxis type. Genetics in medicine : official journal of the American College of Medical Genetics 18 (9) (2016)