about
Systematic association mapping identifies NELL1 as a novel IBD disease geneIndependent and population-specific association of risk variants at the IRGM locus with Crohn's diseaseA Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5Host-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsIL23R variation determines susceptibility but not disease phenotype in inflammatory bowel diseaseAssociation scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsGenome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A regionAssociation of DLG5 R30Q variant with inflammatory bowel diseaseGenetic variation in myosin IXB is associated with ulcerative colitisMeta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibilityA genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study.Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.Altered intestinal microbiota and blood T cell phenotype are shared by patients with Crohn's disease and their unaffected siblings.Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genesPopulation-specific genetic associations with oesophageal squamous cell carcinoma in South Africa.Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease.Effect of communicating DNA based risk assessments for Crohn's disease on smoking cessation: randomised controlled trialDistinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's diseaseGenetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis.Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.The unusual suspects--innate lymphoid cells as novel therapeutic targets in IBD.Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.Defective macrophage handling of Escherichia coli in Crohn's disease.Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfismExploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis.Exome sequencing and genotyping identify a rare variant in NLRP7 gene associated with ulcerative colitis.
P50
Q21090112-3390FF8D-A6C4-4880-BB1F-11445A52EA4BQ22242868-A24A14B6-225D-4662-8E50-460B80DDB076Q22250941-87438767-0A5A-45E7-8A1B-8DDB1E4FF485Q22251082-B1849250-F0B5-41C4-B916-B7B15D5263BCQ24550675-1E94084D-1CF3-420D-A466-B83AF795E177Q24618592-237952F8-F1D4-4BF0-A8A4-E30C598ECE9FQ24628710-956870BC-402D-46CD-A7D9-DDB8E680F66DQ24645890-1D644808-E02C-4E46-AA42-572896CFDE3BQ24646663-CBBF0ACF-F8DB-496C-A737-B0783A4949F3Q24657139-BFE0FFF2-3AFA-4AEC-AB79-BA0EF6964E37Q28246016-FF6480DA-DBA3-4A9F-95FA-7C2C0644A5E1Q28272638-93541252-090D-4747-ABF8-F4957F7D31B3Q28943305-F1EAB458-43DB-4AF0-953E-55B0C3282A60Q29614872-50E559C4-AE80-4EF2-91AE-18F57795245AQ29614873-38BC12BB-E555-45C0-860D-8AD0DB12724BQ30426245-D3FFF4E6-AACF-49E6-A746-E972E098EFB3Q33998487-85406439-5C23-446E-BE13-E9C656342F5CQ34117526-1AB6BECF-92D6-459E-A3DD-28DAD5CFE1D9Q34199869-E0E9F4EE-2BCC-45B6-B220-0FFC10AA849FQ34341147-9EADEA1B-20D6-465A-B71E-4D8369440645Q34899429-D5C6697E-C32F-43E0-BD09-29286EA0BDC6Q35084637-10DD014C-A80F-439C-8247-495CF308BCA1Q35104679-B9279A50-97C1-4521-901A-5CFD400AC250Q35562904-ADA84728-1DFD-4C0A-832C-28213C5FE117Q35681646-D6D9C2DE-DE15-4891-8DEE-337F0BA5FBF8Q36106164-7380AB7B-D8C5-42A7-81D9-F996B5579E32Q36646995-C38EEF78-8C56-457B-A0DE-089DC6E3293BQ36852315-E052F6A0-1A00-477B-8141-ADCB380AEEE0Q37016579-CE676421-8948-4936-97CC-8C389AB2F005Q37156117-B2665A0D-F877-4A99-AE01-698E0C4F7AFCQ37284963-3A1C7EBD-32EE-466C-A45E-CAE796D8EE1CQ38478216-3B482500-A8BA-4D64-B6A6-AC30863839C2Q39031925-C12F9BD9-B5DC-4006-8A09-6567608BABAAQ40021792-819ED958-5A2C-4350-810D-839D76D9EDDFQ41159798-47115B86-E8F2-4FB5-AE87-6D4E9788AB45Q41654115-35A483F0-FE99-4E8B-BACE-7D38DD065F18Q41951157-61AB76A5-AA6E-40A5-BD3F-7AD53A0BAC3BQ42324368-149CE0AF-CCD0-42C1-87F1-49B64F60A906Q46147942-27A0C992-44E8-4283-A76C-2D2BEA9A2979Q46248987-8D9C6F2A-8B23-42A2-B26A-83D83B5FF9D9
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Natalie J Prescott
@nl
Natalie J Prescott
@sl
Natalie J. Prescott
@en
Natalie J. Prescott
@es
Natalie Prescott
@fr
type
label
Natalie J Prescott
@nl
Natalie J Prescott
@sl
Natalie J. Prescott
@en
Natalie J. Prescott
@es
Natalie Prescott
@fr
altLabel
Natalie Joy Prescott
@en
prefLabel
Natalie J Prescott
@nl
Natalie J Prescott
@sl
Natalie J. Prescott
@en
Natalie J. Prescott
@es
Natalie Prescott
@fr
P1053
F-6490-2011
P106
P1153
8964026000
P21
P31
P3829
P496
0000-0002-5901-7371