(Q57155111)

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Closing the gap between genotype and phenotype

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Closing the gap between genotype and phenotype (English)

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Peter K Gregersen

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language of work or name

English

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publication date

September 2009

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published in

Nature Genetics

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volume

41

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issue

9

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page(s)

958-9

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exact match

https://scigraph.springernature.com/pub.10.1038/ng0909-958

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cites work

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

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reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

retrieved

21 January 2018

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

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reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

retrieved

21 January 2018

Recent advances in the genetics of autoimmune disease

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https://api.crossref.org/works/10.1038%2FNG0909-958

retrieved

21 January 2018

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

A prescription for human immunology

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https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Risk alleles for multiple sclerosis identified by a genomewide study

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https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

The biology of interleukin-2.

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https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Homeostatic maintenance of natural Foxp3(+) CD25(+) CD4(+) regulatory T cells by interleukin (IL)-2 and induction of autoimmune disease by IL-2 neutralization

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reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Regulatory T cells are reduced during anti-CD25 antibody treatment of multiple sclerosis.

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reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

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reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0909-958

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21 January 2018

Merging and emerging cohorts: necessary but not sufficient

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19710714

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12 December 2020

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The habitual, diverse and surmountable obstacles to human immunology research

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19710714

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19710714

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19710714

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.1038/NG0909-958

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PubMed publication ID

19710714

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(Q57155111)

Closing the gap between genotype and phenotype

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