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Current Oncology (Toronto, Ont.)
|
March 26, 2025
Barriers and Facilitators to Delivering Multifactorial Risk Assessment and Communication for Personalized Breast Cancer Screening: A Qualitative Study Exploring Implementation in Canada
Meghan J Walker, Anna Neely, Antonis C Antoniou, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 3, 2017
Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome
Christian P Kratz, Maria Isabel Achatz, Laurence Brugières, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
April 18, 2023
Homologous recombination deficiency in newly diagnosed FIGO stage III/IV high-grade epithelial ovarian cancer: a multi-national observational study
Robert D Morgan, Andrew R Clamp, Bethany M Barnes, et al.
Human Mutation
|
October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD
Christopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 17, 2023
Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial
Robert D Morgan, Andrew R Clamp, Daniel J White, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 14, 2025
Psychological and emotional impacts of communicating breast cancer risk using multifactorial assessment with polygenic risk score: findings from PERSPECTIVE I&I
Laurence Lambert-Côté, Annie Turgeon, Kristina M Blackmore, et al.
Ebiomedicine
|
October 21, 2019
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry
Yaohua Yang, Xiang Shu, Xiao-Ou Shu, et al.
Nature Genetics
|
October 26, 2010
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Richard S Houlston, Jeremy Cheadle, Sara E Dobbins, et al.
Nature Genetics
|
April 1, 2008
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Ian P M Tomlinson, Emily Webb, Luis Carvajal-Carmona, et al.
American Journal of Human Genetics
|
January 2, 2018
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848
Magdalena Koczkowska, Yunjia Chen, Tom Callens, et al.
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Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Current Oncology (Toronto, Ont.)
|
March 26, 2025
Barriers and Facilitators to Delivering Multifactorial Risk Assessment and Communication for Personalized Breast Cancer Screening: A Qualitative Study Exploring Implementation in Canada
Meghan J Walker, Anna Neely, Antonis C Antoniou, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 3, 2017
Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome
Christian P Kratz, Maria Isabel Achatz, Laurence Brugières, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
April 18, 2023
Homologous recombination deficiency in newly diagnosed FIGO stage III/IV high-grade epithelial ovarian cancer: a multi-national observational study
Robert D Morgan, Andrew R Clamp, Bethany M Barnes, et al.
Human Mutation
|
October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD
Christopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 17, 2023
Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial
Robert D Morgan, Andrew R Clamp, Daniel J White, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 14, 2025
Psychological and emotional impacts of communicating breast cancer risk using multifactorial assessment with polygenic risk score: findings from PERSPECTIVE I&I
Laurence Lambert-Côté, Annie Turgeon, Kristina M Blackmore, et al.
Ebiomedicine
|
October 21, 2019
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry
Yaohua Yang, Xiang Shu, Xiao-Ou Shu, et al.
Nature Genetics
|
October 26, 2010
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Richard S Houlston, Jeremy Cheadle, Sara E Dobbins, et al.
Nature Genetics
|
April 1, 2008
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Ian P M Tomlinson, Emily Webb, Luis Carvajal-Carmona, et al.
American Journal of Human Genetics
|
January 2, 2018
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848
Magdalena Koczkowska, Yunjia Chen, Tom Callens, et al.
Page
of 11