Published on 09/10/2015
Human Genomics across the Lifespan
Birth Defects and Child Health
Informed choice about Down syndrome screening - Effect of an eHealth tool: A randomized controlled trial.
Skjøth Mette Maria et al. Acta Obstet Gynecol Scand 2015 Aug 31.
Genetic testing in children with autism spectrum disorders.
Çöp Esra et al. Anadolu Psikiyatri Derg 16(6) 426-432
Health professionals' opinions on supporting a cancer biobank: identification of barriers to combat biobanking pitfalls.
Caixeiro Nicole J et al. Eur. J. Hum. Genet. 2015 Sep 2.
Oncotype DX in Bilateral Synchronous Primary Invasive Breast Cancer.
Karsten Maria et al. Ann. Surg. Oncol. 2015 Sep 4.
Molecular Testing for Treatment of Metastatic Non-Small Cell Lung Cancer: How to Implement Evidence-Based Recommendations.
Levy Benjamin P et al. Oncologist 2015 Sep 1.
Cost-effectiveness of Universal BRCA1/2 Screening: Evidence-Based Decision Making.
Long Elisa F et al. JAMA Oncol 2015 Sep 3. 1-2
Systemic Therapy for Stage IV Non-Small-Cell Lung Cancer: American Society of Clinical Oncology Clinical Practice Guideline Update.
Masters Gregory A et al. J. Clin. Oncol. 2015 Aug 31.
The Italian external quality assessment for RAS testing in colorectal carcinoma identifies methods-related inter-laboratory differences.
Normanno Nicola et al. J Transl Med 2015 13287
BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study.
HÃ¸berg-Vetti Hildegunn et al. Eur. J. Hum. Genet. 2015 Sep 9.
Availability and payer coverage of BRCA1/2 tests and gene panels.
Clain Elizabeth et al. Nat. Biotechnol. 2015 Sep 8. 33(9) 900-902
Colonoscopy screening among US adults aged 40 or older with a family history of colorectal cancer.
Tsai Meng-Han et al. Prev Chronic Dis 2015 12E80
Genetic Counselling for Predictive Testing in Huntington's Disease in One Centre since 1993. Gender-Specific Aspects of Decision-Making.
Arning Larissa et al. J Huntingtons Dis 2015 4(1) 87-98
Talking About Type 2 Diabetes: Family Communication From the Perspective of At-Risk Relatives.
Myers Melanie F et al. Diabetes Educ 2015 Aug 31.
The Heart Health Study - increasing cardiovascular risk assessment in family practice for first degree relatives of patients with premature ischaemic heart disease: a randomised controlled trial.
Stocks Nigel P et al. BMC Fam Pract 2015 16(1) 116
Expanded genetic screening panel for the Ashkenazi Jewish population.
Baskovich Brett et al. Genet. Med. 2015 Sep 3.
Prevention for those who can pay: insurance reimbursement of genetic-based preventive interventions in the liminal state between health and disease.
Prince Anya E R et al. J Law Biosci 2015 Jul 1. 2(2) 365-395
Public preferences for communicating personal genomic risk information: a focus group study.
Smit Amelia K et al. Health Expect 2015 Sep 1.
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.
Sanderson Saskia C et al. Genet. Med. 2015 Sep 3.
Enhancing the Collection, Discussion and Use of Family Health History by Consumers, Nurses and Other Health Care Providers: Because Family Health History Matters.
Underwood Sandra Millon et al. Nurs. Clin. North Am. 2015 Sep 50(3) 509-29
ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories.
Wang Jinlian et al. Genome Med 2015 7(1) 77
Newborn screening and the relaxation of one-child policy in mainland China.
Yang H et al. Public Health 2015 Sep 2.
Knowledge of Pharmacogenetics among Healthcare Professionals and Faculty Members of Health Training Institutions in Ghana.
Kudzi W et al. Ghana Med J 2015 Mar 49(1) 50-6
Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Srebniak Malgorzata I et al. Eur. J. Hum. Genet. 2015 Sep 2.
Prenatal Testing in the Genomic Age: Clinical Outcomes, Quality of Life, and Costs.
Kaimal Anjali J et al. Obstet Gynecol 2015 Sep 3.
Six creative ways to teach genetics,
by Zofia Niemtus and Sarah Marsh, the Guardian, September 7, 2015
What's in a phenotype? Next-generation genomic diagnosis,
by Dr Shehla Mohammad and Dr Sobia Raza, PHG Foundation, September 7, 2015
Collaboration Needed To Optimize Role of Genetic Testing
Clinical Oncology September 2015 Volume 10
Universal cholesterol screening in kids IDs genetic dyslipidemia
Medpage Today, September 9, 2015
FDA taking genomic testing to the next level,
by Adam Berger and Zivana Tezak, FDA Voice, September 8, 2015
At the heart of the matter: The genomics underlying cardiovascular disease,
by Jeffrey S. Buguliskis, GEN, September 7, 2015
NIH funds to move precision medicine closer to reality,
by Dr Philippa Brice, PHG Foundation, September 6, 2015
Genetic signature of ageing could also predict dementia risk,
by Dr Philippa Brice, PHG Foundation, September 7, 2015
Genetic testing all women for breast cancer might not be worth the cost,
Science Daily, September 3, 2015
When science fails a scientist.
Hunter-Schaedle Kim et al. Science 2015 Sep 4. 349(6252) 1134
New Cholesterol Drugs Are Vastly Overpriced, Analysis Says,
by Andrew Pollack, New York Times, September 8, 2015