Bert Callewaert - Concepedia

Author

Bert Callewaert

Also Known As

Andi M. Lewis, B Callewaert, B. Callewaert, B.L. Callewaert, BL Callewaert, Bert Callewaert, Bert L Callewaert, Bert L. Callewaert, Bert Louis Callewaert, Callewaert Bert

274

Publications

11.3K

Citations

H-Index

113

Concepts

All Affiliations

Ghent University Hospital Ghent University Inserm Assistance Publique – Hôpitaux de Paris Johns Hopkins University

About

Bert Callewaert is an author at Ghent University Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	38	4.1K
2	Public Health	5	5	1.2K
3	Social Sciences	3	3	69
4	Health Sciences	2	2	402
5	Natural Sciences	1	1	99

Bert Callewaert

Publications

10.1K

Citations

H-Index

Page 1

	Year	Citations
The revised Ghent nosology for the Marfan syndrome: Table 1 Bart Loeys, Harry C. Dietz, Alan C. Braverman, Journal of Medical Genetics	2010	2.2K
Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor Bart Loeys, Ulrike Schwarze, Tammy M. Holm, New England Journal of Medicine	2006	1.6K
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 Laurence Faivre, Gwenaëlle Collod‐Béroud, Bart Loeys, The American Journal of Human Genetics Marfan SyndromeMendelian DisorderGenetic DisorderMedicineGenetics	2007	593
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome Paul Coucke, Andy Willaert, Marja W. Wessels, Nature Genetics Metabolic SyndromeArterial Tortuosity SyndromeMolecular PhysiologyAngiogenesisVascular Adaptation	2006	392
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies Claire Redin, Harrison Brand, Ryan L. Collins, Nature Genetics Human Congenital AnomaliesDevelopmental AnomalyDevelopmental BiologyCytogeneticsGenomic Landscape	2016	346
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection Marjolijn Renard, Catherine Francis, Rajarshi Ghosh, Journal of the American College of Cardiology Clinical ValidityAortic DiseasesGeneticsGenetic EpidemiologyAortic Dissection	2018	289
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly Daniela A. Braun, Jia Rao, Géraldine Mollet, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsNephrotic Syndrome	2017	212
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families Bert Callewaert, Andy Willaert, Wilhelmina S. Kerstjens‐Frederikse, Human Mutation Slc2a10 MutationsGeneticsVascular MalformationPathologyCongenital Heart Anomaly	2007	209
Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations Laurence Faivre, Alice Masurel‐Paulet, Gwenaëlle Collod‐Béroud, PEDIATRICS GeneticsGenetic EpidemiologyPathologyMolecular GeneticsRelated Type	2008	173
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD Marjolijn Renard, Bert Callewaert, Machteld Baetens, International Journal of Cardiology Acta2 MutationsMolecular PhysiologySignal TransductionSignaling PathwayFibroblast Growth Factor	2011	166

Page 1