Published on 11/19/2015
Human Genomics across the Lifespan
Birth Defects and Child Health
The validity of family history as a risk factor in pediatric hearing loss.
Driscoll Carlie et al. International journal of pediatric otorhinolaryngology 2015 May 79(5) 654-9
Carrier testing in children and adolescents.
Vears D F et al. European journal of medical genetics 2015 Nov
Marginally scientific? Genetic testing of children and adolescents for lifestyle and health promotion.
Caulfield Timothy, et al. Journal of law and the biosciences 2015 11 0. (3) 627-644
From Genetics to Genomics: A Short Introduction for Pediatric Neurologists.
Neubauer Bernd A et al. Neuropediatrics 2015 Nov
The Challenges of Precision Oncology Drug Development and Implementation.
Hollingsworth Simon J et al. Public health genomics 2015 Nov
Getting Personal: Accelerating Personalised and Precision Medicine Integration into Clinical Cancer Research and Care in Clinical Trials.
Horgan Denis et al. Public health genomics 2015 Nov
NCCN Oncology Research Program's Investigator Steering Committee and NCCN Best Practices Committee Molecular Profiling Surveys.
Kurzrock Razelle et al. Journal of the National Comprehensive Cancer Network : JNCCN 2015 Nov 13(11) 1337-46
Measuring and Validating a General Cancer Predisposition Perception Scale: An Adaptation of the Revised-IPQ-Genetic Predisposition Scale.
Lam Wendy Wing Tak et al. PloS one 2015 10(11) e0142620
AACR precision medicine series: Highlights of the integrating clinical genomics and cancer therapy meeting.
Maggi Elaine et al. Mutation research 2015 Nov 78244-51
Genomic Correlates to the Newly Proposed Grading Prognostic Groups for Prostate Cancer.
Rubin Mark A et al. European urology 2015 Nov
Integrating Personalized Medicine in the Canadian Environment: Efforts Facilitating Oncology Clinical Research.
Syme Rachel et al. Public health genomics 2015 Nov
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.
Schrader Kasmintan A et al. JAMA oncology 2015 Nov 1-8
A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients.
Sun Jie et al. Scientific reports 2015 516553
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
Gresele P et al. Journal of thrombosis and haemostasis : JTH 2015 Feb 13(2) 314-22
Evaluation of the Families SHARE workbook: an educational tool outlining disease risk and healthy guidelines to reduce risk of heart disease, diabetes, breast cancer and colorectal cancer.
Koehly Laura M et al. BMC public health 2015 15(1) 1120
Performance of Different Diagnostic Criteria for Familial Mediterranean Fever in Children with Periodic Fevers: Results from a Multicenter International Registry.
Demirkaya Erkan et al. The Journal of rheumatology 2015 Nov
Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.
Shelton Celeste A et al. Clinical and translational gastroenterology 2015 6e124
A validated web-based tool to display individualised Crohn's disease predicted outcomes based on clinical, serologic and genetic variables.
Siegel C A et al. Alimentary pharmacology & therapeutics 2015 Nov
Precision medicine ethics: selected issues and developments in next-generation sequencing, clinical oncology, and ethics.
Fiore Robin N et al. Current opinion in oncology 2015 Nov
The Undiagnosed Diseases Network of the National Institutes of Health: A National Extension.
Gahl William A et al. JAMA 2015 Nov 314(17) 1797-8
Genetic Testing Awareness and Attitudes among Latinos: Exploring Shared Perceptions and Gender-Based Differences.
Hamilton Jada G et al. Public health genomics 2015 Nov
TOGGLE: toolbox for generic NGS analyses.
Monat Cécile et al. BMC bioinformatics 2015 16374
Conversations with children about DNA and genes using an original children's book.
Newcomb Patricia et al. Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners 28(6) 497-506
Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice.
Roche Myra I et al. Current genetic medicine reports 3(4) 166-176
Establishing the Evidence Bar for Molecular Diagnostics in Personalised Cancer Care.
Schneider Daniel et al. Public health genomics 2015 Nov 18(6) 29-38
Heart, Lung, Blood and Sleep Diseases
Systematic detection of familial hypercholesterolaemia in primary health care: a community based prospective study of three methods.
Kirke Andrew B et al. Heart, lung & circulation 2015 Mar 24(3) 250-6
Incorporation of pharmacogenetic testing into medication therapy management.
Haga Susanne B et al. Pharmacogenomics 2015 Nov
655: A PILOT STUDY FOR CLINICAL IMPLEMENTATION OF PHARMACOGENOMICS (PGX) IN PERIOPERATIVE CARE.
Hikino Keiko et al. Critical care medicine 2015 Dec 43(12 Suppl 1) 165
Non-invasive prenatal screening for trisomy 21: Consumers' perspectives.
Higuchi Emily C et al. American journal of medical genetics. Part A 2015 Nov
Reproductive Endocrinologists' Utilization of Genetic Counselors for Oncofertility and Preimplantation Genetic Diagnosis (PGD) Treatment of BRCA1/2 Mutation Carriers.
Goetsch Allison L et al. Journal of genetic counseling 2015 Nov
Human genotype-phenotype databases: aims, challenges and opportunities.
Brookes Anthony J et al. Nature reviews. Genetics 2015 Nov
Holidays a good time to focus on family health history,
by David DeMille,the Spectrum, November 17, 2015
NCBI Plans Genomics Hackathon,
BIO IT World, November 16, 2015
Genetic Testing, Genome Sequencing, and the FDA,
National Law Review, November 13, 2015
If You Paid $500 for a Gene Test, Would You Know What to Do With It?
By John Tozzi, Bloomberg, November 16, 2015
Two Boston Hospitals To Sequence Genome Of Newborns For The First Time Ever,
by Dr. Mallika Marshall, CBS Boston, November 12, 2015
'No place' for genetic testing to spot young sporting talent or boost performance,
EurekAlert, November 16, 2015
Cancer researchers band together to pool tumor genome data,
by Jocelyn Kaiser, Science Insider, November 6, 2015
Almost a miracle: gene-edited cells that can cure cancer,
Genomics Education Programme, November 16, 2015
Puppy bred to have muscular dystrophy saved by surprise mutation,
by Ewen Callaway, Nature News, November 12, 2015
Will Layla Save Gene Editing?
DNA Science Blog, November 12, 2015
A Genetic Map Hints At What Makes A Brain Human,
by Jon Hamilton, NPR, November 16, 2015