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Author Details

Carl A Anderson
Wellcome Sanger Institute
2006
66
43
PMIDPaper TitleJournal TitlePublished Year
36634696Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.Lancet Gastroenterol Hepatol2023
34780721An Integrated Taxonomy for Monogenic Inflammatory Bowel Disease.Gastroenterology2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
35288711Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.Nat Genet2022
33022279Underpowered PANTS: A Response to the Conclusions of "Extended Analysis Identifies Drug-Specific Association of Two Distinct HLA Class II Haplotypes for Development of Immunogenicity to Adalimumab and Infliximab".Gastroenterology2021
34226062Somatic mutations provide important and unique insights into the biology of complex diseases.Trends Genet2021
33359885Common and Rare Variant Prediction and Penetrance of IBD in a Large, Multi-ethnic, Health System-based Biobank Cohort.Gastroenterology2021
32697969Somatic Evolution in Non-neoplastic IBD-Affected Colon.Cell2020
30566748Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System.Hepatology2019
31672862Incomplete genetic reconstitution of B cell pools contributes to prolonged immunosuppression after measles.Sci Immunol2019
30806694Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.JAMA2019
31145742Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.PLoS Genet2019
28779025Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.Gut2018
30147686Combined Influence of B-Cell Receptor Rearrangement and Somatic Hypermutation on B-Cell Class-Switch Fate in Health and in Chronic Lymphocytic Leukemia.Front Immunol2018
29894681Consequences of Identifying XIAP Deficiency in an Adult Patient With Inflammatory Bowel Disease.Gastroenterology2018
30507971Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis.PLoS Genet2018
30333321Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.JCI Insight2018
29795570Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.PLoS Genet2018
29091079NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.Mucosal Immunol2018
27992413Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.Nat Genet2017
28658209Fine-mapping inflammatory bowel disease loci to single-variant resolution.Nature2017
28067912Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.Nat Genet2017
28067908Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.Nat Genet2017
28067910Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.Nat Genet2017
27037036Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.BMC Med Genet2016
27619887Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.Nat Commun2016
27503255A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.Nat Commun2016
27525530Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.J Clin Endocrinol Metab2016
27548312A reference panel of 64,976 haplotypes for genotype imputation.Nat Genet2016
24736995Genetics in PSC: what do the "risk genes" teach us?Clin Rev Allergy Immunol2015
26343388Class II HLA interactions modulate genetic risk for multiple sclerosis.Nat Genet2015
26394269International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.Nat Commun2015
26192919Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.Nat Genet2015
24799394Generation of primary human intestinal T cell transcriptomes reveals differential expression at genetic risk loci for immune-mediated disease.Gut2015
24462371Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.Am J Hum Genet2014
25290448Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines.PLoS One2014
24913378Genetic studies of Crohn's disease: past, present and future.Best Pract Res Clin Gastroenterol2014
24906020Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.Am J Hum Genet2014
23603763Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.Nat Genet2013
24076602Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.Nat Genet2013
24035192Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway.Cell2013
22500001optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants.Bioinformatics2012
22961000Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.Nat Genet2012
23104006Genome-wide association meta-analysis identifies new endometriosis risk loci.Nat Genet2012
23128233Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.Nature2012
21267062Synthetic associations are unlikely to account for many common disease genome-wide association signals.PLoS Biol2011
21297633Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.Nat Genet2011
21293453Basic statistical analysis in genetic case-control studies.Nat Protoc2011
21399635Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.Nat Genet2011
21151130Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.Nat Genet2011
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Collaborators

Jeffrey C Barrett
Co-authored papers 27
Judy H Cho
Co-authored papers 16
Christopher G Mathew
Co-authored papers 16
Andre Franke
Institute of Clinical Molecular Biology, Kiel University
Co-authored papers 15
Mark J Daly
Massachusetts General Hospital
Co-authored papers 14
Dermot P B McGovern
F. Widjaja Inflammatory Bowel Disease Institute
Co-authored papers 14
Richard H Duerr
Co-authored papers 14
Mark S Silverberg
Co-authored papers 13
John D Rioux
Co-authored papers 13
Ramnik J Xavier
Broad Institute of MIT and Harvard
Co-authored papers 12
Steven R Brant
Co-authored papers 11
Stefan Schreiber
Co-authored papers 10
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BioMarin Pharmaceutical Inc.
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Talin Haritunians
Co-authored papers 9
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University of Cambridge
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Leonie Schumm
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Andrew P Morris
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Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
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James S Floyd
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Cisca Wijmenga
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Manuel A Rivas
Stanford University School of Medicine
Co-authored papers 6
Aarno Palotie
Co-authored papers 6
Philippe Goyette
Co-authored papers 6
George F Mells
University of Cambridge
Co-authored papers 6
Jonas Halfvarson
Co-authored papers 6
Mauro D'Amato
Co-authored papers 6
David Ellinghaus
Co-authored papers 6
Kent D Taylor
Co-authored papers 5
Peter M Visscher
Co-authored papers 5
Release 1.2