Published on 12/08/2016
Human Genomics across the Lifespan
Birth Defects and Child Health
When One Diagnosis Is Not Enough.
Boycott Kym M, et al. The New England journal of medicine 2017 0 0. (1) 83-85
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Posey Jennifer E, et al. The New England journal of medicine 2017 0 0. (1) 21-31
[New Classification for Advanced Colorectal Cancer Using CancerPlex®Genomic Tests].
Kameyama Hitoshi et al. Gan to kagaku ryoho. Cancer & chemotherapy 2016 Nov 43(11) 1361-1365
Next-generation sequencing in NSCLC and melanoma patients: a cost and budget impact analysis.
van Amerongen Rosa A et al. Ecancermedicalscience 2016 10684
Population-Based Study of Attitudes toward BRCA Genetic Testing among Orthodox Jewish Women.
Tang Eve Y et al. The breast journal 2016 Nov
Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations.
D'Andrea Elvira et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Dec 18(12) 1171-1180
Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience.
Lieberman Sari et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Dec
Health literacy and the perception of risk in a breast cancer family history clinic.
Rutherford E J et al. The surgeon : journal of the Royal Colleges of Surgeons of Edinburgh and Ireland 2016 Nov
The clinical utility of circulating neuroendocrine gene transcript analysis in well-differentiated paragangliomas and pheochromocytomas.
Peczkowska M et al. European journal of endocrinology 2017 Feb 176(2) 143-157
Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening.
Lawson Caitlin E et al. Journal of genetic counseling 2016 Dec
Receptivity and Preferences for Lifestyle Programs to Reduce Cancer Risk among Lung Cancer Family Members.
Howell Lisa A et al. Advances in cancer prevention 2016 Sep 1(3)
Frequency of a positive family history of colorectal cancer in general practice: a cross-sectional study.
Plath Jasper et al. Family practice 2016 Dec
Precision Cancer Diagnostics: Tracking Genomic Evolution in Clinical Trials.
Beca Francisco et al. PLoS medicine 2016 Dec 13(12) e1002177
Sequencing Strategies to Guide Decision Making in Cancer Treatment.
Topham James T et al. PLoS medicine 2016 Dec 13(12) e1002189
Will Diet and Exercise Save Us All?
Monteiro João et al. Cell 2016 Dec 167(6) 1431
Does Gene Testing Spur Healthier Habits? Maybe Not
N Bakalar, New York Times, December 2, 2016
Unpacking Reasons for Genetic Testing of Adoptees.
Lee Richard M et al. The American journal of bioethics : AJOB 2016 Dec 16(12) 39-40
Does Lack of "Genetic-Relative Family Health History" Represent a Potentially Avoidable Health Disparity for Adoptees?
May Thomas et al. The American journal of bioethics : AJOB 2016 Dec 16(12) 33-38
The Need for a Privacy Standard for Medical Devices That Transmit Protected Health Information Used in the Precision Medicine Initiative for Diabetes and Other Diseases.
Klonoff David C et al. Journal of diabetes science and technology 2016 Dec
A Roadmap to Successful Clinical Proteomics.
Wright Ian et al. Clinical chemistry 2016 Nov
Why racial diversity in genetics studies matters in patient care
E Newbern, Genetic Literacy Project, December 7, 2016
Pharmacogenomics and Implications for Nursing Practice.
Cheek Dennis J et al. Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing 2015 Nov 47(6) 496-504
The CRSPR pioneers
Time Magazine, December 2016
Nurses at the front-line of personalised medicine
Genomics England, December 2016
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
Sweet Kevin et al. Journal of genetic counseling 2016 Dec
Ethics of genetic testing and research in sport: a position statement from the Australian Institute of Sport.
Vlahovich Nicole et al. British journal of sports medicine 2016 Nov
Increasing importance of genetics in nursing.
Camak Deborah Jacks et al. Nurse education today 2016 Sep 4486-91
Genomics for Nursing Education and Practice: Measuring Competency.
Anderson Gwen et al. Worldviews on evidence-based nursing 2015 Jun 12(3) 165-75
Heart, Lung, Blood and Sleep Diseases
Attainment of LDL Cholesterol Treatment Goals in Children and Adolescents With Familial Hypercholesterolemia. The SAFEHEART Follow-up Registry.
Saltijeral Adriana et al. Revista espanola de cardiologia (English ed.) 2016 Nov
The response to receiving phenotypic and genetic coronary heart disease risk scores and lifestyle advice - a qualitative study.
Shefer Guy et al. BMC public health 2016 Dec 16(1) 1221
Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC).
Tagliaferri Laura et al. Clinical immunology (Orlando, Fla.) 2016 Dec
Patient Perception of Negative Noninvasive Prenatal Testing Results.
Wittman A Theresa et al. AJP reports 2016 Oct 6(4) e391-e406
A Right to Genetic Family History.
Thomsen Kyle et al. The American journal of bioethics : AJOB 2016 Dec 16(12) 50-52