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Onderzoeker
Rajendra Bahadur Shahi
- Trefwoorden:Geneeskunde
- Disciplines:Bio-informatica van ziekten, Ontwikkeling van bio-informatica software, tools en databases, Medische genomics, Kankerdiagnose, Kankerbiologie, Medische transcriptomics
Affiliaties
- Faculteit van de Geneeskunde en Farmacie (Faculteit)
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Vanaf7 aug 2015 → Heden - Basis (bio)-medische wetenschappen (Departement)
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Vanaf15 mei 2021 → 14 mei 2023 - Basis (bio)-medische wetenschappen (Departement)
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Vanaf8 apr 2019 → 28 mrt 2021 - Basis (bio)-medische wetenschappen (Departement)
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Vanaf15 aug 2018 → 20 okt 2022 - Basis (bio)-medische wetenschappen (Departement)
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Vanaf15 aug 2018 → 9 sep 2018 - Observerende Klinische wetenschappen (Departement)
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Vanaf1 jan 2014 → 30 jun 2018 - Laboratorium Moleculaire Oncologie (Onderzoeksgroep)
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Vanaf1 jan 2012 → 22 mrt 2021 - Inwendige Geneeskundige Specialiteiten (Departement)
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Vanaf15 nov 2011 → 31 dec 2013 - Faculteit van de Geneeskunde en Farmacie (Faculteit)
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Vanaf25 sep 2009 → 16 sep 2011
Publicaties
1 - 5 van 5
- Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers(2024)Gepubliceerd in: BMC CancerISSN: 1471-2407Issue: 1Volume: 24
- Neo-Antigen mRNA Vaccines(2020)Gepubliceerd in: VaccinesISSN: 2076-393XIssue: 4Volume: 8Pagina's: 1-24
- The clinical characteristics of breast cancers with a familial risk in which no BRCA1/2 mutations were found are sometimes suggestive for a genetic etiology(2019)Gepubliceerd in: Journal of molecular and genetic medicineISSN: 1747-0862Issue: 2Volume: 13
- Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families(2019)Gepubliceerd in: BMC CancerISSN: 1471-2407Issue: 1Volume: 19
- Detection of EGFR-TK Domain-activating Mutations in NSCLC With Generic PCR-based Methods(2015)Gepubliceerd in: Applied Immunohistochemistry & Molecular MorphologyISSN: 1541-2016Issue: 3Volume: 23Pagina's: 163-171
Gelinkte datasets
1 - 8 van 8
- Additional file 6: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 1: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 3: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 11: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 5: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 9: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 8: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
- Additional file 4: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families