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JAMA Network Open
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January 9, 2025
Breast Cancer Susceptibility Gene Sequence Variations and Development of Contralateral Breast Cancer
Anne S Reiner, Gordon P Watt, Kathleen E Malone, et al.
Plos One
|
November 26, 2025
CanRisk-GP protocol: A feasibility study of incorporating proactive multifactorial breast cancer risk assessment into general practice
Francisca Stutzin Donoso, Stephanie Archer, Fiona M Walter, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 17, 2008
Large genomic deletions in AIP in pituitary adenoma predisposition
Marianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
Cancer Discovery
|
December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer
Susan M Domchek, Jiangbo Tang, Jill Stopfer, et al.
Trials
|
February 2, 2024
Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocol
Miriam Dixon-Zegeye, Rachel Shaw, Linda Collins, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 9, 2022
CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer
Tommy Nyberg, Mark N Brook, Lorenzo Ficorella, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 22, 2019
Correction: BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 16, 2019
BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, et al.
Human Mutation
|
May 22, 2009
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families
George Chong, Jonathan Jarry, Victoria Marcus, et al.
Nature Genetics
|
January 4, 2007
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Sarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Page
of 26
Search research articles
Search
Showing results (111-120 of 258) with videos related to
Sort By:
Page
of 26
JAMA Network Open
|
January 9, 2025
Breast Cancer Susceptibility Gene Sequence Variations and Development of Contralateral Breast Cancer
Anne S Reiner, Gordon P Watt, Kathleen E Malone, et al.
Plos One
|
November 26, 2025
CanRisk-GP protocol: A feasibility study of incorporating proactive multifactorial breast cancer risk assessment into general practice
Francisca Stutzin Donoso, Stephanie Archer, Fiona M Walter, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 17, 2008
Large genomic deletions in AIP in pituitary adenoma predisposition
Marianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
Cancer Discovery
|
December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer
Susan M Domchek, Jiangbo Tang, Jill Stopfer, et al.
Trials
|
February 2, 2024
Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocol
Miriam Dixon-Zegeye, Rachel Shaw, Linda Collins, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 9, 2022
CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer
Tommy Nyberg, Mark N Brook, Lorenzo Ficorella, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 22, 2019
Correction: BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 16, 2019
BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, et al.
Human Mutation
|
May 22, 2009
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families
George Chong, Jonathan Jarry, Victoria Marcus, et al.
Nature Genetics
|
January 4, 2007
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Sarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Page
of 26