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A Comprehensive Human Gastric Cancer Organoid Biobank Captures Tumor Subtype Heterogeneity and Enables Therapeutic Screening. Yan Helen H N et al. Cell stem cell 2018 Oct Similar articles in PubMed
Breaking bad news in genetic counseling-problems and communication tools. Witt Magdalena M et al. Journal of applied genetics 2018 Nov 59(4) 449-452 Similar articles in PubMed
Framework for Using Risk Stratification to Improve Clinical Preventive Service Guidelines. Lin Jennifer S et al. American journal of preventive medicine 2018 Jan 54(1S1) S26-S37 Similar articles in PubMed
The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages. Jackson Leigh et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul Similar articles in PubMed
Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer. Sernadela Pedro et al. BioMed research international 2017 20178327980 Similar articles in PubMed
A combination test for detection of gene-environment interaction in cohort studies. Coombes Brandon et al. Genetic epidemiology 2017 Jul 41(5) 396-412 Similar articles in PubMed
'IRDiRC Recognized Resources': a new mechanism to support scientists to conduct efficient, high-quality research for rare diseases. Lochmüller Hanns et al. European journal of human genetics : EJHG 2016 Oct Similar articles in PubMed
Supporting families with Cancer: A patient centred survivorship model of care. Craft Emily Victoria et al. Familial cancer 2015 Dec 14(4) 637-40 Similar articles in PubMed
Genetic Test Results That Identify Increased Risk Do Not Change Behavior. Shaughnessy Allen F et al. American family physician 2016 Jul 94(2) 168 Similar articles in PubMed
GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge. Kirkpatrick Brianne E et al. Human mutation 2015 Oct 36(10) 974-8 Similar articles in PubMed
Translation and validation of a Spanish-language genetic health literacy screening tool. Rodríguez Sally Ann et al. Health Psychol 2015 Feb (2) 120-9 Similar articles in PubMed
Toward Global Biobank Integration by Implementation of the Minimum Information About BIobank Data Sharing (MIABIS 2.0 Core). Merino-Martinez Roxana et al. Biopreservation and biobanking 2016 Mar Similar articles in PubMed
Achieving behaviour change for detection of Lynch syndrome using the Theoretical Domains Framework Implementation (TDFI) approach: a study protocol. Taylor Natalie et al. BMC health services research 2016 16(1) 89 Similar articles in PubMed
Evaluation of the Families SHARE workbook: an educational tool outlining disease risk and healthy guidelines to reduce risk of heart disease, diabetes, breast cancer and colorectal cancer. Koehly Laura M et al. BMC public health 2015 15(1) 1120 Similar articles in PubMed
A Family-Centered Model for Sharing Genetic Risk. Daly Mary B et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2015 Sep 43(3) 545-51 Similar articles in PubMed
PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Buske Orion J et al. Hum. Mutat. 2015 Oct 36(10) 931-40 Similar articles in PubMed
SMART on FHIR Genomics: Facilitating standardized clinico-genomic apps. Alterovitz Gil et al. J Am Med Inform Assoc 2015 Jul 21. Similar articles in PubMed
A framework for bridging the gap in the care of familial hypercholesterolaemia in the community: pragmatic and economic perspectives. Purchase Sharon et al. Int J Evid Based Healthc 2014 Dec 12(4) 244-54 Similar articles in PubMed
A one-page summary report of genome sequencing for the healthy adult. Vassy Jason L et al. Public Health Genomics 2015 18(2) 123-9 Similar articles in PubMed
A report template for molecular genetic tests designed to improve communication between the clinician and laboratory. Scheuner Maren T et al. Genet Test Mol Biomarkers 2012 Jul 16(7) 761-9 Similar articles in PubMed
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. Jernigan Terry L et al. Neuroimage 2015 Apr 30. Similar articles in PubMed
Evaluation of a cartoon-based knowledge dissemination intervention on scientific and ethical challenges raised by nutrigenomics/nutrigenetics research. Lafrenière Darquise et al. Eval Program Plann 2014 Oct 46103-14 Similar articles in PubMed
The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic stress disorder enters the age of large-scale genomic collaboration. Logue Mark W et al. Neuropsychopharmacology 2015 Apr 23. Similar articles in PubMed
Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations. Lerner-Ellis Jordan, et al. Journal of medical genetics 2015 7 0. (7) 438-45 Similar articles in PubMed
A systematic approach to the reporting of medically relevant findings from whole genome sequencing. McLaughlin Heather M et al. BMC Med. Genet. 2014 15134 Similar articles in PubMed
Personalized assessment and management of women at risk for breast cancer in North America. Pruthi Sandhya et al. Womens Health (Lond Engl) 2015 Mar 11(2) 213-24 Similar articles in PubMed
An educational module to improve healthcare staffs' attitudes toward sickle cell disease patients. Similar articles in PubMed
Finding genomic function for genetic associations in nicotine addiction research: the ENCODE project's role in future pharmacogenomic analysis. Similar articles in PubMed
openSNP--a crowdsourced web resource for personal genomics. Similar articles in PubMed
Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT). Similar articles in PubMed
Self-guided management of exome and whole-genome sequencing results: changing the results return model. Similar articles in PubMed
Effectiveness of a Web-based genomics training for health educators in Texas. Similar articles in PubMed
A novel clinician interface to improve clinician access to up-to-date genetic results. Similar articles in PubMed
The next controversy in genetic testing: clinical data as trade secrets? Similar articles in PubMed
Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent. Similar articles in PubMed