From CDC-Authored Genomics Publication Database
This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.
- Biobanking, consent, and certificates of confidentiality: does the ANPRM muddy the water?
Williams Brett A et al. J Law Med Ethics 2013 41(2) 440-53
From Implementation Database
This database focuses on state and national activities that integrate genomics into public health programs and clinical practice
- BRCA1 and BRCA2: Information for Health Care Professionals
[Disease: Breast Cancer|Ovarian Cancer; Type: Education; State: Illinois] - Hereditary Colon and Rectal Cancer Registry
[Disease: Lynch syndrome; Type: Data|Program; State: Massachusetts] - BRCA1 & BRCA2
[Disease: Breast Cancer|Ovarian Cancer; Type: Education; State: Illinois] - Genetic Evaluation and Testing for Hereditary Colorectal Cancer: What You Should Know
[Disease: Lynch syndrome; Type: Education; State: Connecticut] - Cancer Genomics Best Practices for Connecticut Healthcare Providers[PDF 7.80 MB]
[Disease: Lynch syndrome|Breast Cancer|Ovarian Cancer; Type: Policy|Program; State: Connecticut]
From Guideline Database
This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.
- Ethics of genetic testing and research in sport: a position statement from the Australian Institute of Sport.
Published 2016 (Australian Institute of Sport) - Prenatal Diagnosis Procedures and Techniques to Obtain a Diagnostic Fetal Specimen or Tissue: Maternal and Fetal Risks and Benefits.
Published 2015 (Society of Obstetricians and Gynaecologists of Canada) - Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Published 2015 (Expert panel) - Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.
Published 2013 (Expert panel) - Recommendations for ethical approaches to genotype-driven research recruitment.
Published 2012 (Expert panel)
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Assessment of the Family History of Patients With Ulcerative Colitis at a Single Center in Japan.
Journal of pediatric gastroenterology and nutrition 2016 Nov 63 (5): 512-515.
Fujii Tohru, Sato Masamichi, Hosoi Kenji, Ohbayashi Naho, Ikuse Tamaki, Jimbo Keisuke, Aoyagi Yo, Kudo Takahiro, Ohtsuka Yoshikazu, Shimizu Toshia - Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study.
Lancet (London, England) 2016 Oct 388 Suppl 1 S80.
Bai Xiaohui, Xu Lei, Zhang Fengguo, Xiao Yun, Li Jianfeng, Wang Hai - Predominant mutations in a hotspot of SERPINC1 associated with venous thromboembolism in the Chinese population: a case-control study.
Lancet (London, England) 2016 Oct 388 Suppl 1 S39.
Tang Liang, Zeng Wei, Wang Qing-Yun, Toderici Mara, de la Morena-Barrio Maria Eugenia, Corral Javier, Hu - First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the BRCA1 gene.
Oncology letters 2016 Aug 12 (2): 1192-1196.
Jouali Farah, Laarabi Fatima-Zahra, Marchoudi Nabila, Ratbi Ilham, Elalaoui Siham Chafai, Rhaissi Houria, Fekkak Jamal, Sefiani Abdelaz - Roles of the Taql and Bsml vitamin D receptor gene polymorphisms in hospital mortality of burn patients.
Clinics (Sa?o Paulo, Brazil) 2016 Aug 71 (8): 470-3.
Nogueira Glaucia R, Azevedo Paula S, Polegato Bertha F, Zornoff Leonardo A M, Paiva Sergio A R, Nogueira Celia R, Araujo Natalia C, Carmona Bruno H M, Conde Sandro J, Minicucci Marcos
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