prof. Jo Van Dorpe
- Work address
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C. Heymanslaan 10, ingang 22 - verdieping 2
9000 Gent - Jo.VanDorpe@UGent.be
- ORCID iD
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0000-0001-8175-2930
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Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophyand hearing loss
(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(Supplement 1). p.45-45 -
- Journal Article
- A1
- open access
Concordance, correlation, and clinical impact of standardized PD-L1 and TIL scoring in SCCHN
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- Journal Article
- open access
Apoptotic enteropathy, gluten intolerance, and IBD-like inflammation associated with lipotoxicity in DGAT1 deficiency–related diarrhea: a case report of a 17-year-old patient and literature review
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Distinct transcriptional programs in ascitic and solid cancer cells induce different responses to chemotherapy in high-grade serous ovarian cancer
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The added value of peroral cholangioscopy to diagnose intraductal papillary neoplasm of the bile duct
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Genomic features of lung-recurrent hormone-sensitive prostate cancer
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Atypical spindle cell/pleomorphic lipomatous tumor with pleomorphic hyalinizing angiectatic tumor-like growth pattern : a search for diagnostic clues
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- Journal Article
- A1
- open access
Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome
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- Journal Article
- A1
- open access
Update of pediatric lipomatous lesions : a clinicopathological, immunohistochemical and molecular overview
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- Journal Article
- A1
- open access
Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières syndrome with severe end-organ involvement