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JAMA Oncology
|
November 12, 2015
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA
Kasmintan A Schrader, Donavan T Cheng, Vijai Joseph, et al.
The New England Journal of Medicine
|
May 28, 2015
Gene-panel sequencing and the prediction of breast-cancer risk
Douglas F Easton, Paul D P Pharoah, Antonis C Antoniou, et al.
European Journal of Cancer (Oxford, England : 1990)
|
May 8, 2019
Addressing the dichotomy between individual and societal approaches to personalised medicine in oncology
Roberto Salgado, David B Solit, David L Rimm, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 21, 2009
Feasibility trial of letrozole in combination with bevacizumab in patients with metastatic breast cancer
Tiffany A Traina, Hope S Rugo, James F Caravelli, et al.
Journal of Medical Genetics
|
April 10, 2019
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report
Amanda B Spurdle, Stephanie Greville-Heygate, Antonis C Antoniou, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
April 6, 2018
Breast Cancer Family History and Contralateral Breast Cancer Risk in Young Women: An Update From the Women's Environmental Cancer and Radiation Epidemiology Study
Anne S Reiner, Julia Sisti, Esther M John, et al.
Journal of the National Cancer Institute
|
July 9, 2021
Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome
Ozge Ceyhan-Birsoy, Pier Selenica, M Herman Chui, et al.
BMJ Open
|
April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
Salma Shickh, Marc Clausen, Chloe Mighton, et al.
Journal of the National Cancer Institute
|
April 5, 2017
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Karoline B Kuchenbaecker, Lesley McGuffog, Daniel Barrowdale, et al.
American Journal of Human Genetics
|
August 7, 2012
Rare de novo germline copy-number variation in testicular cancer
Zsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Page
of 22
Search research articles
Search
Showing results (141-150 of 218) with videos related to
Sort By:
Page
of 22
JAMA Oncology
|
November 12, 2015
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA
Kasmintan A Schrader, Donavan T Cheng, Vijai Joseph, et al.
The New England Journal of Medicine
|
May 28, 2015
Gene-panel sequencing and the prediction of breast-cancer risk
Douglas F Easton, Paul D P Pharoah, Antonis C Antoniou, et al.
European Journal of Cancer (Oxford, England : 1990)
|
May 8, 2019
Addressing the dichotomy between individual and societal approaches to personalised medicine in oncology
Roberto Salgado, David B Solit, David L Rimm, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 21, 2009
Feasibility trial of letrozole in combination with bevacizumab in patients with metastatic breast cancer
Tiffany A Traina, Hope S Rugo, James F Caravelli, et al.
Journal of Medical Genetics
|
April 10, 2019
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report
Amanda B Spurdle, Stephanie Greville-Heygate, Antonis C Antoniou, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
April 6, 2018
Breast Cancer Family History and Contralateral Breast Cancer Risk in Young Women: An Update From the Women's Environmental Cancer and Radiation Epidemiology Study
Anne S Reiner, Julia Sisti, Esther M John, et al.
Journal of the National Cancer Institute
|
July 9, 2021
Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome
Ozge Ceyhan-Birsoy, Pier Selenica, M Herman Chui, et al.
BMJ Open
|
April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
Salma Shickh, Marc Clausen, Chloe Mighton, et al.
Journal of the National Cancer Institute
|
April 5, 2017
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Karoline B Kuchenbaecker, Lesley McGuffog, Daniel Barrowdale, et al.
American Journal of Human Genetics
|
August 7, 2012
Rare de novo germline copy-number variation in testicular cancer
Zsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Page
of 22