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Results: 1 to 20 of 61

Similar articles for PubMed (Select 23247082)

1.
2.

Linkage analysis in the next-generation sequencing era.

Bailey-Wilson JE, Wilson AF.

Hum Hered. 2011;72(4):228-36. doi: 10.1159/000334381. Epub 2011 Dec 23. Review.

3.

Resequencing of the vesicular glutamate transporter 2 gene (VGLUT2) reveals some rare genetic variants that may increase the genetic burden in schizophrenia.

Shen YC, Liao DL, Lu CL, Chen JY, Liou YJ, Chen TT, Chen CH.

Schizophr Res. 2010 Aug;121(1-3):179-86. doi: 10.1016/j.schres.2010.05.015. Epub 2010 Jun 11.

PMID:
20541370
4.

Approaches to the detection of recessive effects using next generation sequencing data from outbred populations.

Curtis D.

Adv Appl Bioinform Chem. 2013 Jun 11;6:29-35. doi: 10.2147/AABC.S44332. Print 2013.

5.

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

Gershon ES, Alliey-Rodriguez N, Liu C.

Am J Psychiatry. 2011 Mar;168(3):253-6. doi: 10.1176/appi.ajp.2010.10091340. Epub 2011 Feb 1. Review.

PMID:
21285144
6.

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.

Need AC, McEvoy JP, Gennarelli M, Heinzen EL, Ge D, Maia JM, Shianna KV, He M, Cirulli ET, Gumbs CE, Zhao Q, Campbell CR, Hong L, Rosenquist P, Putkonen A, Hallikainen T, Repo-Tiihonen E, Tiihonen J, Levy DL, Meltzer HY, Goldstein DB.

Am J Hum Genet. 2012 Aug 10;91(2):303-12. doi: 10.1016/j.ajhg.2012.06.018. Epub 2012 Aug 2.

7.

Narrowing the boundaries of the genetic architecture of schizophrenia.

Wray NR, Visscher PM.

Schizophr Bull. 2010 Jan;36(1):14-23. doi: 10.1093/schbul/sbp137. Epub 2009 Dec 8. Review.

8.

Evaluating rare variants in complex disorders using next-generation sequencing.

Ezewudo M, Zwick ME.

Curr Psychiatry Rep. 2013 Apr;15(4):349. doi: 10.1007/s11920-013-0349-4. Review.

9.

Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Cirulli ET, Goldstein DB.

Nat Rev Genet. 2010 Jun;11(6):415-25. doi: 10.1038/nrg2779. Review.

PMID:
20479773
10.

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J.

PLoS One. 2011;6(8):e23450. doi: 10.1371/journal.pone.0023450. Epub 2011 Aug 11.

11.

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.

Lotta LA, Wang M, Yu J, Martinelli I, Yu F, Passamonti SM, Consonni D, Pappalardo E, Menegatti M, Scherer SE, Lewis LL, Akbar H, Wu Y, Bainbridge MN, Muzny DM, Mannucci PM, Gibbs RA, Peyvandi F.

BMC Med Genomics. 2012 Feb 21;5:7. doi: 10.1186/1755-8794-5-7.

12.

Design considerations for genetic linkage and association studies.

Nsengimana J, Bishop DT.

Methods Mol Biol. 2012;850:237-62. doi: 10.1007/978-1-61779-555-8_13.

PMID:
22307702
13.
14.

A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.

Cheung YH, Wang G, Leal SM, Wang S.

Genet Epidemiol. 2012 Nov;36(7):675-85. doi: 10.1002/gepi.21662. Epub 2012 Aug 3.

PMID:
22865616
15.

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

Sahoo T, Theisen A, Rosenfeld JA, Lamb AN, Ravnan JB, Schultz RA, Torchia BS, Neill N, Casci I, Bejjani BA, Shaffer LG.

Genet Med. 2011 Oct;13(10):868-80. doi: 10.1097/GIM.0b013e3182217a06.

PMID:
21792059
16.
17.

Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence Data.

Curtis D.

Ann Hum Genet. 2015 Mar 27. doi: 10.1111/ahg.12109. [Epub ahead of print]

PMID:
25817274
18.

Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.

Sivakumaran TA, Husami A, Kissell D, Zhang W, Keddache M, Black AP, Tinkle BT, Greinwald JH Jr, Zhang K.

Otolaryngol Head Neck Surg. 2013 Jun;148(6):1007-16. doi: 10.1177/0194599813482294. Epub 2013 Mar 22.

PMID:
23525850
19.

A statistical method for the detection of variants from next-generation resequencing of DNA pools.

Bansal V.

Bioinformatics. 2010 Jun 15;26(12):i318-24. doi: 10.1093/bioinformatics/btq214.

20.

[Polymorphisms of rs4906902 and rs8179184 loci in the promoter of the GABRB3 gene and their relevance with schizophrenia].

Sun XF, Ding M, Sun Y, Pang H, Xuan JF, Xing JX, Li CM, Wang BJ.

Fa Yi Xue Za Zhi. 2012 Jun;28(3):195-7. Chinese.

PMID:
22812221
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