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Results: 10

1.

Annotation of functional variation in personal genomes using RegulomeDB.

Boyle AP, Hong EL, Hariharan M, Cheng Y, Schaub MA, Kasowski M, Karczewski KJ, Park J, Hitz BC, Weng S, Cherry JM, Snyder M.

Genome Res. 2012 Sep;22(9):1790-7. doi: 10.1101/gr.137323.112.

2.

Linking disease associations with regulatory information in the human genome.

Schaub MA, Boyle AP, Kundaje A, Batzoglou S, Snyder M.

Genome Res. 2012 Sep;22(9):1748-59. doi: 10.1101/gr.136127.111.

3.

An integrated encyclopedia of DNA elements in the human genome.

ENCODE Project Consortium.

Nature. 2012 Sep 6;489(7414):57-74. doi: 10.1038/nature11247.

4.

Sex differences in disease risk from reported genome-wide association study findings.

Liu LY, Schaub MA, Sirota M, Butte AJ.

Hum Genet. 2012 Mar;131(3):353-64. doi: 10.1007/s00439-011-1081-y. Epub 2011 Aug 20.

5.

Transmission distortion in Crohn's disease risk gene ATG16L1 leads to sex difference in disease association.

Liu LY, Schaub MA, Sirota M, Butte AJ.

Inflamm Bowel Dis. 2012 Feb;18(2):312-22. doi: 10.1002/ibd.21781. Epub 2011 May 25.

6.

Mutations in 23S rRNA at the peptidyl transferase center and their relationship to linezolid binding and cross-resistance.

Long KS, Munck C, Andersen TM, Schaub MA, Hobbie SN, Böttger EC, Vester B.

Antimicrob Agents Chemother. 2010 Nov;54(11):4705-13. doi: 10.1128/AAC.00644-10. Epub 2010 Aug 9.

7.

Autoimmune disease classification by inverse association with SNP alleles.

Sirota M, Schaub MA, Batzoglou S, Robinson WH, Butte AJ.

PLoS Genet. 2009 Dec;5(12):e1000792. doi: 10.1371/journal.pgen.1000792. Epub 2009 Dec 24.

8.

A Classifier-based approach to identify genetic similarities between diseases.

Schaub MA, Kaplow IM, Sirota M, Do CB, Butte AJ, Batzoglou S.

Bioinformatics. 2009 Jun 15;25(12):i21-9. doi: 10.1093/bioinformatics/btp226.

9.

Qualitative networks: a symbolic approach to analyze biological signaling networks.

Schaub MA, Henzinger TA, Fisher J.

BMC Syst Biol. 2007 Jan 8;1:4.

10.

Subdivision of large introns in Drosophila by recursive splicing at nonexonic elements.

Burnette JM, Miyamoto-Sato E, Schaub MA, Conklin J, Lopez AJ.

Genetics. 2005 Jun;170(2):661-74. Epub 2005 Mar 31.

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