Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis

scientific article published on 7 December 2006

Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/SJ.GENE.6364359
P698PubMed publication ID17159887
P5875ResearchGate publication ID6639594

P50authorTony MerrimanQ37392448
Andrew HarrisonQ43252036
Peter GowQ109592547
Marilyn MerrimanQ108801647
P2093author name stringFitzgerald L
Skolnick MH
Tran T
Iliev D
Steer S
Highton J
O'Donnell J
Lanchbury JS
Chapman P
Cordell HJ
Abkevich V
Rowley KA
Timms KM
Rodger RA
Jones PB
Gutin A
Gendall KL
Kouzmine A
Stamp L
P2860cites workEvidence for a novel rheumatoid arthritis susceptibility locus on chromosome 6p.Q42642429
Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPsQ21266602
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesQ24290189
Delta proteins and MAGI proteins: an interaction of Notch ligands with intracellular scaffolding molecules and its significance for zebrafish developmentQ24309565
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Q24538382
Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scansQ24538972
Complement factor H polymorphism in age-related macular degenerationQ24553334
Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritisQ24611240
Pooled DNA genotyping on Affymetrix SNP genotyping arraysQ25256899
The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritisQ27860872
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritisQ28267921
The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritisQ28306666
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studiesQ29614926
Population structure, differential bias and genomic control in a large-scale, case-control association studyQ29614945
Streamlined analysis of pooled genotype data in SNP-based association studiesQ30982285
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twinsQ31460983
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisQ34114509
Using linkage genome scans to improve power of association in genome scansQ34398834
Association testing by DNA pooling: an effective initial screenQ34430209
Whole genome association study of rheumatoid arthritis using 27 039 microsatellitesQ34431672
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationQ34519498
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) regionQ34525819
Two-stage designs in case-control association analysisQ34898066
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritisQ35834701
Association between PADI4 and rheumatoid arthritis: a meta-analysisQ36383132
PTPN22: setting thresholds for autoimmunityQ36491114
Whole-genome genotyping of haplotype tag single nucleotide polymorphismsQ36503726
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.Q45952965
A genome-wide scalable SNP genotyping assay using microarray technologyQ46111789
Evaluating coverage of genome-wide association studiesQ46423138
Association of the PTPN22 locus with rheumatoid arthritis in a New Zealand Caucasian cohortQ46573581
A common genetic variant is associated with adult and childhood obesityQ46726890
Algorithms for large-scale genotyping microarraysQ47328169
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in childrenQ48242038
Inhibition of genes expression of SARS coronavirus by synthetic small interfering RNAs.Q50774425
SNP allele frequency estimation in DNA pools and variance components analysis.Q51997362
Pedigree disequilibrium tests for multilocus haplotypes.Q52010978
The effect of HLA–DR on susceptibility to rheumatoid arthritis is influenced by the associated lymphotoxin α–tumor necrosis factor haplotypeQ52990092
Dissection of class III major histocompatibility complex haplotypes associated with rheumatoid arthritisQ52990372
Guidelines for conducting and reporting whole genome/large-scale association studies.Q53618040
Association between a variation inLRCH1 and knee osteoarthritis: A genome-wide single-nucleotide polymorphism association study using DNA poolingQ57445855
Association of thePDCD5Locus With Lung Cancer Risk and Prognosis in SmokersQ57763164
HLA class III haplotypes in multicase rheumatoid arthritis familiesQ69639421
Genetics of rheumatoid arthritis (RA): two separate regions in the major histocompatibility complex contribute to susceptibility to RAQ73100407
The telomeric part of the HLA region predisposes to rheumatoid arthritis independently of the class II lociQ73411967
Induction of Notch signaling by tumor necrosis factor in rheumatoid synovial fibroblastsQ79227597
A high-resolution survey of deletion polymorphism in the human genomeQ94465012
P433issue1
P921main subjectrheumatoid arthritisQ187255
whole genome sequencingQ2068526
P304page(s)57-68
P577publication date2006-12-07
P1433published inGenes and ImmunityQ15745246
P1476titleGenomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.
P478volume8

Reverse relations

cites work (P2860)
Q33289150A DArT platform for quantitative bulked segregant analysis
Q48077040A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland
Q33794452A genome-wide association study identifies multiple loci associated with mathematics ability and disability
Q24655759A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
Q28943536A genome-wide association study in 574 schizophrenia trios using DNA pooling
Q30475974A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations
Q33314661A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples
Q30955298A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS).
Q37018101A review of current approaches to identifying human genes involved in myopia.
Q33289927Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studies
Q36709524Assignment of SNP allelic configuration in polyploids using competitive allele-specific PCR: application to citrus triploid progeny
Q40222230Association of PTPN22 Single Nucleotide Polymorphisms with Celiac Disease
Q46923561Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population
Q35130219Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.
Q60924390Comparative study for haplotype block partitioning methods - Evidence from chromosome 6 of the North American Rheumatoid Arthritis Consortium (NARAC) dataset
Q34038213Computational method for estimating DNA copy numbers in normal samples, cancer cell lines, and solid tumors using array comparative genomic hybridization
Q39606833FUT2: filling the gap between genes and environment in Behçet's disease?
Q35694393Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.
Q37032887Genetic developments in autoimmune thyroid disease: an evolutionary process
Q35661517Genetic factors of autoimmune thyroid diseases in Japanese
Q80684055Genetics of chronic obstructive pulmonary disease
Q28943498Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis
Q36593761Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays
Q89965572Identification of 67 Pleiotropic Genes Associated With Seven Autoimmune/Autoinflammatory Diseases Using Multivariate Statistical Analysis
Q36783894Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia
Q28943483Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene
Q35105700Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Q57249724Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans
Q47555364Identifying and exploiting trait-relevant tissues with multiple functional annotations in genome-wide association studies
Q42035322Methodological Issues in Multistage Genome-wide Association Studies
Q30478361Modifiers of hearing impairment in humans and mice
Q36024006Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax
Q41859735Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies
Q48219517NLRP1, PTPN22 and PADI4 gene polymorphisms and rheumatoid arthritis in ACPA-positive Singaporean Chinese
Q34031304PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis
Q40265320PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus
Q52615322PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.
Q33904168Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
Q33970796Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis
Q46147942Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis.
Q82436903Susceptibility influence of a PTPN22 haplotype with thyroid autoimmunity in Koreans
Q37461017Systems biology and heart failure: concepts, methods, and potential research applications
Q33727899The PTPN22 locus and rheumatoid arthritis: no evidence for an effect on risk independent of Arg620Trp
Q40202718The Potential Mutation of GAK Gene in the Typical Sporadic Parkinson's Disease from the Han Population of Chinese Mainland.
Q33735365Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays
Q33517973Validation of pooled genotyping on the Affymetrix 500 k and SNP6.0 genotyping platforms using the polynomial-based probe-specific correction

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