Bert Callewaert
Ghent University Hospital(BE)
Publications by Year
Research Areas
Connective tissue disorders research, Genomics and Rare Diseases, Congenital heart defects research, Genetics and Neurodevelopmental Disorders, Aortic Disease and Treatment Approaches
Most-Cited Works
- → The revised Ghent nosology for the Marfan syndrome: Table 1(2010)2,184 cited
- → Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor(2006)1,629 cited
- → Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study(2007)596 cited
- → Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome(2006)396 cited
- → The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies(2016)350 cited
- → Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection(2018)291 cited
- → Ehlers-Danlos syndromes and Marfan syndrome(2008)254 cited
- → Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly(2017)218 cited
- → Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families(2007)211 cited
- → Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic FBN1 Mutations(2008)173 cited