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.
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Journal ArticleDOI
Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1q
Inga Prokopenko,Eleftheria Zeggini,Eleftheria Zeggini,Robert L. Hanson,Braxton D. Mitchell,N. William Rayner,N. William Rayner,Pelin Akan,Leslie J. Baier,Swapan K Das,Katherine S. Elliott,Mao Fu,Timothy M. Frayling,Christopher J. Groves,Christopher J. Groves,Rhian Gwilliam,Laura J. Scott,Benjamin F. Voight,Benjamin F. Voight,Andrew T. Hattersley,Cheng Hu,Andrew D. Morris,Maggie C.Y. Ng,Colin N. A. Palmer,Colin N. A. Palmer,Marcela K. Tello-Ruiz,M Vaxillaire,Congrong Wang,Lincoln Stein,Juliana C.N. Chan,Weiping Jia,Philippe Froguel,Philippe Froguel,Steven C. Elbein,Panos Deloukas,Clifton Bogardus,Alan R. Shuldiner,Mark I. McCarthy,Mark I. McCarthy +38 more
TL;DR: Detailed fine-mapping of the 23-Mb region of replicated linkage has failed to identify common variant signals contributing to the observed signal, and future studies should focus on identification of causal alleles of lower frequency and higher penetrance.
Journal ArticleDOI
Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro.
Scott Wilson,Scott Wilson,Scott Wilson,Michelle R. Jones,Ben H. Mullin,Ian M. Dick,J. Brent Richards,J. Brent Richards,Tomi Pastinen,Elin Grundberg,Östen Ljunggren,Gabriela L. Surdulescu,Frank Dudbridge,Katherine S. Elliott,Alessandra C. L. Cervino,Tim D. Spector,Richard L. Prince,Richard L. Prince +17 more
TL;DR: Findings suggest common variants in FLNB have effects on bone structure in women, and variation at the 5′ end of the gene may reflect effects on levels of FLNB transcription efficiency.
Journal ArticleDOI
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies.
Robert Lawrence,Robert Lawrence,Aaron G. Day-Williams,Katherine S. Elliott,Andrew P. Morris,Eleftheria Zeggini,Eleftheria Zeggini +6 more
TL;DR: CCRaVAT and QuTie are easy to use software tools that allow users to perform genome-wide association analysis on low frequency and rare variants for both binary and quantitative traits.
Posted ContentDOI
Whole genome sequencing identifies multiple loci for critical illness caused by COVID-19
Athanasios Kousathanas,Erola Pairo-Castineira,Erola Pairo-Castineira,Konrad Rawlik,Alex Stuckey,Christopher A Odhams,Susan P. Walker,Clark D Russell,Tomas Malinauskas,Jonathan E Millar,Katherine S. Elliott,Fiona Griffiths,Wilna Oosthuyzen,Kirstie Morrice,Seán Keating,Bo Wang,Daniel Rhodes,Lucija Klaric,Marie Zechner,Nicholas J. Parkinson,Andrew D. Bretherick,Afshan Siddiq,Peter Goddard,Sally Donovan,David M. Maslove,Alistair Nichol,Malcolm G Semple,Tala Zainy,Fiona Maleady-Crowe,Linda Todd,Shahla Salehi,Julian C. Knight,Greg Elgar,Georgia Chan,Prabhu Arumugam,Tom Fowler,Augusto Rendon,Manu Shankar-Hari,Charlotte Summers,Charles J. Hinds,Peter Horby,Daniel F. McAuley,Hugh Montgomery,Peter J. M. Openshaw,Peter J. M. Openshaw,Yang Wu,Jian Yang,Paul Elliott,Timothy S. Walsh,GenoMICC Investigators,andMe Investigators,Angie Fawkes,Lee Murphy,Kathy Rowan,Chris P. Ponting,Veronique Vitart,James F. Wilson,Richard H Scott,Sara Clohisey,Loukas Moutsianas,Andy Law,Mark J. Caulfield,J Kenneth Baillie +62 more
TL;DR: The GenOMICC (Genetics of Mortality in Critical Care) study is designed to compare genetic variants in critically-ill cases with population controls in order to find underlying disease mechanisms as mentioned in this paper.
Journal ArticleDOI
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (vol 42, pg 579, 2010)
Benjamin F. Voight,Laura J. Scott,Valgerdur Steinthorsdottir,Andrew P. Morris,Christian Dina,Ryan P. Welch,Eleftheria Zeggini,Cornelia Huth,Yurii S. Aulchenko,Gudmar Thorleifsson,Laura J. McCulloch,Teresa Ferreira,Harald Grallert,Najaf Amin,Guanming Wu,Cristen J. Willer,Soumya Raychaudhuri,Steve McCarroll,Claudia Langenberg,Oliver Hofmann,Josée Dupuis,Lu Qi,Ayellet V. Segrè,Mandy van Hoek,Pau Navarro,Kristin G. Ardlie,Beverley Balkau,Rafn Benediktsson,Amanda J. Bennett,Roza Blagieva,Eric Boerwinkle,Lori L. Bonnycastle,Kristina Bengtsson Bostroem,Bert Bravenboer,Suzannah Bumpstead,N P Burtt,Guillaume Charpentier,Peter S. Chines,Marilyn C. Cornelis,David Couper,Gabe Crawford,Alex S. F. Doney,Katherine S. Elliott,Amanda F. Elliott,Michael R. Erdos,Caroline S. Fox,Andrew D. Morris,Igor Rudan,Harry Campbell,James F. Wilson +49 more
TL;DR: The paper was originally published online 15 August 2010 but was corrected after print 27 October 2010 because of a technical error.