David Clayton - Publications, H-index & Citations

David Clayton

University of Cambridge

92H指数

354论文数

4.8W被引数

收录论文 56

发表时间

Myelin Water Fraction of Slowly Evolving Lesions is Associated With Disability in Multiple Sclerosis

NEUROLOGY

IF8.5

2023-04-25

PREAI

Zhuang, Rebecca; Vavasour, Irene; Elliott, Colm; Arnold, Douglas; Clayton, David; Magon, Stefano; Bonati, Ulrike; Bernasconi, Corrado; Gaetano, Laura; Traboulsee, Anthony; Kolind, Shannon

The role of the immune system in kidney disease

CLINICAL AND EXPERIMENTAL IMMUNOLOGY

IF3.8

2018-03-24

166

OAAI

Tecklenborg, J.; Clayton, D.; Siebert, S.; Coley, S. M.

Standardization and Control for Confounding in Observational Studies: A Historical Perspective

STATISTICAL SCIENCE

IF3.4

2014-11-01

OAAI

Keiding, Niels; Clayton, David

A Type I Interferon Transcriptional Signature Precedes Autoimmunity in Children Genetically at Risk for Type 1 Diabetes

DIABETES

IF7.5

2014-06-14

248

OAAI

Ferreira, Ricardo C.; Guo, Hui; Coulson, Richard M. R.; Smyth, Deborah J.; Pekalski, Marcin L.; Burren, Oliver S.; Cutler, Antony J.; Doecke, James D.; Flint, Shaun; McKinney, Eoin F.; Lyons, Paul A.; Smith, Kenneth G. C.; Achenbach, Peter; Beyerlein, Andreas; Dunger, David B.; Clayton, David G.; Wicker, Linda S.; Todd, John A.; Bonifacio, Ezio; Wallace, Chris; Ziegler, Anette-G.

Seven new loci associated with age-related macular degeneration

NATURE GENETICS

IF31.8

2013-03-03

692

OAAI

Fritsche, Lars G.; Chen, Wei; Schu, Matthew; Yaspan, Brian L.; Yu, Yi; Thorleifsson, Gudmar; Zack, Donald J.; Arakawa, Satoshi; Cipriani, Valentina; Ripke, Stephan; Igo, Robert P., Jr.; Buitendijk, Gabrielle H. S.; Sim, Xueling; Weeks, Daniel E.; Guymer, Robyn H.; Merriam, Joanna E.; Francis, Peter J.; Hannum, Gregory; Agarwal, Anita; Armbrecht, Ana Maria; Audo, Isabelle; Aung, Tin; Barile, Gaetano R.; Benchaboune, Mustapha; Bird, Alan C.; Bishop, Paul N.; Branham, Kari E.; Brooks, Matthew; Brucker, Alexander J.; Cade, William H.; Cain, Melinda S.; Campochiaroll, Peter A.; Chan, Chi-Chao; Cheng, Ching-Yu; Chew, Emily Y.; Chin, Kimberly A.; Chowers, Itay; Clayton, David G.; Cojocaru, Radu; Conley, Yvette P.; Cornes, Belinda K.; Daly, Mark J.; Dhillon, Baljean; Edwards, Albert; Evangelou, Evangelos; Fagemess, Jesen; Ferreyra, Henry A.; Friedman, James S.; Geirsdottir, Asbjorg; George, Ronnie J.; Gieger, Christian; Gupta, Neel; Hagstrom, Stephanie A.; Harding, Simon P.; Haritoglou, Christos; Heckenlively, John R.; Hoz, Frank G.; Hughes, Guy; Ioannidis, John P. A.; Ishibashi, Tatsuro; Joseph, Peronne; Jun, Gyungah; Kamatani, Yoichiro; Katsanis, Nicholas; Keilhauer, Claudia N.; Khan, Jane C.; Kim, Ivana K.; Kiyohara, Yutaka; Klein, Barbara E. K.; Klein, Ronald; Kovach, Jaclyn L.; Kozak, Igor; Lee, Clara J.; Lee, Kristine E.; Lichtner, Peter; Lotery, Andrew J.; Meitinger, Thomas; Mitchell, Paul; Mohand-Saied, Saddek; Moore, Anthony T.; Morgan, Denise J.; Morrison, Margaux A.; Myers, Chelsea E.; Naj, Adam C.; Nakamura, Yusuke; Okada, Yukinori; Orlin, Anton; Ortube, M. Carolina; Othman, Mohammad I.; Pappas, Chris; Park, Kyu Hyung; Pauer, Gayle J. T.; Peachey, Neal S.; Poch, Olivier; Priya, Rinki Ratna; Reynolds, Robyn; Richardson, Andrea J.; Ripp, Raymond; Rudolph, Guenther; Ryu, Euijung; Sahel, Jose-Alain; Schaumberg, Debra A.; Scholl, Hendrik P. N.; Schwartz, Stephen G.; Scott, William K.; Shahid, Humma; Sigurdsson, Haraldur; Silvestri, Giuliana; Sivakumaran, Theru A.; Smith, R. Theodore; Sobrin, Lucia; Souied, Eric H.; Stambolian, Dwight E.; Stefansson, Hreinn; Sturgill-Short, Gwen M.; Takahashi, Atsushi; Tosakulwong, Nirubol; Truitt, Barbara J.; Tsironi, Evangelia E.; Uitterlinden, Andre G.; van Duijn, Cornelia M.; Vijaya, Lingam; Vingerling, Johannes R.; Vithana, Eranga N.; Webster, Andrew R.; Wichmann, H-Erich; Winkler, Thomas W.; Wong, Tien Y.; Wright, Alan F.; Zelenika, Diana; Zhang, Ming; Zhao, Ling; Zhang, Kang; Klein, Michael L.; Hageman, Gregory S.; Lathrop, G. Mark; Stefansson, Kari; Allikmets, Rando; Baird, Paul N.; Gorin, Michael B.; Wang, Jie Jin; Klaver, Caroline C. W.; Seddon, Johanna M.; Pericak-Vance, Margaret A.; Iyengar, Sudha K.; Yates, John R. W.; Swaroop, Anand; Weber, Bernhard H. F.; Kubo, Michiaki; DeAngelis, Margaret M.; Leveillard, Thierry; Thorsteinsdottir, Unnur; Haines, Jonathan L.; Farrer, Lindsay A.; Heid, Iris M.; Abecasis, Goncalo R.

Genetically Distinct Subsets within ANCA-Associated Vasculitis

NEW ENGLAND JOURNAL OF MEDICINE

IF78.5

2012-07-19

744

OAAI

Lyons, Paul A.; Rayner, Tim F.; Trivedi, Sapna; Holle, Julia U.; Watts, Richard A.; Jayne, David R. W.; Baslund, Bo; Brenchley, Paul; Bruchfeld, Annette; Chaudhry, Afzal N.; Tervaert, Jan Willem Cohen; Deloukas, Panos; Feighery, Conleth; Gross, Wolfgang L.; Guillevin, Loic; Gunnarsson, Iva; Harper, Lorraine; Hruskova, Zdenka; Little, Mark A.; Martorana, Davide; Neumann, Thomas; Ohlsson, Sophie; Padmanabhan, Sandosh; Pusey, Charles D.; Salama, Alan D.; Sanders, Jan-Stephan F.; Savage, Caroline O.; Segelmark, Mrten; Stegeman, Coen A.; Tesar, Vladimir; Vaglio, Augusto; Wieczorek, Stefan; Wilde, Benjamin; Zwerina, Jochen; Rees, Andrew J.; Clayton, David G.; Smith, Kenneth G. C.

Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXBFKBPLNOTCH4 region of chromosome 6p21.3

HUMAN MOLECULAR GENETICS

IF3.2

2012-06-13

OAAI

Cipriani, Valentina; Leung, Hin-Tak; Plagnol, Vincent; Bunce, Catey; Khan, Jane C.; Shahid, Humma; Moore, Anthony T.; Harding, Simon P.; Bishop, Paul N.; Hayward, Caroline; Campbell, Susan; Armbrecht, Ana Maria; Dhillon, Baljean; Deary, Ian J.; Campbell, Harry; Dunlop, Malcolm; Dominiczak, Anna F.; Mann, Samantha S.; Jenkins, Sharon A.; Webster, Andrew R.; Bird, Alan C.; Lathrop, Mark; Zelenika, Diana; Souied, Eric H.; Sahel, Jose-Alain; Leveillard, Thierry; Cree, Angela J.; Gibson, Jane; Ennis, Sarah; Lotery, Andrew J.; Wright, Alan F.; Clayton, David G.; Yates, John R. W.

Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes

HUMAN MOLECULAR GENETICS

IF3.2

2012-03-08

OAAI

Wallace, Chris; Rotival, Maxime; Cooper, Jason D.; Rice, Catherine M.; Yang, Jennie H. M.; McNeill, Mhairi; Smyth, Deborah J.; Niblett, David; Cambien, Francois; Tiret, Laurence; Todd, John A.; Clayton, David G.; Blankenberg, Stefan

No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degeneration

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2011-10-12

OAAI

Cipriani, Valentina; Matharu, Baljinder K.; Khan, Jane C.; Shahid, Humma; Hayward, Caroline; Wright, Alan F.; Armbrecht, Ana Maria; Dhillon, Baljean; Harding, Simon P.; Bishop, Paul N.; Bunce, Catey; Clayton, David G.; Moore, Anthony T.; Yates, John R. W.

BRITISH JOURNAL OF OPHTHALMOLOGY

IF3.5

2011-08-23

PREAI

Shahid, Humma; Khan, Jane C.; Cipriani, Valentina; Sepp, Tiina; Matharu, Baljinder K.; Bunce, Catey; Harding, Simon P.; Clayton, David G.; Moore, Anthony T.; Yates, John R. W.

Copy number, linkage disequilibrium and disease association in the FCGR locus

HUMAN MOLECULAR GENETICS

IF3.2

2010-05-27

119

OAAI

Niederer, Heather A.; Willcocks, Lisa C.; Rayner, Tim F.; Yang, Wanling; Lau, Yu Lung; Williams, Thomas N.; Scott, J. Anthony G.; Urban, Britta C.; Peshu, Norbert; Dunstan, Sarah J.; Hien, Tran Tinh; Phu, Nguyen Hoan; Padyukov, Leonid; Gunnarsson, Iva; Svenungsson, Elisabet; Savage, Caroline O.; Watts, Richard A.; Lyons, Paul A.; Clayton, David G.; Smith, Kenneth G. C.

The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes

NATURE GENETICS

IF31.8

2009-12-06

281

OAAI

Wallace, Chris; Smyth, Deborah J.; Maisuria-Armer, Meeta; Walker, Neil M.; Todd, John A.; Clayton, David G.

Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing

HUMAN MOLECULAR GENETICS

IF3.2

2009-10-13

117

OAAI

Heap, Graham A.; Yang, Jennie H. M.; Downes, Kate; Healy, Barry C.; Hunt, Karen A.; Bockett, Nicholas; Franke, Lude; Dubois, Patrick C.; Mein, Charles A.; Dobson, Richard J.; Albert, Thomas J.; Rodesch, Matthew J.; Clayton, David G.; Todd, John A.; van Heel, David A.; Plagnol, Vincent

Experimental aspects of copy number variant assays at CCL3L1

NATURE MEDICINE

IF50

2009-10-01

OAAI

Field, Sarah F.; Howson, Joanna M. M.; Maier, Lisa M.; Walker, Susan; Walker, Neil M.; Smyth, Deborah J.; Armour, John A. L.; Clayton, David G.; Todd, John A.

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

NATURE GENETICS

IF31.8

2009-05-10

1.5K

OAAI

Barrett, Jeffrey C.; Clayton, David G.; Concannon, Patrick; Akolkar, Beena; Cooper, Jason D.; Erlich, Henry A.; Julier, Cecile; Morahan, Grant; Nerup, Jorn; Nierras, Concepcion; Plagnol, Vincent; Pociot, Flemming; Schuilenburg, Helen; Smyth, Deborah J.; Stevens, Helen; Todd, John A.; Walker, Neil M.; Rich, Stephen S.

Confirmation of HLA class II independent type 1 diabetes associations in the major histocompatibility complex including HLA-B and HLA-A 在包括hla-b和hla-a在内的主要组织相容性复合体中确认HLA II类独立的1型糖尿病关联

DIABETES OBESITY & METABOLISM

IF5.7

2009-01-12

120

OAAI

Howson, J. M. M.; Walker, N. M.; Clayton, D.; Todd, J. A.

Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease

NEW ENGLAND JOURNAL OF MEDICINE

IF78.5

2008-12-25

615

OAAI

Smyth, Deborah J.; Plagnol, Vincent; Walker, Neil M.; Cooper, Jason D.; Downes, Kate; Yang, Jennie H. M.; Howson, Joanna M. M.; Stevens, Helen; McManus, Ross; Wijmenga, Cisca; Heap, Graham A.; Dubois, Patrick C.; Clayton, David G.; Hunt, Karen A.; van Heel, David A.; Todd, John A.

A robust statistical method for case-control association testing with copy number variation

NATURE GENETICS

IF31.8

2008-09-07

152

OAAI

Barnes, Chris; Plagnol, Vincent; Fitzgerald, Tomas; Redon, Richard; Marchini, Jonathan; Clayton, David; Hurles, Matthew E.

PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes

DIABETES

IF7.5

2008-06-01

OAAI

Smyth, Deborah J.; Cooper, Jason D.; Howson, Joanna M. M.; Walker, Neil M.; Plagnol, Vincent; Stevens, Helen; Clayton, David G.; Todd, John A.

Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study

CLINICAL ENDOCRINOLOGY

IF2.4

2007-08-29

PREAI

Freel, E. M.; Ingram, M.; Friel, E. C.; Fraser, R.; Brown, M.; Samani, N. J.; Caulfield, M.; Munroe, P.; Farrall, M.; Webster, J.; Clayton, D.; Dominiczak, A. F.; Davies, E.; Connell, J. M. C.

研究方向