Health Impact Weekly Scan
About the Genomics & Health Impact Weekly Scan
This weekly update features emerging roles of human genomics, testing and interventions in a wide variety of noncommunicable diseases across the life span, including, birth defects, newborn screening, reproductive health, childhood diseases, cancer, chronic diseases, pharmacogenomics, family health history, guidelines and recommendations. The weekly sweep also includes news, reviews, commentaries, tools and databases.
Human Genomics across the Lifespan
Cancer
- A Family Health Portrait,
by Judith A. Salerno, Huffington Blog Post, May 4, 2016 - Clinical Implications of Genomic Discoveries in Lung Cancer
C Swanton et al, NEJM, May 12, 2016 - Reaching high-risk underserved individuals for cancer genetic counseling by video-teleconferencing.
Mette Lindsey A et al. The Journal of community and supportive oncology 2016 Apr 14(4) 162-8 - Comprehensive Genomic Profiling Facilitates Implementation of the National Comprehensive Cancer Network Guidelines for Lung Cancer Biomarker Testing and Identifies Patients Who May Benefit From Enrollment in Mechanism-Driven Clinical Trials.
Suh James H et al. The oncologist 2016 May - Ovarian cancer in BRCA1/2 mutation carriers: The impact of mutation position and family history on the cancer risk.
Teixeira Natalia et al. Maturitas 2015 Oct 82(2) 197-202 - AGO Austria recommendations for genetic testing of patients with ovarian cancer.
Marth Christian et al. Wiener klinische Wochenschrift 2015 Aug 127(15-16) 652-4 - Fast Screen Identifies Women at Risk for Hereditary Cancers,
by Ingrid Hein, Medscape Today, May 3, 2016 - Facilitating a culture of responsible and effective sharing of cancer genome data.
Siu Lillian L et al. Nature medicine 2016 May 22(5) 464-471 - Patient-Centered Communication for Discussing Oncotype DX Testing.
Roberts Megan C et al. Cancer investigation 2016 Apr 1-8 - Systematic screening for Lynch syndrome in colorectal cancer,
Swiss Med Wkly. 2016;146:w14315v - Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
Maxwell Kara N et al. American journal of human genetics 2016 May 98(5) 801-17
Chronic Diseases
- Draft Recommendation Statement - Celiac Disease: Screening,
U.S. Preventive Services Task Force, May 2016 - Family health history reporting is sensitive to small changes in wording.
Conway-Pearson Liam S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 May - Draft Evidence Review for Celiac Disease: Screening,
U.S. Preventive Services Task Force, May 2016
Ethics, Policy and Law
- Public participation in genetic databases: crossing the boundaries between biobanks and forensic DNA databases through the principle of solidarity.
Machado Helena et al. Journal of medical ethics 2015 Oct 41(10) 820-4 - Informed consent form challenges for genetic research in a developing Arab country with high risk for genetic disease.
Nair Satish Chandrasekhar et al. Journal of genetic counseling 2015 Apr 24(2) 294-9
Genomics in Practice
- Personalized Medicine in the U.S. and Germany: Awareness, Acceptance, Use and Preconditions for the Wide Implementation into the Medical Standard.
Kichko Kateryna et al. Journal of personalized medicine 2016 6(2) - Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study.
Paneque Milena et al. European journal of human genetics : EJHG 2015 Nov 23(11) 1468-72 - Beyond The DNA- Your Informative Guide to Epigenetics & Health
Genetic Alliance, 2016 - What Is Lynch Syndrome?
Dana Farber Blog, May 5, 2016 - Patient-Health Care Provider Conversations About Prenatal Genetic Screening: Recommendation or Personal Choice.
Colicchia Laura C et al. Obstetrics and gynecology 2016 May
Cardiovascular Diseases
- Cardiovascular Cascade Genetic Testing: Exploring the Role of Direct Contact and Technology.
Sturm Amy C et al. Frontiers in cardiovascular medicine 2016 311 - Family communication in a population at risk for hypertrophic cardiomyopathy.
Batte Brittany et al. Journal of genetic counseling 2015 Apr 24(2) 336-48
Newborn Screening
- Cystic fibrosis newborn screening programs: implications of the CFTR variant spectrum in nonwhite patients.
Pique Lynn et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 May - Progress Toward the Control and Management of the Thalassemias.
Fucharoen Suthat et al. Hematology/oncology clinics of North America 2016 Apr 30(2) 359-71 - Healthcare costs and outcomes of managing ß-thalassemia major over 50 years in the United Kingdom.
Weidlich Diana et al. Transfusion 2016 Apr
Pharmacogenomics
- Potential utility of precision medicine for older adults with polypharmacy: a case series study.
Finkelstein Joseph et al. Pharmacogenomics and personalized medicine 2016 931-45
News/Reviews/Commentaries
- Gene Wiki Reviews-Raising the quality and accessibility of information about the human genome.
Tsueng Ginger, Good Benjamin M, Ping Peipei, Golemis Erica, Hanukoglu Israel, van Wijnen Andre J, Su Andrew I Gene 2016 5 0. . - Encore une fois - The genomic era arrives. And this time it’s probably real,
the Economist, May 7, 2016 - Gene Therapy's First Out-and-Out Cure Is Here
MIT Tech Review, May 2016 - Researcher under fire for New Yorker epigenetics article,
by Chris Woolston, Nature News, May 9, 2016
CDC-Authored Genomics Publications
- Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System: A New Model for Biomedical Research.
Chambers David A, Feero W Gregory, Khoury Muin J JAMA 2016 5 0. (18) 1941-1942. - Molecular detection of airborne Coccidioides in Tucson, Arizona.
Chow Nancy A, Griffin Dale W, Barker Bridget M, Loparev Vladimir N, Litvintseva Anastasia P Medical mycology 2016 5 0. . - Three Genome Sequences of Legionella pneumophila subsp. pascullei Associated with Colonization of a Health Care Facility.
Kozak-Muiznieks Natalia A, Morrison Shatavia S, Sammons Scott, Rowe Lori A, Sheth Mili, Frace Michael, Lucas Claressa E, Loparev Vladimir N, Raphael Brian H, Winchell Jonas M Genome announcements 2016 0 0. (3) . - Erratum for Pattabiraman and Bopp, Draft Whole-Genome Sequences of 10 Serogroup O6 Enterotoxigenic Escherichia coli Strains.
Pattabiraman Vaishnavi, Bopp Cheryl A Genome announcements 2016 0 0. (3) .
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