(Q29614873)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17200669%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

title

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

2 references

PubMed

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17200669

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17200669%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

23 December 2019

main subject

0 references

author

Jochen Hampe

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17200669%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

Philip Rosenstiel

3

1 reference

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23 December 2019

Andreas Till

4

1 reference

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23 December 2019

Klaus Huse

6

1 reference

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23 December 2019

Natalie J. Prescott

12

1 reference

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23 December 2019

Thomas Lengauer

17

1 reference

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23 December 2019

Christopher G. Mathew

19

1 reference

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23 December 2019

14

Robert Häsler

1 reference

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23 December 2019

21

Stefan Schreiber

1 reference

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23 December 2019

2

Andre Franke

1 reference

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23 December 2019

author name string

Markus Teuber

5

1 reference

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23 December 2019

Mario Albrecht

7

1 reference

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23 December 2019

Gabriele Mayr

8

1 reference

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23 December 2019

Francisco M De La Vega

9

1 reference

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23 December 2019

Jason Briggs

10

1 reference

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23 December 2019

Simone Günther

11

1 reference

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23 December 2019

Clive M Onnie

13

1 reference

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23 December 2019

Bence Sipos

15

1 reference

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23 December 2019

Ulrich R Fölsch

16

1 reference

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23 December 2019

Matthias Platzer

18

1 reference

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23 December 2019

Michael Krawczak

20

1 reference

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23 December 2019

language of work or name

1 reference

30 April 2017

publication date

31 December 2006

1 reference

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23 December 2019

2 references

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30 April 2017

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23 December 2019

volume

39

2 references

PubMed

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30 April 2017

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23 December 2019

page(s)

207-211

1 reference

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23 December 2019

issue

2

2 references

PubMed

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30 April 2017

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

23 December 2019

cites work

1 reference

7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 reference

7 January 2021

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

7 January 2021

Functional variants of OCTN cation transporter genes are associated with Crohn disease

1 reference

7 January 2021

Genetic variation in DLG5 is associated with inflammatory bowel disease

1 reference

7 January 2021

MDR1 Ala893 polymorphism is associated with inflammatory bowel disease

1 reference

7 January 2021

ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach

1 reference

7 January 2021

Association between the C3435T MDR1 gene polymorphism and susceptibility for ulcerative colitis.

1 reference

7 January 2021

Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease

1 reference

7 January 2021

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing

1 reference

7 January 2021

Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract

1 reference

7 January 2021

Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection

1 reference

7 January 2021

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

1 reference

7 January 2021

NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses

1 reference

7 January 2021

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

1 reference

7 January 2021

High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12

1 reference

7 January 2021

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

1 reference

7 January 2021

Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci

1 reference

7 January 2021

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

1 reference

7 January 2021

Cloning and analysis of human Apg16L

1 reference

7 January 2021

Mouse Apg16L, a novel WD-repeat protein, targets to the autophagic isolation membrane with the Apg12-Apg5 conjugate

1 reference

7 January 2021

An integrated system for high throughput TaqManTM based SNP genotyping

1 reference

7 January 2021

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.

1 reference

7 January 2021

The Sequence of the Human Genome

1 reference

7 January 2021

InSNP: a tool for automated detection and visualization of SNPs and InDels.

1 reference

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

7 January 2021

GENOMIZER: an integrated analysis system for genome-wide association data

1 reference

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17200669

Identifiers

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

314976

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17200669%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

23 December 2019

1020669934

0 references

314976

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17200669

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

314976

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17200669%20AND%20SRC:MED&resulttype=core&format=json