@article {22,
	title = {My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.},
	journal = {Genet Med},
	volume = {19},
	year = {2017},
	month = {2017 Apr},
	pages = {467-475},
	abstract = {<p>A major challenge to implementing precision medicine is the need for an efficient and cost-effective strategy for returning individual genomic test results that is easily scalable and can be incorporated into multiple models of clinical practice. My46 is a Web-based tool for managing the return of genetic results that was designed and developed to support a wide range of approaches to disclosing results, ranging from traditional face-to-face disclosure to self-guided models. My46 has five key functions: set and modify results-return preferences, return results, educate, manage the return of results, and assess the return of results. These key functions are supported by six distinct modules and a suite of features that enhance the user experience, ease site navigation, facilitate knowledge sharing, and enable results-return tracking. My46 is a potentially effective solution for returning results and supports current trends toward shared decision making between patients and providers and patient-driven health management.Genet Med 19 4, 467-475.</p>},
	keywords = {Biomedical Research, Computational Biology, Decision Making, Genomics, Humans, Internet, Medical Informatics, Patient Access to Records, Precision Medicine},
	issn = {1530-0366},
	doi = {10.1038/gim.2016.133},
	author = {Tabor, Holly K and Jamal, Seema M and Yu, Joon-Ho and Crouch, Julia M and Shankar, Aditi G and Dent, Karin M and Anderson, Nick and Miller, Damon A and Futral, Brett T and Bamshad, Michael J}
}
@article {310,
	title = {PhenoDB: a new web-based tool for the collection, storage, and analysis of phenotypic features.},
	journal = {Hum Mutat},
	volume = {34},
	year = {2013},
	month = {2013 Apr},
	pages = {566-71},
	abstract = {<p>To interpret whole exome/genome sequence data for clinical and research purposes, comprehensive phenotypic information, knowledge of pedigree structure, and results of previous clinical testing are essential. With these requirements in mind and to meet the needs of the Centers for Mendelian Genomics project, we have developed PhenoDB (http://phenodb.net), a secure, Web-based portal for entry, storage, and analysis of phenotypic and other clinical information. The phenotypic features are organized hierarchically according to the major headings and subheadings of the Online Mendelian Inheritance in Man (OMIM{\textregistered}) clinical synopses, with further subdivisions according to structure and function. Every string allows for a free-text entry. All of the approximately 2,900 features use the preferred term from Elements of Morphology and are fully searchable and mapped to the Human Phenotype Ontology and Elements of Morphology. The PhenoDB allows for ascertainment of relevant information from a case in a family or cohort, which is then searchable by family, OMIM number, phenotypic feature, mode of inheritance, genes screened, and so on. The database can also be used to format phenotypic data for submission to dbGaP for appropriately consented individuals. PhenoDB was built using Django, an open source Web development tool, and is freely available through the Johns Hopkins McKusick-Nathans Institute of Genetic Medicine (http://phenodb.net).</p>},
	keywords = {Databases, Factual, Genomics, Humans, Internet, Medical Informatics, Phenotype, Software},
	issn = {1098-1004},
	doi = {10.1002/humu.22283},
	author = {Hamosh, Ada and Sobreira, Nara and Hoover-Fong, Julie and Sutton, V Reid and Boehm, Corinne and Schiettecatte, Fran{\c c}ois and Valle, David}
}
