165 related articles for article (PubMed ID: 21362185)
1. CSI-OMIM--Clinical Synopsis Search in OMIM.
Cohen R; Gefen A; Elhadad M; Birk OS
BMC Bioinformatics; 2011 Mar; 12():65. PubMed ID: 21362185
[TBL] [Abstract][Full Text] [Related]
2. Syndrome to gene (S2G): in-silico identification of candidate genes for human diseases.
Gefen A; Cohen R; Birk OS
Hum Mutat; 2010 Mar; 31(3):229-36. PubMed ID: 20052752
[TBL] [Abstract][Full Text] [Related]
3. pyMeSHSim: an integrative python package for biomedical named entity recognition, normalization, and comparison of MeSH terms.
Luo ZH; Shi MW; Yang Z; Zhang HY; Chen ZX
BMC Bioinformatics; 2020 Jun; 21(1):252. PubMed ID: 32552728
[TBL] [Abstract][Full Text] [Related]
4. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.
Amberger JS; Bocchini CA; Schiettecatte F; Scott AF; Hamosh A
Nucleic Acids Res; 2015 Jan; 43(Database issue):D789-98. PubMed ID: 25428349
[TBL] [Abstract][Full Text] [Related]
5. Inferred inheritance of MorbidMap genes without OMIM clinical synopsis.
Shakir A; Ripperger M; Jiang Z; Wierenga KJ
Genet Med; 2018 Apr; 20(4):470-473. PubMed ID: 28837159
[TBL] [Abstract][Full Text] [Related]
6. Pathway networks generated from human disease phenome.
Cirincione AG; Clark KL; Kann MG
BMC Med Genomics; 2018 Sep; 11(Suppl 3):75. PubMed ID: 30255817
[TBL] [Abstract][Full Text] [Related]
7. [Review on the research progress of mining of OMIM data].
Li J; Li Z; Kang Y; Li L
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi; 2014 Dec; 31(6):1400-4. PubMed ID: 25868267
[TBL] [Abstract][Full Text] [Related]
8. The Unified Medical Language System (UMLS): integrating biomedical terminology.
Bodenreider O
Nucleic Acids Res; 2004 Jan; 32(Database issue):D267-70. PubMed ID: 14681409
[TBL] [Abstract][Full Text] [Related]
9. Mapping Phenotypic Information in Heterogeneous Textual Sources to a Domain-Specific Terminological Resource.
Alnazzawi N; Thompson P; Ananiadou S
PLoS One; 2016; 11(9):e0162287. PubMed ID: 27643689
[TBL] [Abstract][Full Text] [Related]
10. A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnostics.
James RA; Campbell IM; Chen ES; Boone PM; Rao MA; Bainbridge MN; Lupski JR; Yang Y; Eng CM; Posey JE; Shaw CA
Genome Med; 2016 Feb; 8(1):13. PubMed ID: 26838676
[TBL] [Abstract][Full Text] [Related]
11. Survey of Natural Language Processing Techniques in Bioinformatics.
Zeng Z; Shi H; Wu Y; Hong Z
Comput Math Methods Med; 2015; 2015():674296. PubMed ID: 26525745
[TBL] [Abstract][Full Text] [Related]
12. CGMIM: automated text-mining of Online Mendelian Inheritance in Man (OMIM) to identify genetically-associated cancers and candidate genes.
Bajdik CD; Kuo B; Rusaw S; Jones S; Brooks-Wilson A
BMC Bioinformatics; 2005 Mar; 6():78. PubMed ID: 15796777
[TBL] [Abstract][Full Text] [Related]
13. Text mining facilitates database curation - extraction of mutation-disease associations from Bio-medical literature.
Ravikumar KE; Wagholikar KB; Li D; Kocher JP; Liu H
BMC Bioinformatics; 2015 Jun; 16():185. PubMed ID: 26047637
[TBL] [Abstract][Full Text] [Related]
14. Textpresso: an ontology-based information retrieval and extraction system for biological literature.
Müller HM; Kenny EE; Sternberg PW
PLoS Biol; 2004 Nov; 2(11):e309. PubMed ID: 15383839
[TBL] [Abstract][Full Text] [Related]
15. Linking the clinical vocabulary of diseases to the genes by mapping UMLS to OMIM allelic variant fields.
Hishiki T; Tamada I
AMIA Annu Symp Proc; 2007 Oct; ():976. PubMed ID: 18694076
[TBL] [Abstract][Full Text] [Related]
16. A random set scoring model for prioritization of disease candidate genes using protein complexes and data-mining of GeneRIF, OMIM and PubMed records.
Jiang L; Edwards SM; Thomsen B; Workman CT; Guldbrandtsen B; Sørensen P
BMC Bioinformatics; 2014 Sep; 15(1):315. PubMed ID: 25253562
[TBL] [Abstract][Full Text] [Related]
17. Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology.
Masino AJ; Dechene ET; Dulik MC; Wilkens A; Spinner NB; Krantz ID; Pennington JW; Robinson PN; White PS
BMC Bioinformatics; 2014 Jul; 15(1):248. PubMed ID: 25047600
[TBL] [Abstract][Full Text] [Related]
18. Inherited disorder phenotypes: controlled annotation and statistical analysis for knowledge mining from gene lists.
Masseroli M; Galati O; Manzotti M; Gibert K; Pinciroli F
BMC Bioinformatics; 2005 Dec; 6 Suppl 4(Suppl 4):S18. PubMed ID: 16351744
[TBL] [Abstract][Full Text] [Related]
19. Improving search over Electronic Health Records using UMLS-based query expansion through random walks.
Martinez D; Otegi A; Soroa A; Agirre E
J Biomed Inform; 2014 Oct; 51():100-6. PubMed ID: 24768598
[TBL] [Abstract][Full Text] [Related]
20. A tool for sharing annotated research data: the "Category 0" UMLS (Unified Medical Language System) vocabularies.
Berman JJ
BMC Med Inform Decis Mak; 2003 Jun; 3():6. PubMed ID: 12809560
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]