scholarly article | Q13442814 |
P50 | author | Tony Merriman | Q37392448 |
Andrew Harrison | Q43252036 | ||
Peter Gow | Q109592547 | ||
Marilyn Merriman | Q108801647 | ||
P2093 | author name string | Fitzgerald 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 | |||
P2860 | cites work | Evidence 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 SNPs | Q21266602 | ||
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes | Q24290189 | ||
Delta proteins and MAGI proteins: an interaction of Notch ligands with intracellular scaffolding molecules and its significance for zebrafish development | Q24309565 | ||
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 PADI4 | Q24538382 | ||
Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans | Q24538972 | ||
Complement factor H polymorphism in age-related macular degeneration | Q24553334 | ||
Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis | Q24611240 | ||
Pooled DNA genotyping on Affymetrix SNP genotyping arrays | Q25256899 | ||
The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritis | Q27860872 | ||
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis | Q28267921 | ||
The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis | Q28306666 | ||
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies | Q29614926 | ||
Population structure, differential bias and genomic control in a large-scale, case-control association study | Q29614945 | ||
Streamlined analysis of pooled genotype data in SNP-based association studies | Q30982285 | ||
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins | Q31460983 | ||
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis | Q34114509 | ||
Using linkage genome scans to improve power of association in genome scans | Q34398834 | ||
Association testing by DNA pooling: an effective initial screen | Q34430209 | ||
Whole genome association study of rheumatoid arthritis using 27 039 microsatellites | Q34431672 | ||
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization | Q34519498 | ||
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region | Q34525819 | ||
Two-stage designs in case-control association analysis | Q34898066 | ||
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis | Q35834701 | ||
Association between PADI4 and rheumatoid arthritis: a meta-analysis | Q36383132 | ||
PTPN22: setting thresholds for autoimmunity | Q36491114 | ||
Whole-genome genotyping of haplotype tag single nucleotide polymorphisms | Q36503726 | ||
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays. | Q45952965 | ||
A genome-wide scalable SNP genotyping assay using microarray technology | Q46111789 | ||
Evaluating coverage of genome-wide association studies | Q46423138 | ||
Association of the PTPN22 locus with rheumatoid arthritis in a New Zealand Caucasian cohort | Q46573581 | ||
A common genetic variant is associated with adult and childhood obesity | Q46726890 | ||
Algorithms for large-scale genotyping microarrays | Q47328169 | ||
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children | Q48242038 | ||
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 haplotype | Q52990092 | ||
Dissection of class III major histocompatibility complex haplotypes associated with rheumatoid arthritis | Q52990372 | ||
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 pooling | Q57445855 | ||
Association of thePDCD5Locus With Lung Cancer Risk and Prognosis in Smokers | Q57763164 | ||
HLA class III haplotypes in multicase rheumatoid arthritis families | Q69639421 | ||
Genetics of rheumatoid arthritis (RA): two separate regions in the major histocompatibility complex contribute to susceptibility to RA | Q73100407 | ||
The telomeric part of the HLA region predisposes to rheumatoid arthritis independently of the class II loci | Q73411967 | ||
Induction of Notch signaling by tumor necrosis factor in rheumatoid synovial fibroblasts | Q79227597 | ||
A high-resolution survey of deletion polymorphism in the human genome | Q94465012 | ||
P433 | issue | 1 | |
P921 | main subject | rheumatoid arthritis | Q187255 |
whole genome sequencing | Q2068526 | ||
P304 | page(s) | 57-68 | |
P577 | publication date | 2006-12-07 | |
P1433 | published in | Genes and Immunity | Q15745246 |
P1476 | title | Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. | |
P478 | volume | 8 |
Q33289150 | A DArT platform for quantitative bulked segregant analysis |
Q48077040 | A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland |
Q33794452 | A genome-wide association study identifies multiple loci associated with mathematics ability and disability |
Q24655759 | A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder |
Q28943536 | A genome-wide association study in 574 schizophrenia trios using DNA pooling |
Q30475974 | A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations |
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Q60924390 | Comparative study for haplotype block partitioning methods - Evidence from chromosome 6 of the North American Rheumatoid Arthritis Consortium (NARAC) dataset |
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Q30478361 | Modifiers of hearing impairment in humans and mice |
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Q48219517 | NLRP1, PTPN22 and PADI4 gene polymorphisms and rheumatoid arthritis in ACPA-positive Singaporean Chinese |
Q34031304 | PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis |
Q40265320 | PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus |
Q52615322 | PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger. |
Q33904168 | Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene |
Q33970796 | Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis |
Q46147942 | Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis. |
Q82436903 | Susceptibility influence of a PTPN22 haplotype with thyroid autoimmunity in Koreans |
Q37461017 | Systems biology and heart failure: concepts, methods, and potential research applications |
Q33727899 | The PTPN22 locus and rheumatoid arthritis: no evidence for an effect on risk independent of Arg620Trp |
Q40202718 | The Potential Mutation of GAK Gene in the Typical Sporadic Parkinson's Disease from the Han Population of Chinese Mainland. |
Q33735365 | Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays |
Q33517973 | Validation of pooled genotyping on the Affymetrix 500 k and SNP6.0 genotyping platforms using the polynomial-based probe-specific correction |
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