Achatz, Maria Isabel
Hospital Sírio-Libanês
6 papers on CoChatORCID 0000-0001-6894-1219
Most cited papers
- Verified
TP53 mutations in human cancers: Functional selection and impact on cancer prognosis and outcomes
Petitjean, A., Achatz, M. I. W., Borresen-Dale, A. L., Hainaut, P., & Olivier, M. (2007) · Oncogene
Cancer-related Molecular PathwaysCancer Genomics and Diagnostics
Cited by 884
- Verified
Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome
Kratz, C. P., Achatz, M. I., Brugières, L., Frebourg, T., Garber, J. E., Greer, M.-L. C., Hansford, J. R., Janeway, K. A., Kohlmann, W. K., McGee, R., et al. (2017) · Clinical Cancer Research
Cancer-related Molecular PathwaysMultiple and Secondary Primary Cancers
Cited by 534
- Verified
Germline Testing in Patients With Breast Cancer: ASCO–Society of Surgical Oncology Guideline
Bedrosian, I., Somerfield, M. R., Achatz, M. I., Boughey, J. C., Curigliano, G., Friedman, S., Kohlmann, W. K., Kurian, A. W., Laronga, C., Lynce, F., et al. (2024) · Journal of Clinical Oncology
BRCA gene mutations in cancerBreast Lesions and Carcinomas
Cited by 216
- Verified
Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect
Garritano, S., Gemignani, F., Palmero, E. I., Olivier, M., Martel-Planche, G., Le Calvez-Kelm, F., Brugiéres, L., Vargas, F. R., Brentani, R. R., Ashton-Prolla, P., et al. (2010) · Human Mutation
Genetic Associations and EpidemiologyCancer-related Molecular Pathways
Cited by 153
- Verified
Clustering of TP53 variants into functional classes correlates with cancer risk and identifies different phenotypes of Li-Fraumeni syndrome
Montellier, E., Lemonnier, N., Penkert, J., Freycon, C., Blanchet, S., Amadou, A., Chuffart, F., Fischer, N. W., Achatz, M.-I., Levine, A. J., et al. (2024) · iScience
Cancer-related Molecular PathwaysGenomics and Rare Diseases
Cited by 29
- Verified
Fine resolution clustering of TP53 variants into functional classes predicts cancer risks and spectra among germline variant carriers
Montellier, E., Lemonnier, N., Penkert, J., Freycon, C., Blanchet, S., Amadou, A., Chuffart, F., Fischer, N., Achatz, M. I., Levine, A., et al. (2023) · iScience
Cancer-related Molecular PathwaysGenomics and Rare Diseases
Cited by 29
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