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Journal of Medical Genetics
|
November 14, 2019
Psychosocial effects of whole-body MRI screening in adult high-risk pathogenic <i>TP53</i> mutation carriers: a case-controlled study (SIGNIFY)
Elizabeth K Bancroft, Sibel Saya, Emma Brown, et al.
Journal of Medical Genetics
|
December 28, 2023
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey
Sophie Allen, Lucy Loong, Alice Garrett, et al.
American Journal of Human Genetics
|
June 19, 2018
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
James Whitworth, Philip S Smith, Jose-Ezequiel Martin, et al.
Journal of Medical Genetics
|
June 4, 2024
Validation of the BOADICEA model in a prospective cohort of <i>BRCA1/2</i> pathogenic variant carriers
Xin Yang, Thea M Mooij, Goska Leslie, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 12, 2021
Clinical practice guidelines for BRCA1 and BRCA2 genetic testing
Pascal Pujol, Massimo Barberis, Philp Beer, et al.
Journal of Clinical Epidemiology
|
October 1, 2024
Corrigendum to "Development of an international glossary for clinical guidelines collaboration" "[Journal of Clinical Epidemiology 158 (2023) 84-91]"
Rachel E Christensen, Michael D Yi, Bianca Y Kang, et al.
Journal of Clinical Epidemiology
|
April 5, 2023
Development of an international glossary for clinical guidelines collaboration
Rachel E Christensen, Michael D Yi, Bianca Y Kang, et al.
Journal of the National Cancer Institute
|
February 29, 2020
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
Xin Yang, Honglin Song, Goska Leslie, et al.
The Lancet. Oncology
|
November 27, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, et al.
NPJ Breast Cancer
|
May 12, 2023
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
Taru A Muranen, Anna Morra, Sofia Khan, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Journal of Medical Genetics
|
November 14, 2019
Psychosocial effects of whole-body MRI screening in adult high-risk pathogenic <i>TP53</i> mutation carriers: a case-controlled study (SIGNIFY)
Elizabeth K Bancroft, Sibel Saya, Emma Brown, et al.
Journal of Medical Genetics
|
December 28, 2023
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey
Sophie Allen, Lucy Loong, Alice Garrett, et al.
American Journal of Human Genetics
|
June 19, 2018
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
James Whitworth, Philip S Smith, Jose-Ezequiel Martin, et al.
Journal of Medical Genetics
|
June 4, 2024
Validation of the BOADICEA model in a prospective cohort of <i>BRCA1/2</i> pathogenic variant carriers
Xin Yang, Thea M Mooij, Goska Leslie, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 12, 2021
Clinical practice guidelines for BRCA1 and BRCA2 genetic testing
Pascal Pujol, Massimo Barberis, Philp Beer, et al.
Journal of Clinical Epidemiology
|
October 1, 2024
Corrigendum to "Development of an international glossary for clinical guidelines collaboration" "[Journal of Clinical Epidemiology 158 (2023) 84-91]"
Rachel E Christensen, Michael D Yi, Bianca Y Kang, et al.
Journal of Clinical Epidemiology
|
April 5, 2023
Development of an international glossary for clinical guidelines collaboration
Rachel E Christensen, Michael D Yi, Bianca Y Kang, et al.
Journal of the National Cancer Institute
|
February 29, 2020
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
Xin Yang, Honglin Song, Goska Leslie, et al.
The Lancet. Oncology
|
November 27, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, et al.
NPJ Breast Cancer
|
May 12, 2023
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
Taru A Muranen, Anna Morra, Sofia Khan, et al.
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of 9