Last Posted: May-13-2019 8AM
Last Posted: May 09, 2019
- Genetics in primary care: validating a tool to pre-symptomatically assess common disease risk using an Australian questionnaire on family history.
Houwink Elisa J F et al. Clinical and translational medicine 2019 May 8(1) 17 - A Two-Way Interactive Text Messaging Application for Low-Income Patients with Chronic Medical Conditions: Design-Thinking Development Approach.
Marko-Holguin Monika et al. JMIR mHealth and uHealth 2019 May 7(5) e11833 - John's story - living with hereditary haemochromatosis.
Graham Julia Vivien et al. Rural and remote health 2019 May 19(2) 4844 - Epigenetics in Human Obesity and Type 2 Diabetes.
Ling Charlotte et al. Cell metabolism 2019 Apr - A review of the reproductive consequences of consanguinity.
Oniya Olubunmi et al. European journal of obstetrics, gynecology, and reproductive biology 2019 Jan 23287-96 - Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform.
Treff Nathan R et al. European journal of medical genetics 2019 Apr - Diabetes: Is there a future for Pharmacogenomics guided treatment?
Pearson Ewan R et al. Clinical pharmacology and therapeutics 2019 Apr - Earlier Detection of Diabetic Retinopathy with Smartphone AI
University of Michigan Health Lab, April 29, 2019 - On the utilization of polygenic risk scores for therapeutic targeting.
Gibson Greg, et al. PLoS genetics 2019 0 0. (4) e1008060 - Future Roadmaps for Precision Medicine Applied to Diabetes: Rising to the Challenge of Heterogeneity.
Bowman P et al. Journal of diabetes research 2018 20183061620
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