- ORCID iD
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0000-0002-5470-3276
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Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11
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- Journal Article
- A2
- open access
Evaluation of relative quantification of alternatively spliced transcripts using droplet digital PCR
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- PhD Thesis
- open access
From human genetics to radiobiology : in vitro radiosensitivity in individuals with a germline defect in DNA damage response genes
(2017) -
- Journal Article
- A1
- open access
Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay
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- Journal Article
- A1
- open access
RENEB accident simulation exercise
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In vitro cellular radiosensitivity in relationship to late normal tissue reactions in breast cancer patients : a multi-endpoint case-control study
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- Journal Article
- A1
- open access
Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation
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The G2 micronucleus-assay for the analysis of in vitro chromosomal radiosensitivity in individuals carrying a BRCA1 mutation
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- Journal Article
- A1
- open access
Hidden genetic variation in LCA9-associated congenital blindness explained by 5′UTR mutations and copy-number variations of NMNAT1
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The G2 micronucleus assay for the analysis of in vitro chromosomal radiosensitivity in individuals carrying a BRCA1 or BRCA2 mutation