All papers authored by Dorien Schepers
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2021
Eline Simons 
,
Alain Labro,
Johan Saenen,
Aleksandra Nijak ,
Ewa Sieliwonczyk ,
Bert Vandendriessche ,
Małgorzata Dąbrowska,
Emeline M. Van Craenenbroeck,
Dorien Schepers ,
Lut Van Laer,
Bart L. Loeys,
Maaike Alaerts
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,
Alain Labro,
Johan Saenen,
Aleksandra Nijak ,
Ewa Sieliwonczyk ,
Bert Vandendriessche ,
Małgorzata Dąbrowska,
Emeline M. Van Craenenbroeck,
Dorien Schepers ,
Lut Van Laer,
Bart L. Loeys,
Maaike Alaerts
Upload
Aleksandra Nijak ,
Johan Saenen,
Alain J. Labro,
Dorien Schepers ,
Bart L. Loeys ,
Maaike Alaerts
,
Johan Saenen,
Alain J. Labro,
Dorien Schepers ,
Bart L. Loeys ,
Maaike Alaerts
iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives
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2018
Dorien Schepers ,
Giada Tortora,
Hiroko Morisaki,
Gretchen MacCarrick,
Mark Lindsay,
David Liang,
Sarju G. Mehta,
Jennifer Hague,
Judith Verhagen ,
Ingrid van de Laar ,
Marja Wessels,
Yvonne Detisch,
Mieke van Haelst,
Annette Baas,
Klaske Lichtenbelt
and 27 other authors
,
Giada Tortora,
Hiroko Morisaki,
Gretchen MacCarrick,
Mark Lindsay,
David Liang,
Sarju G. Mehta,
Jennifer Hague,
Judith Verhagen ,
Ingrid van de Laar ,
Marja Wessels,
Yvonne Detisch,
Mieke van Haelst,
Annette Baas,
Klaske Lichtenbelt
and 27 other authors
A mutation update on the LDS-associated genesTGFB2/3andSMAD2/3
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2012
Alexander J. Doyle,
Jefferson J. Doyle,
Seneca L. Bessling,
Samantha Maragh,
Mark E. Lindsay,
Dorien Schepers ,
Elisabeth Gillis,
Geert Mortier ,
Tessa Homfray,
Kimberly Sauls,
Russell A. Norris,
Nicholas D. Huso,
Dan Leahy,
David W. Mohr,
Mark J. Caulfield
and 9 other authors
,
Elisabeth Gillis,
Geert Mortier ,
Tessa Homfray,
Kimberly Sauls,
Russell A. Norris,
Nicholas D. Huso,
Dan Leahy,
David W. Mohr,
Mark J. Caulfield
and 9 other authors
Mutations in the TGF-β Repressor SKI Cause Shprintzen-Goldberg Syndrome with Aortic Aneurysm
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Mark E. Lindsay,
Dorien Schepers ,
Nikhita Ajit Bolar,
Jefferson J. Doyle,
Elena Gallo,
Justyna Fert-Bober,
Marlies J. E. Kempers,
Elliot K. Fishman,
Yichun Chen,
Loretha Myers,
Nikhita Ajit Bolar,
Djahita Bjeda,
Gretchen Oswald,
Abdullah F. Elias,
Howard P. Levy
and 16 other authors
,
Nikhita Ajit Bolar,
Jefferson J. Doyle,
Elena Gallo,
Justyna Fert-Bober,
Marlies J. E. Kempers,
Elliot K. Fishman,
Yichun Chen,
Loretha Myers,
Nikhita Ajit Bolar,
Djahita Bjeda,
Gretchen Oswald,
Abdullah F. Elias,
Howard P. Levy
and 16 other authors
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm
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