Bauer-Mehren, A., Bundschus, M., Rautschka, M., Mayer, M. A., Sanz, F., & Furlong, L. I. (2011). Gene-disease network analysis reveals functional modules in mendelian, complex and environmental diseases. PloS one, 6(6), e20284.
Bollier, D., & Firestone, C. M. (2010). The promise and peril of big data: Aspen Institute, Communications and Society Program Washington, DC.
Bongers, E. M., Gubler, M. C., & Knoers, N. V. (2002). Nail-patella syndrome. Overview on clinical and molecular findings. Pediatr Nephrol, 17(9), 703-712. doi:10.1007/s00467-002-0911-5
Chen, H., Lun, Y., Ovchinnikov, D., Kokubo, H., Oberg, K. C., Pepicelli, C. V., . . . Johnson, R. L. (1998). Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nat Genet, 19(1), 51-55. doi:10.1038/ng0598-51
Cook, K. ( 2008, Accessed December 3, 2012). Unstructured data and the 80 percent rule. Clarabridge BridgePoints Retrieved from http://clarabridge.com/default.aspx?tabid=137&ModuleID=635&ArticleID=551.
Cox, M., & Ellsworth, D. (1997). Application-controlled demand paging for out-of-core visualization. Paper presented at the Proceedings of the 8th conference on Visualization'97.
Fallik, D. (2014). For big data, big questions remain. Health Aff (Millwood), 33(7), 1111-1114. doi:10.1377/hlthaff.2014.0522
Flicek, P., Amode, M. R., Barrell, D., Beal, K., Billis, K., Brent, S., . . . Searle, S. M. (2014). Ensembl 2014. Nucleic Acids Res, 42(Database issue), D749-755. doi:10.1093/nar/gkt1196
Gentleman, G. R. I. a. R. C. (1993). R language.
Google. (2013). word2vec.
Gray, K. A., Daugherty, L. C., Gordon, S. M., Seal, R. L., Wright, M. W., & Bruford, E. A. (2013). Genenames.org: the HGNC resources in 2013. Nucleic Acids Res, 41(Database issue), D545-552. doi:10.1093/nar/gks1066
Gray, K. A., Yates, B., Seal, R. L., Wright, M. W., & Bruford, E. A. (2015). Genenames.org: the HGNC resources in 2015. Nucleic Acids Res, 43(Database issue), D1079-1085. doi:10.1093/nar/gku1071
Guidera, K. J., Satterwhite, Y., Ogden, J. A., Pugh, L., & Ganey, T. (1991). Nail patella syndrome: a review of 44 orthopaedic patients. J Pediatr Orthop, 11(6), 737-742.
Hamosh, A., Scott, A. F., Amberger, J. S., Bocchini, C. A., & McKusick, V. A. (2005). Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res, 33(Database issue), D514-517. doi:10.1093/nar/gki033
Hartz, A., & Marsh, J. L. (2003). Methodologic issues in observational studies. Clin Orthop Relat Res(413), 33-42. doi:10.1097/01.blo.0000079325.41006.95
Hiatt, R. A., Sulsky, S., Aldrich, M. C., Kreiger, N., & Rothenberg, R. (2013). Promoting innovation and creativity in epidemiology for the 21st century. Ann Epidemiol, 23(7), 452-454. doi:http://dx.doi.org/10.1016/j.annepidem.2013.05.007
Hilbert, M., López, P ( 2012). How to Measure the World’s Technological Capacity to Communicate, Store and Compute Information? Part I: results and scope. . International Journal of Communication.
Hilbert, M., & Lopez, P. (2011). The world's technological capacity to store, communicate, and compute information. Science, 332(6025), 60-65. doi:10.1126/science.1200970
HUGO Gene Nomenclature Committee. (2016).
Jensen, P. B., Jensen, L. J., & Brunak, S. (2012). Mining electronic health records: towards better research applications and clinical care. Nature Reviews Genetics, 13(6), 395-405.
Kay, J., de Sa, D., Shallow, S., Simunovic, N., Safran, M. R., Philippon, M. J., & Ayeni, O. R. (2015). Level of clinical evidence presented at the International Society for Hip Arthroscopy Annual Scientific Meeting over 5 years (2010-2014). J Hip Preserv Surg, 2(4), 332-338. doi:10.1093/jhps/hnv059
Kooistra, B., Dijkman, B., Einhorn, T. A., & Bhandari, M. (2009). How to design a good case series. J Bone Joint Surg Am, 91 Suppl 3, 21-26. doi:10.2106/jbjs.h.01573
Laakso, M., Welling, P., Bukvova, H., Nyman, L., Björk, B.-C., & Hedlund, T. (2011). The development of open access journal publishing from 1993 to 2009. PloS one, 6(6), e20961.
Landrum, M. J., Lee, J. M., Riley, G. R., Jang, W., Rubinstein, W. S., Church, D. M., & Maglott, D. R. (2014). ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res, 42(Database issue), D980-985. doi:10.1093/nar/gkt1113
Laney, D. (2012). The importance of'Big Data': A definition. Gartner. Retrieved, 21.
Lin, Y. C., Wu, Y. H., & Scher, R. K. (2008). Nail changes and association of osteoarthritis in digital myxoid cyst. Dermatol Surg, 34(3), 364-369. doi:10.1111/j.1524-4725.2007.34070.x
Lipscomb, C. E. (2000). Medical Subject Headings (MeSH). Bull Med Libr Assoc, 88(3), 265-266.
Losiewicz, P., Oard, D. W., & Kostoff, R. N. (2000). Textual data mining to support science and technology management. Journal of Intelligent Information Systems, 15(2), 99-119.
Maglott, D., Ostell, J., Pruitt, K. D., & Tatusova, T. (2011). Entrez Gene: gene-centered information at NCBI. Nucleic Acids Res, 39(Database issue), D52-57. doi:10.1093/nar/gkq1237
Mayer Schönberger V, C. K. (2013). Big data: A revolution that will transform how we live, work, and think. Houghton: Mifflin Harcourt.
Meaney, C., Moineddin, R., Voruganti, T., O'Brien, M. A., Krueger, P., & Sullivan, F. (2016). Text mining describes the use of statistical and epidemiological methods in published medical research. J Clin Epidemiol, 74, 124-132. doi:10.1016/j.jclinepi.2015.10.020
Mooney, S. J., Westreich, D. J., & El-Sayed, A. M. (2015). Epidemiology in the Era of Big Data. Epidemiology (Cambridge, Mass.), 26(3), 390-394. doi:10.1097/EDE.0000000000000274
Mork, J. G., Jimeno-Yepes, A., & Aronson, A. R. (2013). The NLM Medical Text Indexer System for Indexing Biomedical Literature. Paper presented at the BioASQ@ CLEF.
Murdoch, T. B., & Detsky, A. S. (2013). The inevitable application of big data to health care. JAMA, 309(13), 1351-1352.
Nadadur, S. S., Miller, C. A., Hopke, P. K., Gordon, T., Vedal, S., Vandenberg, J. J., & Costa, D. L. (2007). The complexities of air pollution regulation: the need for an integrated research and regulatory perspective. Toxicol Sci, 100(2), 318-327. doi:10.1093/toxsci/kfm170
Niu, Y., Otasek, D., & Jurisica, I. (2010). Evaluation of linguistic features useful in extraction of interactions from PubMed; application to annotating known, high-throughput and predicted interactions in I2D. Bioinformatics, 26(1), 111-119. doi:10.1093/bioinformatics/btp602
Piñero, J., Bravo, À., Queralt-Rosinach, N., Gutiérrez-Sacristán, A., Deu-Pons, J., Centeno, E., . . . Furlong, L. I. (2017). DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants. Nucleic Acids Res, 45(D1), D833-D839. doi:10.1093/nar/gkw943
PubGene. (2012). Coremine Medical
Roski, J., Bo-Linn, G. W., & Andrews, T. A. (2014). Creating value in health care through big data: opportunities and policy implications. Health Affairs, 33(7), 1115-1122.
Sacchi, L., & Holmes, J. H. (2016). Progress in Biomedical Knowledge Discovery: A 25-year Retrospective. Yearb Med Inform, Suppl 1, S117-129. doi:10.15265/IYS-2016-s033
Sackett, D. L., Rosenberg, W. M., Gray, J. A., Haynes, R. B., & Richardson, W. S. (1996). Evidence based medicine: what it is and what it isn't. BMJ : British Medical Journal, 312(7023), 71-72.
Salerno, J., Knoppers, B. M., Lee, L. M., Hlaing, W. M., & Goodman, K. W. (2017). Ethics, big data and computing in epidemiology and public health. Ann Epidemiol, 27(5), 297-301. doi:10.1016/j.annepidem.2017.05.002
Schmitt, T., Ogris, C., & Sonnhammer, E. L. (2014). FunCoup 3.0: database of genome-wide functional coupling networks. Nucleic Acids Res, 42(Database issue), D380-388. doi:10.1093/nar/gkt984
Singhal, A., Simmons, M., & Lu, Z. (2016). Text mining for precision medicine: automating disease-mutation relationship extraction from biomedical literature. Journal of the American Medical Informatics Association, ocw041.
Stuart J. Nelson, W. D. J., and Betsy L. Humphreys, & National Library of Medicine, B., MD, USA. Relationships in Medical Subject Headings (MeSH).
Szklarczyk, D., Franceschini, A., Wyder, S., Forslund, K., Heller, D., Huerta-Cepas, J., . . . Tsafou, K. P. (2014). STRING v10: protein–protein interaction networks, integrated over the tree of life. Nucleic Acids Res, gku1003.
The New York Times. (2014). Big Data Compendium. The New York Times.
Tigchelaar, S., Lenting, A., Bongers, E. M. H. F., & van Kampen, A. (2015). Nail patella syndrome: Knee symptoms and surgical outcomes. A questionnaire-based survey. Orthopaedics & Traumatology: Surgery & Research, 101(8), 959-962. doi:http://dx.doi.org/10.1016/j.otsr.2015.09.033
U.S. National Center for Biotechnology Information. (Updated 2017 Mar 14). PubMed Help [Internet].
U.S. National Library of Medicine. Medical Subject Headings.
U.S. National Library of Medicine. (2016). MeSH tree.
Vance, A. (2010). Start-up goes after big data with hadoop helper. New York Times Blog, 22.
Warner, J. L., Jain, S. K., & Levy, M. A. (2016). Integrating cancer genomic data into electronic health records. Genome Medicine, 8, 113. doi:10.1186/s13073-016-0371-3
Weber, G. M., Mandl, K. D., & Kohane, I. S. (2014). FInding the missing link for big biomedical data. JAMA, 311(24), 2479-2480. doi:10.1001/jama.2014.4228
Zuberi, K., Franz, M., Rodriguez, H., Montojo, J., Lopes, C. T., Bader, G. D., & Morris, Q. (2013). GeneMANIA prediction server 2013 update. Nucleic Acids Res, 41(Web Server issue), W115-122. doi:10.1093/nar/gkt533
丁怡婷, & 劉志光. (2010). 文字探勘技術應用於中醫診斷腦中風之研究. Journal of Data Analysis, 5(4), 41-64.
游忠諺. (2016). 醫學電子資源大數據分析模式之建構與應用. (博士), 國立臺灣師範大學, 台北市.