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Items: 1 to 20 of 131

1.

Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains.

Bennett BJ, Davis RC, Civelek M, Orozco L, Wu J, Qi H, Pan C, Packard RR, Eskin E, Yan M, Kirchgessner T, Wang Z, Li X, Gregory JC, Hazen SL, Gargalovic PS, Lusis AJ.

PLoS Genet. 2015 Dec 22;11(12):e1005711. doi: 10.1371/journal.pgen.1005711. eCollection 2015 Dec.

2.

The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants.

Crow AL, Ohmen J, Wang J, Lavinsky J, Hartiala J, Li Q, Li X, Salehide P, Eskin E, Pan C, Lusis AJ, Allayee H, Friedman RA.

G3 (Bethesda). 2015 Sep 4;5(11):2329-39. doi: 10.1534/g3.115.021592.

3.

Genetic and environmental control of host-gut microbiota interactions.

Org E, Parks BW, Joo JW, Emert B, Schwartzman W, Kang EY, Mehrabian M, Pan C, Knight R, Gunsalus R, Drake TA, Eskin E, Lusis AJ.

Genome Res. 2015 Oct;25(10):1558-69. doi: 10.1101/gr.194118.115. Epub 2015 Aug 10.

4.

High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.

Rau CD, Parks B, Wang Y, Eskin E, Simecek P, Churchill GA, Lusis AJ.

G3 (Bethesda). 2015 Jul 28;5(10):2021-6. doi: 10.1534/g3.115.020784.

5.

Quantitative analysis of 3-dimensional facial soft tissue photographic images: technical methods and clinical application.

Nanda V, Gutman B, Bar E, Alghamdi S, Tetradis S, Lusis AJ, Eskin E, Moon W.

Prog Orthod. 2015;16:21. doi: 10.1186/s40510-015-0082-0. Epub 2015 Jul 2.

6.

Identification of causal genes for complex traits.

Hormozdiari F, Kichaev G, Yang WY, Pasaniuc B, Eskin E.

Bioinformatics. 2015 Jun 15;31(12):i206-13. doi: 10.1093/bioinformatics/btv240.

7.

Correction: Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss.

Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA.

PLoS Genet. 2015 Jun 11;11(6):e1005293. doi: 10.1371/journal.pgen.1005293. eCollection 2015 Jun. No abstract available.

8.

The Genetic Landscape of Hematopoietic Stem Cell Frequency in Mice.

Zhou X, Crow AL, Hartiala J, Spindler TJ, Ghazalpour A, Barsky LW, Bennett BJ, Parks BW, Eskin E, Jain R, Epstein JA, Lusis AJ, Adams GB, Allayee H.

Stem Cell Reports. 2015 Jul 14;5(1):125-38. doi: 10.1016/j.stemcr.2015.05.008. Epub 2015 Jun 4.

9.

Accurate and fast multiple-testing correction in eQTL studies.

Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B.

Am J Hum Genet. 2015 Jun 4;96(6):857-68. doi: 10.1016/j.ajhg.2015.04.012. Epub 2015 May 28.

10.

Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss.

Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA.

PLoS Genet. 2015 Apr 16;11(4):e1005094. doi: 10.1371/journal.pgen.1005094. eCollection 2015 Apr. Erratum in: PLoS Genet. 2015 Jun;11(6):e1005293.

11.

Gene-Gene Interactions Detection Using a Two-stage Model.

Wang Z, Sul JH, Snir S, Lozano JA, Eskin E.

J Comput Biol. 2015 Jun;22(6):563-76. doi: 10.1089/cmb.2014.0163. Epub 2015 Apr 14.

PMID:
25871811
12.

Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed model.

Furlotte NA, Eskin E.

Genetics. 2015 May;200(1):59-68. doi: 10.1534/genetics.114.171447. Epub 2015 Feb 27.

PMID:
25724382
13.

Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma.

Luykx JJ, Bakker SC, Visser WF, Verhoeven-Duif N, Buizer-Voskamp JE, den Heijer JM, Boks MP, Sul JH, Eskin E, Ori AP, Cantor RM, Vorstman J, Strengman E, DeYoung J, Kappen TH, Pariama E, van Dongen EP, Borgdorff P, Bruins P, de Koning TJ, Kahn RS, Ophoff RA.

Mol Psychiatry. 2015 Dec;20(12):1557-64. doi: 10.1038/mp.2014.190. Epub 2015 Feb 10.

PMID:
25666758
14.

Memory efficient assembly of human genome.

Hormozdiari F, Eskin E.

J Bioinform Comput Biol. 2015 Apr;13(2):1550008. doi: 10.1142/S0219720015500080. Epub 2014 Dec 17.

PMID:
25603998
15.

Heritability of periodontal bone loss in mice.

Hiyari S, Atti E, Camargo PM, Eskin E, Lusis AJ, Tetradis S, Pirih FQ.

J Periodontal Res. 2015 Dec;50(6):730-6. doi: 10.1111/jre.12258. Epub 2015 Jan 12.

PMID:
25581386
16.

IPED2X: a robust pedigree reconstruction algorithm for complicated pedigrees.

He D, Eskin E.

J Bioinform Comput Biol. 2014 Dec;12(6):1442007. doi: 10.1142/S0219720014420074.

PMID:
25553812
17.

A spatial haplotype copying model with applications to genotype imputation.

Yang WY, Hormozdiari F, Eskin E, Pasaniuc B.

J Comput Biol. 2015 May;22(5):451-62. doi: 10.1089/cmb.2014.0151. Epub 2014 Dec 19.

PMID:
25526526
18.

Spatial localization of recent ancestors for admixed individuals.

Yang WY, Platt A, Chiang CW, Eskin E, Novembre J, Pasaniuc B.

G3 (Bethesda). 2014 Nov 3;4(12):2505-18. doi: 10.1534/g3.114.014274.

19.

Integrating functional data to prioritize causal variants in statistical fine-mapping studies.

Kichaev G, Yang WY, Lindstrom S, Hormozdiari F, Eskin E, Price AL, Kraft P, Pasaniuc B.

PLoS Genet. 2014 Oct 30;10(10):e1004722. doi: 10.1371/journal.pgen.1004722. eCollection 2014 Oct.

20.

Identifying causal variants at loci with multiple signals of association.

Hormozdiari F, Kostem E, Kang EY, Pasaniuc B, Eskin E.

Genetics. 2014 Oct;198(2):497-508. doi: 10.1534/genetics.114.167908. Epub 2014 Aug 7.

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