Research output per year
Research output per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
External positions
Visiting Professor of Computational Biology and Artificial Intelligence, Computational Biology Research Group, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DS, UK.
1-Sept-2020 → 1-Sept-2023
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Dive into the research topics where Gerton Lunter is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Addition of tumor microenvironment immune cell composition to improve the performance of a predictive model for oral squamous cell carcinoma
Bisheshar, S. K., van der Kamp, M. F., de Vries, J., Slagter-Menkema, L., Schuuring, E. M. D., Lunter, G. A., Halmos, G. B. & van der Vegt, B., Jun-2024, In: Oral Oncology. 153, 7 p., 106830.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile2 Citations (Scopus)26 Downloads (Pure) -
Insertions and Deletions: Computational Methods, Evolutionary Dynamics, and Biological Applications
Redelings, B. D., Holmes, I., Lunter, G., Pupko, T. & Anisimova, M., Sept-2024, In: Molecular Biology and Evolution. 41, 9, 24 p., msae177.Research output: Contribution to journal › Review article › peer-review
Open AccessFile1 Citation (Scopus) -
Genetic association studies in critically ill patients: protocol for a systematic review
Cox, E. G. M., Zhang, W., van der Voort, P. H. J., Lunter, G., Keus, F. & Snieder, H., Dec-2023, In: Systematic Reviews. 12, 5 p., 233.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile62 Downloads (Pure) -
Lifestyle factors related to prevalent chronic disease multimorbidity: A population-based cross-sectional study
Niebuur, J., Vonk, J. M., Du, Y., de Bock, G. H., Lunter, G., Krabbe, P. F. M., Alizadeh, B. Z., Snieder, H., Smidt, N., Boezen, M. & Corpeleijn, E., 24-Jul-2023, In: PLoS ONE. 18, 7, 15 p., e0287263.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile6 Citations (Scopus)83 Downloads (Pure) -
Reliability of panel-based mutational signatures for immune-checkpoint-inhibition efficacy prediction in non-small cell lung cancer
Donker, H. C., Cuppens, K., Froyen, G., Groen, H. J. M., Hiltermann, T. J. N., Maes, B., Schuuring, E., Volders, P. J., Lunter, G. A. & van Es, B., Aug-2023, In: Lung Cancer. 182, 7 p., 107286.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile1 Citation (Scopus)95 Downloads (Pure)
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The impact of indels on bioinformatics, health, and evolution
Lunter, G. (Invited speaker)
23-Jul-2023Activity: Talk and presentation › Academic presentation › Academic
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Teaching machine learning: what and to whom?
Lunter, G. (Invited speaker)
3-Nov-2023Activity: Talk and presentation › Academic presentation › Academic
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Biology (Journal)
Lunter, G. (Editorial board member)
2017 → …Activity: Peer-review and editorial work › Editorial work › Academic
Datasets
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Additional file 3 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Pagnamenta, A. T. (Creator), Camps, C. (Creator), Giacopuzzi, E. (Creator), Taylor, J. M. (Creator), Hashim, M. (Creator), Calpena, E. (Creator), Kaisaki, P. J. (Creator), Hashimoto, A. (Creator), Yu, J. (Creator), Sanders, E. (Creator), Schwessinger, R. (Creator), Hughes, J. R. (Creator), Lunter, G. (Creator), Dreau, H. (Creator), Ferla, M. (Creator), Lange, L. (Creator), Kesim, Y. (Creator), Ragoussis, V. (Creator), Vavoulis, D. V. (Creator), Allroggen, H. (Creator), Ansorge, O. (Creator), Babbs, C. (Creator), Banka, S. (Creator), Baños-Piñero, B. (Creator), Beeson, D. (Creator), Ben-Ami, T. (Creator), Bennett, D. L. (Creator), Bento, C. (Creator), Blair, E. (Creator), Brasch-Andersen, C. (Creator), Bull, K. R. (Creator), Cario, H. (Creator), Cilliers, D. (Creator), Conti, V. (Creator), Davies, E. G. (Creator), Dhalla, F. (Creator), Dacal, B. D. (Creator), Dong, Y. (Creator), Dunford, J. E. (Creator), Guerrini, R. (Creator), Harris, A. L. (Creator), Hartley, J. (Creator), Hollander, G. (Creator), Javaid, K. (Creator), Kane, M. (Creator), Kelly, D. (Creator), Kelly, D. (Creator), Knight, S. J. L. (Creator), Kreins, A. Y. (Creator), Kvikstad, E. M. (Creator), Langman, C. B. (Creator), Lester, T. (Creator), Lines, K. E. (Creator), Lord, S. R. (Creator), Lu, X. (Creator), Mansour, S. (Creator), Manzur, A. (Creator), Maroofian, R. (Creator), Marsden, B. (Creator), Mason, J. (Creator), McGowan, S. J. (Creator), Mei, D. (Creator), Mlcochova, H. (Creator), Murakami, Y. (Creator), Németh, A. H. (Creator), Okoli, S. (Creator), Ormondroyd, E. (Creator), Ousager, L. B. (Creator), Palace, J. (Creator), Patel, S. Y. (Creator), Pentony, M. M. (Creator), Pugh, C. (Creator), Rad, A. (Creator), Ramesh, A. (Creator), Riva, S. G. (Creator), Roberts, I. (Creator), Roy, N. (Creator), Salminen, O. (Creator), Schilling, K. D. (Creator), Scott, C. (Creator), Sen, A. (Creator), Smith, C. (Creator), Stevenson, M. (Creator), Thakker, R. V. (Creator), Twigg, S. R. F. (Creator), Uhlig, H. H. (Creator), van Wijk, R. (Creator), Vona, B. (Creator), Wall, S. (Creator), Wang, J. (Creator), Watkins, H. (Creator), Zak, J. (Creator), Schuh, A. H. (Creator), Kini, U. (Creator), Wilkie, A. O. M. (Creator), Popitsch, N. (Creator) & Taylor, J. C. (Creator), figshare, 11-Sept-2024
DOI: 10.6084/m9.figshare.26990317.v1, https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Structural_and_non-coding_variants_increase_the_diagnostic_yield_of_clinical_whole_genome_sequencing_for_rare_diseases/26990317/1
Dataset
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Additional file 3 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Pagnamenta, A. T. (Creator), Camps, C. (Creator), Giacopuzzi, E. (Creator), Taylor, J. M. (Creator), Hashim, M. (Creator), Calpena, E. (Creator), Kaisaki, P. J. (Creator), Hashimoto, A. (Creator), Yu, J. (Creator), Sanders, E. (Creator), Schwessinger, R. (Creator), Hughes, J. R. (Creator), Lunter, G. (Creator), Dreau, H. (Creator), Ferla, M. (Creator), Lange, L. (Creator), Kesim, Y. (Creator), Ragoussis, V. (Creator), Vavoulis, D. V. (Creator), Allroggen, H. (Creator), Ansorge, O. (Creator), Babbs, C. (Creator), Banka, S. (Creator), Baños-Piñero, B. (Creator), Beeson, D. (Creator), Ben-Ami, T. (Creator), Bennett, D. L. (Creator), Bento, C. (Creator), Blair, E. (Creator), Brasch-Andersen, C. (Creator), Bull, K. R. (Creator), Cario, H. (Creator), Cilliers, D. (Creator), Conti, V. (Creator), Davies, E. G. (Creator), Dhalla, F. (Creator), Dacal, B. D. (Creator), Dong, Y. (Creator), Dunford, J. E. (Creator), Guerrini, R. (Creator), Harris, A. L. (Creator), Hartley, J. (Creator), Hollander, G. (Creator), Javaid, K. (Creator), Kane, M. (Creator), Kelly, D. (Creator), Kelly, D. (Creator), Knight, S. J. L. (Creator), Kreins, A. Y. (Creator), Kvikstad, E. M. (Creator), Langman, C. B. (Creator), Lester, T. (Creator), Lines, K. E. (Creator), Lord, S. R. (Creator), Lu, X. (Creator), Mansour, S. (Creator), Manzur, A. (Creator), Maroofian, R. (Creator), Marsden, B. (Creator), Mason, J. (Creator), McGowan, S. J. (Creator), Mei, D. (Creator), Mlcochova, H. (Creator), Murakami, Y. (Creator), Németh, A. H. (Creator), Okoli, S. (Creator), Ormondroyd, E. (Creator), Ousager, L. B. (Creator), Palace, J. (Creator), Patel, S. Y. (Creator), Pentony, M. M. (Creator), Pugh, C. (Creator), Rad, A. (Creator), Ramesh, A. (Creator), Riva, S. G. (Creator), Roberts, I. (Creator), Roy, N. (Creator), Salminen, O. (Creator), Schilling, K. D. (Creator), Scott, C. (Creator), Sen, A. (Creator), Smith, C. (Creator), Stevenson, M. (Creator), Thakker, R. V. (Creator), Twigg, S. R. F. (Creator), Uhlig, H. H. (Creator), van Wijk, R. (Creator), Vona, B. (Creator), Wall, S. (Creator), Wang, J. (Creator), Watkins, H. (Creator), Zak, J. (Creator), Schuh, A. H. (Creator), Kini, U. (Creator), Wilkie, A. O. M. (Creator), Popitsch, N. (Creator) & Taylor, J. C. (Creator), figshare, 11-Sept-2024
DOI: 10.6084/m9.figshare.26990317, https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Structural_and_non-coding_variants_increase_the_diagnostic_yield_of_clinical_whole_genome_sequencing_for_rare_diseases/26990317
Dataset
Press/Media
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AIHACKCOVID | Outcomes and winning team
19/07/2021
1 item of Media coverage
Press/Media: Expert Comment › Popular