Published on in Vol 5, No 2 (2016): Apr-Jun

Information Needs in the Precision Medicine Era: How Genetics Home Reference Can Help

Information Needs in the Precision Medicine Era: How Genetics Home Reference Can Help

Information Needs in the Precision Medicine Era: How Genetics Home Reference Can Help

Journals

  1. Vo T, Bell G, Owusu Obeng A, Hicks J, Dunnenberger H. Pharmacogenomics Implementation: Considerations for Selecting a Reference Laboratory. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy 2017;37(9):1014 View
  2. Famiglietti M, Estreicher A, Breuza L, Poux S, Redaschi N, Xenarios I, Bridge A. An enhanced workflow for variant interpretation in UniProtKB/Swiss-Prot improves consistency and reuse in ClinVar. Database 2019;2019 View
  3. Anderson D, Bousman C, Chapman K. Engaging in building the educational support needed to deliver precision health in Canada. Healthcare Management Forum 2020;33(3):135 View
  4. Zhang C, Mao Y, Song L. Precise treatments for schizophrenia: where is the way forward?. General Psychiatry 2018;31(1):e000002 View
  5. Hillyer G, Schmitt K, Reyes A, Cruz A, Lizardo M, Schwartz G, Terry M. Community education to enhance the more equitable use of precision medicine in Northern Manhattan. Journal of Genetic Counseling 2020;29(2):247 View
  6. Qiu B, Jiang W, Qiu W, Mu W, Qin Y, Zhu Y, Zhang J, Wang Q, Liu D, Qu Z. Pine needle oil induces G2/M arrest of HepG2 cells by activating the ATM pathway. Experimental and Therapeutic Medicine 2017 View
  7. Kolasa K, Goettsch W, Petrova G, Berler A. ‘Without data, you’re just another person with an opinion’. Expert Review of Pharmacoeconomics & Outcomes Research 2020;20(2):147 View
  8. Burghardt T. Demographic model for inheritable cardiac disease. Archives of Biochemistry and Biophysics 2019;672:108056 View
  9. Brown S, Jouni H, Marroush T, Kullo I. Effect of Disclosing Genetic Risk for Coronary Heart Disease on Information Seeking and Sharing. Circulation: Cardiovascular Genetics 2017;10(4) View
  10. McCarthy M, Walsh T. The fungal meningitis outbreak five years later: what have we learned aboutExserohilum rostratum?. Expert Review of Precision Medicine and Drug Development 2017;2(6):321 View
  11. de Carvalho J, de Morais G, Vieira T, Rabelo N, Llerena J, Gonzalez S, de Vasconcelos A. miRNA Genetic Variants Alter Their Secondary Structure and Expression in Patients With RASopathies Syndromes. Frontiers in Genetics 2019;10 View
  12. Ray S, Goyal S. Precision medicine: From concept to clinical practice – A promising challenge!!. Journal of Marine Medical Society 2020;22(1):1 View
  13. Abdul Rahim H, Ismail S, Hassan A, Fadl T, Khaled S, Shockley B, Nasrallah C, Qutteina Y, Elmaghraby E, Yasin H, Darwish D, Fakhro K, Badji R, Al-Muftah W, Afifi N, Althani A. Willingness to participate in genome testing: a survey of public attitudes from Qatar. Journal of Human Genetics 2020;65(12):1067 View
  14. Burl R, Clough S, Sendler E, Estill M, Krawetz S. Sperm RNA elements as markers of health. Systems Biology in Reproductive Medicine 2018;64(1):25 View
  15. Babac A, Litzkendorf S, Schmidt K, Pauer F, Damm K, Frank M, Graf von der Schulenburg J. Shaping an Effective Health Information Website on Rare Diseases Using a Group Decision-Making Tool: Inclusion of the Perspectives of Patients, Their Family Members, and Physicians. Interactive Journal of Medical Research 2017;6(2):e23 View
  16. Melocchi A, Briatico-Vangosa F, Uboldi M, Parietti F, Turchi M, von Zeppelin D, Maroni A, Zema L, Gazzaniga A, Zidan A. Quality considerations on the pharmaceutical applications of fused deposition modeling 3D printing. International Journal of Pharmaceutics 2021;592:119901 View
  17. Doña I, Jurado-Escobar R, Pérez-Sánchez N, Laguna J, Bartra J, Testera-Montes A, de Santa María R, Torres M, Cornejo-García J. Genetic Variants Associated With Drug-Induced Hypersensitivity Reactions: towards Precision Medicine?. Current Treatment Options in Allergy 2021;8(1):42 View
  18. Rovira‐Moreno E, Abuli A, Codina‐Sola M, Valenzuela I, Serra‐Juhe C, Cuscó I, Borregán M, Cueto‐González A, Vendrell T, López‐Grondona F, Brun‐Gasca C, Brignani E, Martínez‐Ribot L, Garci‐Espejo R, Cruz J, García‐Arumí E, Tizzano E. Beyond the disease itself: A cross‐cutting educational initiative for patients and families with rare diseases. Journal of Genetic Counseling 2021;30(3):693 View
  19. Voigt I, Inojosa H, Dillenseger A, Haase R, Akgün K, Ziemssen T. Digital Twins for Multiple Sclerosis. Frontiers in Immunology 2021;12 View

Books/Policy Documents

  1. Videira N, Tramontina R, Sodré V, Contesini F. Bioprocessing for Biomolecules Production. View
  2. Hersh W. Information Retrieval: A Biomedical and Health Perspective. View
  3. Gammal R, Dunnenberger H, Caudle K, Swen J. Pharmacogenomics. View
  4. Bogdan B. MedRevolution. View