Last Posted: Dec 12, 2018
- Developing a Process for Returning Medically Actionable Genomic Variants to Latino Patients in a Federally Qualified Health Center.
Shaibi Gabriel Q et al. Public health genomics 2018 Dec 1-8 - White Paper: Pathways to Progress in Newborn Screening for Sickle Cell Disease in Sub-Saharan Africa.
Hsu Lewis et al. Journal of tropical diseases & public health 2018 6(2) 260 - Women's preferences for and experiences with prenatal genetic testing decision making: Sociodemographic disparities in preference-concordant decision making.
Molina Fabiola et al. Patient education and counseling 2018 Oct - Data resource profile: Cardiovascular H3Africa Innovation Resource (CHAIR)
MO Owalabi et al, Int J EPi, December 5, 2018 - A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults
M. Murray and the Genomics and Population Health Action Collaborative, National Academies of Medicine, December 3, 2018 - Perceived Unfair Treatment by Police, Race, and Telomere Length: A Nashville Community-based Sample of Black and White Men.
McFarland Michael J et al. Journal of health and social behavior 2018 Nov 22146518811144 - Data-Driven Medicine Will Help People — But Can It Do So Equally?
New York Times, November 2018 - A Recurrent BRCA2 Mutation Explains the Majority of Hereditary Breast and Ovarian Cancer Syndrome Cases in Puerto Rico.
Diaz-Zabala Hector J et al. Cancers 2018 Nov 10(11) - Understanding Disparities in Access to Genomic Medicine: Proceedings of a Workshop
NASEM workshop, November 2018 - Disparities in genetic services utilization in a random sample of young breast cancer survivors.
Nikolaidis Christos et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Nov
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