T
Tugce Karaderi
Researcher at Wellcome Trust Centre for Human Genetics
Publications - 52
Citations - 5330
Tugce Karaderi is an academic researcher from Wellcome Trust Centre for Human Genetics. The author has contributed to research in topics: Genome-wide association study & Ankylosing spondylitis. The author has an hindex of 21, co-authored 50 publications receiving 4604 citations. Previous affiliations of Tugce Karaderi include Royal National Hospital for Rheumatic Diseases & University of Copenhagen.
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Journal ArticleDOI
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
David M. Evans,Spencer Cca.,J J Pointon,Zhan Su,D Harvey,Grazyna Kochan,Udo Oppermann,Alexander T. Dilthey,Matti Pirinen,Millicent A. Stone,L H Appleton,Loukas Moutsianas,Stephen Leslie,T. W. H. Wordsworth,Tony J. Kenna,Tugce Karaderi,Gethin P. Thomas,Minghong Ward,Michael H. Weisman,C. Farrar,Linda A. Bradbury,Patrick Danoy,Robert D. Inman,Walter P. Maksymowych,Dafna D. Gladman,Proton Rahman,Ann W. Morgan,Helena Marzo-Ortega,Paul Bowness,Karl Gaffney,Gaston Jsh.,Malcolm D. Smith,Jácome Bruges-Armas,Couto A-R.,Rosa Sorrentino,Fabiana Paladini,Manuel A. R. Ferreira,Huji Xu,Yu Liu,L. Jiang,Carlos López-Larrea,Roberto Díaz-Peña,Antonio López-Vázquez,Tetyana Zayats,Céline Bellenguez,Hannah Blackburn,Jenefer M. Blackwell,Elvira Bramon,Suzannah Bumpstead,Juan P. Casas,Aiden Corvin,N. Craddock,Panagiotis Deloukas,Serge Dronov,Audrey Duncanson,Sarah Edkins,Colin Freeman,Matthew W. Gillman,Emma Gray,R. Gwilliam,Naomi Hammond,Sarah E. Hunt,Janusz Jankowski,Alagurevathi Jayakumar,Cordelia Langford,Jennifer Liddle,Hugh S. Markus,Christopher G. Mathew,O. T. McCann,Mark I. McCarthy,Palmer Cna.,Leena Peltonen,Robert Plomin,Simon C. Potter,Anna Rautanen,Radhi Ravindrarajah,Michelle Ricketts,Nilesh J. Samani,Stephen Sawcer,A. Strange,Richard C. Trembath,Ananth C. Viswanathan,Ananth C. Viswanathan,Matthew Waller,Paul A. Weston,Pamela Whittaker,Sara Widaa,Nicholas W. Wood,Gil McVean,John D. Reveille,B P Wordsworth,Matthew A. Brown,Peter Donnelly +92 more
TL;DR: In this paper, the identification of three variants in the RUNX3, LTBR-TNFRSF1A and IL12B regions convincingly associated with ankylosing spondylitis (P < 5 x 10(-8) in the combined discovery and replication datasets) and a further four loci at PTGER4, TBKBP1, ANTXR2 and CARD9 that show strong association across all their datasets (p < 5x 10(-6) overall, with support in each of the three datasets studied).
Journal ArticleDOI
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci.
Adrian Cortes,Johanna Hadler,J.P. Pointon,Philip Robinson,Tugce Karaderi,Paul Leo,Katie Cremin,Karena Pryce,Jessica Harris,Sang-Gug Lee,Kyung Bin Joo,Shim S-C.,Michael H. Weisman,Minghong Ward,Xiaodong Zhou,Garchon H-J.,Gilles Chiocchia,Johannes C. Nossent,Benedicte A. Lie,Øystein Førre,J. Tuomilehto,J. Tuomilehto,J. Tuomilehto,K. Laiho,Lei Jiang,Yu Liu,Xin Wu,Linda A. Bradbury,Dirk Elewaut,Ruben Burgos-Vargas,Simon Stebbings,Louise Appleton,Claire Farrah,J. Lau,Tony J. Kenna,Nigil Haroon,Manuel A. R. Ferreira,Jian Yang,J Mulero,José Luis Fernández-Sueiro,Miguel A. Gonzalez-Gay,Carlos López-Larrea,Panagiotis Deloukas,Peter Donnelly,Paul Bowness,Karl Gafney,Hill Gaston,Dafna D. Gladman,Dafna D. Gladman,Proton Rahman,Walter P. Maksymowych,Huji Xu,Crusius Jba.,I E van der Horst-Bruinsma,Chou C-T.,R. Valle-Oñate,Consuelo Romero-Sánchez,Inger Myrnes Hansen,Fernando Pimentel-Santos,Robert D. Inman,Vibeke Videm,Javier Martín,Maxime Breban,Maxime Breban,J. D. Reveille,David M. Evans,Kim T-H.,B P Wordsworth,Matthew A. Brown +68 more
TL;DR: In this paper, the authors used the Illumina Immunochip microarray to perform a case-control association study involving 10,619 individuals with ankylosing spondylitis (cases) and 15,145 controls.
Journal ArticleDOI
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
John D. Reveille,Anne Marie Sims,Patrick Danoy,David M. Evans,Paul Leo,J J Pointon,Rui Jin,Xiaodong Zhou,Linda A. Bradbury,L H Appleton,John C. Davis,Laura Diekman,Tracey Doan,Alison Dowling,Ran Duan,Emma L. Duncan,C Farrar,Johanna Hadler,David Harvey,Tugce Karaderi,R Mogg,Emma Pomeroy,Karena Pryce,Jacqueline Taylor,L. Savage,Panos Deloukas,Vasudev Kumanduri,Leena Peltonen,Susan M. Ring,Pamela Whittaker,Evgeny A. Glazov,Gethin P. Thomas,Walter P. Maksymowych,Robert D. Inman,Michael M. Ward,Millicent A. Stone,Millicent A. Stone,Michael H. Weisman,B. Paul Wordsworth,Matthew A. Brown,Matthew A. Brown +40 more
TL;DR: In this article, the authors conducted a genome-wide association study in 2,053 unrelated ankylosing spondylitis cases among people of European descent and 5,140 ethnically matched controls.
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
John D. Reveille,A. M. Sims,Patrick Danoy,David M. Evans,Paul Leo,J J Pointon,R. Jin,Xiaodong Zhou,Linda A. Bradbury,L H Appleton,J. C. Davis,Laura Diekman,Tracy Doan,Alison Dowling,Ran Duan,Emma L. Duncan,C Farrar,Johanna Hadler,David Harvey,Tugce Karaderi,R Mogg,Emma Pomeroy,Karena Pryce,Jenny C. Taylor,L. Savage,Panagiotis Deloukas,Vasudev Kumanduri,Leena Peltonen,S.M. Ring,Pamela Whittaker,Evgeny A. Glazov,Gethin P. Thomas,Walter P. Maksymowych,Robert D. Inman,M. M. Ward,Millicent A. Stone,Michael H. Weisman,B P Wordsworth,Matthew A. Brown +38 more
TL;DR: Four genetic loci associated with ankylosing spondylitis risk are reported and a major role for the interleukin (IL)-23 and IL-1 cytokine pathways in disease susceptibility is identified.
Rare and low-frequency coding variants alter human adult height
Eirini Marouli,Mariaelisa Graff,Carolina Medina-Gomez,Ken Sin Lo,Andrew R. Wood,Troels R. Kjaer,Rebecca S. Fine,Yingchang Lu,Claudia Schurmann,Heather M. Highland,Sina Rüeger,Gudmar Thorleifsson,Anne E. Justice,David Lamparter,Kathleen Stirrups,Valérie Turcot,Kristin L. Young,Thomas W. Winkler,Tõnu Esko,Tugce Karaderi,Adam E. Locke,Nicholas G. D. Masca,Maggie C.Y. Ng,Poorva Mudgal,Manuel A. Rivas,Sailaja Vedantam,Anubha Mahajan,Xiuqing Guo,Gonçalo R. Abecasis,Katja K.H. Aben,Linda S. Adair,Dewan S. Alam,Eva Albrecht,Kristine H. Allin,Matthew A. Allison,Philippe Amouyel,Emil V. R. Appel,Dominique Arveiler,Folkert W. Asselbergs,Paul L. Auer,Beverley Balkau,Bernhard Banas,Lia E. Bang,Marianne Benn,Sven Bergmann,Lawrence F. Bielak,Matthias Blueher,Heiner Boeing,Eric Boerwinkle,Carsten A. Boeger,Lori L. Bonnycastle,Jette Bork-Jensen,Michiel L. Bots,Erwin P. Bottinger,Donald W. Bowden,Ivan Brandslund,Gerome Breen,Murray H. Brilliant,Linda Broer,Amber A. Burt,Adam S. Butterworth,David J. Carey,Mark J. Caulfield,John C. Chambers,Daniel I. Chasman,Yii-Der Ida Chen,Rajiv Chowdhury,Cramer Christensen,Audrey Y. Chu,Massimiliano Cocca,Francis S. Collins,James P. Cook,Janie Corley,Jordi Corominas Galbany,Amanda J. Cox,Gabriel Cuellar-Partida,John Danesh,Gail Davies,Paul I.W. de Bakker,Gert J. de Borst,Simon de Denus,Mark C.H. De Groot,Renée de Mutsert,Ian J. Deary,George Dedoussis,Ellen W. Demerath,Anneke I. den Hollander,Joe Dennis,Emanuele Di Angelantonio,Fotios Drenos,Mengmeng Du,Alison M. Dunning,Douglas F. Easton,Tapani Ebeling,Todd L. Edwards,Patrick T. Ellinor,Paul Elliott,Evangelos Evangelou,Aliki-Eleni Farmaki,Jessica D. Faul,Mary F. Feitosa,Shuang Feng,Ele Ferrannini,Marco M Ferrario,Jean Ferrières,Jose C. Florez,Ian Ford,Myriam Fornage,Paul W. Franks,Ruth Frikke-Schmidt,Tessel E. Galesloot,Wei Gan,Ilaria Gandin,Paolo Gasparini,Vilmantas Giedraitis,Ayush Giri,Giorgia Girotto,Scott D. Gordon,Penny Gordon-Larsen,Mathias Gorski,Niels Grarup,Megan L. Grove,Vilmundur Gudnason,Stefan Gustafsson,Torben Hansen,Kathleen Mullan Harris,Tamara B. Harris,Andrew T. Hattersley,Caroline Hayward,Liang He,Iris M. Heid,Kauko Heikkilä,Øyvind Helgeland,Jussi Hernesniemi,Alex W. Hewitt,Lynne J. Hocking,Mette Hollensted,Oddgeir L. Holmen,G. Kees Hovingh,Joanna M. M. Howson,Carel B. Hoyng,Paul L. Huang,Kristian Hveem,M. Arfan Ikram,Erik Ingelsson,Anne U. Jackson,Jan-Håkan Jansson,Gail P. Jarvik,Gorm B. Jensen,Min A. Jhun,Yucheng Jia,Xuejuan Jiang,Stefan Johansson,Marit E. Jørgensen,Torben Jørgensen,Pekka Jousilahti,J. Wouter Jukema,Bratati Kahali,René S. Kahn,Mika Kähönen,Pia R. Kamstrup,Stavroula Kanoni,Jaakko Kaprio,Maria Karaleftheri,Sharon L.R. Kardia,Fredrik Karpe,Frank Kee,Renske Keeman,Lambertus A. Kiemeney,Hidetoshi Kitajima,Kirsten B. Kluivers,Thomas D. Kocher,Pirjo Komulainen,Jukka Kontto,Jaspal S. Kooner,Charles Kooperberg,Peter Kovacs,Jennifer Kriebel,Helena Kuivaniemi,Sébastien Küry,Johanna Kuusisto,Martina La Bianca,Markku Laakso,Timo A. Lakka,Ethan M. Lange,Leslie A. Lange,Carl D. Langefeld,Claudia Langenberg,Eric B. Larson,I-Te Lee,Terho Lehtimäki,Cora E. Lewis,Huaixing Li,Jin Li,Ruifang Li-Gao,Honghuang Lin,Li-An Lin,Xu Lin,Lars Lind,Jaana Lindström,Allan Linneberg,Y Liu,Yongmei Liu,Artitaya Lophatananon,Jian'an Luan,Steven A. Lubitz,Leo-Pekka Lyytikäinen,David A. Mackey,Pamela A. F. Madden,Alisa K. Manning,Satu Männistö,Gaëlle Marenne,Jonathan Marten,Nicholas G. Martin,Angela L. Mazul,Karina Meidtner,Andres Metspalu,Paul Mitchell,Karen L. Mohlke,Dennis O. Mook-Kanamori,Anna Morgan,Andrew D. Morris,Andrew P. Morris,Martina Mueller-Nurasyid,Patricia B. Munroe,Mike A. Nalls,Matthias Nauck,Christopher P. Nelson,Matt Neville,Sune F. Nielsen,Kjell Nikus,Pål R. Njølstad,Børge G. Nordestgaard,Ioanna Ntalla,Jeffrey R. O'Connel,Heikki Oksa,Loes M. Olde Loohuis,Roel A. Ophoff,Katharine R. Owen,Chris J. Packard,Sandosh Padmanabhan,Colin N. A. Palmer,Gerard Pasterkamp,Aniruddh P. Patel,Alison Pattie,Oluf Pedersen,Peggy L. Peissig,Gina M. Peloso,Craig E. Pennell,Markus Perola,James A. Perry,John R. B. Perry,Thomas N. Person,Ailith Pirie,Ozren Polasek,Danielle Posthuma,Olli T. Raitakari,Asif Rasheed,Rainer Rauramaa,Dermot F. Reilly,Alexander P. Reiner,Frida Renström,Paul M. Ridker,John D. Rioux,Neil Robertson,Antonietta Robino,Olov Rolandsson,Igor Rudan,Katherine S. Ruth,Danish Saleheen,Veikko Salomaa,Nilesh J. Samani,Kevin Sandow,Yadav Sapkota,Naveed Sattar,Marjanka K. Schmidt,Pamela J. Schreiner,Matthias B. Schulze,Robert A. Scott,Marcelo P. Segura-Lepe,Svati H. Shah,Xueling Sim,Suthesh Sivapalaratnam,Kerrin S. Small,Albert V. Smith,Jennifer A. Smith,Lorraine Southam,Tim D. Spector,Elizabeth K. Speliotes,John M. Starr,Valgerdur Steinthorsdottir,Heather M. Stringham,Michael Stumvoll,Praveen Surendran,Leen M 't Hart,Katherine E. Tansey,Jean-Claude Tardif,Kent D. Taylor,Alexander Teumer,Deborah J. Thompson,Unnur Thorsteinsdottir,Betina H. Thuesen,Anke Toenjes,Gerard Tromp,Stella Trompet,Emmanouil Tsafantakis,Jaakko Tuomilehto,Anne Tybjærg-Hansen,Jonathan Tyrer,Rudolf Uher,André G. Uitterlinden,Sheila Ulivi,Sander W. van der Laan,Andries R. van der Leij,Cornelia M. van Duijn,Natasja M. van Schoor,Jessica van Setten,Anette Varbo,Tibor V. Varga,Rohit Varma,Digna R. Velez Edwards,Sita H. Vermeulen,Henrik Vestergaard,Veronique Vitart,Thomas F. Vogt,Diego Vozzi,Mark Walker,Feijie Wang,Carol A. Wang,Shuai Wang,Yiqin Wang,Nicholas J. Wareham,Helen R. Warren,Jennifer Wessel,Sara M. Willems,James G. Wilson,Daniel R. Witte,Michael O. Woods,Ying Wu,Hanieh Yaghootkar,Jie Yao,Pang Yao,Laura M. Yerges-Armstrong,Robin Young,Eleftheria Zeggini,Xiaowei Zhan,Weihua Zhang,Jing Hua Zhao,Wei Zhao,He Zheng,Wei Zhou,Jerome I. Rotter,Michael Boehnke,Sekar Kathiresan,Mark I. McCarthy,Cristen J. Willer,Kari Stefansson,Ingrid B. Borecki,Dajiang J. Liu,Kari E. North,Nancy L. Heard-Costa,Tune H. Pers,Cecilia M. Lindgren,Claus Oxvig,Zoltán Kutalik,Fernando Rivadeneira,Ruth J. F. Loos,Timothy M. Frayling,Joel N. Hirschhorn,Panos Deloukas,Guillaume Lettre +370 more
TL;DR: The results demonstrate that sufficiently large sample sizes can uncover rare and low-frequency variants of moderate-to-large effect associated with polygenic human phenotypes, and that these variants implicate relevant genes and pathways.