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Results: 1 to 20 of 127

1.

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 Dec;16(1):82. doi: 10.1186/s40510-015-0082-0. Epub 2015 Jul 2.

2.

Identification of causal genes for complex traits.

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

Bioinformatics. 2015 Jun 15;31(12):i206-i213. doi: 10.1093/bioinformatics/btv240.

3.

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.

4.

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.

5.

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.

PMID:
26027500
6.

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.

7.

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
8.

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
9.

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 Feb 10. doi: 10.1038/mp.2014.190. [Epub ahead of print]

PMID:
25666758
10.

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
11.

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 Jan 12. doi: 10.1111/jre.12258. [Epub ahead of print]

PMID:
25581386
12.

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
13.

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
14.

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.

15.

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.

16.

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.

PMID:
25104515
17.

Accurate viral population assembly from ultra-deep sequencing data.

Mangul S, Wu NC, Mancuso N, Zelikovsky A, Sun R, Eskin E.

Bioinformatics. 2014 Jun 15;30(12):i329-37. doi: 10.1093/bioinformatics/btu295.

18.

Privacy preserving protocol for detecting genetic relatives using rare variants.

Hormozdiari F, Joo JW, Wadia A, Guan F, Ostrosky R, Sahai A, Eskin E.

Bioinformatics. 2014 Jun 15;30(12):i204-11. doi: 10.1093/bioinformatics/btu294.

19.

Allele-specific expression and eQTL analysis in mouse adipose tissue.

Hasin-Brumshtein Y, Hormozdiari F, Martin L, van Nas A, Eskin E, Lusis AJ, Drake TA.

BMC Genomics. 2014 Jun 13;15:471. doi: 10.1186/1471-2164-15-471.

20.

Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies.

Joo JW, Sul JH, Han B, Ye C, Eskin E.

Genome Biol. 2014 Apr 7;15(4):r61. doi: 10.1186/gb-2014-15-4-r61.

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