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Items: 1 to 20 of 92

1.

Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.

Sellick GS, Longman C, Tolmie J, Newbury-Ecob R, Geenhalgh L, Hughes S, Whiteford M, Garrett C, Houlston RS.

Nucleic Acids Res. 2004 Nov 23;32(20):e164.

2.

A novel gene for neonatal diabetes maps to chromosome 10p12.1-p13.

Sellick GS, Garrett C, Houlston RS.

Diabetes. 2003 Oct;52(10):2636-8.

3.

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites.

John S, Shephard N, Liu G, Zeggini E, Cao M, Chen W, Vasavda N, Mills T, Barton A, Hinks A, Eyre S, Jones KW, Ollier W, Silman A, Gibson N, Worthington J, Kennedy GC.

Am J Hum Genet. 2004 Jul;75(1):54-64. Epub 2004 May 20.

4.

A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer.

Middeldorp A, Jagmohan-Changur S, Helmer Q, van der Klift HM, Tops CM, Vasen HF, Devilee P, Morreau H, Houwing-Duistermaat JJ, Wijnen JT, van Wezel T.

BMC Cancer. 2007 Jan 12;7:6.

5.

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
6.

[Advances in high-density whole genome-wide single nucleotide polymorphism array in cancer research].

Zeng ZY, Xiong W, Zhou YH, Li XL, Li GY.

Ai Zheng. 2006 Nov;25(11):1454-8. Review. Chinese.

PMID:
17094921
7.

Design of tag SNP whole genome genotyping arrays.

Peiffer DA, Gunderson KL.

Methods Mol Biol. 2009;529:51-61. doi: 10.1007/978-1-59745-538-1_4.

PMID:
19381970
8.

Single nucleotide polymorphism mapping array assay.

Zhou X, Wong DT.

Methods Mol Biol. 2007;396:295-314.

PMID:
18025700
9.

Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies.

Gonzalez-Neira A, Rosa-Rosa JM, Osorio A, Gonzalez E, Southey M, Sinilnikova O, Lynch H, Oldenburg RA, van Asperen CJ, Hoogerbrugge N, Pita G, Devilee P, Goldgar D, Benitez J.

BMC Genomics. 2007 Aug 30;8:299.

10.

Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference.

Saunders IW, Brohede J, Hannan GN.

Genomics. 2007 Sep;90(3):291-6. Epub 2007 Jun 27.

11.

Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

Arinami T, Ohtsuki T, Ishiguro H, Ujike H, Tanaka Y, Morita Y, Mineta M, Takeichi M, Yamada S, Imamura A, Ohara K, Shibuya H, Ohara K, Suzuki Y, Muratake T, Kaneko N, Someya T, Inada T, Yoshikawa T, Toyota T, Yamada K, Kojima T, Takahashi S, Osamu O, Shinkai T, Nakamura M, Fukuzako H, Hashiguchi T, Niwa SI, Ueno T, Tachikawa H, Hori T, Asada T, Nanko S, Kunugi H, Hashimoto R, Ozaki N, Iwata N, Harano M, Arai H, Ohnuma T, Kusumi I, Koyama T, Yoneda H, Fukumaki Y, Shibata H, Kaneko S, Higuchi H, Yasui-Furukori N, Numachi Y, Itokawa M, Okazaki Y; Japanese Schizophrenia Sib-Pair Linkage Group.

Am J Hum Genet. 2005 Dec;77(6):937-44. Epub 2005 Oct 12.

12.

Hot topic: performance of bovine high-density genotyping platforms in Holsteins and Jerseys.

Rincon G, Weber KL, Eenennaam AL, Golden BL, Medrano JF.

J Dairy Sci. 2011 Dec;94(12):6116-21. doi: 10.3168/jds.2011-4764.

PMID:
22118099
13.

SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data.

Huentelman MJ, Craig DW, Shieh AD, Corneveaux JJ, Hu-Lince D, Pearson JV, Stephan DA.

BMC Genomics. 2005 Oct 31;6:149.

14.

Application of genomewide SNP arrays for detection of simulated susceptibility loci.

Kulle B, Schirmer M, Toliat MR, Suk A, Becker C, Tzvetkov MV, Brockmöller J, Bickeböller H, Hasenfuss G, Nürnberg P, Wojnowski L.

Hum Mutat. 2005 Jun;25(6):557-65.

PMID:
15880731
15.

Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families.

Suh I, Filetti S, Vriens MR, Guerrero MA, Tumino S, Wong M, Shen WT, Kebebew E, Duh QY, Clark OH.

Surgery. 2009 Dec;146(6):1073-80. doi: 10.1016/j.surg.2009.09.012.

PMID:
19958934
16.

A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.

Xiao Y, Segal MR, Yang YH, Yeh RF.

Bioinformatics. 2007 Jun 15;23(12):1459-67. Epub 2007 Apr 25.

17.

Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.

Wong KK, Tsang YT, Shen J, Cheng RS, Chang YM, Man TK, Lau CC.

Nucleic Acids Res. 2004 May 17;32(9):e69.

18.

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans.

Meaburn E, Butcher LM, Schalkwyk LC, Plomin R.

Nucleic Acids Res. 2006 Feb 14;34(4):e27.

19.

A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility loci.

Sellick GS, Webb EL, Allinson R, Matutes E, Dyer MJ, Jonsson V, Langerak AW, Mauro FR, Fuller S, Wiley J, Lyttelton M, Callea V, Yuille M, Catovsky D, Houlston RS.

Am J Hum Genet. 2005 Sep;77(3):420-9. Epub 2005 Aug 2.

20.

Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.

Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C, Romanos J, Palmason H, Reif A, Heine M, Windemuth-Kieselbach C, Vogler C, Sigmund J, Warnke A, Schäfer H, Meyer J, Stephan DA, Lesch KP.

Mol Psychiatry. 2008 May;13(5):522-30. doi: 10.1038/mp.2008.12. Epub 2008 Feb 26.

PMID:
18301393
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