Shifman S - Search Results

1

Widespread Allelic Heterogeneity in Complex Traits.

Hormozdiari F, Zhu A, Kichaev G, Ju CJ, Segrè AV, Joo JWJ, Won H, Sankararaman S, Pasaniuc B, Shifman S, Eskin E. Hormozdiari F, et al. Among authors: shifman s. Am J Hum Genet. 2017 May 4;100(5):789-802. doi: 10.1016/j.ajhg.2017.04.005. Am J Hum Genet. 2017. PMID: 28475861 Free PMC article.

2

A highly significant association between a COMT haplotype and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A. Shifman S, et al. Am J Hum Genet. 2002 Dec;71(6):1296-302. doi: 10.1086/344514. Epub 2002 Oct 25. Am J Hum Genet. 2002. PMID: 12402217 Free PMC article.

3

Linkage disequilibrium patterns of the human genome across populations.

Shifman S, Kuypers J, Kokoris M, Yakir B, Darvasi A. Shifman S, et al. Hum Mol Genet. 2003 Apr 1;12(7):771-6. doi: 10.1093/hmg/ddg088. Hum Mol Genet. 2003. PMID: 12651872

4

Mouse inbred strain sequence information and yin-yang crosses for quantitative trait locus fine mapping.

Shifman S, Darvasi A. Shifman S, et al. Genetics. 2005 Feb;169(2):849-54. doi: 10.1534/genetics.104.032474. Epub 2004 Nov 1. Genetics. 2005. PMID: 15520253 Free PMC article.

5

Further tests of the association between schizophrenia and single nucleotide polymorphism markers at the catechol-O-methyltransferase locus in an Askenazi Jewish population using microsatellite markers.

Horowitz A, Shifman S, Rivlin N, Pisanté A, Darvasi A. Horowitz A, et al. Among authors: shifman s. Psychiatr Genet. 2005 Sep;15(3):163-9. doi: 10.1097/00041444-200509000-00005. Psychiatr Genet. 2005. PMID: 16094249

6

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia.

Shifman S, Levit A, Chen ML, Chen CH, Bronstein M, Weizman A, Yakir B, Navon R, Darvasi A. Shifman S, et al. Hum Genet. 2006 Sep;120(2):160-70. doi: 10.1007/s00439-006-0195-0. Epub 2006 Jun 17. Hum Genet. 2006. PMID: 16783572

7

Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.

Ben-David E, Granot-Hershkovitz E, Monderer-Rothkoff G, Lerer E, Levi S, Yaari M, Ebstein RP, Yirmiya N, Shifman S. Ben-David E, et al. Among authors: shifman s. Hum Mol Genet. 2011 Sep 15;20(18):3632-41. doi: 10.1093/hmg/ddr283. Epub 2011 Jun 16. Hum Mol Genet. 2011. PMID: 21680558

8

Allelic expression analysis in the brain suggests a role for heterogeneous insults affecting epigenetic processes in autism spectrum disorders.

Ben-David E, Shohat S, Shifman S. Ben-David E, et al. Among authors: shifman s. Hum Mol Genet. 2014 Aug 1;23(15):4111-24. doi: 10.1093/hmg/ddu128. Epub 2014 Mar 21. Hum Mol Genet. 2014. PMID: 24659497

9

Discovering Single Nucleotide Polymorphisms Regulating Human Gene Expression Using Allele Specific Expression from RNA-seq Data.

Kang EY, Martin LJ, Mangul S, Isvilanonda W, Zou J, Ben-David E, Han B, Lusis AJ, Shifman S, Eskin E. Kang EY, et al. Among authors: shifman s. Genetics. 2016 Nov;204(3):1057-1064. doi: 10.1534/genetics.115.177246. Epub 2016 Oct 7. Genetics. 2016. PMID: 27765809 Free PMC article.

10

ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues.

Mangul S, Yang HT, Strauli N, Gruhl F, Porath HT, Hsieh K, Chen L, Daley T, Christenson S, Wesolowska-Andersen A, Spreafico R, Rios C, Eng C, Smith AD, Hernandez RD, Ophoff RA, Santana JR, Levanon EY, Woodruff PG, Burchard E, Seibold MA, Shifman S, Eskin E, Zaitlen N. Mangul S, et al. Among authors: shifman s. Genome Biol. 2018 Feb 15;19(1):36. doi: 10.1186/s13059-018-1403-7. Genome Biol. 2018. PMID: 29548336 Free PMC article.

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