The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
2016 · Nature Genetics · 350 citations
https://doi.org/10.1038/ng.3720
B
Bert Callewaert
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
272
Papers
11.4K
Citations
47
h-index
113
i10-index
Bert Callewaert is an academic researcher from Ghent University Hospital. The author has contributed to research in topics: Connective tissue disorders research & Genomics and Rare Diseases & Congenital heart defects research. The author has an h-index of 47, co-authored 232 publications.
ORCID: 0000-0002-9743-4205Papers by this author
worksPhenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
2018 · Genetics in Medicine · 106 citations
https://doi.org/10.1038/gim.2017.221
Redefining the MED13L syndrome
2015 · European Journal of Human Genetics · 80 citations
https://doi.org/10.1038/ejhg.2015.26
Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients
2016 · Genetics in Medicine · 55 citations
https://doi.org/10.1038/gim.2016.176
Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1
2014 · Molecular Genetics and Metabolism · 44 citations
https://doi.org/10.1016/j.ymgme.2014.05.003
Genes Associated With Hypertrophic Cardiomyopathy
2025 · Journal of the American College of Cardiology · 44 citations
https://doi.org/10.1016/j.jacc.2024.12.010
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat