dr. Kim De Leeneer
- ORCID iD
- 0000-0002-9319-411X
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BeSolveRD : the Belgian genome resource to resolve rare diseases
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.573-574 -
- Journal Article
- A1
- open access
ENIGMA CHEK2gether Project : a comprehensive study identifies functionally impaired CHEK2 germline missense variants associated with increased breast cancer risk
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- Journal Article
- A1
- open access
Noncoding aberrations in mismatch repair genes underlie a substantial part of the missing heritability in Lynch syndrome
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- Journal Article
- A1
- open access
Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores
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CRISPR-SID : identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping
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- Journal Article
- A1
- open access
Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients
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Integration of genomics and transcriptomics allows the identification of rare DNA damage defects in PID patients with a cancer predisposition
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Integration of genomics and transcriptomics to identify DNA damage defects in PID patients prone to cancer
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Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients
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Dealing with pseudogenes in in the next generation sequencing era