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Journal of Medical Genetics
|
October 12, 2012
Rare variants in XRCC2 as breast cancer susceptibility alleles
Florentine S Hilbers, Juul T Wijnen, Nicoline Hoogerbrugge, et al.
NPJ Precision Oncology
|
November 19, 2025
Paired tumor-normal sequencing provides insights into the CDKN2A-associated tumor spectrum
Kelsey E Breen, Nikita Mehta, Vignesh Ravichandran, et al.
Human Mutation
|
August 25, 2019
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma
Liying Zhang, Michael F Walsh, Sowmya Jairam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 6, 2018
Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future
Laura V Milko, Birgit H Funke, Ray E Hershberger, et al.
Journal of Hematology & Oncology
|
January 6, 2026
Multiple myeloma risk linked to DNA damage response genes
Michael Conry, Irina Ostrovnaya, Yelena Kemel, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 30, 2016
Reliable Detection of Mismatch Repair Deficiency in Colorectal Cancers Using Mutational Load in Next-Generation Sequencing Panels
Zsofia K Stadler, Francesca Battaglin, Sumit Middha, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 8, 2022
NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects
Sami Belhadj, Aliya Khurram, Chaitanya Bandlamudi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2024
Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors
Brent Mabey, Elisha Hughes, Matthew Kucera, et al.
JCO Precision Oncology
|
November 4, 2022
Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition
Elisha Hughes, Susanne Wagner, Dmitry Pruss, et al.
International Journal of Cancer
|
June 30, 2005
Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers
Carey A Cullinane, Jan Lubinski, Susan L Neuhausen, et al.
Page
of 43
Search research articles
Search
Showing results (211-220 of 429) with videos related to
Sort By:
Page
of 43
Journal of Medical Genetics
|
October 12, 2012
Rare variants in XRCC2 as breast cancer susceptibility alleles
Florentine S Hilbers, Juul T Wijnen, Nicoline Hoogerbrugge, et al.
NPJ Precision Oncology
|
November 19, 2025
Paired tumor-normal sequencing provides insights into the CDKN2A-associated tumor spectrum
Kelsey E Breen, Nikita Mehta, Vignesh Ravichandran, et al.
Human Mutation
|
August 25, 2019
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma
Liying Zhang, Michael F Walsh, Sowmya Jairam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 6, 2018
Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future
Laura V Milko, Birgit H Funke, Ray E Hershberger, et al.
Journal of Hematology & Oncology
|
January 6, 2026
Multiple myeloma risk linked to DNA damage response genes
Michael Conry, Irina Ostrovnaya, Yelena Kemel, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 30, 2016
Reliable Detection of Mismatch Repair Deficiency in Colorectal Cancers Using Mutational Load in Next-Generation Sequencing Panels
Zsofia K Stadler, Francesca Battaglin, Sumit Middha, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 8, 2022
NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects
Sami Belhadj, Aliya Khurram, Chaitanya Bandlamudi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2024
Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors
Brent Mabey, Elisha Hughes, Matthew Kucera, et al.
JCO Precision Oncology
|
November 4, 2022
Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition
Elisha Hughes, Susanne Wagner, Dmitry Pruss, et al.
International Journal of Cancer
|
June 30, 2005
Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers
Carey A Cullinane, Jan Lubinski, Susan L Neuhausen, et al.
Page
of 43