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L Nathanson

Showing results (371-380 of 528) with videos related to

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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 29, 2011
Genetic variation in IGF2 and HTRA1 and breast cancer risk among BRCA1 and BRCA2 carriersSusan L Neuhausen, Sean Brummel, Yuan Chun Ding, et al.
Cancer Cell|February 7, 2017
Comprehensive Molecular Characterization of Pheochromocytoma and ParagangliomaLauren Fishbein, Ignaty Leshchiner, Vonn Walter, et al.
Nature|January 8, 2025
Functional evaluation and clinical classification of BRCA2 variantsHuaizhi Huang, Chunling Hu, Jie Na, et al.
NPJ Breast Cancer|November 10, 2017
Erratum: Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer riskThomas P Slavin, Kara N Maxwell, Jenna Lilyquist, et al.
NPJ Breast Cancer|June 27, 2017
The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer riskThomas P Slavin, Kara N Maxwell, Jenna Lilyquist, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Implementation Science : IS|November 6, 2023
Protocol to evaluate sequential electronic health record-based strategies to increase genetic testing for breast and ovarian cancer risk across diverse patient populations in gynecology practicesHeather Symecko, Robert Schnoll, Rinad S Beidas, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 23, 2023
Uptake of Genetic Research Results and Patient-Reported Outcomes With Return of Results Incorporating Web-Based Predisclosure EducationMadison Kilbride, Brian L Egleston, Wendy K Chung, et al.
Breast Cancer Research and Treatment|January 4, 2012
The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriersYael Laitman, Karoline B Kuchenbaecker, Johanna Rantala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2014
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibilityAngela R Bradbury, Linda Patrick-Miller, Jessica Long, et al.
Pageof 53

Showing results (371-380 of 528) with videos related to

Sort By:
Pageof 53
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 29, 2011
Genetic variation in IGF2 and HTRA1 and breast cancer risk among BRCA1 and BRCA2 carriersSusan L Neuhausen, Sean Brummel, Yuan Chun Ding, et al.
Cancer Cell|February 7, 2017
Comprehensive Molecular Characterization of Pheochromocytoma and ParagangliomaLauren Fishbein, Ignaty Leshchiner, Vonn Walter, et al.
Nature|January 8, 2025
Functional evaluation and clinical classification of BRCA2 variantsHuaizhi Huang, Chunling Hu, Jie Na, et al.
NPJ Breast Cancer|November 10, 2017
Erratum: Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer riskThomas P Slavin, Kara N Maxwell, Jenna Lilyquist, et al.
NPJ Breast Cancer|June 27, 2017
The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer riskThomas P Slavin, Kara N Maxwell, Jenna Lilyquist, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Implementation Science : IS|November 6, 2023
Protocol to evaluate sequential electronic health record-based strategies to increase genetic testing for breast and ovarian cancer risk across diverse patient populations in gynecology practicesHeather Symecko, Robert Schnoll, Rinad S Beidas, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 23, 2023
Uptake of Genetic Research Results and Patient-Reported Outcomes With Return of Results Incorporating Web-Based Predisclosure EducationMadison Kilbride, Brian L Egleston, Wendy K Chung, et al.
Breast Cancer Research and Treatment|January 4, 2012
The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriersYael Laitman, Karoline B Kuchenbaecker, Johanna Rantala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2014
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibilityAngela R Bradbury, Linda Patrick-Miller, Jessica Long, et al.
Pageof 53