Lindblom, Annika
Harvard University · University of Washington · Karolinska Institutet
10 papers on CoChatORCID 0000-0001-7675-7569
Most cited papers
- Verified
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer
Stacey, S. N., Manolescu, A., Sulem, P., Rafnar, T., Gudmundsson, J., Gudjonsson, S. A., Masson, G., Jakobsdottir, M., Thorlacius, S., Helgason, A., et al. (2007) · Nature Genetics
Genetic Associations and EpidemiologyBRCA gene mutations in cancer
Cited by 786
- Verified
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Vasen, H. F. A., Blanco, I., Aktan-Collan, K., Gopie, J. P., Alonso, A., Aretz, S., Bernstein, I., Bertario, L., Burn, J., Capella, G., et al. (2013) · Gut
Genetic factors in colorectal cancerBRCA gene mutations in cancer
Cited by 746
- Verified
Associations of breast cancer risk factors with tumor subtypes: A pooled analysis from the breast cancer association consortium studies
Yang, X. R., Chang-Claude, J., Goode, E. L., Couch, F. J., Nevanlinna, H., Milne, R. L., Gaudet, M., Schmidt, M. K., Broeks, A., Cox, A., et al. (2011) · JNCI: Journal of the National Cancer Institute
Cancer Risks and FactorsBreast Cancer Treatment Studies
Cited by 691
- Verified
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Study, A. O. C., Perry, J. R. B., The GENICA Network, kConFab, Study, T. L. C., The InterAct Consortium, Early Growth Genetics (EGG) Consortium, Day, F., Elks, C. E., Sulem, P., et al. (2014) · Nature
Hypothalamic control of reproductive hormonesGenetic Associations and Epidemiology
Cited by 604
- Verified
Age- and Tumor Subtype–Specific Breast Cancer Risk Estimates for CH EK 2 *1100delC Carriers
Schmidt, M. K., Hogervorst, F., van Hien, R., Cornelissen, S., Broeks, A., Adank, M. A., Meijers, H., Waisfisz, Q., Hollestelle, A., Schutte, M., et al. (2016) · Journal of Clinical Oncology
BRCA gene mutations in cancerBreast Lesions and Carcinomas
Cited by 173
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
EMBRACE, Dunning, A. M., Collaborators, G. S., HEBON, kConFab Investigators, Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., et al. (2016) · Nature Genetics
Genetic Associations and EpidemiologyEstrogen and related hormone effects
Cited by 161
- Verified
Body mass index and breast cancer survival: a Mendelian randomization analysis
Guo, Q., Burgess, S., Turman, C., Bolla, M. K., Wang, Q., Lush, M., Abraham, J., Aittomäki, K., Andrulis, I. L., Apicella, C., et al. (2017) · International Journal of Epidemiology
Cancer Risks and FactorsGenetic Associations and Epidemiology
Cited by 64
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Regulator of Chromosome Condensation 2 Identifies High-Risk Patients within Both Major Phenotypes of Colorectal Cancer
Bruun, J., Kolberg, M., Ahlquist, T. C., Røyrvik, E. C., Nome, T., Leithe, E., Lind, G. E., Merok, M. A., Rognum, T. O., Bjørkøy, G., et al. (2015) · Clinical Cancer Research
Genetic factors in colorectal cancerColorectal Cancer Treatments and Studies
Cited by 41
- Verified
No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast‐cancer families linked to 17q22
Luo, L., Lei, H., Du, Q., von Wachenfeldt, A., Kockum, I., Luthman, H., Vorechovsky, I., & Lindblom, A. (2002) · International Journal of Cancer
BRCA gene mutations in cancerDNA Repair Mechanisms
Cited by 28
- Verified
Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden
Wendt, C., Lindblom, A., Arver, B., von Wachenfeldt, A., & Margolin, S. (2015) · Hereditary Cancer in Clinical Practice
BRCA gene mutations in cancerMultiple and Secondary Primary Cancers
Cited by 16
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