Identification of disease causing loci using an array-based genotyping approach on pooled DNA

[1]  P. Sham,et al.  SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. , 2005, Human molecular genetics.

[2]  Robert Plomin,et al.  Genotyping DNA pools on microarrays: Tackling the QTL problem of large samples and large numbers of SNPs , 2005, BMC Genomics.

[3]  I. Craig,et al.  Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms , 2005, Molecular Psychiatry.

[4]  M. Owen,et al.  Streamlined analysis of pooled genotype data in SNP‐based association studies , 2005, Genetic epidemiology.

[5]  Claire L. Simpson,et al.  A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays , 2005, Nucleic acids research.

[6]  M. Daly,et al.  Genome-wide association studies for common diseases and complex traits , 2005, Nature Reviews Genetics.

[7]  S. P. Fodor,et al.  Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays , 2004, Nature Methods.

[8]  D. Cox,et al.  Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels , 2004, Human Genomics.

[9]  I. Craig,et al.  Genotyping Pooled DNA on Microarrays: A Systematic Genome Screen of Thousands of SNPs in Large Samples to Detect QTLs for Complex Traits , 2004, Behavior genetics.

[10]  Winnie S. Liang,et al.  Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[11]  C. Carlson,et al.  Mapping complex disease loci in whole-genome association studies , 2004, Nature.

[12]  Jing Huang,et al.  Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array. , 2004, Genome research.

[13]  E. Puffenberger,et al.  Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania , 2003, American journal of medical genetics. Part C, Seminars in medical genetics.

[14]  G. Marnellos,et al.  High-throughput SNP analysis for genetic association studies. , 2003, Current opinion in drug discovery & development.

[15]  P. Visscher,et al.  SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. , 2002, Nucleic acids research.

[16]  G. Kirov,et al.  Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools , 2002, Human Genetics.

[17]  L. Cardon,et al.  Association study designs for complex diseases , 2001, Nature Reviews Genetics.

[18]  B. Hoogendoorn,et al.  Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography. , 2001, Journal of biochemical and biophysical methods.

[19]  Michael Owen,et al.  Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools , 2000, Human Genetics.

[20]  N Risch,et al.  The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling. , 1998, Genome research.

[21]  D Bentley,et al.  Highly parallel SNP genotyping. , 2003, Cold Spring Harbor symposia on quantitative biology.