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MutationTaster evaluates disease-causing potential of sequence alterations.
Schwarz JM, Rödelsperger C, Schuelke M, Seelow D. Schwarz JM, et al. Among authors: Seelow D. Nat Methods. 2010 Aug;7(8):575-6. doi: 10.1038/nmeth0810-575. Nat Methods. 2010. PMID: 20676075 No abstract available.
MutationTaster2: mutation prediction for the deep-sequencing age.
Schwarz JM, Cooper DN, Schuelke M, Seelow D. Schwarz JM, et al. Among authors: Seelow D. Nat Methods. 2014 Apr;11(4):361-2. doi: 10.1038/nmeth.2890. Nat Methods. 2014. PMID: 24681721 No abstract available.
Improved exome prioritization of disease genes through cross-species phenotype comparison.
Robinson PN, Köhler S, Oellrich A; Sanger Mouse Genetics Project, Wang K, Mungall CJ, Lewis SE, Washington N, Bauer S, Seelow D, Krawitz P, Gilissen C, Haendel M, Smedley D. Robinson PN, et al. Among authors: Seelow D. Genome Res. 2014 Feb;24(2):340-8. doi: 10.1101/gr.160325.113. Epub 2013 Oct 25. Genome Res. 2014. PMID: 24162188 Free PMC article.
AssociationDB: web-based exploration of genomic association.
Seelow D, Hoffmann K, Lindner TH. Seelow D, et al. Bioinformatics. 2007 Oct 1;23(19):2643-4. doi: 10.1093/bioinformatics/btm376. Epub 2007 Jul 27. Bioinformatics. 2007. PMID: 17660207
Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticus.
Knierim E, Seelow D, Gill E, von Moers A, Schuelke M. Knierim E, et al. Among authors: Seelow D. Mitochondrion. 2015 Jan;20:1-6. doi: 10.1016/j.mito.2014.10.007. Epub 2014 Nov 4. Mitochondrion. 2015. PMID: 25446393
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