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Items: 1 to 20 of 87

1.

Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19).

Ma L, Semick SA, Chen Q, Li C, Tao R, Price AJ, Shin JH, Jia Y; BrainSeq Consortium, Brandon NJ, Cross AJ, Hyde TM, Kleinman JE, Jaffe AE, Weinberger DR, Straub RE.

Mol Psychiatry. 2019 Jan 11. doi: 10.1038/s41380-018-0293-0. [Epub ahead of print]

PMID:
30635639
2.

Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci.

Fullard JF, Giambartolomei C, Hauberg ME, Xu K, Voloudakis G, Shao Z, Bare C, Dudley JT, Mattheisen M, Robakis NK, Haroutunian V, Roussos P.

Hum Mol Genet. 2017 May 15;26(10):1942-1951. doi: 10.1093/hmg/ddx103.

3.

Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia.

Law AJ, Kleinman JE, Weinberger DR, Weickert CS.

Hum Mol Genet. 2007 Jan 15;16(2):129-41. Epub 2006 Dec 12.

PMID:
17164265
4.

Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets.

Olsson AH, Volkov P, Bacos K, Dayeh T, Hall E, Nilsson EA, Ladenvall C, Rönn T, Ling C.

PLoS Genet. 2014 Nov 6;10(11):e1004735. doi: 10.1371/journal.pgen.1004735. eCollection 2014 Nov. Erratum in: PLoS Genet. 2014 Dec;10(12):e1004886.

5.

Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.

Martin RI, Babaei MS, Choy MK, Owens WA, Chico TJ, Keenan D, Yonan N, Koref MS, Keavney BD.

J Mol Cell Cardiol. 2015 Aug;85:207-14. doi: 10.1016/j.yjmcc.2015.06.005. Epub 2015 Jun 11.

PMID:
26073630
6.

Endometrial vezatin and its association with endometriosis risk.

Holdsworth-Carson SJ, Fung JN, Luong HT, Sapkota Y, Bowdler LM, Wallace L, Teh WT, Powell JE, Girling JE, Healey M, Montgomery GW, Rogers PA.

Hum Reprod. 2016 May;31(5):999-1013. doi: 10.1093/humrep/dew047. Epub 2016 Mar 22.

PMID:
27005890
7.

Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe.

Blauwendraat C, Francescatto M, Gibbs JR, Jansen IE, Simón-Sánchez J, Hernandez DG, Dillman AA, Singleton AB, Cookson MR, Rizzu P, Heutink P.

Genome Med. 2016 Jun 10;8(1):65. doi: 10.1186/s13073-016-0320-1.

8.

Association between SNPs and gene expression in multiple regions of the human brain.

Kim S, Cho H, Lee D, Webster MJ.

Transl Psychiatry. 2012 May 8;2:e113. doi: 10.1038/tp.2012.42.

9.

Quantitative Trait Locus and Brain Expression of HLA-DPA1 Offers Evidence of Shared Immune Alterations in Psychiatric Disorders.

Morgan LZ, Rollins B, Sequeira A, Byerley W, DeLisi LE, Schatzberg AF, Barchas JD, Myers RM, Watson SJ, Akil H, Bunney WE Jr, Vawter MP.

Microarrays (Basel). 2016 Mar;5(1). pii: 6. Epub 2016 Mar 7.

10.

Variants at IRX4 as prostate cancer expression quantitative trait loci.

Xu X, Hussain WM, Vijai J, Offit K, Rubin MA, Demichelis F, Klein RJ.

Eur J Hum Genet. 2014 Apr;22(4):558-63. doi: 10.1038/ejhg.2013.195. Epub 2013 Sep 11.

11.

Characterization of genomic organization of the adenosine A2A receptor gene by molecular and bioinformatics analyses.

Yu L, Frith MC, Suzuki Y, Peterfreund RA, Gearan T, Sugano S, Schwarzschild MA, Weng Z, Fink JS, Chen JF.

Brain Res. 2004 Mar 12;1000(1-2):156-73.

PMID:
15053963
13.

Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia.

Lin D, Chen J, Perrone-Bizzozero N, Bustillo JR, Du Y, Calhoun VD, Liu J.

Genome Med. 2018 Feb 26;10(1):13. doi: 10.1186/s13073-018-0519-4.

14.

Identification of human-specific transcript variants induced by DNA insertions in the human genome.

Kim DS, Hahn Y.

Bioinformatics. 2011 Jan 1;27(1):14-21. doi: 10.1093/bioinformatics/btq612. Epub 2010 Oct 29.

PMID:
21037245
15.

Transcript-specific associations of SLC12A5 (KCC2) in human prefrontal cortex with development, schizophrenia, and affective disorders.

Tao R, Li C, Newburn EN, Ye T, Lipska BK, Herman MM, Weinberger DR, Kleinman JE, Hyde TM.

J Neurosci. 2012 Apr 11;32(15):5216-22. doi: 10.1523/JNEUROSCI.4626-11.2012.

16.

Functional evaluation of genetic variants associated with endometriosis near GREB1.

Fung JN, Holdsworth-Carson SJ, Sapkota Y, Zhao ZZ, Jones L, Girling JE, Paiva P, Healey M, Nyholt DR, Rogers PA, Montgomery GW.

Hum Reprod. 2015 May;30(5):1263-75. doi: 10.1093/humrep/dev051. Epub 2015 Mar 18.

PMID:
25788566
17.

Integrative modeling of eQTLs and cis-regulatory elements suggests mechanisms underlying cell type specificity of eQTLs.

Brown CD, Mangravite LM, Engelhardt BE.

PLoS Genet. 2013;9(8):e1003649. doi: 10.1371/journal.pgen.1003649. Epub 2013 Aug 1.

18.

Genetic risk mechanisms of posttraumatic stress disorder in the human brain.

Bharadwaj RA, Jaffe AE, Chen Q, Deep-Soboslay A, Goldman AL, Mighdoll MI, Cotoia JA, Brandtjen AC, Shin J, Hyde TM, Mattay VS, Weinberger DR, Kleinman JE.

J Neurosci Res. 2018 Jan;96(1):21-30. doi: 10.1002/jnr.23957. Epub 2016 Oct 24.

PMID:
27775175
19.

DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia.

Numata S, Ye T, Herman M, Lipska BK.

Front Genet. 2014 Aug 26;5:280. doi: 10.3389/fgene.2014.00280. eCollection 2014.

20.

Computational discovery of human coding and non-coding transcripts with conserved splice sites.

Rose D, Hiller M, Schutt K, Hackermüller J, Backofen R, Stadler PF.

Bioinformatics. 2011 Jul 15;27(14):1894-900. doi: 10.1093/bioinformatics/btr314. Epub 2011 May 26.

PMID:
21622663

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