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September 28, 2021
Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel-Lindau Disease
Hugh Furness, Louay Salfity, Johanna Devereux, et al.
Journal of Medical Genetics
|
November 19, 2020
Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations
Alice Garrett, Miranda Durkie, Alison Callaway, et al.
The Lancet. Oncology
|
May 13, 2023
Utility of polygenic risk scores in UK cancer screening: a modelling analysis
Catherine Huntley, Bethany Torr, Amit Sud, et al.
European Urology Oncology
|
December 14, 2019
Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals
Claire Forde, Derek H K Lim, Yousef Alwan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2024
Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK)
Alice Garrett, Sophie Allen, Miranda Durkie, et al.
Journal of Genetic Counseling
|
August 7, 2025
Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study
Kelly Kohut, Kate Morton, Lesley Turner, et al.
British Journal of Haematology
|
February 6, 2023
Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group
Beverley Speight, Helen Hanson, Clare Turnbull, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
September 10, 2020
Preventing Ovarian Cancer through early Excision of Tubes and late Ovarian Removal (PROTECTOR): protocol for a prospective non-randomised multi-center trial
Faiza Gaba, Sadiyah Robbani, Naveena Singh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 5, 2024
Management of individuals with heterozygous germline pathogenic variants in ATM: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Tuya Pal, Katherine R Schon, Esteban Astiazaran-Symonds, et al.
American Journal of Human Genetics
|
September 9, 2025
Availability of benign missense variant "truthsets" for validation of functional assays: Current status and a systematic approach
Charlie F Rowlands, Sophie Allen, Alice Garrett, et al.
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Search research articles
Search
Showing results (41-50 of 85) with videos related to
Sort By:
Page
of 9
Genes
|
September 28, 2021
Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel-Lindau Disease
Hugh Furness, Louay Salfity, Johanna Devereux, et al.
Journal of Medical Genetics
|
November 19, 2020
Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations
Alice Garrett, Miranda Durkie, Alison Callaway, et al.
The Lancet. Oncology
|
May 13, 2023
Utility of polygenic risk scores in UK cancer screening: a modelling analysis
Catherine Huntley, Bethany Torr, Amit Sud, et al.
European Urology Oncology
|
December 14, 2019
Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals
Claire Forde, Derek H K Lim, Yousef Alwan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2024
Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK)
Alice Garrett, Sophie Allen, Miranda Durkie, et al.
Journal of Genetic Counseling
|
August 7, 2025
Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study
Kelly Kohut, Kate Morton, Lesley Turner, et al.
British Journal of Haematology
|
February 6, 2023
Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group
Beverley Speight, Helen Hanson, Clare Turnbull, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
September 10, 2020
Preventing Ovarian Cancer through early Excision of Tubes and late Ovarian Removal (PROTECTOR): protocol for a prospective non-randomised multi-center trial
Faiza Gaba, Sadiyah Robbani, Naveena Singh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 5, 2024
Management of individuals with heterozygous germline pathogenic variants in ATM: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Tuya Pal, Katherine R Schon, Esteban Astiazaran-Symonds, et al.
American Journal of Human Genetics
|
September 9, 2025
Availability of benign missense variant "truthsets" for validation of functional assays: Current status and a systematic approach
Charlie F Rowlands, Sophie Allen, Alice Garrett, et al.
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