Volume 35 Number 11 September 10-17, 2015
Human Genomics across the Lifespan
Birth Defects and Child Health
Genetic testing in children with autism spectrum disorders.
Çöp E et al. Anadolu Psikiyatri Derg 16(6) 426-432
Çöp E et al. Anadolu Psikiyatri Derg 16(6) 426-432
Informed choice about Down syndrome screening - Effect of an eHealth tool: A randomized controlled trial.
Skjøth MM et al. Acta Obstet Gynecol Scand 2015 Aug 31.
Skjøth MM et al. Acta Obstet Gynecol Scand 2015 Aug 31.
Cancer
Availability and payer coverage of BRCA1/2 tests and gene panels.
Clain E et al. Nat. Biotechnol. 2015 Sep 8. 33(9) 900-902
Clain E et al. Nat. Biotechnol. 2015 Sep 8. 33(9) 900-902
BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study
Høberg-Vetti H, et al. European Journal of Human Genetics 2015 Sep 9
Høberg-Vetti H, et al. European Journal of Human Genetics 2015 Sep 9
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
Tsai Meng-Han et al. Prev Chronic Dis 2015 12E80
Cost-effectiveness of universal BRCA1/2 screening: evidence-based decision making.
Long EF et al. JAMA Oncol 2015 Sep 3. 1-2
Long EF et al. JAMA Oncol 2015 Sep 3. 1-2
Health professionals' opinions on supporting a cancer biobank: identification of barriers to combat biobanking pitfalls.
Caixeiro NJ et al. Eur. J. Hum. Genet. 2015 Sep 2.
Caixeiro NJ et al. Eur. J. Hum. Genet. 2015 Sep 2.
Molecular testing for treatment of metastatic non-small cell lung cancer: How to implement evidence-based recommendations.
Levy BP et al. Oncologist 2015 Sep 1.
Levy BP et al. Oncologist 2015 Sep 1.
Oncotype DX in bilateral synchronous primary invasive breast cancer.
Karsten M et al. Ann. Surg. Oncol. 2015 Sep 4.
Karsten M et al. Ann. Surg. Oncol. 2015 Sep 4.
Systemic therapy for stage IV non-small-cell lung cancer: American Society of Clinical Oncology Clinical Practice guideline update.
Masters GA et al. J. Clin. Oncol. 2015 Aug 31.
Masters GA 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 N et al. J Transl Med 2015 13287
Normanno N et al. J Transl Med 2015 13287
Chronic Diseases
Genetic counselling for predictive testing in Huntington's disease in one centre since 1993. Gender-specific aspects of decision-making.
Arning L et al. J Huntingtons Dis 2015 4(1) 87-98
Arning L 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 MF et al. Diabetes Educ 2015 Aug 31.
Myers MF et al. Diabetes Educ 2015 Aug 31.
Genomics in Practice
ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories.
Wang J et al. Genome Med 2015 7(1) 77
Wang J et al. Genome Med 2015 7(1) 77
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.
Sanderson SC et al. Genet. Med. 2015 Sep 3.
Sanderson SC et al. Genet. Med. 2015 Sep 3.
Enhancing the collection, discussion and use of family health gistory by consumers, nurses and other health care providers: Because family health history matters.
Underwood SM et al. Nurs. Clin. North Am. 2015 Sep 50(3) 509-29
Underwood SM et al. Nurs. Clin. North Am. 2015 Sep 50(3) 509-29
Expanded genetic screening panel for the Ashkenazi Jewish population.
Baskovich B et al. Genet. Med. 2015 Sep 3.
Baskovich B 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 AER et al. J Law Biosci 2015 Jul 1. 2(2) 365-395
Prince AER 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 AK et al. Health Expect 2015 Sep 1.
Smit AK et al. Health Expect 2015 Sep 1.
Newborn Screening
Newborn screening and the relaxation of one-child policy in mainland China.
Yang H et al. Public Health 2015 Sep 2.
Yang H et al. Public Health 2015 Sep 2.
Pharmacogenomics
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
Kudzi W et al. Ghana Med J 2015 Mar 49(1) 50-6
Reproductive Health
Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Srebniak MI et al. Eur. J. Hum. Genet. 2015 Sep 2.
Srebniak MI et al. Eur. J. Hum. Genet. 2015 Sep 2.
Prenatal testing in the genomic age: Clinical outcomes, quality of life, and costs.
Kaimal AJ et al. Obstet Gynecol 2015 Sep 3.
Kaimal AJ et al. Obstet Gynecol 2015 Sep 3.
Reviews, News and Commentaries
When science fails a scientist.
Hunter-Schaedle Kim et al. Science 2015 Sep 4. 349(6252) 1134
Hunter-Schaedle Kim et al. Science 2015 Sep 4. 349(6252) 1134
Why do we pay for information that we won't use? A cognitive-based explanation for genetic information seeking
Gorini A, et al. European Journal of Human Genetics 2015 Sept 9
Gorini A, et al. European Journal of Human Genetics 2015 Sept 9
Collaboration needed to optimize role of genetic testing
Clinical Oncology September 2015 Volume 10
Clinical Oncology September 2015 Volume 10
Remembering Dr. Kenneth Pass, a newborn screening champion, APHL, September 9, 2015
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
New cholesterol drugs are vastly overpriced, analysis says, by Andrew Pollack, New York Times, September 8, 2015
At the heart of the matter: The genomics underlying cardiovascular disease, by Jeffrey S. Buguliskis, GEN, September 7, 2015
Genetic signature of ageing could also predict dementia risk, by Dr Philippa Brice, PHG Foundation, September 7, 2015
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
NIH funds to move precision medicine closer to reality, by Dr Philippa Brice, PHG Foundation, September 6, 2015
Genetic testing all women for breast cancer might not be worth the cost, Science Daily, September 3, 2015
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