Schork NJ - Search Results

1

Comprehensive analysis of treatment response phenotypes in rheumatoid arthritis for pharmacogenetic studies.

Standish KA, Huang CC, Curran ME, Schork NJ. Standish KA, et al. Among authors: schork nj. Arthritis Res Ther. 2017 May 12;19(1):90. doi: 10.1186/s13075-017-1299-8. Arthritis Res Ther. 2017. PMID: 28494788 Free PMC article. Clinical Trial.

2

Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls.

Buckley AR, Standish KA, Bhutani K, Ideker T, Lasken RS, Carter H, Harismendy O, Schork NJ. Buckley AR, et al. Among authors: schork nj. BMC Genomics. 2017 Jun 12;18(1):458. doi: 10.1186/s12864-017-3770-y. BMC Genomics. 2017. PMID: 28606096 Free PMC article.

3

Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies.

Standish KA, Carland TM, Lockwood GK, Pfeiffer W, Tatineni M, Huang CC, Lamberth S, Cherkas Y, Brodmerkel C, Jaeger E, Smith L, Rajagopal G, Curran ME, Schork NJ. Standish KA, et al. Among authors: schork nj. BMC Bioinformatics. 2015 Sep 22;16(1):304. doi: 10.1186/s12859-015-0736-4. BMC Bioinformatics. 2015. PMID: 26395405 Free PMC article.

4

Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population.

Fan X, Wang H, Sun L, Zheng X, Yin X, Zuo X, Peng Q, Standish KA, Cheng H, Zhang Y, Wang Z, Xiao F, Yang S, Zhang X, Schork NJ. Fan X, et al. Among authors: schork nj. Epigenomics. 2019 Feb;11(4):455-467. doi: 10.2217/epi-2018-0131. Epub 2019 Feb 20. Epigenomics. 2019. PMID: 30785334 Free PMC article.

5

Genotype-based risk and pharmacogenetic sampling in clinical trials.

Schork NJ, Topol EJ. Schork NJ, et al. J Biopharm Stat. 2010 Mar;20(2):315-33. doi: 10.1080/10543400903572779. J Biopharm Stat. 2010. PMID: 20309761 Free PMC article.

6

Genome-wide association study of paliperidone efficacy.

Li Q, Wineinger NE, Fu DJ, Libiger O, Alphs L, Savitz A, Gopal S, Cohen N, Schork NJ. Li Q, et al. Among authors: schork nj. Pharmacogenet Genomics. 2017 Jan;27(1):7-18. doi: 10.1097/FPC.0000000000000250. Pharmacogenet Genomics. 2017. PMID: 27846195 Free PMC article.

7

Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites.

Long T, Hicks M, Yu HC, Biggs WH, Kirkness EF, Menni C, Zierer J, Small KS, Mangino M, Messier H, Brewerton S, Turpaz Y, Perkins BA, Evans AM, Miller LA, Guo L, Caskey CT, Schork NJ, Garner C, Spector TD, Venter JC, Telenti A. Long T, et al. Among authors: schork nj. Nat Genet. 2017 Apr;49(4):568-578. doi: 10.1038/ng.3809. Epub 2017 Mar 6. Nat Genet. 2017. PMID: 28263315

8

Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population.

Peng Q, Schork NJ, Wilhelmsen KC, Ehlers CL. Peng Q, et al. Among authors: schork nj. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):435-450. doi: 10.1002/ajmg.b.32533. Epub 2017 Apr 24. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28436151 Free PMC article.

9

Effective discovery of rare variants by pooled target capture sequencing: A comparative analysis with individually indexed target capture sequencing.

Ryu S, Han J, Norden-Krichmar TM, Schork NJ, Suh Y. Ryu S, et al. Among authors: schork nj. Mutat Res. 2018 May;809:24-31. doi: 10.1016/j.mrfmmm.2018.03.007. Epub 2018 Mar 30. Mutat Res. 2018. PMID: 29677560 Free PMC article.

10

Pathway and network analysis with high-density allelic association data.

Torkamani A, Schork NJ. Torkamani A, et al. Among authors: schork nj. Methods Mol Biol. 2009;563:289-301. doi: 10.1007/978-1-60761-175-2_16. Methods Mol Biol. 2009. PMID: 19597792

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