Published on 10/15/2015
Human Genomics across the Lifespan
Birth Defects and Child Health
Clinical utility gene card for: acrodermatitis enteropathica - update 2015.
KÃ¼ry SÃ©bastien et al. European journal of human genetics : EJHG 2015 Oct
Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
Peshkin Beth N et al. Journal of genetic counseling 2015 Oct
BRCA1 and BRCA2 mutations in Japanese patients with ovarian, fallopian tube, and primary peritoneal cancer.
Sakamoto Ikuko et al. Cancer 2015 Oct
Communication Between Breast Cancer Patients Who Received Inconclusive Genetic Test Results and Their Daughters and Sisters Years After Testing.
Baars Jessica E et al. Journal of genetic counseling 2015 Oct
Uptake of risk-reducing salpingo-oophorectomy among female BRCA mutation carriers: experience at the National Cancer Center of Korea.
Kim Se Ik et al. Journal of cancer research and clinical oncology 2015 Oct
Genetic testing for Lynch syndrome: family communication and motivation.
Leenen Celine H M et al. Familial cancer 2015 Oct
Genetic Counselors' Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels.
Mets Sarah et al. Journal of genetic counseling 2015 Oct
FDA's Proposed Guidance for Laboratory Developed Tests: How Should Regulators Balance the Risks and Promise of Innovation in Clinical Genetics?
Bayefsky Michelle et al. FDLI's food and drug policy forum 2015 Mar 5(2)
Your DNA is not your diagnosis: getting diagnoses right following secondary genomic findings.
Murray Michael F et al. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Oct
CRCDA-Comprehensive resources for cancer NGS data analysis.
Thangam Manonanthini et al. Database : the journal of biological databases and curation 2015 2015
Overview of 'Omics Technologies for Military Occupational Health Surveillance and Medicine.
Bradburne Christopher et al. Military medicine 2015 Oct 180(10 Suppl) 34-48
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery.
European journal of human genetics : EJHG 2015 Oct
Million Veteran Program (MVP): A Mega-Biobank to Study Genetic Influences On Health and Disease.
Gaziano John Michael et al. Journal of clinical epidemiology 2015 Oct
Components of genetic counsellor education: A systematic review of the peer-reviewed literature.
Ingvoldstad C et al. Journal of community genetics 2015 Oct
Review of Current International Decision-Making Processes for Newborn Screening: Lessons for Australia.
Metternick-Jones Selina Carolyne et al. Frontiers in public health 2015 3214
The Newborn Screening Paradox: Sensitivity vs. Overdiagnosis in VLCAD Deficiency.
Diekman Eugene et al. JIMD reports 2015 Oct
A Naturalistic Study of the Effectiveness of Pharmacogenetic Testing to Guide Treatment in Psychiatric Patients With Mood and Anxiety Disorders.
Brennan Francis X et al. The primary care companion for CNS disorders 2015 17(2)
Premarital genetic screening for beta thalassemia carrier status of indexed families using HbA2 electrophoresis.
Nosheen Aneeqa et al. JPMA. The Journal of the Pakistan Medical Association 2015 Oct 65(10) 1047-9
Committee Opinion No. 643: Identification and Referral of Maternal Genetic Conditions in Pregnancy.
et al. Obstetrics and gynecology 2015 Oct 126(4) e49-51
Contingent non-invasive prenatal testing: An opportunity to improve non-genetic aspects of fetal aneuploidy screening.
Gyselaers Wilfried et al. Prenatal diagnosis 2015 Oct
Estonia wants to collect the DNA of all its citizens,
by Katharine Schwab, the Atlantic, October 8, 2015
Human Longevity, Inc. launches the health nucleus, a comprehensive and personalized health platform for individuals,
Human Longevity, October 13, 2015
The rise of DIY genetic testing,
by Emily Matchar, Smithsonian.com, October 13, 2015
Scientists hope to attract millions to 'DNA.LAND',
by Erika Check Hayden, Nature News, October 9, 2015
Human genetics: Strength in numbers in the low-frequency spectrum.
Skipper Magdalena et al. Nature reviews. Genetics 2015 Oct
Epigenetic study of histone modifications and DNA damage could lead to new cancer treatments,
by Bailey Kirkpatrick, What is Epigenetics, October 13, 2015
Gene therapy staves off blindness from retinitis pigmentosa in canine model,
NIH News, October 13, 2015
CDC enters into research collaboration with Edico Genome to evaluate performance of DRAGEN hardware platform,
PR Newswire, October 9, 2015
The tantalizing links between gut microbes and the brain.
Smith Peter Andrey, et al. Nature 2015 10 0. (7573) 312-4
Study shows BRCA mutation screening needed despite family history,
by Leah Lawrence, Cancer Network, October 13, 2015
UT Southwestern investigators develop new strategy to classify cancers caused by KRAS mutations,
News- Medical.net, October 8, 2015
FDA approves the first disease screening by gene testing company,
by Charles Margulis, World Tech Today, October 8, 2015
Sharing genomic data in the precision medicine era,
by Scott Edmunds, Giga Blogs, October 9, 2015
National Academies Human Gene-Editing Initiative holds public meeting,
by Chloe Poston, Genes to Genomes, October 6, 2015
What You Need to Know About Genetic Counseling,
by Georgia Hurst, the Cure, October 8, 2015
Diagnostic developers target antibiotic resistance,
by Viviane Callier, Nature News, October 9, 2015
5 major breast cancer advancements you need to know about,
by Anna Almendrala, Huffington Post, October 7, 2015
Precision medicine: what it is and how it will be achieved?
Genomics Education Programme, October 12, 2015
Genomics and Evolution of Pathogens and Hosts
November 9-21, 2015 ~ Atlanta, GA