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Cancer

Last data update: Oct 15, 2021. (Total: 42864 Documents since 2012)
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Query Trace: all[original query]>>Guidelines Related[Product Type]
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe.
Marmolejo David Humberto et al. European journal of medical genetics 2021 104350
Update Swiss guideline for counselling and testing for predisposition to breast, ovarian, pancreatic and prostate cancer.
Stoll Susanna et al. Swiss medical weekly 2021 151w30038
Exploring Gene-Specific Guidelines for Risk Management of Gynecological Cancer in Lynch Syndrome.
Petelin Lara et al. JAMA network open 2021 4(9) e2124384
Genetic risk assessment for hereditary renal cell carcinoma: Clinical consensus statement.
Bratslavsky Gennady et al. Cancer 2021
Evaluation and comparison of hereditary Cancer guidelines in the population.
Ritchie Jordon B et al. Hereditary cancer in clinical practice 2021 19(1) 31
Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2020 for the Clinical Practice of Hereditary Colorectal Cancer.
Tomita Naohiro et al. International journal of clinical oncology 2021
Uptake and timing of risk-reducing salpingo-oophorectomy among patients with BRCA1/2 mutations.
Smith Maria J et al. American journal of obstetrics and gynecology 2021
Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Mao Rong et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
R Mao et al, Genetics in Medicine, June 17, 2021
Recent Insights on Genetic Testing in Primary Prostate Cancer.
Kafka Mona et al. Molecular diagnosis & therapy 2021
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
Seppälä T T et al. The British journal of surgery 2021 108(5) 484-498
International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers.
Amar Laurence et al. Nature reviews. Endocrinology 2021
Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Tischkowitz Marc et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2021 325(19) 1965-1977
ACG Clinical Report and Recommendations on Transition of Care in Children and Adolescents With Hereditary Polyposis Syndromes.
Attard Thomas M et al. The American journal of gastroenterology 2021 116(4) 638-646
Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
M Tishkowitz et al, Genetics in Medicine, May 11, 2021
Chronic cor pulmonale in pulmonary sarcoidosis.
Battesti J P et al. Thorax 1978 33(1) 76-84
Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group.
Aronson Melyssa et al. Journal of medical genetics 2021
[Dihydropyrimidine déhydrogenase (DPD) deficiency screening and securing of fluoropyrimidine-based chemotherapies: Update and recommendations of the French GPCO-Unicancer and RNPGx networks].
Loriot Marie-Anne et al. Bulletin du cancer 2018 105(4) 397-407
Recommendations from the European Commission Initiative on Breast Cancer for multigene testing to guide the use of adjuvant chemotherapy in patients with early breast cancer, hormone receptor positive, HER-2 negative.
Giorgi Rossi Paolo et al. British journal of cancer 2021 Feb
Update: variable implementation of the 2018 UKCGG/UKGTN guidelines for breast cancer gene panel tests offered by UK genetics services.
Wedderburn Sarah et al. Journal of medical genetics 2021 Feb
British Gynaecological Cancer Society/British Association of Gynaecological Pathology consensus for germline and tumor testing for BRCA 1/2 variants in ovarian cancer in the United Kingdom.
Sundar Sudha et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2021 Jan
Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
Daly Mary B et al. Journal of the National Comprehensive Cancer Network : JNCCN 2021 Jan 19(1) 77-102
Recommendations to researchers for aiding in increasing American Indian representation in genetic research and personalized medicine.
Carroll Dana M et al. Personalized medicine 2020 Dec
Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.
Fortuno Cristina et al. Human mutation 2020 Dec
Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment (edition 2.1).
Naito Yoichi et al. International journal of clinical oncology 2020 Nov
NCCN Updates Guidelines for Hereditary Cancer Risks.
et al. American journal of medical genetics. Part A 2020 Dec 182(12) 2813-2814
Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations.
Garrett Alice et al. Journal of medical genetics 2020 Nov
Public Comment on Draft Recommendation Statement, Draft Evidence Review, and Draft Modeling Report: Screening for Colorectal Cancer
This document is available for Public Comments until Nov 23, 2020 11:59 PM EDT
Testing strategies for Lynch syndrome in people with endometrial cancer
NICE, October 28, 2020
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