Published on 07/20/2016
Human Genomics across the Lifespan
Birth Defects and Child Health
The fragile X mental retardation 1 gene (FMR1): historical perspective, phenotypes, mechanism, pathology, and epidemiology.
Grigsby Jim et al. The Clinical neuropsychologist 2016 Aug 30(6) 815-33
Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis.
Tridello Gloria et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2016 Jul
Celebrity Influence and Identification: A Test of the Angelina Effect.
Kosenko Kami A et al. Journal of health communication 2016 21(3) 318-26
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.
George Angela et al. Scientific reports 2016 629506
Breast Cancer in Africa: Limitations and Opportunities for Application of Genomic Medicine.
Silverstein Allison et al. International journal of breast cancer 2016 20164792865
Streamlined genetic testing pathway is developed for women with ovarian cancer.
Wise Jacqui et al. BMJ (Clinical research ed.) 2016 354i3900
Video-assisted genetic counseling in patients with ovarian, fallopian and peritoneal carcinoma.
Watson Catherine H et al. Gynecologic oncology 2016 Jul
A Prospective Blinded Evaluation of Urine-DNA Testing for Detection of Urothelial Bladder Carcinoma in Patients with Gross Hematuria.
Dahmcke Christina M et al. European urology 2016 Jul
Hereditary Cancer: Example of a Public Health Approach to Ensure Population Health Benefits of Genetic Medicine.
Cragun Deborah et al. Healthcare (Basel, Switzerland) 2016 4(1)
Expert and Advocacy Group Consensus Findings on the Horizon of Public Health Genetic Testing.
Modell Stephen M et al. Healthcare (Basel, Switzerland) 2016 4(1)
Public Health Approaches and Barriers to Educating Providers about Hereditary Breast and Ovarian Cancer Syndrome.
Trepanier Angela M et al. Healthcare (Basel, Switzerland) 2016 4(1)
Understanding the Needs of Young Women Regarding Breast Cancer Risk Assessment and Genetic Testing: Convergence and Divergence among Patient-Counselor Perceptions and the Promise of Peer Support.
Evans Chalanda et al. Healthcare (Basel, Switzerland) 2016 4(3)
Brain changes wrought by gene linked to Alzheimers may begin in childhood, scientists say
K Kaplan, LA Times, July 13, 2016
Epigenetic epidemiology as a tool to understand the role of immunity in chronic disease.
Nelson Heather H et al. Epigenomics 2016 Jul
The critical role of epigenetics in systemic lupus erythematosus and autoimmunity.
Long Hai et al. Journal of autoimmunity 2016 Jul
Type 2 diabetes: genetic data sharing to advance complex disease research.
Flannick Jason et al. Nature reviews. Genetics 2016 Jul
Inflammation and epigenetic regulation in osteoarthritis.
Shen Jie et al. Connective tissue research 2016 Jul
The effect of communicating the genetic risk of cardiometabolic disorders on motivation and actual engagement in preventative lifestyle modification and clinical outcome: a systematic review and meta-analysis of randomised controlled trials.
Li Sherly X et al. The British journal of nutrition 2016 Jul 1-11
A preliminary study to evaluate the strategy of combining clinical criteria and next generation sequencing (NGS) for the identification of monogenic diabetes among multi-ethnic Asians.
Ang Su Fen et al. Diabetes research and clinical practice 2016 Jul 11913-22
The ethics of conducting molecular autopsies in the cases of sudden death in the young.
McGuire Amy et al. Genome research 2016 Jul
Ethics, Guidelines for Molecular Autopsy in Youth Sudden Death Explored by Texas Team,
Genome Web, July 15, 2016
Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Chalmers Don et al. BMC medical ethics 2016 17(1) 39
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine.
Petrovski Slavé, et al. Genome biology 2016 0 0. (1) 157
Crowdsourcing biomedical research: leveraging communities as innovation engines.
Saez-Rodriguez Julio et al. Nature reviews. Genetics 2016 Jul 17(8) 470-86
The Qatar genome: a population-specific tool for precision medicine in the Middle East.
Fakhro Khalid A et al. Human genome variation 2016 316016
How digitizing you and me could revolutionize medicine. At least in theory
Stat News, July 2016
Contribution of Genetic Background and Clinical Risk Factors to Low-Trauma Fractures in Human Immunodeficiency Virus (HIV)-Positive Persons: The Swiss HIV Cohort Study.
Junier Thomas et al. Open forum infectious diseases 2016 Apr 3(2) ofw101
Genetic Test Results That Identify Increased Risk Do Not Change Behavior.
Shaughnessy Allen F et al. American family physician 2016 Jul 94(2) 168
User-centered design of multi-gene sequencing panel reports for clinicians.
Cutting Elizabeth et al. Journal of biomedical informatics 2016 Jul
Evaluation of a New Genetic Epidemiology Resource: The Intermountain Genealogy Registry.
Knight Stacey et al. Human heredity 2016 Jul 81(1) 1-10
Heart, Lung, Blood and Sleep Diseases
Statins in Familial Hypercholesterolemia: Consequences for Coronary Artery Disease and All-Cause Mortality.
Besseling Joost et al. Journal of the American College of Cardiology 2016 Jul 68(3) 252-60
Morphologic features of culprit lesions in sudden coronary death with family history of premature coronary artery disease.
Zhang Ming Chang et al. Forensic science international 2016 Jul 266412-415
Pharmacogenomics in type 2 diabetes: oral antidiabetic drugs.
Daniels M A, et al. The pharmacogenomics journal 2016 10 0. (5) 399-410
Cost-Effectiveness of Pharmacogenomic and Pharmacogenetic Test-Guided Personalized Therapies: A Systematic Review of the Approved Active Substances for Personalized Medicine in Germany.
Plöthner Marika et al. Advances in therapy 2016 Jul
Assessment of pharmacogenomic agreement.
Safikhani Zhaleh et al. F1000Research 2016 5825
What Do Parents Think about Chromosomal Microarray Testing? A Qualitative Report from Parents of Children with Autism Spectrum Disorders.
Xu Lei et al. Autism research and treatment 2016 20166852539
Clinical experience of unexpected findings in prenatal array testing.
Joosten Marieke et al. Biomarkers in medicine 2016 Aug 10(8) 831-840
Epigenetics: A key paradigm in reproductive health.
Bunkar Neha et al. Clinical and experimental reproductive medicine 2016 Jun 43(2) 59-81
Implementing PGD/PGD-A in IVF clinics: considerations for the best laboratory approach and management.
Capalbo Antonio et al. Journal of assisted reproduction and genetics 2016 Jul
The White House Is Pushing Precision Medicine, but It Wont Happen for Years,
by Mike Orcutt, Technology Review, July 18, 2016
Do CRISPR enthusiasts have their head in the sand about the safety of gene editing?
S Begley, StatNews, July 18, 2016
Mendelian randomization in (epi)genetic epidemiology: an effective tool to be handled with care.
Latvala Antti et al. Genome biology 2016 17(1) 156