(Q28271903)

20

0 references

Philip Rosenstiel

8

0 references

Christian Gieger

19

0 references

Michael Nothnagel

4

0 references

David Ellinghaus

3

0 references

Anders Eklund

17

Anders Eklund

0 references

Joachim Müller-Quernheim

23

Joachim Müller-Quernheim

0 references

Gernot Zissel

Gernot Zissel

9

0 references

Leonid Padyukov

Leonid Padyukov

18

0 references

Almut Nebel

21

Almut Nebel

0 references

Stefan Schreiber

25

Stefan Schreiber

0 references

Johan Grunewald

15

Johan Grunewald

0 references

Andre Franke

22

Andre Franke

0 references

Annegret Fischer

1

Annegret Fischer

0 references

Manfred Schürmann

6

Manfred Schürmann

0 references

Simone Lipinski

7

Simone Lipinski

0 references

Kerstin Höhne

10

Kerstin Höhne

0 references

Martin Petrek

11

Martin Petrek

0 references

Christian Grohé

14

Christian Grohé

0 references

Marcus Ronninger

16

Marcus Ronninger

0 references

author name string

Benjamin Schmid

2

0 references

Karoline I Gaede

5

0 references

Vitezslav Kolek

12

0 references

Stefan Pabst

13

0 references

Sylvia Hofmann

American Journal of Respiratory and Critical Care Medicine

24

0 references

language of work or name

English

0 references

publication date

1 November 2012

0 references

published in

0 references

volume

186

0 references

issue

9

0 references

page(s)

877-85

0 references

cites work

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The BTNL2 gene and sarcoidosis susceptibility in African Americans and Whites

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Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis

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First independent replication study confirms the strong genetic association of ANXA11 with sarcoidosis.

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A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1.

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Statement on Sarcoidosis

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Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes.

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Female-specific association of C-C chemokine receptor 5 gene polymorphisms with Löfgren's syndrome.

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A new model for an etiology of rheumatoid arthritis: smoking may trigger HLA-DR (shared epitope)-restricted immune reactions to autoantigens modified by citrullination

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Principal components analysis corrects for stratification in genome-wide association studies

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A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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Haploview: analysis and visualization of LD and haplotype maps

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Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences

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The UCSC Genome Browser Database: update 2006

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SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels

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Genomic control for association studies

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Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2.

21 January 2018

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Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

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Genome-wide association study in alopecia areata implicates both innate and adaptive immunity

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

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Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy

21 January 2018

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Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci

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The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

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Protective role of Gipie, a Girdin family protein, in endoplasmic reticulum stress responses in endothelial cells

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Cloning and expression of human TRAAK, a polyunsaturated fatty acids-activated and mechano-sensitive K(+) channel

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Expression of mechanogated two-pore domain potassium channels in mouse lungs: special reference to mechanosensory airway receptors

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Peroxiredoxin 5: structure, mechanism, and function of the mammalian atypical 2-Cys peroxiredoxin

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Leukocyte oxidase: defective activity in chronic granulomatous disease

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Phospholipase cbeta is critical for T cell chemotaxis.

21 January 2018

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Phospholipase C beta3 deficiency leads to macrophage hypersensitivity to apoptotic induction and reduction of atherosclerosis in mice

21 January 2018

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Heredity in sarcoidosis: a registry-based twin study

21 January 2018

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Caspase recruitment domain 15 gene haplotypes in sarcoidosis

21 January 2018

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