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BMC Cancer
|
February 23, 2019
Are rare cancer survivors at elevated risk of subsequent new cancers?
Dianne M Finkelstein, Nora K Horick, Ritesh Ramchandani, et al.
European Urology Oncology
|
February 17, 2026
Expanding Risk-adapted Early Detection of Prostate Cancer: A Call to Action for Men at High Risk
Maike K Klett, Peter Albers, Adam Kibel, et al.
Cancer
|
December 7, 2021
Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Breast Cancer Research and Treatment
|
May 13, 2023
Correction to: Pathogenic variants among females with breast cancer and a non‑breast cancer reveal opportunities for cancer interception
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Breast Cancer Research and Treatment
|
March 1, 2023
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 12, 2026
The biology of hypomorphic TP53 variants and implications for clinical management
Renyta Moses, Jacquelyn Powers, Alison S Levine, et al.
Data in Brief
|
December 22, 2021
Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data
Danielle K Manning, Priyanka Shivdasani, Diane R Koeller, et al.
JCO Precision Oncology
|
January 7, 2022
Evaluation of <i>TP53</i> Variants Detected on Peripheral Blood or Saliva Testing: Discerning Germline From Somatic <i>TP53</i> Variants
Alison N Schwartz, Sophie R Hyman, Samantha M Stokes, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2025
Low allele frequency variants identified on germline multi-gene panel testing for cancer predisposition can suggest the presence of constitutional mosaicism
Adela Rodriguez-Hernandez, Linda M Polfus, Brittany L Bychkovsky, et al.
Cancer Genetics
|
November 11, 2022
Concurrent Pathogenic Variants of BRCA1, MUTYH and CHEK2 in a Hereditary Cancer Family
Nihat Bugra Agaoglu, Ozden Hatirnaz Ng, Busra Unal, et al.
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of 8
Search research articles
Search
Showing results (11-20 of 75) with videos related to
Sort By:
Page
of 8
BMC Cancer
|
February 23, 2019
Are rare cancer survivors at elevated risk of subsequent new cancers?
Dianne M Finkelstein, Nora K Horick, Ritesh Ramchandani, et al.
European Urology Oncology
|
February 17, 2026
Expanding Risk-adapted Early Detection of Prostate Cancer: A Call to Action for Men at High Risk
Maike K Klett, Peter Albers, Adam Kibel, et al.
Cancer
|
December 7, 2021
Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Breast Cancer Research and Treatment
|
May 13, 2023
Correction to: Pathogenic variants among females with breast cancer and a non‑breast cancer reveal opportunities for cancer interception
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Breast Cancer Research and Treatment
|
March 1, 2023
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception
Brittany L Bychkovsky, Min-Tzu Lo, Amal Yussuf, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 12, 2026
The biology of hypomorphic TP53 variants and implications for clinical management
Renyta Moses, Jacquelyn Powers, Alison S Levine, et al.
Data in Brief
|
December 22, 2021
Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data
Danielle K Manning, Priyanka Shivdasani, Diane R Koeller, et al.
JCO Precision Oncology
|
January 7, 2022
Evaluation of <i>TP53</i> Variants Detected on Peripheral Blood or Saliva Testing: Discerning Germline From Somatic <i>TP53</i> Variants
Alison N Schwartz, Sophie R Hyman, Samantha M Stokes, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2025
Low allele frequency variants identified on germline multi-gene panel testing for cancer predisposition can suggest the presence of constitutional mosaicism
Adela Rodriguez-Hernandez, Linda M Polfus, Brittany L Bychkovsky, et al.
Cancer Genetics
|
November 11, 2022
Concurrent Pathogenic Variants of BRCA1, MUTYH and CHEK2 in a Hereditary Cancer Family
Nihat Bugra Agaoglu, Ozden Hatirnaz Ng, Busra Unal, et al.
Page
of 8