Volume 35 Number 1 July 2-9, 2015
Human Genomics across the Lifespan
Birth Defects and Child Health
Duchenne muscular dystrophy: High-resolution melting curve analysis as an affordable diagnostic mutation scanning tool in a South African cohort.
Esterhuizen AI et al. S. Afr. Med. J. 2014 Nov 104(11) 779-84
Esterhuizen AI et al. S. Afr. Med. J. 2014 Nov 104(11) 779-84
Genetic and clinical profile of patients of Duchenne muscular dystrophy: Experience from a tertiary care center in Eastern India.
Dey S et al. Indian Pediatr 2015 Jun 8. 52(6) 481-4
Dey S et al. Indian Pediatr 2015 Jun 8. 52(6) 481-4
Can genetics predict response to complex behavioral interventions? evidence from a genetic analysis of the Fast Track randomized control trial.
Albert D et al. J Policy Anal Manage 2015 34(3) 497-518
Albert D et al. J Policy Anal Manage 2015 34(3) 497-518
Findings from the National Birth Defects Prevention Study: Interpretation and translation for the clinician.
Alwan S et al. Birth Defects Res. Part A Clin. Mol. Teratol. 2015 Jun 25.
Alwan S 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 IA et al. Biochim. Biophys. Acta 2015 Jun 24.
Cismondi IA et al. Biochim. Biophys. Acta 2015 Jun 24.
Cancer
A family history of lethal prostate cancer and risk of aggressive prostate cancer in patients undergoing radical prostatectomy.
Raheem OA et al. Sci Rep 2015 510544
Raheem OA et al. Sci Rep 2015 510544
Patients with non-small cell lung cancer analyzed for EGFR: Adherence to guidelines, prevalence and outcome.
Sandelin M et al. Anticancer Res. 2015 Jul 35(7) 3979-85
Sandelin M 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 A et al. Acta Oncol 2015 Jun 26. 1-10
Visser A et al. Acta Oncol 2015 Jun 26. 1-10
Genomics in Practice
Design of a genomics curriculum: Competencies for practicing pathologists.
Laudadio J et al. Arch. Pathol. Lab. Med. 2015 Jul 139(7) 894-900
Laudadio J 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 YP et al. Nurs Outlook 2015 Jun 12.
Conley YP et al. Nurs Outlook 2015 Jun 12.
The support of human genetic evidence for approved drug indications.
Nelson MR et al. Nat. Genet. 2015 Jun 29.
Nelson MR et al. Nat. Genet. 2015 Jun 29.
Newborn Screening
Framing optional genetic testing in the context of mandatory newborn screening tests.
Lillie SE et al. BMC Med Inform Decis Mak 2015 15(1) 50
Lillie SE et al. BMC Med Inform Decis Mak 2015 15(1) 50
Reproductive Health
Committee opinion: Cell-free DNA screening for fetal aneuploidy.
Obstet Gynecol. 2015 Jun 25.
Obstet Gynecol. 2015 Jun 25.
What patients are reading about noninvasive prenatal testing: an evaluation of Internet content and implications for patient-centered care.
Mercer MB et al. Prenat. Diagn. 2014 Oct 34(10) 986-93
Mercer MB et al. Prenat. Diagn. 2014 Oct 34(10) 986-93
Reviews, News and Commentaries
Computational biology: Moving into the future one click at a time.
Fogg CN, et al. PLoS Comput Biol. 2015 Jun 24;11(6):e1004323.
Fogg CN, et al. PLoS Comput Biol. 2015 Jun 24;11(6):e1004323.
Transformation medicine genomically informed and personally precise, by Stephen C. Peiper and Erica S. Johnson, GEN, July 2
Should babies have their genomes sequenced? By Anna Nowogrodzki, MIT Technology Review, July 2
Should everyone be tested for high-risk cancer genes? by Marie Delaney, Genetic Literacy Project, July 2
Oncology dominates personalized medicine, Applied Clinical Trials, June 1
Another 5 things to know about meta-analysis, by Hilda Bastian, PLoS Blogs, June 30
Genomics and the trouble with ‘N of 1’ trials, Genomics Education Programme, June 29
Scientific ethical divide between China and West, by Didi Kirsten Tatlow, The New York Times, June 29
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
Report from the Festival of Genomics, Bio IT World, June 26
Genetics and cancer risk: More options, more tests, more prevention, more survivors, the Monitor, June 25
The promise and peril of Crispr, by John Lauerman and Caroline Chen, Bloomberg, June 25
CRISPR: Science can't solve it, by Daniel Sarewitz, Nature News, June 23
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
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