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  • In silico guided reconstruction and analysis of ICAM-1-binding var genes from Plasmodium falciparum.

    Carrington E, Otto TD, Szestak T, Lennartz F, Higgins MK et al.

    Scientific reports 2018;8;1;3282

  • Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.

    Corbin LJ, Tan VY, Hughes DA, Wade KH, Paul DS et al.

    Nature communications 2018;9;1;711

  • The Impact of NOD2 Variants on Fecal Microbiota in Crohn's Disease and Controls Without Gastrointestinal Disease.

    Kennedy NA, Lamb CA, Berry SH, Walker AW, Mansfield J et al.

    Inflammatory bowel diseases 2018;24;3;583-592

  • Emergence of an Extensively Drug-Resistant<i>Salmonella enterica</i>Serovar Typhi Clone Harboring a Promiscuous Plasmid Encoding Resistance to Fluoroquinolones and Third-Generation Cephalosporins.

    Klemm EJ, Shakoor S, Page AJ, Qamar FN, Judge K et al.

    mBio 2018;9;1

  • Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome.

    Menke LA, DDD study, Gardeitchik T, Hammond P, Heimdal KR et al.

    American journal of medical genetics. Part A 2018

  • Convergent amino acid signatures in polyphyletic Campylobacter jejuni sub-populations suggest human niche tropism.

    Méric G, McNally A, Pessia A, Mourkas E, Pascoe B et al.

    Genome biology and evolution 2018

  • Gut microbiota trajectory in early life may predict development of celiac disease.

    Olivares M, Walker AW, Capilla A, Benítez-Páez A, Palau F et al.

    Microbiome 2018;6;1;36

  • Superbubbles, Ultrabubbles, and Cacti.

    Paten B, Eizenga JM, Rosen YM, Novak AM, Garrison E and Hickey G

    Journal of computational biology : a journal of computational molecular cell biology 2018

  • Origins and genetic legacies of the Caribbean Taino.

    Schroeder H, Sikora M, Gopalakrishnan S, Cassidy LM, Maisano Delser P et al.

    Proceedings of the National Academy of Sciences of the United States of America 2018

  • APPLaUD: access for patients and participants to individual level uninterpreted genomic data.

    Thorogood A, Bobe J, Prainsack B, Middleton A, Scott E et al.

    Human genomics 2018;12;1;7