-
1
-
-
10944272139
-
Friends and neighbors on the web
-
Adamic, L. A., and Adar, E. (2003). Friends and neighbors on the web. Soc. Netw. 25, 211-230. doi: 10.1016/S0378-8733(03)00009-1
-
(2003)
Soc. Netw
, vol.25
, pp. 211-230
-
-
Adamic, L.A.1
Adar, E.2
-
2
-
-
0034994570
-
Healthy lifestyles in europe: prevention of obesity and type ii diabetes by diet and physical activity
-
Astrup, A. (2001). Healthy lifestyles in europe: prevention of obesity and type ii diabetes by diet and physical activity. Public Health Nutr. 4, 499-515. doi: 10.1079/PHN2001136
-
(2001)
Public Health Nutr
, vol.4
, pp. 499-515
-
-
Astrup, A.1
-
3
-
-
79955548007
-
The genetic effect of copy number variations on the risk of type 2 diabetes in a korean population
-
Bae, J. S., Cheong, H. S., Kim, J.-H., Park, B. L., Kim, J.-H., Park, T. J., et al. (2011). The genetic effect of copy number variations on the risk of type 2 diabetes in a korean population. PLoS ONE 6:e19091. doi: 10.1371/journal.pone.0019091
-
(2011)
PLoS ONE
, vol.6
-
-
Bae, J.S.1
Cheong, H.S.2
Kim, J.-H.3
Park, B.L.4
Kim, J.-H.5
Park, T.J.6
-
4
-
-
78650373804
-
Network medicine: a network-based approach to human disease
-
Barabási, A.-L., Gulbahce, N., and Loscalzo, J. (2011). Network medicine: a network-based approach to human disease. Nat. Rev. Genet. 12, 56-68. doi: 10.1038/nrg2918
-
(2011)
Nat. Rev. Genet
, vol.12
, pp. 56-68
-
-
Barabási, A.-L.1
Gulbahce, N.2
Loscalzo, J.3
-
5
-
-
78149236787
-
Disgenet: a cytoscape plugin to visualize, integrate, search and analyze gene-disease networks
-
Bauer-Mehren, A., Rautschka, M., Sanz, F., and Furlong, L. I. (2010). Disgenet: a cytoscape plugin to visualize, integrate, search and analyze gene-disease networks. Bioinformatics 26, 2924-2926. doi: 10.1093/bioinformatics/btq538
-
(2010)
Bioinformatics
, vol.26
, pp. 2924-2926
-
-
Bauer-Mehren, A.1
Rautschka, M.2
Sanz, F.3
Furlong, L.I.4
-
6
-
-
2442604715
-
The genetic association database
-
Becker, K. G., Barnes, K. C., Bright, T. J., and Wang, S. A. (2004). The genetic association database. Nat. Genet. 36, 431-432. doi: 10.1038/ng0504-431
-
(2004)
Nat. Genet
, vol.36
, pp. 431-432
-
-
Becker, K.G.1
Barnes, K.C.2
Bright, T.J.3
Wang, S.A.4
-
7
-
-
70449356774
-
Quickgo: a web-based tool for gene ontology searching
-
Binns, D., Dimmer, E., Huntley, R., Barrell, D., O'Donovan, C., and Apweiler, R. (2009). Quickgo: a web-based tool for gene ontology searching. Bioinformatics 25, 3045-3046. doi: 10.1093/bioinformatics/btp536
-
(2009)
Bioinformatics
, vol.25
, pp. 3045-3046
-
-
Binns, D.1
Dimmer, E.2
Huntley, R.3
Barrell, D.4
O'Donovan, C.5
Apweiler, R.6
-
8
-
-
84909980102
-
The structure and dynamics of multilayer networks
-
Boccaletti, S., Bianconi, G., Criado, R., Del Genio, C., Gómez-Gardeñes, J., Romance, M., et al. (2014). The structure and dynamics of multilayer networks. Phys. Rep. 544, 1. doi: 10.1016/j.physrep.2014.07.001
-
(2014)
Phys. Rep
, vol.544
, pp. 1
-
-
Boccaletti, S.1
Bianconi, G.2
Criado, R.3
Del Genio, C.4
Gómez-Gardeñes, J.5
Romance, M.6
-
9
-
-
78049469708
-
Time to care: a collaborative engine for practical disease prediction
-
Davis, D. A., Chawla, N. V., Christakis, N. A., and Barabási, A.-L. (2010). Time to care: a collaborative engine for practical disease prediction. Data Mining Knowl. Discov. 20, 388-415. doi: 10.1007/s10618-009-0156-z
-
(2010)
Data Mining Knowl. Discov
, vol.20
, pp. 388-415
-
-
Davis, D.A.1
Chawla, N.V.2
Christakis, N.A.3
Barabási, A.-L.4
-
10
-
-
0026639706
-
Adapting a clinical comorbidity index for use with icd-9-cm administrative databases
-
Deyo, R. A., Cherkin, D. C., and Ciol, M. A. (1992). Adapting a clinical comorbidity index for use with icd-9-cm administrative databases. J. Clin. Epidemiol. 45, 613-619. doi: 10.1016/0895-4356(92)90133-8
-
(1992)
J. Clin. Epidemiol
, vol.45
, pp. 613-619
-
-
Deyo, R.A.1
Cherkin, D.C.2
Ciol, M.A.3
-
11
-
-
84891650295
-
Findzebra: a search engine for rare diseases
-
Dragusin, R., Petcu, P., Lioma, C., Larsen, B., Jørgensen, H. L., Cox, I. J., et al. (2013). Findzebra: a search engine for rare diseases. Int. J. Med. Inform. 82, 528-538. doi: 10.1016/j.ijmedinf.2013.01.005
-
(2013)
Int. J. Med. Inform
, vol.82
, pp. 528-538
-
-
Dragusin, R.1
Petcu, P.2
Lioma, C.3
Larsen, B.4
Jørgensen, H.L.5
Cox, I.J.6
-
12
-
-
0031613172
-
Comorbidity measures for use with administrative data
-
Elixhauser, A., Steiner, C., Harris, D. R., and Coffey, R. M. (1998). Comorbidity measures for use with administrative data. Med. Care 36, 8-27. doi: 10.1097/00005650-199801000-00004
-
(1998)
Med. Care
, vol.36
, pp. 8-27
-
-
Elixhauser, A.1
Steiner, C.2
Harris, D.R.3
Coffey, R.M.4
-
13
-
-
84899752592
-
Communicability reveals a transition to coordinated behavior in multiplex networks
-
Estrada, E., and Gómez-Gardeñes, J. (2014). Communicability reveals a transition to coordinated behavior in multiplex networks. Phys. Rev. E 89:042819. doi: 10.1103/PhysRevE.89.042819
-
(2014)
Phys. Rev. E
, vol.89
-
-
Estrada, E.1
Gómez-Gardeñes, J.2
-
14
-
-
0036081484
-
Hgvbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources
-
Fredman, D., Siegfried, M., Yuan, Y. P., Bork, P., Lehväslaiho, H., and Brookes, A. J. (2002). Hgvbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources. Nucleic Acids Res. 30, 387-391. doi: 10.1093/nar/30.1.387
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 387-391
-
-
Fredman, D.1
Siegfried, M.2
Yuan, Y.P.3
Bork, P.4
Lehväslaiho, H.5
Brookes, A.J.6
-
15
-
-
28744458859
-
Bioconductor: open software development for computational biology and bioinformatics
-
Gentleman, R. C., Carey, V. J., Bates, D. M., Bolstad, B., Dettling, M., Dudoit, S., et al. (2004). Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 5:R80. doi: 10.1186/gb-2004-5-10-r80
-
(2004)
Genome Biol
, vol.5
, pp. R80
-
-
Gentleman, R.C.1
Carey, V.J.2
Bates, D.M.3
Bolstad, B.4
Dettling, M.5
Dudoit, S.6
-
16
-
-
34547140875
-
The human disease network
-
Goh, K.-I., Cusick, M. E., Valle, D., Childs, B., Vidal, M., and Barabasi, A.-L. (2007). The human disease network. Proc. Natl. Acad. Sci. U.S.A. 104, 8685-8690. doi: 10.1073/pnas.0701361104
-
(2007)
Proc. Natl. Acad. Sci. U.S.A
, vol.104
, pp. 8685-8690
-
-
Goh, K.-I.1
Cusick, M.E.2
Valle, D.3
Childs, B.4
Vidal, M.5
Barabasi, A.-L.6
-
17
-
-
66249129037
-
A dynamic network approach for the study of human phenotypes
-
Hidalgo, C. A., Blumm, N., Barabási, A.-L., and Christakis, N. A. (2009). A dynamic network approach for the study of human phenotypes. PLoS Comput. Biol. 5:e1000353. doi: 10.1371/journal.pcbi.1000353
-
(2009)
PLoS Comput. Biol
, vol.5
-
-
Hidalgo, C.A.1
Blumm, N.2
Barabási, A.-L.3
Christakis, N.A.4
-
18
-
-
0036087166
-
Jsnp: a database of common gene variations in the japanese population
-
Hirakawa, M., Tanaka, T., Hashimoto, Y., Kuroda, M., Takagi, T., and Nakamura, Y. (2002). Jsnp: a database of common gene variations in the japanese population. Nucleic Acids Res. 30, 158-162. doi: 10.1093/nar/30.1.158
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 158-162
-
-
Hirakawa, M.1
Tanaka, T.2
Hashimoto, Y.3
Kuroda, M.4
Takagi, T.5
Nakamura, Y.6
-
19
-
-
68449088145
-
Human disease-drug network based on genomic expression profiles
-
Hu, G., and Agarwal, P. (2009). Human disease-drug network based on genomic expression profiles. PLoS ONE 4:e6536. doi: 10.1371/journal.pone.0006536
-
(2009)
PLoS ONE
, vol.4
-
-
Hu, G.1
Agarwal, P.2
-
20
-
-
84903473624
-
Temporal disease trajectories condensed from population-wide registry data covering 6.2 million patients
-
Jensen, A. B., Moseley, P. L., Oprea, T. I., Ellesøe, S. G., Eriksson, R., Schmock, H., et al. (2014). Temporal disease trajectories condensed from population-wide registry data covering 6.2 million patients. Nat. Commun. 5:4022. doi: 10.1038/ncomms5022
-
(2014)
Nat. Commun
, vol.5
, pp. 4022
-
-
Jensen, A.B.1
Moseley, P.L.2
Oprea, T.I.3
Ellesøe, S.G.4
Eriksson, R.5
Schmock, H.6
-
21
-
-
77953888015
-
Prioritization of disease micrornas through a human phenome-micrornaome network
-
Jiang, Q., Hao, Y., Wang, G., Juan, L., Zhang, T., Teng, M., et al. (2010). Prioritization of disease micrornas through a human phenome-micrornaome network. BMC Syst. Biol. 4(Suppl. 1):S2. doi: 10.1186/1752-0509-4-S1-S2
-
(2010)
BMC Syst. Biol
, vol.4
, pp. S2
-
-
Jiang, Q.1
Hao, Y.2
Wang, G.3
Juan, L.4
Zhang, T.5
Teng, M.6
-
22
-
-
58149179989
-
mir2disease: a manually curated database for microrna deregulation in human disease
-
Jiang, Q., Wang, Y., Hao, Y., Juan, L., Teng, M., Zhang, X., et al. (2009). mir2disease: a manually curated database for microrna deregulation in human disease. Nucleic Acids Res. 37(Suppl. 1), D98-D104. doi: 10.1093/nar/gkn714
-
(2009)
Nucleic Acids Res
, vol.37
, pp. D98-D104
-
-
Jiang, Q.1
Wang, Y.2
Hao, Y.3
Juan, L.4
Teng, M.5
Zhang, X.6
-
23
-
-
33845881411
-
Mechanisms linking obesity to insulin resistance and type 2 diabetes
-
Kahn, S. E., Hull, R. L., and Utzschneider, K. M. (2006). Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature 444, 840-846. doi: 10.1038/nature05482
-
(2006)
Nature
, vol.444
, pp. 840-846
-
-
Kahn, S.E.1
Hull, R.L.2
Utzschneider, K.M.3
-
24
-
-
70350474767
-
Clinical diagnostics in human genetics with semantic similarity searches in ontologies
-
Köhler, S., Schulz, M. H., Krawitz, P., Bauer, S., Dölken, S., Ott, C. E., et al. (2009). Clinical diagnostics in human genetics with semantic similarity searches in ontologies. Am. J. Hum. Genet. 85, 457-464. doi: 10.1016/j.ajhg.2009.09.003
-
(2009)
Am. J. Hum. Genet
, vol.85
, pp. 457-464
-
-
Köhler, S.1
Schulz, M.H.2
Krawitz, P.3
Bauer, S.4
Dölken, S.5
Ott, C.E.6
-
25
-
-
78651293534
-
mirbase: integrating microrna annotation and deep-sequencing data
-
Kozomara, A., and Griffiths-Jones, S. (2011). mirbase: integrating microrna annotation and deep-sequencing data. Nucleic Acids Res. 39, D152-D157. doi: 10.1093/nar/gkq1027
-
(2011)
Nucleic Acids Res
, vol.39
, pp. D152-D157
-
-
Kozomara, A.1
Griffiths-Jones, S.2
-
26
-
-
48249158278
-
The implications of human metabolic network topology for disease comorbidity
-
Lee, D.-S., Park, J., Kay, K., Christakis, N., Oltvai, Z., and Barabási, A.-L. (2008). The implications of human metabolic network topology for disease comorbidity. Proc. Natl. Acad. Sci. U.S.A. 105, 9880-9885. doi: 10.1073/pnas.0802208105
-
(2008)
Proc. Natl. Acad. Sci. U.S.A
, vol.105
, pp. 9880-9885
-
-
Lee, D.-S.1
Park, J.2
Kay, K.3
Christakis, N.4
Oltvai, Z.5
Barabási, A.-L.6
-
27
-
-
80455145185
-
Prediction of disease and phenotype associations from genome-wide association studies
-
Lewis, S. N., Nsoesie, E., Weeks, C., Qiao, D., and Zhang, L. (2011). Prediction of disease and phenotype associations from genome-wide association studies. PLoS ONE 6:e27175. doi: 10.1371/journal.pone.0027175
-
(2011)
PLoS ONE
, vol.6
-
-
Lewis, S.N.1
Nsoesie, E.2
Weeks, C.3
Qiao, D.4
Zhang, L.5
-
28
-
-
84891781832
-
Hmdd v2 0, a database for experimentally supported human microrna and disease associations
-
Li, Y., Qiu, C., Tu, J., Geng, B., Yang, J., Jiang, T., et al. (2014). Hmdd v2. 0: a database for experimentally supported human microrna and disease associations. Nucleic Acids Res. 42, D1070-D1074. doi: 10.1093/nar/gkt1023
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D1070-D1074
-
-
Li, Y.1
Qiu, C.2
Tu, J.3
Geng, B.4
Yang, J.5
Jiang, T.6
-
29
-
-
63049094002
-
The etiome: identification and clustering of human disease etiological factors
-
Liu, Y. I., Wise, P. H., and Butte, A. J. (2009). The etiome: identification and clustering of human disease etiological factors. BMC Bioinform. 10(Suppl. 2):S14. doi: 10.1186/1471-2105-10-S2-S14
-
(2009)
BMC Bioinform
, vol.10
, pp. S14
-
-
Liu, Y.I.1
Wise, P.H.2
Butte, A.J.3
-
30
-
-
54849408182
-
An analysis of human microrna and disease associations
-
Lu, M., Zhang, Q., Deng, M., Miao, J., Guo, Y., Gao, W., et al. (2008). An analysis of human microrna and disease associations. PLoS ONE 3:e3420. doi: 10.1371/journal.pone.0003420
-
(2008)
PLoS ONE
, vol.3
-
-
Lu, M.1
Zhang, Q.2
Deng, M.3
Miao, J.4
Guo, Y.5
Gao, W.6
-
31
-
-
84891783452
-
The database of genomic variants: a curated collection of structural variation in the human genome
-
MacDonald, J. R., Ziman, R., Yuen, R. K., Feuk, L., and Scherer, S. W. (2014). The database of genomic variants: a curated collection of structural variation in the human genome. Nucleic Acids Res. 42, D986-D992. doi: 10.1093/nar/gkt958
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D986-D992
-
-
MacDonald, J.R.1
Ziman, R.2
Yuen, R.K.3
Feuk, L.4
Scherer, S.W.5
-
32
-
-
34347353237
-
Copy-number variation and association studies of human disease
-
McCarroll, S. A., and Altshuler, D. M. (2007). Copy-number variation and association studies of human disease. Nat. Genet. 39, S37-S42. doi: 10.1038/ng2080
-
(2007)
Nat. Genet
, vol.39
, pp. S37-S42
-
-
McCarroll, S.A.1
Altshuler, D.M.2
-
33
-
-
34147122065
-
Mendelian inheritance in man and its online version, omim
-
McKusick, V. A. (2007). Mendelian inheritance in man and its online version, omim. Am. J. Hum. Genet. 80, 588. doi: 10.1086/514346
-
(2007)
Am. J. Hum. Genet
, vol.80
, pp. 588
-
-
McKusick, V.A.1
-
34
-
-
84988810041
-
comor: a software for disease comorbidity risk assessment
-
Moni, M. A., and Lio, P. (2014). comor: a software for disease comorbidity risk assessment. J. Clin. Bioinform. 4:8. doi: 10.1186/2043-9113-4-8
-
(2014)
J. Clin. Bioinform
, vol.4
, pp. 8
-
-
Moni, M.A.1
Lio, P.2
-
35
-
-
64349109427
-
The impact of cellular networks on disease comorbidity
-
Park, J., Lee, D.-S., Christakis, N. A., and Barabási, A.-L. (2009). The impact of cellular networks on disease comorbidity. Mol. Syst. Biol. 5, 262. doi: 10.1038/msb.2009.16
-
(2009)
Mol. Syst. Biol
, vol.5
, pp. 262
-
-
Park, J.1
Lee, D.-S.2
Christakis, N.A.3
Barabási, A.-L.4
-
36
-
-
47149083877
-
Metrics for go based protein semantic similarity: a systematic evaluation
-
Pesquita, C., Faria, D., Bastos, H., Ferreira, A. E., Falcão, A. O., and Couto, F. M. (2008). Metrics for go based protein semantic similarity: a systematic evaluation. BMC Bioinform. 9(Suppl. 5):S4. doi: 10.1186/1471-2105-9-S5-S4
-
(2008)
BMC Bioinform
, vol.9
, pp. S4
-
-
Pesquita, C.1
Faria, D.2
Bastos, H.3
Ferreira, A.E.4
Falcão, A.O.5
Couto, F.M.6
-
37
-
-
84954358609
-
The human phenotype ontology: a tool for annotating and analyzing human hereditary disease
-
Robinson, P. N., Köhler, S., Bauer, S., Seelow, D., Horn, D., and Mundlos, S. (2008). The human phenotype ontology: a tool for annotating and analyzing human hereditary disease. Am. J. Hum. Genet. 83, 610-615. doi: 10.1016/j.ajhg.2008.09.017
-
(2008)
Am. J. Hum. Genet
, vol.83
, pp. 610-615
-
-
Robinson, P.N.1
Köhler, S.2
Bauer, S.3
Seelow, D.4
Horn, D.5
Mundlos, S.6
-
38
-
-
77953936166
-
The human phenotype ontology
-
Robinson, P. N., and Mundlos, S. (2010). The human phenotype ontology. Clin. Genet. 77, 525-534
-
(2010)
Clin. Genet
, vol.77
, pp. 525-534
-
-
Robinson, P.N.1
Mundlos, S.2
-
39
-
-
70249134919
-
Molecular networks as sensors and drivers of common human diseases
-
Schadt, E. E. (2009). Molecular networks as sensors and drivers of common human diseases. Nature 461, 218-223. doi: 10.1111/j.1399-0004.2010.01436.x
-
(2009)
Nature
, vol.461
, pp. 218-223
-
-
Schadt, E.E.1
-
40
-
-
0035173378
-
dbsnp: the ncbi database of genetic variation
-
Sherry, S. T., Ward, M.-H., Kholodov, M., Baker, J., Phan, L., Smigielski, E. M., et al. (2001). dbsnp: the ncbi database of genetic variation. Nucleic Acids Res. 29, 308-311. doi: 10.1093/nar/29.1.308
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.-H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
-
41
-
-
84907033471
-
'Automated hypothesis generation based on mining scientific literature'
-
(ACM)
-
Spangler, S., Wilkins, A. D., Bachman, B. J., Nagarajan, M., Dayaram, T., Haas, P., et al. (2014). 'Automated hypothesis generation based on mining scientific literature'. in Proceedings of the 20th ACM SIGKDD International Conference on Knowledge Discovery and Data Mining (ACM), 1877-1886
-
(2014)
Proceedings of the 20th ACM SIGKDD International Conference on Knowledge Discovery and Data Mining
, pp. 1877-1886
-
-
Spangler, S.1
Wilkins, A.D.2
Bachman, B.J.3
Nagarajan, M.4
Dayaram, T.5
Haas, P.6
-
42
-
-
27344435774
-
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles
-
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., et al. (2005). Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl. Acad. Sci. U.S.A. 102, 15545-15550. doi: 10.1073/pnas.0506580102
-
(2005)
Proc. Natl. Acad. Sci. U.S.A
, vol.102
, pp. 15545-15550
-
-
Subramanian, A.1
Tamayo, P.2
Mootha, V.K.3
Mukherjee, S.4
Ebert, B.L.5
Gillette, M.A.6
-
43
-
-
77649222972
-
Network-based elucidation of human disease similarities reveals common functional modules enriched for pluripotent drug targets
-
Suthram, S., Dudley, J. T., Chiang, A. P., Chen, R., Hastie, T. J., and Butte, A. J. (2010). Network-based elucidation of human disease similarities reveals common functional modules enriched for pluripotent drug targets. PLoS Comput. Biol. 6:e1000662. doi: 10.1371/journal.pcbi.1000662
-
(2010)
PLoS Comput. Biol
, vol.6
-
-
Suthram, S.1
Dudley, J.T.2
Chiang, A.P.3
Chen, R.4
Hastie, T.J.5
Butte, A.J.6
-
45
-
-
79955023439
-
Emerging landscape of genomics in the electronic health record for personalized medicine
-
Ullman-Cullere, M. H., and Mathew, J. P. (2011). Emerging landscape of genomics in the electronic health record for personalized medicine. Hum. Mutat. 32, 512-516. doi: 10.1002/humu.21456
-
(2011)
Hum. Mutat
, vol.32
, pp. 512-516
-
-
Ullman-Cullere, M.H.1
Mathew, J.P.2
-
46
-
-
77954193356
-
Inferring the human microrna functional similarity and functional network based on microrna-associated diseases
-
Wang, D., Wang, J., Lu, M., Song, F., and Cui, Q. (2010). Inferring the human microrna functional similarity and functional network based on microrna-associated diseases. Bioinformatics 26, 1644-1650. doi: 10.1093/bioinformatics/btq241
-
(2010)
Bioinformatics
, vol.26
, pp. 1644-1650
-
-
Wang, D.1
Wang, J.2
Lu, M.3
Song, F.4
Cui, Q.5
-
47
-
-
34447294237
-
A new method to measure the semantic similarity of go terms
-
Wang, J. Z., Du, Z., Payattakool, R., Philip, S. Y., and Chen, C.-F. (2007). A new method to measure the semantic similarity of go terms. Bioinformatics 23, 1274-1281. doi: 10.1093/bioinformatics/btm087
-
(2007)
Bioinformatics
, vol.23
, pp. 1274-1281
-
-
Wang, J.Z.1
Du, Z.2
Payattakool, R.3
Philip, S.Y.4
Chen, C.-F.5
-
48
-
-
57649232146
-
An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases
-
Yang, J. O., Hwang, S., Oh, J., Bhak, J., and Sohn, T.-K. (2008). An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases. BMC Bioinform. 9(Suppl. 12):S19. doi: 10.1186/1471-2105-9-S12-S19
-
(2008)
BMC Bioinform
, vol.9
, pp. S19
-
-
Yang, J.O.1
Hwang, S.2
Oh, J.3
Bhak, J.4
Sohn, T.-K.5
-
49
-
-
84928658738
-
DOSE: an R/Bioconductor package for disease ontology semantic and enrichment analysis
-
Yu, G., Wang, L. G., Yan, G. R., and He, Q. Y. (2015). DOSE: an R/Bioconductor package for disease ontology semantic and enrichment analysis. Bioinformatics 31, 608-609. doi: 10.1093/bioinformatics/btu684
-
(2015)
Bioinformatics
, vol.31
, pp. 608-609
-
-
Yu, G.1
Wang, L.G.2
Yan, G.R.3
He, Q.Y.4
-
50
-
-
77956151027
-
'A novel computational method for predicting disease genes based on functional similarity'
-
With Aspects of Artificial Intelligence (Springer)
-
Yuan, F., Wang, R., Guan, M., and He, G. (2010). 'A novel computational method for predicting disease genes based on functional similarity'. in Advanced Intelligent Computing Theories and Applications. With Aspects of Artificial Intelligence (Springer), 42-51
-
(2010)
Advanced Intelligent Computing Theories and Applications
, pp. 42-51
-
-
Yuan, F.1
Wang, R.2
Guan, M.3
He, G.4
-
51
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
Zhang, F., Gu, W., Hurles, M. E., and Lupski, J. R. (2009). Copy number variation in human health, disease, and evolution. Annu. Rev. Genomics Hum. Genet. 10, 451-481. doi: 10.1146/annurev.genom.9.081307.164217
-
(2009)
Annu. Rev. Genomics Hum. Genet
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.E.3
Lupski, J.R.4
-
52
-
-
77955663914
-
From phenotype to gene: detecting disease-specific gene functional modules via a text-based human disease phenotype network construction
-
Zhang, S.-H., Wu, C., Li, X., Chen, X., Jiang, W., Gong, B.-S., et al. (2010). From phenotype to gene: detecting disease-specific gene functional modules via a text-based human disease phenotype network construction. FEBS Lett. 584, 3635-3643. doi: 10.1016/j.febslet.2010.07.038
-
(2010)
FEBS Lett
, vol.584
, pp. 3635-3643
-
-
Zhang, S.-H.1
Wu, C.2
Li, X.3
Chen, X.4
Jiang, W.5
Gong, B.-S.6
-
53
-
-
84889679014
-
Discovering disease-disease associations by fusing systems-level molecular data
-
Žitnik, M., Janjic, V., Larminie, C., Zupan, B., and Pržulj, N. (2013). Discovering disease-disease associations by fusing systems-level molecular data. Sci. Rep. 3:3202. doi: 10.1038/srep03202
-
(2013)
Sci. Rep
, vol.3
, pp. 3202
-
-
Žitnik, M.1
Janjic, V.2
Larminie, C.3
Zupan, B.4
Pržulj, N.5
|