104 Results

People

  1. Offit
    Offit
  2. Robson
    Robson
  3. Stadler
    Stadler
  4. Kauff
    Kauff
  5. Ellis
    Ellis
  6. Boyd
    Boyd
  7. Norton
    Norton
  8. Barakat
    Barakat
  9. Nafa
    Nafa
  10. Borgen
    Borgen

Groups

  1. Clinical Genetics Service (104)
  2. Department of Medicine (104)
  3. Population Sciences Research Program (104)
  4. Solid Tumor Oncology Division (104)
  5. Survivorship Research (101)
  6. GSK Faculty (96)
  7. Breast Medicine Service (47)
  8. Surgery (43)
  9. Center for Pancreatic Cancer Research (24)
  10. Epidemiology and Biostatistics (18)
  1. "middle aged"
  2. "Clinical Genetics Service"
Formats
  1. Journal Article (104)
Groups
  1. Clinical Genetics Service (104)
  2. Department of Medicine (104)
  3. Population Sciences Research Program (104)
  4. Solid Tumor Oncology Division (104)
  5. Survivorship Research (101)
  6. GSK Faculty (96)

More Groups

People
  1. Kenneth Offit (94)
  2. Mark Robson (43)
  3. Zsofia Stadler (22)
  4. Noah Kauff (21)
  5. Nathan Ellis (16)
  6. Khedoudja Nafa (15)

More People

Years
  1. 2023 (4)
  2. 2022 (4)
  3. 2021 (2)
  4. 2020 (1)
  5. 2019 (2)
  6. 2018 (1)

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Publications
  1. Breast Cancer Research and Treatment (6)
  2. Cancer (6)
  3. Cancer Epidemiology Biomarkers and Prevention (6)
  4. Cancer Research (6)
  5. Clinical Cancer Research (6)
  6. Journal of Clinical Oncology (6)

More Publications

Publishers
  1. American Association for Cancer Research (18)
  2. American Society of Clinical Oncology (10)
  3. Springer (9)
  4. Wiley Blackwell (7)
  5. Elsevier Inc. (6)
  6. Oxford University Press (6)

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Results (104)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
    Journal Article

    Levi, H.; Carmi, S.; Rosset, S.; Yerushalmi, R.; Zick, A.; Yablonski-Peretz, T.; The BCAC Consortium; Wang, Q.; Bolla, M. K.; Dennis, J.; more...
    Journal of Medical Genetics (2023)

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  • Summary of the experiences, knowledge, medical management, and family communication of monoallelic MUTYH carriers
    Journal Article

    McKenna, D. B.; Sanchez, P.; Powers, J.; Brower, J.; Wang, L.; Mueller, R.; Symecko, H.; Hamilton, J. G.; Wildman, T.; Domchek, S. M.; more...
    Journal of Genetic Counseling (2023)

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  • Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family
    Journal Article

    Yang, C.; Misyura, M.; Kane, S.; Rai, V.; Latham, A.; Zhang, L.
    Molecular Genetics and Genomic Medicine (2023)

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  • Gene-based confirmatory germline testing following tumor-only sequencing of prostate cancer
    Journal Article

    Truong, H.; Breen, K.; Nandakumar, S.; Sjoberg, D. D.; Kemel, Y.; Mehta, N.; Lenis, A. T.; Reisz, P. A.; Carruthers, J.; Benfante, N.; more...
    European Urology (2023)

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  • Methylation analyses reveal promoter hypermethylation as a rare cause of “second hit” in germline BRCA1-associated pancreatic ductal adenocarcinoma
    Journal Article

    Zheng-Lin, B.; Rainone, M.; Varghese, A. M.; Yu, K. H.; Park, W.; Berger, M.; Mehine, M.; Chou, J.; Capanu, M.; Mandelker, D.; more...
    Molecular Diagnosis and Therapy (2022)

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  • Inherited TP53 variants and risk of prostate cancer
    Journal Article

    Maxwell, K. N.; Cheng, H. H.; Powers, J.; Gulati, R.; Ledet, E. M.; Morrison, C.; Le, A.; Hausler, R.; Stopfer, J.; Hyman, S.; more...
    European Urology (2022)

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  • Simplified graded infusion strategy for mitigation of oxaliplatin hypersensitivity
    Journal Article

    Alonso Martinez, S.; Segal, N. H.; Cercek, A.; Yaeger, R.; Stadler, Z.; Kemeny, N. E.; Nusrat, M.; Shahrokni, A.; Connell, L.; Saltz, L. B.
    Clinical Colorectal Cancer (2022)

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  • Factors influencing patient preferences for telehealth cancer genetic counseling during the COVID-19 pandemic
    Journal Article

    Breen, K. E.; Tuman, M.; Bertelsen, C. E.; Sheehan, M.; Wylie, D.; Fleischut, M. H.; Offit, K.; Stadler, Z. K.; Salo-Mullen, E. E.; Hamilton, J. G.
    JCO Oncology Practice (2022)

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  • The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer
    Journal Article

    Yang, C.; Arnold, A. G.; Catchings, A.; Rai, V.; Stadler, Z. K.; Zhang, L.
    Breast Cancer Research and Treatment (2021)

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  • A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
    Journal Article

    Coignard, J.; Lush, M.; Beesley, J.; O’Mara, T. A.; Dennis, J.; Tyrer, J. P.; Barnes, D. R.; McGuffog, L.; Leslie, G.; Bolla, M. K.; more...
    Nature Communications (2021)

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