-
1
-
-
0034069495
-
Gene ontology: Tool for the unification of biology
-
Ashburner, M., Ball, C.A., Blake, J.A., Botstein, D., Butler, H., Cherry, J.M., Davis, A.P., Dolinski, K., Dwight, S.S. and Eppig, J. T. et al. (2000) 'Gene ontology: tool for the unification of biology', Nature genetics, Vol. 25, No. 1, pp.25-29.
-
(2000)
Nature Genetics
, vol.25
, Issue.1
, pp. 25-29
-
-
Ashburner, M.1
Ball, C.A.2
Blake, J.A.3
Botstein, D.4
Butler, H.5
Cherry, J.M.6
Davis, A.P.7
Dolinski, K.8
Dwight, S.S.9
Eppig, J.T.10
-
2
-
-
84977754786
-
Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency
-
Bone, W.P., Washington, N.L., Buske, O.J., Adams, D.R., Davis, J., Draper, D., Flynn, E.D., Girdea, M., Godfrey, R. and Golas G. et al. (2015) 'Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency', Genetics in Medicine.
-
(2015)
Genetics in Medicine
-
-
Bone, W.P.1
Washington, N.L.2
Buske, O.J.3
Adams, D.R.4
Davis, J.5
Draper, D.6
Flynn, E.D.7
Girdea, M.8
Godfrey, R.9
Golas, G.10
-
3
-
-
84905044212
-
Gossto: A stand-alone application and a web tool for calculating semantic similarities on the gene ontology
-
Caniza, H., Romero, A.E., Heron, S., Yang, H., Devoto, A., Frasca, M., Mesiti, M., Valentini, G. and Paccanaro, A. (2014) 'Gossto: a stand-alone application and a web tool for calculating semantic similarities on the gene ontology', Bioinformatics, Vol. 30, No. 15, pp.2235-2236.
-
(2014)
Bioinformatics
, vol.30
, Issue.15
, pp. 2235-2236
-
-
Caniza, H.1
Romero, A.E.2
Heron, S.3
Yang, H.4
Devoto, A.5
Frasca, M.6
Mesiti, M.7
Valentini, G.8
Paccanaro, A.9
-
4
-
-
84961707370
-
Using semantic association to extend and infer literature-oriented relativity between terms
-
Cheng, L. Li, J., Hu, Y., Jiang, Y., Liu, Y. Chu, Y., Wang, Z. and Wang, Y. (2015) 'Using semantic association to extend and infer literature-oriented relativity between terms', IEEE/ACM Transactions on Computational Biology and Bioinformatics, Vol. 12, No. 6, pp.1219-1226.
-
(2015)
IEEE/ACM Transactions On Computational Biology and Bioinformatics
, vol.12
, Issue.6
, pp. 1219-1226
-
-
Cheng Li L, J.1
Hu, Y.2
Jiang, Y.3
Liu Chu Y, Y.4
Wang, Z.5
Wang, Y.6
-
5
-
-
84979523479
-
Dissim: An online system for exploring significant similar diseases and exhibiting potential therapeutic drugs
-
Cheng, L., Jiang, Y., Wang, Z., Shi, H., Sun, J., Yang, H., Zhang, S., Hu, Y. and Zhou, M. (2016) 'Dissim: an online system for exploring significant similar diseases and exhibiting potential therapeutic drugs', Scientific Reports, Vol. 6.
-
(2016)
Scientific Reports
, vol.6
-
-
Cheng, L.1
Jiang, Y.2
Wang, Z.3
Shi, H.4
Sun, J.5
Yang, H.6
Zhang, S.7
Hu, Y.8
Zhou, M.9
-
6
-
-
84903289028
-
Semfunsim: A new method for measuring disease similarity by integrating semantic and gene functional association
-
Cheng, L., Li, J., Ju, P., Peng, J. and Wang, Y. (2014) 'Semfunsim: a new method for measuring disease similarity by integrating semantic and gene functional association', PloS one, Vol. 9, No. 6, p.e99415.
-
(2014)
PloS One
, vol.9
, Issue.6
, pp. e99415
-
-
Cheng, L.1
Li, J.2
Ju, P.3
Peng, J.4
Wang, Y.5
-
7
-
-
84990026548
-
Oahg: An integrated resource for annotating human genes with multi-level ontologies
-
Cheng, L., Sun, J., Xu, W., Dong, L., Hu, Y. and Zhou, M. (2016) 'Oahg: an integrated resource for annotating human genes with multi-level ontologies', Scientific Reports, Vol. 6.
-
(2016)
Scientific Reports
, vol.6
-
-
Cheng, L.1
Sun, J.2
Xu, W.3
Dong, L.4
Hu, Y.5
Zhou, M.6
-
8
-
-
84975266625
-
Dynamic environmental photosynthetic imaging reveals emergent phenotypes
-
Cruz, J.A., Savage, L.J., Zegarac, R., Hall, C.C., Satoh-Cruz, M., Davis, G.A., Kovac, W.K., Chen, J. and Kramer, D.M. (2016) 'Dynamic environmental photosynthetic imaging reveals emergent phenotypes', Cell Systems, Vol. 2, No. 6, pp.365-377.
-
(2016)
Cell Systems
, vol.2
, Issue.6
, pp. 365-377
-
-
Cruz, J.A.1
Savage, L.J.2
Zegarac, R.3
Hall, C.C.4
Satoh-Cruz, M.5
Davis, G.A.6
Kovac, W.K.7
Chen, J.8
Kramer, D.M.9
-
9
-
-
84868686559
-
Diagnostic exome sequencing in persons with severe intellectual disability
-
De Ligt, J., Willemsen, M.H., van Bon, B.W., Kleefstra, T., Yntema, H.G., Kroes, T., Vulto-van Silfhout, A.T., Koolen, D.A., de Vries, P., Gilissen, C. et al. (2012) 'Diagnostic exome sequencing in persons with severe intellectual disability', New England Journal of Medicine, Vol. 367, No. 20, pp.1921-1929.
-
(2012)
New England Journal of Medicine
, vol.367
, Issue.20
, pp. 1921-1929
-
-
De Ligt, J.1
Willemsen, M.H.2
Van Bon, B.W.3
Kleefstra, T.4
Yntema, H.G.5
Kroes, T.6
Vulto-Van Silfhout, A.T.7
Koolen, D.A.8
De Vries, P.9
Gilissen, C.10
-
10
-
-
84922593366
-
Hposim: An r package for phenotypic similarity measure and enrichment analysis based on the human phenotype ontology
-
Deng, Y., Gao, L., Wang, B. and Guo, X. (2015) 'Hposim: an r package for phenotypic similarity measure and enrichment analysis based on the human phenotype ontology', PloS one, Vol. 10, No. 2, p.e0115692.
-
(2015)
PloS One
, vol.10
, Issue.2
, pp. e0115692
-
-
Deng, Y.1
Gao, L.2
Wang, B.3
Guo, X.4
-
11
-
-
84872198906
-
A gene ontology inferred from molecular networks
-
Dutkowski, J. Kramer, M., Surma, M.A., Balakrishnan, R., Cherry, J.M., Krogan, N.J. and Ideker, T. (2013) 'A gene ontology inferred from molecular networks', Nature biotechnology, Vol. 31, No. 1, pp. 38-45.
-
(2013)
Nature Biotechnology
, vol.31
, Issue.1
, pp. 38-45
-
-
Dutkowski, J.1
Kramer, M.2
Surma, M.A.3
Balakrishnan, R.4
Cherry, J.M.5
Krogan, N.J.6
Ideker, T.7
-
12
-
-
84959927017
-
Inter-functional analysis of high-throughput phenotype data by non-parametric clustering and its application to photosynthesis
-
Gao, Q., Ostendorf, E., Cruz, J.A., Jin, R., Kramer, D.M. and Chen, J. (2016) 'Inter-functional analysis of high-throughput phenotype data by non-parametric clustering and its application to photosynthesis', Bioinformatics, Vol. 32, No. 1, pp. 67-76.
-
(2016)
Bioinformatics
, vol.32
, Issue.1
, pp. 67-76
-
-
Gao, Q.1
Ostendorf, E.2
Cruz, J.A.3
Jin, R.4
Kramer, D.M.5
Chen, J.6
-
13
-
-
84937523757
-
The human phenotype ontology: Semantic unification of common and rare disease
-
Groza, T., Köhler, S., Moldenhauer, D., Vasilevsky, N., Baynam, G., Zemojtel, T., Schriml, L.M., Kibbe, W.A., Schofield, P.N., Beck T. et al. (2015) 'The human phenotype ontology: semantic unification of common and rare disease', The American Journal of Human Genetics, Vol. 97, No. 1, pp.111-124.
-
(2015)
The American Journal of Human Genetics
, vol.97
, Issue.1
, pp. 111-124
-
-
Groza, T.1
Köhler, S.2
Moldenhauer, D.3
Vasilevsky, N.4
Baynam, G.5
Zemojtel, T.6
Schriml, L.M.7
Kibbe, W.A.8
Schofield, P.N.9
Beck, T.10
-
14
-
-
0024904643
-
Similarity measures in scientometric research: The jaccard index versus salton's cosine formula
-
Hamers, L., Hemeryck, Y., Herweyers, G., Janssen, M., Keters, H., Rousseau, R. and Vanhoutte, A. (1989) 'Similarity measures in scientometric research: the jaccard index versus salton's cosine formula', Information Processing & Management, Vol. 25, No. 3, pp.315-318.
-
(1989)
Information Processing & Management
, vol.25
, Issue.3
, pp. 315-318
-
-
Hamers, L.1
Hemeryck, Y.2
Herweyers, G.3
Janssen, M.4
Keters, H.5
Rousseau, R.6
Vanhoutte, A.7
-
15
-
-
13444266370
-
Online mendelian inheritance in man (omim), a knowledgebase of human genes and genetic disorders
-
Hamosh, A., Scott, A.F., Amberger, J.S., Bocchini, C.A. and McKusick, V. A. (2005) 'Online mendelian inheritance in man (omim), a knowledgebase of human genes and genetic disorders', Nucleic acids research, Vol. 33, No. suppl 1, pp.D514-D517.
-
(2005)
Nucleic Acids Research
, vol.33
, pp. D514-D517
-
-
Hamosh, A.1
Scott, A.F.2
Amberger, J.S.3
Bocchini, C.A.4
McKusick, V.A.5
-
16
-
-
85006041139
-
The dynamics of reinforcement social learning in networked cooperative multiagent systems
-
Hao, J., Huang, D., Cai, Y. and Lueng, H.-F. (2017) 'The dynamics of reinforcement social learning in networked cooperative multiagent systems', Engineering Application of Artificial Intelligence, Vol. 58, pp.111-122.
-
(2017)
Engineering Application of Artificial Intelligence
, vol.58
, pp. 111-122
-
-
Hao, J.1
Huang, D.2
Cai, Y.3
Lueng, H.-F.4
-
17
-
-
80054087451
-
Phenomenet: A whole-phenome approach to disease gene discovery
-
Hoehndorf, R., Schofield, P.N. and Gkoutos, G.V. (2011) 'Phenomenet: a whole-phenome approach to disease gene discovery', Nucleic acids research, Vol. 39, No. 18, pp.e119-e119.
-
(2011)
Nucleic Acids Research
, vol.39
, Issue.18
, pp. e119-e119
-
-
Hoehndorf, R.1
Schofield, P.N.2
Gkoutos, G.V.3
-
18
-
-
84985916601
-
Annotating the function of the human genome with gene ontology and disease ontology
-
Hu, Y., Zhou, W., Ren, J., Dong, L., Wang, Y., Jin, S. and Cheng, L. (2016) 'Annotating the function of the human genome with gene ontology and disease ontology', BioMed Research International, Vol. 2016, No. 8.
-
(2016)
BioMed Research International
, vol.2016
, Issue.8
-
-
Hu, Y.1
Zhou, W.2
Ren, J.3
Dong, L.4
Wang, Y.5
Jin, S.6
Cheng, L.7
-
20
-
-
84970940026
-
Phenostruct: Prediction of human phenotype ontology terms using heterogeneous data sources
-
Kahanda, I. Funk, C., Verspoor, K. and Ben-Hur, A. (2015) 'Phenostruct: Prediction of human phenotype ontology terms using heterogeneous data sources', F1000Research, Vol. 4.
-
(2015)
F1000Research
, vol.4
-
-
Kahanda Funk, C.1
Verspoor, K.2
Ben-Hur, A.3
-
21
-
-
84908334056
-
The human phenotype ontology project: Linking molecular biology and disease through phenotype data
-
Kohler, S., Doelken, S.C., Mungall, C.J., Bauer, S., Firth, H.V., Bailleul-Forestier, I., Black, G.C., Brown, D. L., Brudno, M. and Campbell J. et al. (2013) 'The human phenotype ontology project: linking molecular biology and disease through phenotype data', Nucleic acids research, p.gkt1026.
-
(2013)
Nucleic Acids Research
, pp. gkt1026
-
-
Kohler, S.1
Doelken, S.C.2
Mungall, C.J.3
Bauer, S.4
Firth, H.V.5
Bailleul-Forestier, I.6
Black, G.C.7
Brown, D.L.8
Brudno, M.9
Campbell, J.10
-
22
-
-
70350474767
-
Clinical diagnostics in human genetics with semantic similarity searches in ontologies
-
Kohler, S., Schulz, M.H., Krawitz, P. Bauer, S., Dolken, S., Ott, C.E., Mundlos, C., Horn, D., Mundlos, S. and Robinson, P.N. (2009) 'Clinical diagnostics in human genetics with semantic similarity searches in ontologies', The American Journal of Human Genetics, Vol. 85, No. 4, pp.457-464.
-
(2009)
The American Journal of Human Genetics
, vol.85
, Issue.4
, pp. 457-464
-
-
Kohler, S.1
Schulz, M.H.2
Krawitz Bauer P, S.3
Dolken, S.4
Ott, C.E.5
Mundlos, C.6
Horn, D.7
Mundlos, S.8
Robinson, P.N.9
-
23
-
-
0005180705
-
An information-theoretic definition of similarity
-
Citeseer
-
Lin, D. (1998) 'An information-theoretic definition of similarity'. in ICML, Vol. 98. Citeseer, pp.296-304.
-
(1998)
ICML
, vol.98
, pp. 296-304
-
-
Lin, D.1
-
24
-
-
84904445954
-
Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology
-
Masino, A.J., Dechene, E.T., Dulik, M.C., Wilkens, A., Spinner, N.B., Krantz, I.D., Pennington, J.W., Robinson, P.N. and White, P. S. (2014) 'Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology', BMC bioinformatics, Vol. 15, No. 1, p.1.
-
(2014)
BMC Bioinformatics
, vol.15
, Issue.1
, pp. 1
-
-
Masino, A.J.1
Dechene, E.T.2
Dulik, M.C.3
Wilkens, A.4
Spinner, N.B.5
Krantz, I.D.6
Pennington, J.W.7
Robinson, P.N.8
White, P.S.9
-
25
-
-
33847243488
-
Analysis and visualization of network data using jung
-
O'Madadhain, J., Fisher, D., Smyth, P., White, S., and Boey, Y.-B. (2005) 'Analysis and visualization of network data using jung', Journal of Statistical Software, Vol. 10, No. 2, pp.1-35.
-
(2005)
Journal of Statistical Software
, vol.10
, Issue.2
, pp. 1-35
-
-
O'Madadhain, J.1
Fisher, D.2
Smyth, P.3
White, S.4
Boey, Y.-B.5
-
26
-
-
77953537026
-
Node centrality in weighted networks: Generalizing degree and shortest paths
-
Opsahl, T., Agneessens, F. and Skvoretz, J. (2010) 'Node centrality in weighted networks: Generalizing degree and shortest paths', Social networks, Vol. 32, No. 3, pp.245-251.
-
(2010)
Social Networks
, vol.32
, Issue.3
, pp. 245-251
-
-
Opsahl, T.1
Agneessens, F.2
Skvoretz, J.3
-
27
-
-
0003780986
-
-
Page, L., Brin, S., Motwani, R. and Winograd, T. (1999) 'The pagerank citation ranking: bringing order to the web'.
-
(1999)
The Pagerank Citation Ranking: Bringing Order to the Web
-
-
Page, L.1
Brin, S.2
Motwani, R.3
Winograd, T.4
-
28
-
-
85013325042
-
Predicting disease-related genes using integrated biomedical networks
-
Peng, J., Bai, K., Shang, X., Wang, G., Xue, H., Jin, S., Cheng, L., Wang, Y. and Chen, J. (2016) 'Predicting disease-related genes using integrated biomedical networks'. BMC Genomics, Vol. 17, No. 11, p. 40.
-
(2016)
BMC Genomics
, vol.17
, Issue.11
, pp. 40
-
-
Peng, J.1
Bai, K.2
Shang, X.3
Wang, G.4
Xue, H.5
Jin, S.6
Cheng, L.7
Wang, Y.8
Chen, J.9
-
29
-
-
84884184167
-
Identifying cross-category relations in gene ontology and constructing genome-specific term association networks
-
Peng, J., Chen, J. and Wang, Y. (2013) 'Identifying cross-category relations in gene ontology and constructing genome-specific term association networks', BMC bioinformatics, Vol. 14, No. 2, p.1.
-
(2013)
BMC Bioinformatics
, vol.14
, Issue.2
, pp. 1
-
-
Peng, J.1
Chen, J.2
Wang, Y.3
-
30
-
-
84961595200
-
An integrative approach for measuring semantic similarities using gene ontology
-
Peng, J., Li, H., Jiang, Q. Wang, Y. and Chen, J. (2014) 'An integrative approach for measuring semantic similarities using gene ontology', BMC systems biology, Vol. 8, No. Suppl 5, p.S8.
-
(2014)
BMC Systems Biology
, vol.8
, pp. S8
-
-
Peng, J.1
Li, H.2
Jiang, Q.3
Wang, Y.4
Chen, J.5
-
31
-
-
84984700595
-
Intego2: A web tool for measuring and visualizing gene semantic similarities using gene ontology
-
Peng, J., Li, H., Liu, Y., Juan, L., Jiang, Q., Wang, Y. and Chen, J. (2016) 'Intego2: a web tool for measuring and visualizing gene semantic similarities using gene ontology', BMC Genomics, Vol. 17, No. 5, p.530.
-
(2016)
BMC Genomics
, vol.17
, Issue.5
, pp. 530
-
-
Peng, J.1
Li, H.2
Liu, Y.3
Juan, L.4
Jiang, Q.5
Wang, Y.6
Chen, J.7
-
32
-
-
84924071510
-
Measuring semantic similarities by combining gene ontology annotations and gene co-function networks
-
Peng, J., Uygun, S., Kim, T., Wang, Y., Rhee, S.Y. and Chen, J. (2015) 'Measuring semantic similarities by combining gene ontology annotations and gene co-function networks', BMC bioinformatics, Vol. 16, No. 1, p.1.
-
(2015)
BMC Bioinformatics
, vol.16
, Issue.1
, pp. 1
-
-
Peng, J.1
Uygun, S.2
Kim, T.3
Wang, Y.4
Rhee, S.Y.5
Chen, J.6
-
33
-
-
84966570660
-
Extending gene ontology with gene association networks
-
Peng, J., Wang, T., Wang, J., Wang, Y. and Chen, J. (2016) 'Extending gene ontology with gene association networks', Bioinformatics, Vol. 32, No. 8, pp.1185-1194.
-
(2016)
Bioinformatics
, vol.32
, Issue.8
, pp. 1185-1194
-
-
Peng, J.1
Wang, T.2
Wang, J.3
Wang, Y.4
Chen, J.5
-
34
-
-
84901254443
-
Towards integrative gene functional similarity measurement
-
Peng, J., Wang, Y. and Chen, J. (2014) 'Towards integrative gene functional similarity measurement', BMC Bioinformatics, Vol. 15, No. 2, p.1.
-
(2014)
BMC Bioinformatics
, vol.15
, Issue.2
, pp. 1
-
-
Peng, J.1
Wang, Y.2
Chen, J.3
-
35
-
-
85019666274
-
An online tool for measuring and visualizing phenotype similarities using HPO
-
press
-
Peng, J., Xue, H., Chen, B., Jiang, Q., Shang, X. and Wang, Y. (2017) 'An online tool for measuring and visualizing phenotype similarities using HPO', BMC Bioinformatics, in press.
-
(2017)
BMC Bioinformatics
-
-
Peng, J.1
Xue, H.2
Chen, B.3
Jiang, Q.4
Shang, X.5
Wang, Y.6
-
36
-
-
79956272259
-
Evaluating go-based semantic similarity measures
-
Pesquita, C., Faria, D., Bastos, H., Falcao, A. and Couto, F. (2007) 'Evaluating go-based semantic similarity measures', in Proc. 10th Annual BioOntologies Meeting, Vol. 37, No. 40, p.38.
-
(2007)
Proc. 10th Annual BioOntologies Meeting
, vol.37
, Issue.40
, pp. 38
-
-
Pesquita, C.1
Faria, D.2
Bastos, H.3
Falcao, A.4
Couto, F.5
-
37
-
-
84907291749
-
Phenomics and the interpretation of personal genomes
-
Petrovski S. and Goldstein, D. B. (2014) 'Phenomics and the interpretation of personal genomes', Science translational medicine, Vol. 6, No. 254, pp.254fs35-254fs35.
-
(2014)
Science Translational Medicine
, vol.6
, Issue.254
, pp. 254fs35-254fs35
-
-
Petrovski, S.1
Goldstein, D.B.2
-
38
-
-
34748862927
-
Ontoquest: A physician decision support system based on ontological queries of the hospital database
-
American Medical Informatics Association
-
Popescu, M. and Arthur, G. (2006) 'Ontoquest: A physician decision support system based on ontological queries of the hospital database', in AMIA Annual Symposium Proceedings, Vol. 2006. American Medical Informatics Association, p.639.
-
(2006)
AMIA Annual Symposium Proceedings
, vol.2006
, pp. 639
-
-
Popescu, M.1
Arthur, G.2
-
39
-
-
84954358609
-
The human phenotype ontology: A tool for annotating and analyzing human hereditary disease
-
Robinson, P.N., Kohler, S., Bauer, S., Seelow, D., Horn, D. and Mundlos, S. (2008) 'The human phenotype ontology: a tool for annotating and analyzing human hereditary disease', The American Journal of Human Genetics, Vol. 83, No. 5, pp.610-615.
-
(2008)
The American Journal of Human Genetics
, vol.83
, Issue.5
, pp. 610-615
-
-
Robinson, P.N.1
Kohler, S.2
Bauer, S.3
Seelow, D.4
Horn, D.5
Mundlos, S.6
-
40
-
-
33748335463
-
A new measure for functional similarity of gene products based on gene ontology
-
Schlicker, A., Domingues, F. S., Rahnenfiihrer, J. and Lengauer, T. (2006) 'A new measure for functional similarity of gene products based on gene ontology', BMC bioinformatics, Vol. 7, No. 1, p.1.
-
(2006)
BMC Bioinformatics
, vol.7
, Issue.1
, pp. 1
-
-
Schlicker, A.1
Domingues, F.S.2
Rahnenfiihrer, J.3
Lengauer, T.4
-
41
-
-
84859699832
-
Disease ontology: A backbone for disease semantic integration
-
Schriml, L.M., Arze, C., Nadendla, S., Chang, Y.-W.W., Mazaitis, M., Felix, V., Feng, G. and Kibbe, W.A. (2012) 'Disease ontology: a backbone for disease semantic integration', Nucleic acids research, Vol. 40, No. D1, pp.D940-D946.
-
(2012)
Nucleic Acids Research
, vol.40
, Issue.D1
, pp. D940-D946
-
-
Schriml, L.M.1
Arze, C.2
Nadendla, S.3
Chang, Y.-W.W.4
Mazaitis, M.5
Felix, V.6
Feng, G.7
Kibbe, W.A.8
-
42
-
-
84947907035
-
Next-generation diagnostics and disease-gene discovery with the exomiser
-
Smedley, D., Jacobsen, J.O., Jager, M., Kohler, S., Holtgrewe, M., Schubach, M., Siragusa, E., Zemojtel, T., Buske, O.J., Washington, N.L. et al. (2015) 'Next-generation diagnostics and disease-gene discovery with the exomiser', Nature protocols, Vol. 10, No. 12, pp. 2004-2015.
-
(2015)
Nature Protocols
, vol.10
, Issue.12
, pp. 2004-2015
-
-
Smedley, D.1
Jacobsen, J.O.2
Jager, M.3
Kohler, S.4
Holtgrewe, M.5
Schubach, M.6
Siragusa, E.7
Zemojtel, T.8
Buske, O.J.9
Washington, N.L.10
-
43
-
-
84929590712
-
Improving egt-based robustness analysis of negotiation strategies in multi-agent systems via model checking
-
Song, S., Hao, J., Liu, Y., Zhang, J., and Lueng, H.-F. (2016) 'Improving egt-based robustness analysis of negotiation strategies in multi-agent systems via model checking', IEEE Transactions on Human-Machine Systems, Vol. 46, No. 2, pp.197-208.
-
(2016)
IEEE Transactions On Human-Machine Systems
, vol.46
, Issue.2
, pp. 197-208
-
-
Song, S.1
Hao, J.2
Liu, Y.3
Zhang, J.4
Lueng, H.-F.5
-
44
-
-
84924666082
-
Large-scale discovery of novel genetic causes of developmental disorders
-
Study, T.D.D.D. (2015) 'Large-scale discovery of novel genetic causes of developmental disorders', Nature, Vol. 519, No. 7542, pp.223-228.
-
(2015)
Nature
, vol.519
, Issue.7542
, pp. 223-228
-
-
Study, T.D.D.D.1
-
45
-
-
84878328074
-
Measuring gene functional similarity based on group-wise comparison of go terms
-
Teng, Z., Guo, M., Liu, X., Dai, Q., Wang, C. and Xuan, P. (2013) 'Measuring gene functional similarity based on group-wise comparison of go terms', Bioinformatics, p.btt160.
-
(2013)
Bioinformatics
, pp. btt160
-
-
Teng, Z.1
Guo, M.2
Liu, X.3
Dai, Q.4
Wang, C.5
Xuan, P.6
-
46
-
-
84945401367
-
Standardized phenotyping enhances mendelian disease gene identification
-
Vissers, L.E. and Veltman, J.A. (2015) 'Standardized phenotyping enhances mendelian disease gene identification', Nature genetics, Vol. 47, No. 11, pp.1222-1224.
-
(2015)
Nature Genetics
, vol.47
, Issue.11
, pp. 1222-1224
-
-
Vissers, L.E.1
Veltman, J.A.2
-
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, Vol.23, No.10, pp.1274-1281.
-
(2007)
Bioinformatics
, vol.23
, Issue.10
, pp. 1274-1281
-
-
Wang, J.Z.1
Du, Z.2
Payattakool, R.3
Philip, S.Y.4
Chen, C.-F.5
-
48
-
-
72949116593
-
Linking human diseases to animal models using ontology-based phenotype annotation
-
Washington, N.L., Haendel, M.A., Mungall, C.J., Ashburner, M., Westerfield, M. and Lewis, S.E. (2009) 'Linking human diseases to animal models using ontology-based phenotype annotation', PLoS Biol, Vol. 7, No. 11, p.e1000247.
-
(2009)
PLoS Biol
, vol.7
, Issue.11
, pp. e1000247
-
-
Washington, N.L.1
Haendel, M.A.2
Mungall, C.J.3
Ashburner, M.4
Westerfield, M.5
Lewis, S.E.6
-
49
-
-
84940611109
-
Phenolyzer: Phenotype-based prioritization of candidate genes for human diseases
-
Yang, H., Robinson, P.N. and Wang, K. (2015) 'Phenolyzer: phenotype-based prioritization of candidate genes for human diseases', Nature methods, Vol. 12, No. 9, pp.841-843.
-
(2015)
Nature Methods
, vol.12
, Issue.9
, pp. 841-843
-
-
Yang, H.1
Robinson, P.N.2
Wang, K.3
-
50
-
-
84918771753
-
Molecular findings among patients referred for clinical whole-exome sequencing
-
Yang, Y., Muzny, D.M., Xia, F., Niu, Z., Person, R., Ding, Y., Ward, P., Braxton, A., Wang, M., Buhay, C. et al. (2014) 'Molecular findings among patients referred for clinical whole-exome sequencing', Jama, Vol. 312, No. 18, pp.1870-1879.
-
(2014)
Jama
, vol.312
, Issue.18
, pp. 1870-1879
-
-
Yang, Y.1
Muzny, D.M.2
Xia, F.3
Niu, Z.4
Person, R.5
Ding, Y.6
Ward, P.7
Braxton, A.8
Wang, M.9
Buhay, C.10
-
51
-
-
84907284564
-
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome
-
Zemojtel, T., Köhler, S., Mackenroth, L., Jager, M., Hecht, J., Krawitz, P., Graul-Neumann, Doelken, S. Ehmke, N., Spielmann M. et al. (2014) 'Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome', Science translational medicine, Vol. 6, No. 252, pp. 252ra123-252ra123.
-
(2014)
Science Translational Medicine
, vol.6
, Issue.252
, pp. 252ra123-252ra123
-
-
Zemojtel, T.1
Köhler, S.2
Mackenroth, L.3
Jager, M.4
Hecht, J.5
Krawitz, P.6
Graul-Neumann, D.S.7
Ehmke, N.8
Spielmann, M.9
-
52
-
-
84903639346
-
Human symptoms-disease network
-
Zhou, X., Menche, J., Barabasi, A.-L. and Sharma, A. (2014) 'Human symptoms-disease network', Nature communications, Vol. 5.
-
(2014)
Nature Communications
, vol.5
-
-
Zhou, X.1
Menche, J.2
Barabasi, A.-L.3
Sharma, A.4
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