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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 prediction
Anja 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 Patients
Anne 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 example
Leila 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 alleles
Francisco 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 patients
Heleen 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 history
Encarna 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 syndrome
Juul 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 statement
Nora 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 statement
Nora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Page
of 29
Search research articles
Search
Showing results (111-120 of 282) with videos related to
Sort By:
Page
of 29
Breast (Edinburgh, Scotland)
|
December 7, 2023
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction
Anja 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 Patients
Anne 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 example
Leila 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 alleles
Francisco 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 patients
Heleen 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 history
Encarna 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 syndrome
Juul 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 statement
Nora 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 statement
Nora Pashayan, Antonis C Antoniou, Urska Ivanus, et al.
Page
of 29