Published on 09/28/2016
Human Genomics across the Lifespan
Birth Defects and Child Health
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The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort.
Walker Caroline E et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep -
Psychosocial outcomes and counselee satisfaction following genetic counseling for hereditary breast and ovarian cancer: A patient-reported outcome study.
Oberguggenberger Anne et al. Journal of psychosomatic research 2016 Oct 8939-45
Cancer
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Common cancers share familial susceptibility: implications for cancer genetics and counselling.
Yu Hongyao et al. Journal of medical genetics 2016 Sep -
How Are Information Seeking, Scanning, and Processing Related to Beliefs About the Roles of Genetics and Behavior in Cancer Causation?
Waters Erika A et al. Journal of health communication 2016 Sep 1-10 -
Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening.
Paluch-Shimon S et al. Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2016 Sep 27(suppl 5) v103-v110
Chronic Disease
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Phenomenology of Schizophrenia and the Representativeness of Modern Diagnostic Criteria.
Kendler Kenneth S et al. JAMA psychiatry 2016 Sep -
Genetic and epigenetic analysis of schizophrenia in blood-a no-brainer?
Jaffe Andrew E et al. Genome medicine 8(1) 96 -
Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.
Schmitt Andrea et al. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2016 Sep 17(6) 406-28 -
Reviewing the epigenetics of schizophrenia.
Cromby John et al. Journal of mental health (Abingdon, England) 2016 Aug 1-9 -
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.
Wolfe Kate et al. European journal of human genetics : EJHG 2016 Sep -
Is the gut microbiome an important cause of obesity
StatNews, September 22, 2016
Ethics/Policy/Law
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Participants' Role Expectations in Genetics Research and Re-consent: Revising the Theory and Methods of Mental Models Research Relating to Roles.
Condit Celeste M et al. Journal of health communication 2016 Sep 1-9 -
Ethical considerations for genetic testing in the context of mandated cardiac screening before athletic participation.
Magavern Emma F et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep -
A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research.
O'Daniel Julianne M et al. Genome medicine 8(1) 95
Practice
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Leveling the Playing Field: Closing the Gap in Public Awareness of Genetics between the Well Served and Underserved.
Kung Johnny et al. The Hastings Center report 2016 Sep 46(5) 17-20 -
From "Personalized" to "Precision" Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine.
Juengst Eric et al. The Hastings Center report 2016 Sep 46(5) 21-33 -
Genetics and genomic medicine in the Philippines.
Padilla Carmencita D et al. Molecular genetics & genomic medicine 2016 Sep 4(5) 494-503 -
Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER.
Rasmussen Luke V et al. Applied clinical informatics 2016 7(3) 870-82 -
Genetic Testing in Dermatology: A Survey Analyzing Obstacles to Appropriate Care.
Shagalov Devorah R et al. Pediatric dermatology 2016 Sep -
All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms.
Laestadius Linnea I et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep -
Realizing the Full Potential of Precision Medicine in Health and Health Care.
Dzau Victor J et al. JAMA 2016 Sep -
Implementation of a Multicenter Biobanking Collaboration for Next-Generation Sequencing-Based Biomarker Discovery Based on Fresh Frozen Pretreatment Tumor Tissue Biopsies.
Bins Sander et al. The oncologist 2016 Sep -
Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.
Messner Donna A et al. Applied & translational genomics 2016 Sep 1019-24 -
A Partnership Approach to Genetic and Genomic Graduate Nursing Curriculum: Report of a New Course's Impact on Student Confidence.
Williams Tamara et al. The Journal of nursing education 2016 Oct 55(10) 574-578 -
Precision Medicine: New Paradigms, Risks and Opportunities
Knowledge@Wharton, September 2016 -
All About Genetic Counselors
From the National Society for Genetic Counselors
Heart, Lung, Blood and Sleep Diseases
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Personal Stories of Patients with Familial Hypercholesterolemia
The FH Foundation -
The cards I was dealt: my life with familial hypercholesterolemia.
Ames Mackenzie et al. Circulation. Cardiovascular quality and outcomes 2015 Mar 8(2) 218-9 -
Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting.
Christiansen Sofie Lindgren et al. European journal of human genetics : EJHG 2016 Sep
Pharmacogenomics
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Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study.
Carere Deanna Alexis et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep
Reproductive Health
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Payer decision making for next-generation sequencing-based genetic tests: insights from cell-free DNA prenatal screening.
Dervan Andrew P et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep