Research output per year
Research output per year
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Dive into the research topics where Arpad Danos 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
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CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase
Krysiak, K., Danos, A. M., Saliba, J., McMichael, J. F., Coffman, A. C., Kiwala, S., Barnell, E. K., Sheta, L., Grisdale, C. J., Kujan, L., Pema, S., Lever, J., Ridd, S., Spies, N. C., Andric, V., Chiorean, A., Rieke, D. T., Clark, K. A., Reisle, C. & Venigalla, A. C. & 45 others, , Jan 6 2023, In: Nucleic acids research. 51, 1 D, p. D1230-D1241Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
A community approach to the cancer-variant-interpretation bottleneck
Krysiak, K., Danos, A. M., Kiwala, S., McMichael, J. F., Coffman, A. C., Barnell, E. K., Sheta, L., Saliba, J., Grisdale, C. J., Kujan, L., Pema, S., Lever, J., Spies, N. C., Chiorean, A., Rieke, D. T., Clark, K. A., Jani, P., Takahashi, H., Horak, P. & Ritter, D. I. & 32 others, , May 2022, In: Nature Cancer. 3, 5, p. 522-525 4 p.Research output: Contribution to journal › Comment/debate
Open Access3 Scopus citations -
Erratum: Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC) (Genetics in Medicine (2022) 24(5) (986–998), (S1098360022000016), (10.1016/j.gim.2022.01.001))
Horak, P., Griffith, M., Danos, A. M., Pitel, B. A., Madhavan, S., Liu, X., Chow, C., Williams, H., Carmody, L., Barrow-Laing, L., Rieke, D., Kreutzfeldt, S., Stenzinger, A., Tamborero, D., Benary, M., Rajagopal, P. S., Ida, C. M., Lesmana, H., Satgunaseelan, L. & Merker, J. D. & 27 others, , Sep 2022, In: Genetics in Medicine. 24, 9, p. 1991 1 p.Research output: Contribution to journal › Comment/debate
Open Access10 Scopus citations -
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease
Chiorean, A., Farncombe, K. M., Delong, S., Andric, V., Ansar, S., Chan, C., Clark, K., Danos, A. M., Gao, Y., Giles, R. H., Goldenberg, A., Jani, P., Krysiak, K., Kujan, L., Macpherson, S., Maher, E. R., McCoy, L. G., Salama, Y., Saliba, J. & Sheta, L. & 5 others, , Sep 2022, In: Human mutation. 43, 9, p. 1268-1285 18 p.Research output: Contribution to journal › Article › peer-review
Open Access7 Scopus citations -
Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions
Saliba, J., Church, A. J., Rao, S., Danos, A., Furtado, L. V., Laetsch, T., Zhang, L., Nardi, V., Lin, W. H., Ritter, D. I., Madhavan, S., Li, M. M., Griffith, O. L., Griffith, M., Raca, G. & Roy, A., Jun 2022, In: Cancer Genetics. 264-265, p. 50-59 10 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations