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Marc Tischkowitz

Showing results (111-120 of 258) with videos related to

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JAMA Network Open|January 9, 2025
Breast Cancer Susceptibility Gene Sequence Variations and Development of Contralateral Breast CancerAnne 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 practiceFrancisca 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 predispositionMarianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
Cancer Discovery|December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancerSusan 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 protocolMiriam 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 CancerTommy 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 factorsAndrew 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 factorsAndrew 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 familiesGeorge 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 cancerSarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Pageof 26

Showing results (111-120 of 258) with videos related to

Sort By:
Pageof 26
JAMA Network Open|January 9, 2025
Breast Cancer Susceptibility Gene Sequence Variations and Development of Contralateral Breast CancerAnne 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 practiceFrancisca 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 predispositionMarianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
Cancer Discovery|December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancerSusan 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 protocolMiriam 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 CancerTommy 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 factorsAndrew 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 factorsAndrew 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 familiesGeorge 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 cancerSarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Pageof 26