Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy.

Autor: Olga Gorlova, Jose-Ezequiel Martin, Blanca Rueda, Bobby P. C. Koeleman, Jun Ying, Maria Teruel, Lina-Marcela Diaz-Gallo, Jasper C. Broen, Madelon C. Vonk, Carmen P. Simeon, Behrooz Z. Alizadeh, Marieke J. H. Coenen, Alexandre E. Voskuyl, Annemie J. Schuerwegh, Piet L. C. M. van Riel, Marie Vanthuyne, Ruben van 't Slot, Annet Italiaander, Roel A. Ophoff, Nicolas Hunzelmann, Vicente Fonollosa, Norberto Ortego-Centeno, Miguel A. González-Gay, Francisco J. García-Hernández, María F. González-Escribano, Paolo Airo, Jacob van Laar, Jane Worthington, Roger Hesselstrand, Vanessa Smith, Filip de Keyser, Fredric Houssiau, Meng May Chee, Rajan Madhok, Paul G. Shiels, Rene Westhovens, Alexander Kreuter, Elfride de Baere, Torsten Witte, Leonid Padyukov, Annika Nordin, Raffaella Scorza, Claudio Lunardi, Benedicte A. Lie, Anna-Maria Hoffmann-Vold, Øyvind Palm, Paloma García de la Peña, Patricia Carreira, John Varga, Monique Hinchcliff, Annette T. Lee, Pravitt Gourh, Christopher I. Amos, Frederick M. Wigley, Laura K. Hummers, J. Lee Nelson, Gabriella Riemekasten, Ariane Herrick, Lorenzo Beretta, Carmen Fonseca, Christopher P. Denton, Peter K. Gregersen, Sandeep Agarwal, Shervin Assassi, Filemon K. Tan, Frank C. Arnett, Timothy R. D. J. Radstake, Maureen D. Mayes, Javier Martin

Publikováno v: PLoS Genetics, Vol 7, Iss 8 (2011)

Externí odkaz: https://doaj.org/article/4d5606e9cb53448b8c0723d7f6339f4c

Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.

Autor: Olga Gorlova, Jose-Ezequiel Martin, Blanca Rueda, Bobby P C Koeleman, Jun Ying, Maria Teruel, Lina-Marcela Diaz-Gallo, Jasper C Broen, Madelon C Vonk, Carmen P Simeon, Behrooz Z Alizadeh, Marieke J H Coenen, Alexandre E Voskuyl, Annemie J Schuerwegh, Piet L C M van Riel, Marie Vanthuyne, Ruben van 't Slot, Annet Italiaander, Roel A Ophoff, Nicolas Hunzelmann, Vicente Fonollosa, Norberto Ortego-Centeno, Miguel A González-Gay, Francisco J García-Hernández, María F González-Escribano, Paolo Airo, Jacob van Laar, Jane Worthington, Roger Hesselstrand, Vanessa Smith, Filip de Keyser, Fredric Houssiau, Meng May Chee, Rajan Madhok, Paul G Shiels, Rene Westhovens, Alexander Kreuter, Elfride de Baere, Torsten Witte, Leonid Padyukov, Annika Nordin, Raffaella Scorza, Claudio Lunardi, Benedicte A Lie, Anna-Maria Hoffmann-Vold, Oyvind Palm, Paloma García de la Peña, Patricia Carreira, Spanish Scleroderma Group, John Varga, Monique Hinchcliff, Annette T Lee, Pravitt Gourh, Christopher I Amos, Frederick M Wigley, Laura K Hummers, J Lee Nelson, Gabriella Riemekasten, Ariane Herrick, Lorenzo Beretta, Carmen Fonseca, Christopher P Denton, Peter K Gregersen, Sandeep Agarwal, Shervin Assassi, Filemon K Tan, Frank C Arnett, Timothy R D J Radstake, Maureen D Mayes, Javier Martin

Publikováno v: PLoS Genetics, Vol 7, Iss 7, p e1002178 (2011)

The aim of this study was to determine, through a genome-wide association study (GWAS), the genetic components contributing to different clinical sub-phenotypes of systemic sclerosis (SSc). We considered limited (lcSSc) and diffuse (dcSSc) cutaneous

Externí odkaz: https://doaj.org/article/a5f42acd89a14eab989b4aae529eeb02

Identification of an Association ofTNFAIP3Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors

Autor: Syeling Lai, Shervin Assassi, Xiaodong Zhou, Filemon K. Tan, Xinjian Guo, Yang Yang, Mengyuan Liu, Nainan Hei, Peng Wei

Publikováno v: Arthritis & Rheumatology. 68:749-760

Objective Systemic sclerosis (SSc) is a fibrotic disease attributed to both genetic susceptibility and environmental factors. This study was undertaken to investigate the associations between SSc-associated genetic variants and the expression of extr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::58f8aa69e63ef6dcc578b43fc0f0b19c
https://doi.org/10.1002/art.39476

Identification of Cadherin 11 as a Mediator of Dermal Fibrosis and Possible Role in Systemic Sclerosis

Autor: Minghua Wu, Robert Lafyatis, Sandeep K. Agarwal, Filemon K. Tan, Mesias Pedroza, Shervin Assassi, Michael B. Brenner, Anuh T. George, Maureen D. Mayes

Publikováno v: Arthritis & Rheumatology. 66:1010-1021

Objective Systemic sclerosis (SSc) is a chronic autoimmune disease clinically manifesting as progressive fibrosis of the skin and internal organs. Recent microarray studies demonstrated that cadherin 11 (Cad-11) expression is increased in the affecte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::74d3771026d964cfb9f3ca71a68a25c0
https://doi.org/10.1002/art.38275

New insight on the Xq28 association with systemic sclerosis

Autor: Maureen D. Mayes, Gabriela Riemekasten, Alexandre E. Voskuyl, V. Fonollosa, Jane Worthington, Madelon C. Vonk, Miguel A. González-Gay, Christopher P. Denton, José Luis Callejas-Rubio, Alexander Kreuter, Javier Martin, F. David Carmona, Annemie J. Schuerwegh, Jasper C A Broen, Patricia Carreira, Rajan Madhok, Timothy R D J Radstake, Paul G. Shiels, Lina-Marcela Diaz-Gallo, Frank C. Arnett, Jörg H W Distler, Carmen P. Simeon, Nicolas Hunzelmann, Jacob M van Laar, Torsten Witte, Filemon K. Tan, M. Carmen Cénit, Carmen Fonseca, Shervin Assassi, Ariane L. Herrick, Francisco Javier López-Longo

Publikováno v: Carmona, F D, Cenit, M C, Diaz-Gallo, L M, Broen, J C A, Simeon, C P, Carreira, P E, Callejas-Rubio, J L, Fonollosa, V, Lopez-Longo, F J, Gonzalez-Gay, M A, Hunzelmann, N, Riemekasten, G, Witte, T, Kreuter, A, Distler, J H W, Madhok, R, Shiels, P, van Laar, J M, Schuerwegh, A J, Vonk, M C, Voskuyl, A E, Fonseca, C, Denton, C P, Herrick, A, Worthington, J, Arnett, F C, Tan, F K, Assassi, S, Radstake, T R D J, Mayes, M D & Martin, J 2013, ' New insight on the Xq28 association with systemic sclerosis ', Annals of the Rheumatic Diseases, vol. 72, no. 12, pp. 2032-2038 . https://doi.org/10.1136/annrheumdis-2012-202742
Annals of the Rheumatic Diseases, 72, 12, pp. 2032-8
Annals of the Rheumatic Diseases, 72(12), 2032-2038. BMJ Publishing Group
Annals of the Rheumatic Diseases, 72, 2032-8

ObjectiveTo evaluate whether the systemic sclerosis (SSc)-associated IRAK1 non-synonymous single-nucleotide polymorphism rs1059702 is responsible for the Xq28 association with SSc or whether there are other independent signals in the nearby methyl-Cp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::878658de3daa7a65af224b40b6db94e5
https://doi.org/10.1136/annrheumdis-2012-202742