K
Katherine S. Elliott
Researcher at University of Oxford
Publications - 51
Citations - 14778
Katherine S. Elliott is an academic researcher from University of Oxford. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 26, co-authored 43 publications receiving 13239 citations. Previous affiliations of Katherine S. Elliott include Wellcome Trust Centre for Human Genetics.
Papers
More filters
Journal ArticleDOI
IFITM3 and Susceptibility to Respiratory Viral Infections in the Community
Tara C. Mills,Anna Rautanen,Katherine S. Elliott,Tom Parks,Vivek Naranbhai,Margareta Ieven,Christopher C Butler,Paul Little,Theo J M Verheij,Christopher S. Garrard,Charles J. Hinds,Herman Goossens,Stephen J Chapman,Adrian V. S. Hill +13 more
TL;DR: Evidence is found of an association between rs12252 rare allele homozygotes and susceptibility to mild influenza (in patients attending primary care) but could not confirm a previously reported association between this single-nucleotide polymorphism and susceptible to severe H1N1 infection.
Journal ArticleDOI
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Bendik S. Winsvold,Christopher P. Nelson,Rainer Malik,Padhraig Gormley,Verneri Anttila,Jason A. Vander Heiden,Katherine S. Elliott,L.M. Jacobsen,Priit Palta,Najaf Amin,Boukje de Vries,Eija Hämäläinen,Tobias Freilinger,M. Arfan Ikram,Thorsten Kessler,Markku Koiranen,Lannie Ligthart,George McMahon,Linda M. Pedersen,Christina Willenborg,Hong-Hee Won,Jes Olesen,Ville Artto,Themistocles L. Assimes,Stefan Blankenberg,Dorret I. Boomsma,Lynn Cherkas,George Davey Smith,Stephen E. Epstein,Jeanette Erdmann,Michel D. Ferrari,Hartmut Göbel,Alistair S. Hall,Marjo-Riitta Järvelin,Mikko Kallela,Jaakko Kaprio,Sekar Kathiresan,Terho Lehtimäki,Ruth McPherson,Winfried März,Dale R. Nyholt,Christopher J. O'Donnell,Lydia Quaye,Daniel J. Rader,Olli T. Raitakari,Robert Roberts,Heribert Schunkert,Markus Schürks,Alexandre F.R. Stewart,Gisela M. Terwindt,Unnur Thorsteinsdottir,Arn M. J. M. van den Maagdenberg,Cornelia M. van Duijn,Maija Wessman,Tobias Kurth,Christian Kubisch,Martin Dichgans,Daniel I. Chasman,Chris Cotsapas,John-Anker Zwart,Nilesh J. Samani,Aarno Palotie +61 more
TL;DR: In this paper, the authors apply genetic analysis of genome-wide association data to study the extent and nature of a shared biological basis between migraine and coronary artery disease (CAD).
Journal ArticleDOI
Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22
Eric K. Moses,E. Fitzpatrick,Katy A. Freed,Thomas D. Dyer,S. Forrest,Katherine S. Elliott,Matthew P. Johnson,John Blangero,Shaun P. Brennecke +8 more
TL;DR: An objective prioritization strategy that integrates quantitative bioinformatics, assessment of differential gene expression and association analysis of single-nucleotide polymorphisms (SNPs) was applied, and highest priority was assigned to the activin receptor gene ACVR2.
Journal ArticleDOI
Genome-wide association study to identify common variants associated with brachial circumference: A meta-analysis of 14 cohorts
Vesna Boraska,Vesna Boraska,Aaron G. Day-Williams,Christopher S. Franklin,Katherine S. Elliott,Kalliope Panoutsopoulou,Ioanna Tachmazidou,Eva Albrecht,Stefania Bandinelli,Lawrence J. Beilin,Murielle Bochud,Gemma Cadby,Florian Ernst,David M. Evans,Caroline Hayward,Andrew A. Hicks,Jennifer E. Huffman,Cornelia Huth,Alan James,Alan James,Norman Klopp,Ivana Kolcic,Zoltán Kutalik,Debbie A Lawlor,Arthur W. Musk,Arthur W. Musk,Marina Pehlić,Craig E. Pennell,John R. B. Perry,John R. B. Perry,Annette Peters,Ozren Polasek,Beate St Pourcain,Susan M. Ring,Erika Salvi,Sabine Schipf,Jan A. Staessen,Jan A. Staessen,Alexander Teumer,Nicholas J. Timpson,Veronique Vitart,Nicole M. Warrington,Hanieh Yaghootkar,Tatijana Zemunik,Lina Zgaga,Lina Zgaga,Ping An,Verneri Anttila,Verneri Anttila,Ingrid B. Borecki,Jostein Holmen,Ioanna Ntalla,Aarno Palotie,Kirsi H. Pietiläinen,Kirsi H. Pietiläinen,Juho Wedenoja,Bendik S. Winsvold,Bendik S. Winsvold,George Dedoussis,Jaakko Kaprio,Jaakko Kaprio,Michael A. Province,John-Anker Zwart,Michel Burnier,Harry Campbell,Daniele Cusi,George Davey Smith,Timothy M. Frayling,Christian Gieger,Lyle J. Palmer,Peter P. Pramstaller,Igor Rudan,Igor Rudan,Henry Völzke,H.-Erich Wichmann,Alan F. Wright,Eleftheria Zeggini +76 more
TL;DR: This first GWAS meta-analysis for BC has not identified any genome-wide significant signals and do not observe robust association of previously established obesity loci with BC, suggesting large-scale collaborations will be necessary to achieve higher power to detect loci underlying BC.
Journal ArticleDOI
Early-onset autoimmunity associated with SOCS1 haploinsufficiency
Jérôme Hadjadj,Carla N. Castro,Maud Tusseau,Marie-Claude Stolzenberg,Fabienne Mazerolles,Nathalie Aladjidi,Martin Armstrong,Houman Ashrafian,Ioana Cutcutache,Georg Ebetsberger-Dachs,Katherine S. Elliott,Isabelle Durieu,Nicole Fabien,Mathieu Fusaro,Maximilian Heeg,Yohan Schmitt,Marc Bras,Julian C. Knight,Jean-Christophe Lega,Gaetan Lesca,Anne-Laure Mathieu,Marion Moreews,Baptiste Moreira,Audrey Nosbaum,Matthew Page,Cécile Picard,T. Ronan Leahy,Isabelle Rouvet,Ethel Ryan,Damien Sanlaville,Klaus Schwarz,Andrew J. Skelton,Jean-François Viallard,Sébastien Viel,Marine Villard,Isabelle Callebaut,Capucine Picard,Thierry Walzer,Stephan Ehl,Alain Fischer,Alain Fischer,Bénédicte Neven,Alexandre Belot,Frédéric Rieux-Laucat +43 more
TL;DR: Heterozygous, autosomal-dominant, germline loss-of-function mutations in the SOCS1 gene in ten patients from five unrelated families with early onset autoimmune manifestations causes a dominantly inherited predisposition toEarly onset autoimmune diseases related to cytokine hypersensitivity of immune cells.