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Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma.
Nat Commun. 2015 Jan 16;6:5965. doi: 10.1038/ncomms6965.
Nat Commun. 2015.
PMID: 25591454
Free PMC article.
PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.
Livne OE, Han L, Alkorta-Aranburu G, Wentworth-Sheilds W, Abney M, Ober C, Nicolae DL.
Livne OE, et al.
PLoS Comput Biol. 2015 Mar 3;11(3):e1004139. doi: 10.1371/journal.pcbi.1004139. eCollection 2015 Mar.
PLoS Comput Biol. 2015.
PMID: 25735005
Free PMC article.
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Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, Churchhouse C, Fontanillas P, King R, Lee S, Lincoln SE, Trubetskoy V, DePristo M, Fingerlin T, Grossman R, Grundstad J, Heath A, Kim J, Kim YJ, Laramie J, Lee J, Li H, Liu X, Livne O, Locke AE, Maller J, Mazur A, Morris AP, Pollin TI, Ragona D, Reich D, Rivas MA, Scott LJ, Sim X, Tearle RG, Teo YY, Williams AL, Zöllner S, Curran JE, Peralta J, Akolkar B, Bell GI, Burtt NP, Cox NJ, Florez JC, Hanis CL, McKeon C, Mohlke KL, Seielstad M, Wilson JG, Atzmon G, Below JE, Dupuis J, Nicolae DL, Lehman D, Park T, Won S, Sladek R, Altshuler D, McCarthy MI, Duggirala R, Boehnke M, Frayling TM, Abecasis GR, Blangero J.
Jun G, et al.
Proc Natl Acad Sci U S A. 2018 Jan 9;115(2):379-384. doi: 10.1073/pnas.1705859115. Epub 2017 Dec 26.
Proc Natl Acad Sci U S A. 2018.
PMID: 29279374
Free PMC article.
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes.
Majithia AR, Flannick J, Shahinian P, Guo M, Bray MA, Fontanillas P, Gabriel SB; GoT2D Consortium; NHGRI JHS/FHS Allelic Spectrum Project; SIGMA T2D Consortium; T2D-GENES Consortium; Rosen ED, Altshuler D.
Majithia AR, et al.
Proc Natl Acad Sci U S A. 2014 Sep 9;111(36):13127-32. doi: 10.1073/pnas.1410428111. Epub 2014 Aug 25.
Proc Natl Acad Sci U S A. 2014.
PMID: 25157153
Free PMC article.
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A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.
Kim YJ, Lee J, Kim BJ; T2D-Genes Consortium; Park T.
Kim YJ, et al.
BMC Genomics. 2015 Dec 29;16:1109. doi: 10.1186/s12864-015-2192-y.
BMC Genomics. 2015.
PMID: 26715385
Free PMC article.
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Federating clinical data from six pediatric hospitals: process and initial results from the PHIS+ Consortium.
Narus SP, Srivastava R, Gouripeddi R, Livne OE, Mo P, Bickel JP, de Regt D, Hales JW, Kirkendall E, Stepanek RL, Toth J, Keren R.
Narus SP, et al. Among authors: livne oe.
AMIA Annu Symp Proc. 2011;2011:994-1003. Epub 2011 Oct 22.
AMIA Annu Symp Proc. 2011.
PMID: 22195159
Free PMC article.
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Federated querying architecture with clinical & translational health IT application.
Livne OE, Schultz ND, Narus SP.
Livne OE, et al.
J Med Syst. 2011 Oct;35(5):1211-24. doi: 10.1007/s10916-011-9720-3. Epub 2011 May 3.
J Med Syst. 2011.
PMID: 21537849
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Architecture of a federated query engine for heterogeneous resources.
Bradshaw RL, Matney S, Livne OE, Bray BE, Mitchell JA, Narus SP.
Bradshaw RL, et al. Among authors: livne oe.
AMIA Annu Symp Proc. 2009 Nov 14;2009:70-4.
AMIA Annu Symp Proc. 2009.
PMID: 20351825
Free PMC article.
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