All papers authored by Guy Van Camp
Refreshing results…
2021
Lisse J. M. Tavernier 
,
Erik Fransen ,
Hanne Valgaeren ,
Guy Van Camp
,
Erik Fransen ,
Hanne Valgaeren ,
Guy Van Camp
Genetics of otosclerosis: finally catching up with other complex traits?
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Erik Fransen,
Hanne Valgaeren,
Katleen Janssens,
Manou Sommen,
Raphael De Ridder ,
Geert Vandeweyer,
Luigi Bisceglia,
Vincent Soler,
Alexander Hoischen ,
Geert Mortier,
François Malecaze,
Carina Koppen ,
Guy Van Camp
,
Geert Vandeweyer,
Luigi Bisceglia,
Vincent Soler,
Alexander Hoischen ,
Geert Mortier,
François Malecaze,
Carina Koppen ,
Guy Van Camp
Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes
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2019
Andries Paul Nagtegaal ,
Linda Broer ,
Nuno R. Zilhao,
Johanna Jakobsdottir,
Charles E. Bishop,
Marco Brumat,
Mark W. Christiansen,
Massimiliano Cocca ,
Yan Gao,
Nancy L. Heard-Costa ,
Daniel S. Evans,
Nathan Pankratz,
Sheila R. Pratt,
T. Ryan Price,
Christopher Spankovich
and 27 other authors
,
Linda Broer ,
Nuno R. Zilhao,
Johanna Jakobsdottir,
Charles E. Bishop,
Marco Brumat,
Mark W. Christiansen,
Massimiliano Cocca ,
Yan Gao,
Nancy L. Heard-Costa ,
Daniel S. Evans,
Nathan Pankratz,
Sheila R. Pratt,
T. Ryan Price,
Christopher Spankovich
and 27 other authors
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
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Lieselot Croes,
Erik Fransen,
Marieke Hylebos,
Kimberly Buys,
Christophe Hermans,
Glenn Broeckx ,
Marc Peeters,
Patrick Pauwels,
Ken Op de Beeck ,
Guy Van Camp
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,
Marc Peeters,
Patrick Pauwels,
Ken Op de Beeck ,
Guy Van Camp
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Hanne Valgaeren ,
Manou Sommen ,
Matthias Beyens ,
Geert Vandeweyer ,
Isabelle Schrauwen ,
Anne Schepers,
Isabelle Schatteman,
Vedat Topsakal ,
Ingeborg Dhooge ,
Henricus Kunst ,
Diego Zanetti ,
Alexander M. Huber ,
Alexander Hoischen ,
Erik Fransen ,
Guy Van Camp
,
Manou Sommen ,
Matthias Beyens ,
Geert Vandeweyer ,
Isabelle Schrauwen ,
Anne Schepers,
Isabelle Schatteman,
Vedat Topsakal ,
Ingeborg Dhooge ,
Henricus Kunst ,
Diego Zanetti ,
Alexander M. Huber ,
Alexander Hoischen ,
Erik Fransen ,
Guy Van Camp
Insufficient evidence for a role of SERPINF1 in otosclerosis
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Matias Morin,
Andrea M. Oza,
Rebecca K. Siegert,
Ahmad N. Abou Tayoun,
Tatsuo Matsunaga,
Jun Shen,
Wenying Zhang,
Lisa A. Schimmenti,
Mustafa Tekin,
Heidi L. Rehm,
Ignacio del Castillo,
Lim Jiin Ying,
Suzanne Leal,
Morag Lewis,
Xue Zhong Liu
and 58 other authors
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs
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2018
Gitta Boons,
Timon Vandamme,
Marc Peeters,
Katrien Janssens,
Karen Zwaenepoel,
Geert Roeyen,
Guy Van Camp ,
Ken Op de Beeck,
Matthias Beyens,
Ann Driessen
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,
Ken Op de Beeck,
Matthias Beyens,
Ann Driessen
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Isabelle Schrauwen,
Hanne Valgaeren,
Laura Tomas-Roca,
Manou Sommen,
Umut Altunoglu,
Mieke Wesdorp,
Matthias Beyens,
Erik Fransen,
Abdul Nasir,
Geert Vandeweyer,
Anne Schepers,
Malika Rahmoun,
Ellen van Beusekom,
Matt J. Huentelman,
Erwin Offeciers
and 16 other authors
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Anna Rita Fetoni,
Veronica Zorzi,
Fabiola Paciello,
Gaia Ziraldo,
Chiara Peres,
Marcello Raspa,
Ferdinando Scavizzi,
Anna Maria Salvatore,
Giulia Crispino,
Gabriella Tognola ,
Giulia Gentile,
Antonio Gianmaria Spampinato,
Denis Cuccaro,
Maria Guarnaccia,
Giovanna Morello
and 8 other authors
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,
Giulia Gentile,
Antonio Gianmaria Spampinato,
Denis Cuccaro,
Maria Guarnaccia,
Giovanna Morello
and 8 other authors
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Nele Boeckx ,
Reija Koukakis,
Ken Op de Beeck ,
Christian Rolfo ,
Guy Van Camp ,
Salvatore Siena,
Josep Tabernero,
Jean-Yves Douillard,
Thierry André ,
Marc Peeters
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,
Reija Koukakis,
Ken Op de Beeck ,
Christian Rolfo ,
Guy Van Camp ,
Salvatore Siena,
Josep Tabernero,
Jean-Yves Douillard,
Thierry André ,
Marc Peeters
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Behrouz Hassannia,
Bartosz Wiernicki,
Irina Ingold,
Feng Qu,
Simon Van Herck,
Yulia Y. Tyurina,
Hülya Bayır,
Behnaz A. Abhari,
Jose Pedro Friedmann Angeli,
Sze Men Choi,
Eline Meul,
Karen Heyninck,
Ken Declerck,
Chandra Sekhar Chirumamilla,
Maija Lahtela-Kakkonen
and 10 other authors
and 10 other authors
Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma
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