Published on 07/02/2015
Human Genomics across the Lifespan
Birth Defects and Child Health
Genetic and Clinical Profile of Patients of Duchenne Muscular Dystrophy: Experience from a Tertiary Care Center in Eastern India.
Dey Sadanand et al. Indian Pediatr 2015 Jun 8. 52(6) 481-4
Duchenne muscular dystrophy: High-resolution melting curve analysis as an affordable diagnostic mutation scanning tool in a South African cohort.
Esterhuizen A I et al. S. Afr. Med. J. 2014 Nov 104(11) 779-84
Findings from the National Birth Defects Prevention Study: Interpretation and translation for the clinician.
Alwan Sura et al. Birth Defects Res. Part A Clin. Mol. Teratol. 2015 Jun 25.
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder.
Cismondi Inés Adriana et al. Biochim. Biophys. Acta 2015 Jun 24.
Can genetics predict response to complex behavioral interventions? evidence from a genetic analysis of the Fast Track randomized control trial.
Albert Dustin et al. J Policy Anal Manage 2015 34(3) 497-518
Patients with Non-small Cell Lung Cancer Analyzed for EGFR: Adherence to Guidelines, Prevalence and Outcome.
Sandelin Martin et al. Anticancer Res. 2015 Jul 35(7) 3979-85
Peer support and additional information in group medical consultations (GMCs) for BRCA1/2 mutation carriers: A randomized controlled trial.
Visser Annemiek et al. Acta Oncol 2015 Jun 26. 1-10
A Family History of Lethal Prostate Cancer and Risk of Aggressive Prostate Cancer in Patients Undergoing Radical Prostatectomy.
Raheem Omer A et al. Sci Rep 2015 510544
Prospective Clinical Utility Study of the Use of the 21-Gene Assay in Adjuvant Clinical Decision Making in Women With Estrogen Receptor-Positive Early Invasive Breast Cancer: Results From the SWITCH Study.
Gligorov Joseph et al. Oncologist 2015 Jun 25.
Design of a Genomics Curriculum: Competencies for Practicing Pathologists.
Laudadio Jennifer et al. Arch. Pathol. Lab. Med. 2015 Jul 139(7) 894-900
Educating future nursing scientists: Recommendations for integrating omics content in PhD programs.
Conley Yvette P et al. Nurs Outlook 2015 Jun 12.
The support of human genetic evidence for approved drug indications.
Nelson Matthew R et al. Nat. Genet. 2015 Jun 29.
Framing optional genetic testing in the context of mandatory newborn screening tests.
Lillie Sarah E et al. BMC Med Inform Decis Mak 2015 15(1) 50
What patients are reading about noninvasive prenatal testing: an evaluation of Internet content and implications for patient-centered care.
Mercer M B et al. Prenat. Diagn. 2014 Oct 34(10) 986-93
Committee Opinion No. 640: Cell-free DNA Screening for Fetal Aneuploidy.
Obstet Gynecol 2015 Jun 29.
Should everyone be tested for high-risk cancer genes?
By Maria Delaney, Genetic Literacy Project, July 2
Oncology dominates personalized medicine,
Applied Clinical Trials, June 1
Transformation Medicine Genomically Informed and Personally Precise,
by Stephen C. Peiper and Erica S. Johnson, GEN, July 2
Genomics and the trouble with 'N of 1' trials,
Genomics Education Programme, June 29
CRISPR: Science can't solve it,
by Daniel Sarewitz, Nature News, June 23
Computational Biology: Moving into the Future One Click at a Time.
Fogg Christiana N et al. PLoS Comput. Biol. 2015 Jun 11(6) e1004323
Navigators have a key role in using genetics and genomics for cancer risk identification,
by Joyce Pagan, Oncology Nurse Advisor, June 28
Would you be willing to reveal your genetic code to your employer?
By Fintan Burke, Irish Times, June 28
Genomic hype translates, slowly, into hope,
by Alex Philippidis, GEN, June 23
Consumers of commercial genetic tests understand more than many believe,
Michigan University News, June 22
Another 5 things to know about meta-analysis,
by Hilda Bastian, PLoS Blogs, June 30
Scientific ethical divide between China and West,
by Didi Kirsten Tatlow, The New York Times, June 29
Report from the Festival of Genomics,
Bio IT World, June 26