Halperin E - Search Results

1

Remote blood collection from older adults in the Brain Health Registry for plasma biomarker and genetic analysis.

Fockler J, Ashford MT, Eichenbaum J, Howell T, Ekanem A, Flenniken D, Happ A, Truran D, Mackin RS, Blennow K, Halperin E, Coppola G, Weiner MW, Nosheny RL. Fockler J, et al. Among authors: halperin e. Alzheimers Dement. 2022 Dec;18(12):2627-2636. doi: 10.1002/alz.12617. Epub 2022 Feb 28. Alzheimers Dement. 2022. PMID: 35226409 Free PMC article.

2

A model-based approach for analysis of spatial structure in genetic data.

Yang WY, Novembre J, Eskin E, Halperin E. Yang WY, et al. Among authors: halperin e. Nat Genet. 2012 May 20;44(6):725-31. doi: 10.1038/ng.2285. Nat Genet. 2012. PMID: 22610118 Free PMC article.

3

Phenome-Wide Association Study of Polygenic Risk Score for Alzheimer's Disease in Electronic Health Records.

Fu M; UCLA Precision Health Data Discovery Repository Working Group; UCLA Precision Health ATLAS Working Group; Chang TS. Fu M, et al. Front Aging Neurosci. 2022 Mar 15;14:800375. doi: 10.3389/fnagi.2022.800375. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35370621 Free PMC article.

4

Methylation risk scores are associated with a collection of phenotypes within electronic health record systems.

Thompson M, Hill BL, Rakocz N, Chiang JN, Geschwind D, Sankararaman S, Hofer I, Cannesson M, Zaitlen N, Halperin E. Thompson M, et al. Among authors: halperin e. NPJ Genom Med. 2022 Aug 25;7(1):50. doi: 10.1038/s41525-022-00320-1. NPJ Genom Med. 2022. PMID: 36008412 Free PMC article.

5

Genotyping common and rare variation using overlapping pool sequencing.

He D, Zaitlen N, Pasaniuc B, Eskin E, Halperin E. He D, et al. Among authors: halperin e. BMC Bioinformatics. 2011;12 Suppl 6(Suppl 6):S2. doi: 10.1186/1471-2105-12-S6-S2. Epub 2011 Jul 28. BMC Bioinformatics. 2011. PMID: 21989232 Free PMC article.

6

CNVeM: copy number variation detection using uncertainty of read mapping.

Wang Z, Hormozdiari F, Yang WY, Halperin E, Eskin E. Wang Z, et al. Among authors: halperin e. J Comput Biol. 2013 Mar;20(3):224-36. doi: 10.1089/cmb.2012.0258. Epub 2013 Feb 19. J Comput Biol. 2013. PMID: 23421794 Free PMC article.

7

Rare variant association testing under low-coverage sequencing.

Navon O, Sul JH, Han B, Conde L, Bracci PM, Riby J, Skibola CF, Eskin E, Halperin E. Navon O, et al. Among authors: halperin e. Genetics. 2013 Jul;194(3):769-79. doi: 10.1534/genetics.113.150169. Epub 2013 May 1. Genetics. 2013. PMID: 23636738 Free PMC article.

8

Learning natural selection from the site frequency spectrum.

Ronen R, Udpa N, Halperin E, Bafna V. Ronen R, et al. Among authors: halperin e. Genetics. 2013 Sep;195(1):181-93. doi: 10.1534/genetics.113.152587. Epub 2013 Jun 14. Genetics. 2013. PMID: 23770700 Free PMC article.

9

eALPS: estimating abundance levels in pooled sequencing using available genotyping data.

Eskin I, Hormozdiari F, Conde L, Riby J, Skibola CF, Eskin E, Halperin E. Eskin I, et al. Among authors: halperin e. J Comput Biol. 2013 Nov;20(11):861-77. doi: 10.1089/cmb.2013.0105. Epub 2013 Oct 21. J Comput Biol. 2013. PMID: 24144111 Free PMC article.

10

Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies.

Rahmani E, Zaitlen N, Baran Y, Eng C, Hu D, Galanter J, Oh S, Burchard EG, Eskin E, Zou J, Halperin E. Rahmani E, et al. Among authors: halperin e. Nat Methods. 2016 May;13(5):443-5. doi: 10.1038/nmeth.3809. Epub 2016 Mar 28. Nat Methods. 2016. PMID: 27018579 Free PMC article.

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