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Author Details

Eivind Hovig
Center for Bioinformatics, University of Oslo
1987
235
47
PMIDPaper TitleJournal TitlePublished Year
37962376JASPAR 2024: 20th anniversary of the open-access database of transcription factor binding profiles.Nucleic Acids Res2024
36251678Cooperative induction of receptor tyrosine kinases contributes to adaptive MAPK drug resistance in melanoma through the PI3K pathway.Cancer Rep (Hoboken)2023
37627152A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population.Cancers (Basel)2023
37622176Chromosomal instability and a deregulated cell cycle are intrinsic features of high-risk gastrointestinal stromal tumours with a metastatic potential.Mol Oncol2023
37181409Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.EClinicalMedicine2023
37467208hGSuite HyperBrowser: A web-based toolkit for hierarchical metadata-informed analysis of genomic tracks.PLoS One2023
36608656The genetic history of Scandinavia from the Roman Iron Age to the present.Cell2023
36573326screenwerk: a modular tool for the design and analysis of drug combination screens.Bioinformatics2023
35047825A comprehensive framework for analysis of microRNA sequencing data in metastatic colorectal cancer.NAR Cancer2022
35841045Correction to: Improving public cancer care by implementing precision medicine in Norway: IMPRESS-Norway.J Transl Med2022
35613827Durable and dynamic hTERT immune responses following vaccination with the long-peptide cancer vaccine UV1: long-term follow-up of three phase I clinical trials.J Immunother Cancer2022
35643867Clonal evolution after treatment pressure in multiple myeloma: heterogenous genomic aberrations and transcriptomic convergence.Leukemia2022
36428697Genetic Characterization in High-Risk Individuals from a Low-Resource City of Peru.Cancers (Basel)2022
36523963Mutational analysis and protein profiling predict drug sensitivity in multiple myeloma cell lines.Front Oncol2022
36182700The population genomic legacy of the second plague pandemic.Curr Biol2022
36163057Functional precision cancer medicine: drug sensitivity screening enabled by cell culture models.Trends Pharmacol Sci2022
36089578Characterization of the T cell receptor repertoire and melanoma tumor microenvironment upon combined treatment with ipilimumab and hTERT vaccination.J Transl Med2022
35948919Clonal evolution in primary breast cancers under sequential epirubicin and docetaxel monotherapy.Genome Med2022
34850127MirGeneDB 2.1: toward a complete sampling of all major animal phyla.Nucleic Acids Res2022
33257847Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Genet Med2021
33743481Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Eur J Cancer2021
33574832Editorial: Genomic Colocalization and Enrichment Analyses.Front Genet2021
33922147The Quandary of DNA-Based Treatment Assessment in De Novo Metastatic Prostate Cancer in the Era of Precision Oncology.J Pers Med2021
34046035Combining a Universal Telomerase Based Cancer Vaccine With Ipilimumab in Patients With Metastatic Melanoma - Five-Year Follow Up of a Phase I/IIa Trial.Front Immunol2021
34249331Recommendations for the FAIRification of genomic track metadata.F1000Res2021
34290704Telomerase as a Target for Therapeutic Cancer Vaccines and Considerations for Optimizing Their Clinical Potential.Front Immunol2021
34203177No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database Study.J Clin Med2021
34310709Cancer Predisposition Sequencing Reporter (CPSR): A flexible variant report engine for high-throughput germline screening in cancer.Int J Cancer2021
34002043The genetic structure of Norway.Eur J Hum Genet2021
31337882Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.Genet Med2020
34367618The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.F1000Res2020
31642479MirGeneDB 2.0: the metazoan microRNA complement.Nucleic Acids Res2020
31927437Computational approaches in cancer multidrug resistance research: Identification of potential biomarkers, drug targets and drug-target interactions.Drug Resist Updat2020
32050665Correction: Møller, P.; et al. Causes for Frequent Pathogenic <i>BRCA1</i> Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. <i>Cancers</i> 2019, <i>11</i>, 132.Cancers (Basel)2020
33214604Accuracy and efficiency of germline variant calling pipelines for human genome data.Sci Rep2020
32690931Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.Genet Med2020
32605315Dysregulation of MITF Leads to Transformation in MC1R-Defective Melanocytes.Cancers (Basel)2020
32939053Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor status.Br J Cancer2020
32365348Loss of Snord116 impacts lateral hypothalamus, sleep, and food-related behaviors.JCI Insight2020
32332858Tankyrase inhibition sensitizes melanoma to PD-1 immune checkpoint blockade in syngeneic mouse models.Commun Biol2020
32208873Molecularly matched therapy in the context of sensitivity, resistance, and safety; patient outcomes in end-stage cancer - the MetAction study.Acta Oncol2020
32374878Mutational dynamics and immune evasion in diffuse large B-cell lymphoma explored in a relapse-enriched patient series.Blood Adv2020
31598695MirGeneDB 2.0: the metazoan microRNA complement.Nucleic Acids Res2020
30303536From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America.Int J Cancer2019
31849974Diagnostic Profiling of the Human Public IgM Repertoire With Scalable Mimotope Libraries.Front Immunol2019
31704995PathTracer: High-sensitivity detection of differential pathway activity in tumours.Sci Rep2019
31442815A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries.Eur J Cancer2019
30988515Roadmap for a precision-medicine initiative in the Nordic region.Nat Genet2019
30862609Integrative genomic analysis of peritoneal malignant mesothelioma: understanding a case with extraordinary chemotherapy response.Cold Spring Harb Mol Case Stud2019
30804006Responsiveness to PD-1 Blockade in End-Stage Colon Cancer with Gene Locus 9p24.1 Copy-Number Gain.Cancer Immunol Res2019
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Collaborators

University of Oslo
Co-authored papers 37
Institute for Cancer Research, Oslo University Hospital
Co-authored papers 33
Institute for Cancer Research, Oslo University Hospital
Co-authored papers 22
Institute for Cancer Research, Oslo University Hospital
Co-authored papers 20
University of Oslo
Co-authored papers 19
Norwegian University of Science and Technology
Co-authored papers 14
Institute for Cancer Research, Oslo University Hospital
Co-authored papers 12
Center for Bioinformatics, University of Oslo
Co-authored papers 12
University of Mainz
Co-authored papers 12
Institute for Cancer Research, Norwegian Radium Hospital
Co-authored papers 10
Population Health Sciences Institute, Newcastle University
Co-authored papers 10
University of Oslo
Co-authored papers 8
Harvard School of Dental Medicine
Co-authored papers 7
University of Oslo
Co-authored papers 6
Mayo Clinic
Co-authored papers 6
NTNU - Norwegian University of Science and Technology
Co-authored papers 6
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers 6
Co-authored papers 6
University of Oslo
Co-authored papers 6
Mayo Clinic
Co-authored papers 6
Co-authored papers 5
Oslo University Hospital
Co-authored papers 5
University of Iceland
Co-authored papers 5
Co-authored papers 5
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Oslo University Hospital & Institute of Clinical Medicine, University of Oslo
Co-authored papers 4
Radiumhospitalet, Oslo University Hosptial
Co-authored papers 4
University of Iceland
Co-authored papers 4