Anderson, Carl A
Wellcome Sanger Institute
23 papers on CoChatORCID 0000-0003-1719-7009
Most cited papers
- Verified
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
The International IBD Genetics Consortium (IIBDGC), Jostins, L., Ripke, S., Weersma, R. K., Duerr, R. H., McGovern, D. P., Hui, K. Y., Lee, J. C., Philip Schumm, L., Sharma, Y., et al. (2012) · Nature
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 4,722
- Verified
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Liu, J. Z., van Sommeren, S., Huang, H., Ng, S. C., Alberts, R., Takahashi, A., Ripke, S., Lee, J. C., Jostins, L., Shah, T., et al. (2015) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 2,603
- Verified
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
the NIDDK IBD Genetics Consortium, Barrett, J. C., the Belgian-French IBD Consortium, the Wellcome Trust Case Control Consortium, Hansoul, S., Nicolae, D. L., Cho, J. H., Duerr, R. H., Rioux, J. D., Brant, S. R., et al. (2008) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 2,593
- Verified
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Franke, A., McGovern, D. P. B., Barrett, J. C., Wang, K., Radford-Smith, G. L., Ahmad, T., Lees, C. W., Balschun, T., Lee, J., Roberts, R., et al. (2010) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 2,520
- Verified
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange, K. M., Moutsianas, L., Lee, J. C., Lamb, C. A., Luo, Y., Kennedy, N. A., Jostins, L., Rice, D. L., Gutierrez-Achury, J., Ji, S.-G., et al. (2017) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 1,445
- Verified
Data quality control in genetic case-control association studies
Anderson, C. A., Pettersson, F. H., Clarke, G. M., Cardon, L. R., Morris, A. P., & Zondervan, K. T. (2010) · Nature Protocols
Genetic Associations and EpidemiologyGenetic diversity and population structure
Cited by 1,318
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The UK10K project identifies rare variants in health and disease
The UK10K Consortium, Writing group, Walter, K., Min, J. L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J. R. B., Xu, C., et al. (2015) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 1,040
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Meta-analysis and imputation refines the association of 15q25 with smoking quantity
The Wellcome Trust Case Control Consortium, Liu, J. Z., Tozzi, F., Waterworth, D. M., Pillai, S. G., Muglia, P., Middleton, L., Berrettini, W., Knouff, C. W., Yuan, X., et al. (2010) · Nature Genetics
Genetic Associations and EpidemiologySmoking Behavior and Cessation
Cited by 614
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Fine-mapping inflammatory bowel disease loci to single-variant resolution
International Inflammatory Bowel Disease Genetics Consortium, Huang, H., Fang, M., Jostins, L., Umićević Mirkov, M., Boucher, G., Anderson, C. A., Andersen, V., Cleynen, I., Cortes, A., et al. (2017) · Nature
Genetic Associations and EpidemiologyInflammatory Bowel Disease
Cited by 611
- Verified
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
The UK PBC Consortium, Mells, G. F., The Wellcome Trust Case Control Consortium 3, Floyd, J. A. B., Morley, K. I., Cordell, H. J., Franklin, C. S., Shin, S.-Y., Heneghan, M. A., Neuberger, J. M., et al. (2011) · Nature Genetics
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 464
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Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
The UK-PSCSC Consortium, Liu, J. Z., The International IBD Genetics Consortium, The International PSC Study Group, Hov, J. R., Folseraas, T., Ellinghaus, E., Rushbrook, S. M., Doncheva, N. T., Andreassen, O. A., et al. (2013) · Nature Genetics
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 391
- Verified
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
The UK-PSC Consortium, Ji, S.-G., The International IBD Genetics Consortium, The International PSC Study Group, Juran, B. D., Mucha, S., Folseraas, T., Jostins, L., Melum, E., Kumasaka, N., et al. (2017) · Nature Genetics
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 357
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Genome-wide association meta-analysis identifies new endometriosis risk loci
Nyholt, D. R., Low, S.-K., Anderson, C. A., Painter, J. N., Uno, S., Morris, A. P., MacGregor, S., Gordon, S. D., Henders, A. K., Martin, N. G., et al. (2012) · Nature Genetics
Endometriosis Research and TreatmentGenetic Associations and Epidemiology
Cited by 315
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Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis
Painter, J. N., Anderson, C. A., Nyholt, D. R., Macgregor, S., Lin, J., Lee, S. H., Lambert, A., Zhao, Z. Z., Roseman, F., Guo, Q., et al. (2011) · Nature Genetics
Endometriosis Research and TreatmentGenetic Associations and Epidemiology
Cited by 308
- Verified
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease
Lee, J. C., Biasci, D., Roberts, R., Gearry, R. B., Mansfield, J. C., Ahmad, T., Prescott, N. J., Satsangi, J., Wilson, D. C., Jostins, L., et al. (2017) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 304
- Verified
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Cordell, H. J., Han, Y., Mells, G. F., Li, Y., Hirschfield, G. M., Greene, C. S., Xie, G., Juran, B. D., Zhu, D., Qian, D. C., et al. (2015) · Nature Communications
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 287
- Verified
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
The UK Primary Biliary Cirrhosis (PBC) Consortium, Liu, J. Z., The Wellcome Trust Case Control Consortium 3, Almarri, M. A., Gaffney, D. J., Mells, G. F., Jostins, L., Cordell, H. J., Ducker, S. J., Day, D. B., et al. (2012) · Nature Genetics
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 274
- Verified
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7
Luo, Y., de Lange, K. M., Jostins, L., Moutsianas, L., Randall, J., Kennedy, N. A., Lamb, C. A., McCarthy, S., Ahmad, T., Edwards, C., et al. (2017) · Nature Genetics
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 162
- Verified
Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals
Anderson, C. A., Soranzo, N., Zeggini, E., & Barrett, J. C. (2011) · PLoS Biology
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 114
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Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
Nicholas, A. K., Serra, E. G., Cangul, H., Alyaarubi, S., Ullah, I., Schoenmakers, E., Deeb, A., Habeb, A. M., Almaghamsi, M., Peters, C., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 112
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Whole-genome sequence-based analysis of thyroid function
Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., et al. (2015) · Nature Communications
Genetic Associations and EpidemiologyThyroid Disorders and Treatments
Cited by 104
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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Rivas, M. A., Avila, B. E., Koskela, J., Huang, H., Stevens, C., Pirinen, M., Haritunians, T., Neale, B. M., Kurki, M., Ganna, A., et al. (2018) · PLoS Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 87
- Verified
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Cangul, H., Liao, X.-H., Schoenmakers, E., Kero, J., Barone, S., Srichomkwun, P., Iwayama, H., Serra, E. G., Saglam, H., Eren, E., et al. (2018) · JCI Insight
Thyroid Disorders and TreatmentsChemical Analysis and Environmental Impact
Cited by 69
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