Gorka Alkorta‐Aranburu

Navarre Institute of Health Research — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index4.1kcitations61works6.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(11), Genetic Associations and Epidemiology(6), Genetic and phenotypic traits in livestock(5), Pancreatic function and diabetes(5), CRISPR and Genetic Engineering(5)

Publications61 total

Water Kefir and Olive Leaf Polyphenols Attenuate Body Weight Gain and Excessive Adiposity in Diet-Induced Obese Rats
Nutraceuticals·2026Open Access
Familial mast cell–mediated angioedema: Description of 4 families
The Journal of Allergy and Clinical Immunology In Practice·2025
Mutational Analysis of Bile Cell‐Free DNA in Primary Sclerosing Cholangitis: A Pilot Study
Liver International·2025· 3 citedOpen Access
318 Comparison of two Automated Real-time PCR Systems on Cytological Smears in NSCLC: IDYLLA™ and AmoyDx® Pan Lung Cancer Panel
Laboratory Investigation·2025Open Access
Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma
Scientific Reports·2024· 5 citedOpen Access
Gut microbiota produces biofilm-associated amyloids with potential for neurodegeneration
Nature Communications·2024· 41 citedOpen Access
Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma
Research Square (Research Square)·2024Open Access
Continued lessons from the INS gene: An intronic mutation causing diabetes through a novel mechanism
UNC Libraries·2024· 2 citedOpen Access
Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma
EBioMedicine·2024· 2 citedOpen Access
Liquid biopsy for monitoring minimal residual disease in localized and locally-advanced non-small cell lung cancer after radical-intent treatment
The Journal of Liquid Biopsy·2024· 7 citedOpen Access
232P Identification of ‘secondary’ germline cancer predisposition variants from somatic tumour testing: Should we evolve towards universal screening?
Annals of Oncology·2023Open Access
Next-generation sequencing improves precision medicine in hearing loss
Frontiers in Genetics·2023· 6 citedOpen Access
Whole exome sequencing and machine learning germline analysis of individuals presenting with phenotypes of extreme high and low risk of developing tobacco-induced lung adenocarcinoma.
Journal of Clinical Oncology·2023Open Access
Laboratory Cross-Comparison and Ring Test Trial for Tumor BRCA Testing in a Multicenter Epithelial Ovarian Cancer Series: The BORNEO GEICO 60-0 Study
Journal of Personalized Medicine·2022· 3 citedOpen Access
NGS-Based Molecular Karyotyping of Multiple Myeloma: Results from the GEM12 Clinical Trial
Cancers·2022· 12 citedOpen Access
Primary trimethylaminuria syndrome: more than an unpleasant odor
International Journal of Dermatology·2022· 1 cited
Familial primary cutaneous amyloidosis: Caspase activation may be involved in amyloid formation
Experimental Dermatology·2022· 1 citedOpen Access
Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma
New England Journal of Medicine·2022· 244 citedOpen Access
Epitope spreading driven by the joint action of CART cells and pharmacological STING stimulation counteracts tumor escape via antigen-loss variants
Journal for ImmunoTherapy of Cancer·2021· 48 citedOpen Access
Next-generation sequencing of bile cell-free DNA for the early detection of patients with malignant biliary strictures
Gut·2021· 84 citedOpen Access
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Frequent Co-authors

Anna Di Rienzo(11), David Carmody(9), Ana Patiño‐García(9), David Witonsky(8), Daniela del Gaudio(8), Siri Atma W. Greeley(7), Cynthia M. Beall(6), Amha Gebremedhin(5), Jonathan K. Pritchard(5), R. I. Sukernik(4), Eric Shifrut(4), Laurence Pellerin(4), Baz Smith(4), Michael Haugwitz(4), Kathrin Schumann(4), Rosa Bacchetta(4), Eric Meffre(4), Neil Romberg(4), Alexander Marson(4), Soma Das(4)