This page is being kept as a historical record of the research conducted at the Sanger Institute. This page is no longer being updated and was last edited Summer 2013.

Publications

  • The GENCODE exome: sequencing the complete human exome.

    Coffey AJ, Kokocinski F, Calafato MS, Scott CE, Palta P et al.

    European journal of human genetics : EJHG 2011;19;7;827-31

  • Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

    Chasman DI, Schürks M, Anttila V, de Vries B, Schminke U et al.

    Nature genetics 2011;43;7;695-8

  • Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

    Anttila V, Stefansson H, Kallela M, Todt U, Terwindt GM et al.

    Nature genetics 2010;42;10;869-73

  • Integrating common and rare genetic variation in diverse human populations.

    International HapMap 3 Consortium, Altshuler DM, Gibbs RA, Peltonen L, Altshuler DM et al.

    Nature 2010;467;7311;52-8

  • An immune response network associated with blood lipid levels.

    Inouye M, Silander K, Hamalainen E, Salomaa V, Harald K et al.

    PLoS genetics 2010;6;9;e1001113

  • Distinct variants at LIN28B influence growth in height from birth to adulthood.

    Widén E, Ripatti S, Cousminer DL, Surakka I, Lappalainen T et al.

    American journal of human genetics 2010;86;5;773-82

  • Target-enrichment strategies for next-generation sequencing.

    Mamanova L, Coffey AJ, Scott CE, Kozarewa I, Turner EH et al.

    Nature methods 2010;7;2;111-8

  • Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.

    McCarroll SA, Bradner JE, Turpeinen H, Volin L, Martin PJ et al.

    Nature genetics 2009;41;12;1341-4

  • The genome-wide patterns of variation expose significant substructure in a founder population.

    Jakkula E, Rehnström K, Varilo T, Pietiläinen OP, Paunio T et al.

    American journal of human genetics 2008;83;6;787-94

  • Susceptibility loci for intracranial aneurysm in European and Japanese populations.

    Bilguvar K, Yasuno K, Niemelä M, Ruigrok YM, von Und Zu Fraunberg M et al.

    Nature genetics 2008;40;12;1472-7

  • A high-density association screen of 155 ion transport genes for involvement with common migraine.

    Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V et al.

    Human molecular genetics 2008;17;21;3318-31

  • Consistently replicating locus linked to migraine on 10q22-q23.

    Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S et al.

    American journal of human genetics 2008;82;5;1051-63