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Results: 1 to 20 of 128

1.

DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism.

Aguiar D, Halldórsson BV, Morrow EM, Istrail S.

Bioinformatics. 2012 Jun 15;28(12):i154-62. doi: 10.1093/bioinformatics/bts234.

PMID:
22689755
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
[PubMed - indexed for MEDLINE]
3.

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.

Mefford HC, Cooper GM, Zerr T, Smith JD, Baker C, Shafer N, Thorland EC, Skinner C, Schwartz CE, Nickerson DA, Eichler EE.

Genome Res. 2009 Sep;19(9):1579-85. doi: 10.1101/gr.094987.109. Epub 2009 Jun 8.

PMID:
19506092
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

An algorithm for detecting high frequency copy number polymorphisms using SNP arrays.

Halldórsson BV, Gudbjartsson DF.

J Comput Biol. 2011 Aug;18(8):955-66. doi: 10.1089/cmb.2010.0317. Epub 2011 Jul 5.

PMID:
21728861
[PubMed - indexed for MEDLINE]
5.

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.

Eckel-Passow JE, Atkinson EJ, Maharjan S, Kardia SL, de Andrade M.

BMC Bioinformatics. 2011 May 31;12:220. doi: 10.1186/1471-2105-12-220.

PMID:
21627824
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.

Rudan I.

Psychiatr Danub. 2010 Jun;22(2):190-2. Review.

PMID:
20562745
[PubMed - indexed for MEDLINE]
Free Article
7.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays.

Hua J, Craig DW, Brun M, Webster J, Zismann V, Tembe W, Joshipura K, Huentelman MJ, Dougherty ER, Stephan DA.

Bioinformatics. 2007 Jan 1;23(1):57-63. Epub 2006 Oct 24.

PMID:
17062589
[PubMed - indexed for MEDLINE]
Free Article
8.

Genome-wide algorithm for detecting CNV associations with diseases.

Xu Y, Peng B, Fu Y, Amos CI.

BMC Bioinformatics. 2011 Aug 9;12:331. doi: 10.1186/1471-2105-12-331.

PMID:
21827692
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A genotype resource for postmortem brain samples from the Autism Tissue Program.

Wintle RF, Lionel AC, Hu P, Ginsberg SD, Pinto D, Thiruvahindrapduram B, Wei J, Marshall CR, Pickett J, Cook EH, Scherer SW.

Autism Res. 2011 Apr;4(2):89-97. doi: 10.1002/aur.173. Epub 2011 Jan 19. Erratum in: Autism Res. 2011 Aug;4(4):314.

PMID:
21254448
[PubMed - indexed for MEDLINE]
10.

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.

Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT.

BMC Pregnancy Childbirth. 2012 Jun 29;12:61.

PMID:
22748001
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis.

Wu CC, Shete S, Jo EJ, Xu Y, Lu EY, Chen WV, Amos CI.

Hum Mol Genet. 2013 Mar 15;22(6):1249-61. doi: 10.1093/hmg/dds512. Epub 2012 Dec 6.

PMID:
23223014
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.

Valsesia A, Stevenson BJ, Waterworth D, Mooser V, Vollenweider P, Waeber G, Jongeneel CV, Beckmann JS, Kutalik Z, Bergmann S.

BMC Genomics. 2012 Jun 15;13:241. doi: 10.1186/1471-2164-13-241.

PMID:
22702538
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

A flexible rank-based framework for detecting copy number aberrations from array data.

LaFramboise T, Winckler W, Thomas RK.

Bioinformatics. 2009 Mar 15;25(6):722-8. doi: 10.1093/bioinformatics/btp063. Epub 2009 Jan 28.

PMID:
19176555
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic studies of complex human diseases: characterizing SNP-disease associations using Bayesian networks.

Han B, Chen XW, Talebizadeh Z, Xu H.

BMC Syst Biol. 2012;6 Suppl 3:S14. doi: 10.1186/1752-0509-6-S3-S14. Epub 2012 Dec 17.

PMID:
23281790
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
16.

Robust relationship inference in genome-wide association studies.

Manichaikul A, Mychaleckyj JC, Rich SS, Daly K, Sale M, Chen WM.

Bioinformatics. 2010 Nov 15;26(22):2867-73. doi: 10.1093/bioinformatics/btq559. Epub 2010 Oct 5.

PMID:
20926424
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Genomic selection and complex trait prediction using a fast EM algorithm applied to genome-wide markers.

Shepherd RK, Meuwissen TH, Woolliams JA.

BMC Bioinformatics. 2010 Oct 22;11:529. doi: 10.1186/1471-2105-11-529.

PMID:
20969788
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Detection of copy number variation using SNP genotyping.

Cooper GM, Mefford HC.

Methods Mol Biol. 2011;767:243-52. doi: 10.1007/978-1-61779-201-4_18.

PMID:
21822880
[PubMed - indexed for MEDLINE]
19.

Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis.

Wu CC, Shete S, Chen WV, Peng B, Lee AT, Ma J, Gregersen PK, Amos CI.

Hum Genet. 2009 Aug;126(2):303-15. doi: 10.1007/s00439-009-0672-3. Epub 2009 May 5.

PMID:
19415332
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.

Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH Jr, Stankiewicz P, State MW, Beaudet AL.

Hum Mol Genet. 2011 Nov 15;20(22):4360-70. doi: 10.1093/hmg/ddr363. Epub 2011 Aug 24.

PMID:
21865298
[PubMed - indexed for MEDLINE]
Free PMC Article

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