日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Exposure to Occupational Inhalants and the Risk of Developing Rheumatoid Arthritis: A Systematic Review and Meta-Analysis

职业性吸入物暴露与类风湿性关节炎发病风险:系统评价和荟萃分析

Liu, Qianwen; Song, Xin; Mauro, Emily; Jiang, Yuan; Shchetynsky, Klementy; Klareskog, Lars; Alfredsson, Lars; Jiang, Xia

Depression Polygenicity and Disease Activity and Disability Worsening in Multiple Sclerosis

抑郁症的多基因性与多发性硬化症的疾病活动度和残疾恶化

Manouchehrinia, Ali; Fitzgerald, Kathryn C; Salter, Amber; Marrie, Ruth Ann; Alfredsson, Lars; Bernstein, Charles N; Bolton, James M; Cutter, Gary; Fisk, John D; Graff, Lesley A; Hitchon, Carol A; Hillert, Jan; Kockum, Ingrid; Lu, Yi; Lublin, Fred D; McKay, Kyla; Olsson, Tomas; Patten, Scott; Patki, Amit; Riel, Hayley; Shchetynsky, Klementy; Stridh, Pernilla; Tiwari, Hemant K; Wolinsky, Jerry S; Kowalec, Kaarina

Genetic Risk Variants for Multiple Sclerosis and Other Loci Linked to Intrathecal Immunoglobulin G Synthesis

多发性硬化症的遗传风险变异及其他与鞘内免疫球蛋白G合成相关的基因位点

Pukaj, Albert; Harroud, Adil; Shchetynsky, Klementy; Wirsching, Laura; Peters, Lucy; Andlauer, Till F M; Pääkkönen, Kimmo; Bos, Steffan D; Moylett, Sinéad; Dubois, Bénédicte; Llufriu, Sara; Luessi, Felix; Tackenberg, Björn; Kowarik, Markus C; Then Bergh, Florian; Trebst, Corinna; Tumani, Hayrettin; Wildemann, Brigitte; Bayas, Antonios; Havla, Joachim; Kümpfel, Tania; Knop, Matthias; Genetics Center, Regeneron; Stridh, Pernilla; Hillert, Jan A; Olsson, Tomas; Alfredsson, Lars; Cotsapas, Chris; Flinstad Harbo, Hanne; Zipp, Frauke; Saarela, Janna; Baranzini, Sergio E; Berthele, Achim; Kockum, Ingrid; Hemmer, Bernhard; Gasperi, Christiane

Correction: Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study

更正:多发性硬化症患者对那他珠单抗临床反应的药物基因组学:一项全基因组多中心关联研究

Clarelli, Ferdinando; Corona, Andrea; Pääkkönen, Kimmo; Sorosina, Melissa; Zollo, Alen; Piehl, Fredrik; Olsson, Tomas; Stridh, Pernilla; Jagodic, Maja; Hemmer, Bernhard; Gasperi, Christiane; Harroud, Adil; Shchetynsky, Klementy; Mingione, Alessandra; Mascia, Elisabetta; Misra, Kaalindi; Giordano, Antonino; Mazzieri, Maria Laura Terzi; Priori, Alberto; Saarela, Janna; Kockum, Ingrid; Filippi, Massimo; Esposito, Federica; Martinelli Boneschi, Filippo

A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis

1q21.1 位点的遗传-表观遗传相互作用是 CHD1L 介导的原发性进行性多发性硬化症易感性的基础

Pahlevan Kakhki, Majid; Giordano, Antonino; Starvaggi Cucuzza, Chiara; Venkata S Badam, Tejaswi; Samudyata, Samudyata; Lemée, Marianne Victoria; Stridh, Pernilla; Gkogka, Asimenia; Shchetynsky, Klementy; Harroud, Adil; Gyllenberg, Alexandra; Liu, Yun; Boddul, Sanjaykumar; James, Tojo; Sorosina, Melissa; Filippi, Massimo; Esposito, Federica; Wermeling, Fredrik; Gustafsson, Mika; Casaccia, Patrizia; Hillert, Jan; Olsson, Tomas; Kockum, Ingrid; Sellgren, Carl M; Golzio, Christelle; Kular, Lara; Jagodic, Maja

Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study

多发性硬化症患者对那他珠单抗临床反应的药物基因组学:一项全基因组多中心关联研究

Clarelli, Ferdinando; Corona, Andrea; Pääkkönen, Kimmo; Sorosina, Melissa; Zollo, Alen; Piehl, Fredrik; Olsson, Tomas; Stridh, Pernilla; Jagodic, Maja; Hemmer, Bernhard; Gasperi, Christiane; Harroud, Adil; Shchetynsky, Klementy; Mingione, Alessandra; Mascia, Elisabetta; Misra, Kaalindi; Giordano, Antonino; Mazzieri, Maria Laura Terzi; Priori, Alberto; Saarela, Janna; Kockum, Ingrid; Filippi, Massimo; Esposito, Federica; Boneschi, Filippo Giovanni Martinelli

A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy

一种与多发性硬化症严重程度相关的遗传风险变异与脑萎缩有关

Gasperi, Christiane; Wiltgen, Tun; McGinnis, Julian; Cerri, Stefano; Moridi, Thomas; Ouellette, Russell; Pukaj, Albert; Voon, Cuici; Bafligil, Cemsel; Lauerer, Markus; Andlauer, Till F M; Held, Friederike; Aly, Lilian; Shchetynsky, Klementy; Stridh, Pernilla; Harroud, Adil; Wiestler, Benedikt; Kirschke, Jan S; Zimmer, Claus; Baras, Aris; Piehl, Fredrik; Berthele, Achim; Granberg, Tobias; Kockum, Ingrid; Hemmer, Bernhard; Mühlau, Mark

Simultaneous detection of DNA variation and methylation at HLA class II locus and immune gene promoters using targeted SureSelect Methyl-Sequencing

利用靶向SureSelect甲基测序技术同时检测HLA II类基因座和免疫基因启动子的DNA变异和甲基化

Maria Kalomoiri ,Chandana Rao Prakash ,Sonja Lagström ,Kai Hauschulz ,Ewoud Ewing ,Klementy Shchetynsky ,Lara Kular ,Maria Needhamsen ,Maja Jagodic

Endophilin A2 deficiency protects rodents from autoimmune arthritis by modulating T cell activation

Endophilin A2 缺乏通过调节 T 细胞活化保护啮齿动物免受自身免疫性关节炎的侵害

Ulrika Norin, Carola Rintisch, Liesu Meng, Florian Forster, Diana Ekman, Jonatan Tuncel, Katrin Klocke, Johan Bäcklund, Min Yang, Michael Y Bonner, Gonzalo Fernandez Lahore, Jaime James, Klementy Shchetynsky, Maria Bergquist, Inger Gjertsson, Norbert Hubner, Liselotte Bäckdahl, Rikard Holmdahl2

Systematic approach demonstrates enrichment of multiple interactions between non-HLA risk variants and HLA-DRB1 risk alleles in rheumatoid arthritis

系统性研究表明,类风湿性关节炎中非HLA风险变异与HLA-DRB1风险等位基因之间存在多种相互作用。

Diaz-Gallo, Lina-Marcela; Ramsköld, Daniel; Shchetynsky, Klementy; Folkersen, Lasse; Chemin, Karine; Brynedal, Boel; Uebe, Steffen; Okada, Yukinori; Alfredsson, Lars; Klareskog, Lars; Padyukov, Leonid