Gao, Jianjiong
Caris Life Sciences (United States)
30 papers on CoChatORCID 0000-0002-5739-1781
Most cited papers
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Multimodal data integration using machine learning improves risk stratification of high-grade serous ovarian cancer
Boehm, K. M., Aherne, E. A., Ellenson, L., Nikolovski, I., Alghamdi, M., Vázquez-García, I., Zamarin, D., Long Roche, K., Liu, Y., Patel, D., et al. (2022) · Nature Cancer
Ovarian cancer diagnosis and treatmentRadiomics and Machine Learning in Medical Imaging
Cited by 357
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Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Akdemir, K. C., Le, V. T., Chandran, S., Li, Y., Verhaak, R. G., Beroukhim, R., Campbell, P. J., Chin, L., Dixon, J. R., Futreal, P. A., et al. (2020) · Nature Genetics
Genomics and Chromatin DynamicsChromatin Remodeling and Cancer
Cited by 283
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Automated Real-World Data Integration Improves Cancer Outcome Prediction
Jee, J., Fong, C., Pichotta, K., Tran, T. N., Luthra, A., Waters, M., Fu, C., Altoe, M., Liu, S.-Y., Maron, S. B., et al. (2024) · Nature
Machine Learning in HealthcareCancer Genomics and Diagnostics
Cited by 188
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Comprehensive pan-genomic characterization of adrenocortical carcinoma
Zheng, S., Cherniack, A. D., Dewal, N., Moffitt, R. A., Danilova, L., Murray, B. A., Lerario, A. M., Else, T., Knijnenburg, T. A., Ciriello, G., et al. (2016) · Cancer Cell
Adrenal and Paraganglionic TumorsChromatin Remodeling and Cancer
Cited by 165
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A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
Variant Interpretation for Cancer Consortium, Wagner, A. H., Walsh, B., Mayfield, G., Tamborero, D., Sonkin, D., Krysiak, K., Deu-Pons, J., Duren, R. P., Gao, J., et al. (2020) · Nature Genetics
Genomics and Rare DiseasesCancer Genomics and Diagnostics
Cited by 164
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Abstract 99: Evolution of OncoKB, a precision oncology knowledgebase
Suehnholz, S. P., Kundra, R., Zhang, H., Smith, S., Nissan, M., Yao, Y., LaFave, L., Gala, K., Miles, L., Arcila, M. E., et al. (2021) · Cancer Research
Cancer Genomics and DiagnosticsGenomics and Rare Diseases
Cited by 3
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