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Author Details

Evangelos Bellos
Imperial College London
2012
11
7
PMIDPaper TitleJournal TitlePublished Year
37744344Neuroinflammation, autoinflammation, splenomegaly and anemia caused by bi-allelic mutations in <i>IRAK4</i>.Front Immunol2023
37744344Neuroinflammation, autoinflammation, splenomegaly and anemia caused by bi-allelic mutations in <i>IRAK4</i>.Front Immunol2023
36007525Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations.Am J Hum Genet2022
36007525Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations.Am J Hum Genet2022
33772158Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease.Eur J Hum Genet2021
33772158Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease.Eur J Hum Genet2021
32185379Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study.Clin Infect Dis2020
32185379Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study.Clin Infect Dis2020
29330469Mycobacterium tuberculosis Exploits a Molecular Off Switch of the Immune System for Intracellular Survival.Sci Rep2018
29330469Mycobacterium tuberculosis Exploits a Molecular Off Switch of the Immune System for Intracellular Survival.Sci Rep2018
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
25161258cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data.Bioinformatics2014
25228465cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.Nucleic Acids Res2014
25161258cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data.Bioinformatics2014
25228465cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.Nucleic Acids Res2014
23221639A population model for genotyping indels from next-generation sequence data.Nucleic Acids Res2013
23221639A population model for genotyping indels from next-generation sequence data.Nucleic Acids Res2013
23101505Bioinformatics: living on the edge.Genome Biol2012
23259578cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data.Genome Biol2012
23259578cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data.Genome Biol2012
23101505Bioinformatics: living on the edge.Genome Biol2012
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Co-authored papers 9
Victoria J Wright
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Co-authored papers 4
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London School of Hygiene and Tropical Medicine
Co-authored papers 3
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Co-authored papers 2
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Co-authored papers 1
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Co-authored papers 1
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Instituto de Investigacion Sanitaria de Santiago
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Neaman Center for Personalized Medicine, NorthShore University HealthSystem
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Oregon Health & Science University
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University of Utah
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Kimberly Gilmour
NIHR Great Ormond Street Hospital BRC
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Jacqueline Armstrong
SA Pathology at the Women's and Children's Hospital
Co-authored papers 1
Stacey L Edwards
QIMR Berghofer Medical Research Institute
Co-authored papers 1
Gregory M Goldgof
University of California san francisco
Co-authored papers 1
Jonathan Beesley
QIMR Berghofer Medical Research Institute
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Amanda B Spurdle
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Sunil R Lakhani
University of Queensland
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Theo Heller
National Institute of Diabetes and Digestive and Kidney Diseases
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Alireza Heravi-Moussavi
Ferdowsi University of Mashhad
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Release 1.2