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Peter Devilee

Showing results (111-120 of 282) with videos related to

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Breast (Edinburgh, Scotland)|December 7, 2023
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk predictionAnja Tüchler, Antoine De Pauw, Corinna Ernst, et al.
Plos One|June 15, 2016
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome PatientsAnne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, et al.
BMC Cancer|July 1, 2009
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an exampleLeila Mohammadi, Maaike P Vreeswijk, Rogier Oldenburg, et al.
Journal of Personalized Medicine|July 2, 2021
Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I)Jennifer D Brooks, Hermann H Nabi, Irene L Andrulis, et al.
Plos One|February 15, 2013
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility allelesFrancisco Javier Gracia-Aznarez, Victoria Fernandez, Guillermo Pita, et al.
Human Mutation|February 27, 2010
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patientsHeleen M van der Klift, Carli M J Tops, Elsa C Bik, et al.
Breast Cancer Research : BCR|February 10, 2009
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family historyEncarna B Gómez García, Jan C Oosterwijk, Maarten Timmermans, et al.
Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.
Nature Reviews. Clinical Oncology|July 1, 2020
Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statementNora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Nature Reviews. Clinical Oncology|June 20, 2020
Personalized early detection and prevention of breast cancer: ENVISION consensus statementNora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Pageof 29

Showing results (111-120 of 282) with videos related to

Sort By:
Pageof 29
Breast (Edinburgh, Scotland)|December 7, 2023
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk predictionAnja Tüchler, Antoine De Pauw, Corinna Ernst, et al.
Plos One|June 15, 2016
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome PatientsAnne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, et al.
BMC Cancer|July 1, 2009
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an exampleLeila Mohammadi, Maaike P Vreeswijk, Rogier Oldenburg, et al.
Journal of Personalized Medicine|July 2, 2021
Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I)Jennifer D Brooks, Hermann H Nabi, Irene L Andrulis, et al.
Plos One|February 15, 2013
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility allelesFrancisco Javier Gracia-Aznarez, Victoria Fernandez, Guillermo Pita, et al.
Human Mutation|February 27, 2010
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patientsHeleen M van der Klift, Carli M J Tops, Elsa C Bik, et al.
Breast Cancer Research : BCR|February 10, 2009
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family historyEncarna B Gómez García, Jan C Oosterwijk, Maarten Timmermans, et al.
Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.
Nature Reviews. Clinical Oncology|July 1, 2020
Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statementNora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Nature Reviews. Clinical Oncology|June 20, 2020
Personalized early detection and prevention of breast cancer: ENVISION consensus statementNora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Pageof 29