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Cindy Badoer

Observed name: C. Badoer
OpenAlex ID: A5041559459
Digenic inheritance of human primary microcephaly delineates centrosomal and non‐centrosomal pathways
2019 · Sarah Duerinckx, Valérie Jacquemin, et al. · Human Mutation · 25
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Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy
2021 · Sarah Duerinckx, Julie Désir, et al. · Molecular Genetics & Genomic Medicine · 20
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POT1 tumour predisposition: a broader spectrum of associated malignancies and proposal for additional screening program
2024 · Marta Baptista Freitas, Laurence Desmyter, et al. · European Journal of Human Genetics · 15
Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders
2025 · Sebastian Neuens, Julie Soblet, et al. · European Journal of Medical Genetics · 10
Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samples
2016 · Cindy Badoer, Céline Garrec, et al. · Oncotarget · 10
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Prevalence and clinical impact of BRCA1/2 mutations in patients with de novo metastatic hormone-sensitive prostate cancer (mHSPC).
2020 · Nieves Martinez Chanza, Marie Tkint De Roodenbeke, et al. · Journal of Clinical Oncology · 2
Broader gene panels in carrier screening: Insights from the Belgian BeGECS cohort of 1,700 preconception couples
2026 · Rani Deventer, Hannah Verdin, et al. · Research Square
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P004 Newborn screening for cystic fibrosis (CF-NBS) in Wallonia-Brussels Federation (Belgium): report of first evaluation after 3 years
2024 · M. Thimmesch, G. Luis, et al. · Journal of Cystic Fibrosis
Phenotypes and genotypes in outbred and inbred Primary microcephaly: high incidence of epilepsy
2021 · Sarah Duerinckx, Julie Désir, et al.
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Works count: 9
Citation count: 82
H-index: 5
I10-index: 5
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