Introduction to SNPs: discovery of markers for disease.

[1]  A. Børresen-Dale,et al.  High-throughput methods for detection of genetic variation. , 2001, BioTechniques.

[2]  J. Todd,et al.  Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation. , 2000, Genome research.

[3]  Pardis C Sabeti,et al.  Linkage disequilibrium in the human genome , 2001, Nature.

[4]  P. Kwok,et al.  Fluorescence polarization in homogeneous nucleic acid analysis. , 1999, Genome research.

[5]  M. Weiner,et al.  Multiplexed single nucleotide polymorphism genotyping by oligonucleotide ligation and flow cytometry. , 2000, Cytometry.

[6]  E. Marshall.  Drug Firms to Create Public Database of Genetic Mutations , 1999, Science.

[7]  Eric Lander,et al.  Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland , 1992, Nature Genetics.

[8]  D. Sarracino,et al.  Rapid genotyping by MALDI-monitored nuclease selection from probe libraries , 2000, Nature Biotechnology.

[9]  Roger S Lasken,et al.  High-throughput genotyping of single nucleotide polymorphisms with rolling circle amplification , 2001, BMC Genomics.

[10]  S. P. Fodor,et al.  Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.

[11]  M M Shi,et al.  Enabling large-scale pharmacogenetic studies by high-throughput mutation detection and genotyping technologies. , 2001, Clinical chemistry.

[12]  D. Harold,et al.  Determining SNP allele frequencies in DNA pools. , 2000, BioTechniques.

[13]  Peter Beighton,et al.  de la Chapelle, A. , 1997 .

[14]  H A Erlich,et al.  Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[15]  L. Tsui,et al.  Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.

[16]  U Landegren,et al.  A ligase-mediated gene detection technique. , 1988, Science.

[17]  Jörg Schmidtke,et al.  An estimate of unique DNA sequence heterozygosity in the human genome , 2004, Human Genetics.

[18]  Timothy B. Stockwell,et al.  The Sequence of the Human Genome , 2001, Science.

[19]  A. Roses,et al.  The use of single nucleotide polymorphisms in the isolation of common disease genes. , 2000, Pharmacogenomics.

[20]  John P Nolan,et al.  Suspension array technology: evolution of the flat-array paradigm. , 2002, Trends in biotechnology.

[21]  Ivo G Gut,et al.  Large-scale genotyping by mass spectrometry: experience, advances and obstacles. , 2002, Current opinion in chemical biology.

[22]  J. Drabek,et al.  A commented dictionary of techniques for genotyping , 2001, Electrophoresis.

[23]  E Lai,et al.  A 4-Mb high-density single nucleotide polymorphism-based map around human APOE. , 1998, Genomics.

[24]  F. Crick,et al.  Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid , 1953, Nature.

[25]  Sinead B. O'Leary,et al.  Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease , 2001, Nature Genetics.

[26]  A. Mazumder,et al.  Suspension arrays for high throughput, multiplexed single nucleotide polymorphism genotyping. , 2000, Cytometry.

[27]  A Chakravarti,et al.  Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. , 2000, Genome research.

[28]  I. Gut,et al.  Automation in genotyping of single nucleotide polymorphisms , 2001, Human mutation.

[29]  Fred Russell Kramer,et al.  Multicolor molecular beacons for allele discrimination , 1998, Nature Biotechnology.

[30]  M. Daly,et al.  High-resolution haplotype structure in the human genome , 2001, Nature Genetics.

[31]  E S Lander,et al.  Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci. , 2000, American journal of human genetics.

[32]  G. Mátyás,et al.  Quantification of single nucleotide polymorphisms: A novel method that combines primer extension assay and capillary electrophoresis , 2002, Human mutation.

[33]  E Lai,et al.  Application of SNP technologies in medicine: lessons learned and future challenges. , 2001, Genome research.

[34]  E. Boerwinkle,et al.  Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene. , 2000, Genome research.

[35]  M. Goldrick.  RNase cleavage‐based methods for mutation/SNP detection, past and present , 2001, Human mutation.

[36]  T M McHugh,et al.  Flow microsphere immunoassay for the quantitative and simultaneous detection of multiple soluble analytes. , 1994, Methods in cell biology.

[37]  Manish S. Shah,et al.  A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes , 1993, Cell.

[38]  A. Syvänen.  From gels to chips: “Minisequencing” primer extension for analysis of point mutations and single nucleotide polymorphisms , 1999, Human mutation.

[39]  John A. Todd,et al.  Towards fully automated genome–wide polymorphism screening , 1995, Nature Genetics.

[40]  A Chakravarti,et al.  High-throughput variation detection and genotyping using microarrays. , 2001, Genome research.

[41]  T. Sekiya,et al.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[42]  P. Kwok,et al.  High-throughput genotyping assay approaches. , 2000, Pharmacogenomics.

[43]  Charles R. Cantor,et al.  Sequencing exons 5 to 8 of the p53 gene by MALDI-TOF mass spectrometry , 1998, Nature Biotechnology.

[44]  P. Kwok,et al.  Methods for genotyping single nucleotide polymorphisms. , 2003, Annual review of genomics and human genetics.

[45]  I. Gut,et al.  Facile method for automated genotyping of single nucleotide polymorphisms by mass spectrometry. , 2002, Nucleic acids research.

[46]  L. Helmuth.  Map of the Human Genome 3.0 , 2001, Science.

[47]  F. Collins,et al.  New goals for the U.S. Human Genome Project: 1998-2003. , 1998, Science.

[48]  K. Gunderson,et al.  Mutation detection by ligation to complete n-mer DNA arrays. , 1998, Genome research.

[49]  Rolf Hilfiker,et al.  The use of single-nucleotide polymorphism maps in pharmacogenomics , 2000, Nature Biotechnology.