Published on 09/15/2016
Human Genomics across the Lifespan
Birth Defects and Child Health
-
Public Health Research, Epidemiology, and Surveillance for Hemoglobinopathies (PHRESH)
-
FASD Awareness
-
Sickle Cell Awareness
-
An Update on Fetal Alcohol Syndrome-Pathogenesis, Risks, and Treatment.
Gupta Keshav K et al. Alcoholism, clinical and experimental research 2016 Aug 40(8) 1594-602 -
The Genetics of Fetal Alcohol Spectrum Disorders.
Eberhart Johann K et al. Alcoholism, clinical and experimental research 2016 Jun 40(6) 1154-65 -
Prevalence of Sickle Cell Trait and Reliability of Self-Reported Status among Expectant Parents in Nigeria: Implications for Targeted Newborn Screening.
Burnham-Marusich Amanda R et al. Public health genomics 2016 Sep 19(5)
Cancer
-
Therapeutic and Preventive Implications of Moonshot in Hereditary Cancer Syndromes.
Diab Osama et al. JAMA oncology 2016 Sep -
In honor of Ovarian Cancer Awareness Month
G Hurst, Cure today, Sepetember 2016 -
Facing my fear: did I have the cancer mutation that killed my dad?
JH Edelestein, The Guardian, September 9, 2016 -
Insurers May Insist On Counseling Before Genetic Tests For Breast Cancer
M Andrews, Kaiser Health News, September 13, 2016 -
Inactivation of Cancer Mutations Utilizing CRISPR/Cas9.
Gebler Christina et al. Journal of the National Cancer Institute 2017 Jan 109(1) -
A 19-Gene expression signature as a predictor of survival in colorectal cancer.
Abdul Aziz Nurul Ainin et al. BMC medical genomics 2016 9(1) 58 -
Prognostic significance of performing universal HER2 testing in cases of advanced gastric cancer.
Jiménez-Fonseca Paula et al. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2016 Sep -
Bilateral Oophorectomy and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
Kotsopoulos Joanne et al. Journal of the National Cancer Institute 2017 Jan 109(1) -
National Prociency Testing Result of CYP2D6*10 Genotyping for Adjuvant Tamoxifen Therapy in China.
Lin Guigao et al. PloS one 2016 11(9) e0162361 -
Prostate Cancer Prevention (PDQ®)–Patient Version
NCI, September 8, 2016 -
Increasing Appropriate BRCA1/2 Mutation Testing: The Role of Family History Documentation and Genetic Counseling in a Multidisciplinary Clinic.
Kishan Amar U et al. Annals of surgical oncology 2016 Sep
Chronic Disease
-
Implications of Personal Genomic Testing for Health Behaviors: The Case of Smoking.
Olfson Emily et al. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2016 Jul -
A microRNA plays role in major depression,
Science, September 9, 2016 -
Early Childhood Environment and Genetic Interactions: the Diathesis for Suicidal Behavior.
Brodsky Beth S et al. Current psychiatry reports 2016 Sep 18(9) 86
Ethics/Policy/Law
-
Privacy: The myth of anonymity.
Savage Neil et al. Nature 2016 537(7619) S70-2 -
Ethical issues in pediatric genetic testing and screening.
Botkin Jeffrey R et al. Current opinion in pediatrics 2016 Sep -
Ethical issues in the evaluation of adults with suspected genetic neuromuscular disorders.
Su Xiaowei et al. Muscle & nerve 2016 Sep
Practice
-
A special Nature Outlook Supplement on Precision Medicine
Nature Outlook, September 2016 -
NHS England sets out its vision for personalised medicine,
by Rebecca Bazeley, PHG Foundation, September 8, 2016 -
Americans are keen to take part in a national precision medicine program
E Dishman, STat News, September 8, 2016 -
The impact of personal genomics on risk perceptions and medical decision-making.
Krieger Joshua L et al. Nature biotechnology 2016 Sep 34(9) 912-8 -
Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information.
Oliveri Serena et al. Public health genomics 2016 Sep 19(5) -
Public Awareness of Direct-to-Consumer Genetic Tests: Findings from the 2013 U.S. Health Information National Trends Survey.
Agurs-Collins Tanya et al. Journal of cancer education : the official journal of the American Association for Cancer Education 2015 Dec 30(4) 799-807 -
Assessing multilevel determinants of adoption and implementation of genomic medicine: an organizational mixed-methods approach.
Oishi Sabine M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Nov 17(11) 919-26 -
Five-Year Bibliometric Review of Genomic Nursing Science Research.
Williams Janet K et al. Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau 2016 Mar 48(2) 179-86 -
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing.
Balmaña Judith et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Sep
Heart, Lung, Blood and Sleep Diseases
-
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Liu Chunyu et al. Nature genetics 2016 Sep -
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
Surendran Praveen et al. Nature genetics 2016 Sep -
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Alfares Ahmed A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Nov 17(11) 880-8
Newborn Screening
-
A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis.
Bombard Yvonne et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep -
Lab Quality Program Important to Newborn Screening
Pharmacogenomics
-
Clinical Utility of Combinatorial Pharmacogenomics-Guided Antidepressant Therapy: Evidence from Three Clinical Studies.
Altar C Anthony et al. Molecular neuropsychiatry 2015 Oct 1(3) 145-55
Reproductive Health
-
Prenatal and pre-implantation genetic diagnosis.
Vermeesch Joris Robert, et al. Nature reviews. Genetics 2016 0 0. (10) 643-56 -
A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan.
Yotsumoto Junko et al. Journal of human genetics 2016 Sep -
Prenatal Carrier Screening for Spinal Muscular Atrophy.
Wood S Lindsay et al. American journal of perinatology 2016 Sep -
'It made you think twice' - an interview study of women's perception of a web-based decision aid concerning screening and diagnostic testing for fetal anomalies.
Åhman Annika et al. BMC pregnancy and childbirth 2016 16267
News/ Reviews/Comments
-
Applications of CRISPR technologies in research and beyond.
Barrangou Rodolphe et al. Nature biotechnology 2016 Sep 933-941