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The Lancet. Oncology
|
May 10, 2025
Long-term health outcomes of bilateral salpingo-oophorectomy in BRCA1 and BRCA2 pathogenic variant carriers with personal history of breast cancer: a retrospective cohort study using linked electronic health records
Hend Hassan, Isaac Allen, Tameera Rahman, et al.
Journal of Medical Genetics
|
November 30, 2021
Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors
Andrew Lee, Xin Yang, Jonathan Tyrer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 11, 2007
Analysis of PALB2/FANCN-associated breast cancer families
Marc Tischkowitz, Bing Xia, Nelly Sabbaghian, 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.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>ATM</i> sequence variants
Marcy E Richardson, Megan Holdren, Terra Brannan, et al.
Journal of Medical Genetics
|
October 21, 2024
Lynch syndrome diagnostic testing pathways in endometrial cancers: a nationwide English registry-based study
Lucy Loong, Catherine Huntley, Joanna Pethick, et al.
Journal of Medical Genetics
|
September 26, 2022
Enhancing the BOADICEA cancer risk prediction model to incorporate new data on <i>RAD51C</i>, <i>RAD51D</i>, <i>BARD1</i> updates to tumour pathology and cancer incidence
Andrew Lee, Nasim Mavaddat, Alex Cunningham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2022
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
Lucy Loong, Alice Garrett, Sophie Allen, et al.
American Journal of Human Genetics
|
September 24, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants
Marcy E Richardson, Megan Holdren, Terra Brannan, et al.
Genes
|
February 25, 2023
Molecular Genetic Characteristics of <i>FANCI</i>, a Proposed New Ovarian Cancer Predisposing Gene
Caitlin T Fierheller, Wejdan M Alenezi, Corinne Serruya, et al.
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of 26
Search research articles
Search
Showing results (131-140 of 258) with videos related to
Sort By:
Page
of 26
The Lancet. Oncology
|
May 10, 2025
Long-term health outcomes of bilateral salpingo-oophorectomy in BRCA1 and BRCA2 pathogenic variant carriers with personal history of breast cancer: a retrospective cohort study using linked electronic health records
Hend Hassan, Isaac Allen, Tameera Rahman, et al.
Journal of Medical Genetics
|
November 30, 2021
Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors
Andrew Lee, Xin Yang, Jonathan Tyrer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 11, 2007
Analysis of PALB2/FANCN-associated breast cancer families
Marc Tischkowitz, Bing Xia, Nelly Sabbaghian, 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.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>ATM</i> sequence variants
Marcy E Richardson, Megan Holdren, Terra Brannan, et al.
Journal of Medical Genetics
|
October 21, 2024
Lynch syndrome diagnostic testing pathways in endometrial cancers: a nationwide English registry-based study
Lucy Loong, Catherine Huntley, Joanna Pethick, et al.
Journal of Medical Genetics
|
September 26, 2022
Enhancing the BOADICEA cancer risk prediction model to incorporate new data on <i>RAD51C</i>, <i>RAD51D</i>, <i>BARD1</i> updates to tumour pathology and cancer incidence
Andrew Lee, Nasim Mavaddat, Alex Cunningham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2022
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
Lucy Loong, Alice Garrett, Sophie Allen, et al.
American Journal of Human Genetics
|
September 24, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants
Marcy E Richardson, Megan Holdren, Terra Brannan, et al.
Genes
|
February 25, 2023
Molecular Genetic Characteristics of <i>FANCI</i>, a Proposed New Ovarian Cancer Predisposing Gene
Caitlin T Fierheller, Wejdan M Alenezi, Corinne Serruya, et al.
Page
of 26