(Q37102159)

18 August 2017

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title

Primer: SNP-associated studies and what they can teach us. (English)

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18 August 2017

Ryo Yamada

1

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18 August 2017

publication date

4 March 2008

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Nature Clinical Practice Rheumatology

18 August 2017

published in

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18 August 2017

volume

4

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18 August 2017

issue

4

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18 August 2017

page(s)

210-217

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A promoter haplotype of the immunoreceptor tyrosine-based inhibitory motif-bearing FcgammaRIIb alters receptor expression and associates with autoimmunity. I. Regulatory FCGR2B polymorphisms and their association with systemic lupus erythematosus

18 August 2017

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7 January 2021

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Adjusting the focus on human variation

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Human genome sequence variation and the influence of gene history, mutation and recombination

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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Structural variation in the human genome

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7 January 2021

Structural variation in the human genome

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7 January 2021

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

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7 January 2021

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

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7 January 2021

Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

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7 January 2021

A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

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7 January 2021

Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus

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7 January 2021

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

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7 January 2021

Fcgamma receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility

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7 January 2021

Loss of function of a lupus-associated FcγRIIb polymorphism through exclusion from lipid rafts

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7 January 2021

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

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7 January 2021

Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis

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7 January 2021

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

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7 January 2021

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

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7 January 2021

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

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7 January 2021

Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs

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7 January 2021

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

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7 January 2021

Leveraging the HapMap correlation structure in association studies

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7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

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7 January 2021

A tutorial on statistical methods for population association studies

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7 January 2021

Complement factor H polymorphism in age-related macular degeneration

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7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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7 January 2021

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

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7 January 2021

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

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7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

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7 January 2021

A genome-wide association study identifies novel risk loci for type 2 diabetes

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7 January 2021

The pharmacogenetics research network: from SNP discovery to clinical drug response.

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7 January 2021

Will tomorrow's medicines work for everyone?

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7 January 2021

Potential genetic causes of heterogeneity of treatment effects

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7 January 2021

Association of CFH Y402H and LOC387715 A69S with progression of age-related macular degeneration

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7 January 2021

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

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7 January 2021

Common deletion polymorphisms in the human genome.

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7 January 2021

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0757

7 January 2021

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

1 reference

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7 January 2021

STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

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7 January 2021

TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

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7 January 2021

Identifiers

DOI

10.1038/NCPRHEUM0757

1 reference

Dimensions Publication ID

18 August 2017

1023138758

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Fatcat ID

release_3ekcoyo4dvgfhod5w5uo7xyutm

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3ekcoyo4dvgfhod5w5uo7xyutm

24 November 2022

mapped directly with Wikidata item

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