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

Novel hypermorphic variants in IRF2BP2 identified in patients with common variable immunodeficiency and autoimmunity

在患有常见变异性免疫缺陷和自身免疫的患者中发现 IRF2BP2 的新型高态变异

Manfred Anim, Georgios Sogkas, Nadezhda Camacho-Ordonez, Gunnar Schmidt, Abdulwahab Elsayed, Michele Proietti, Torsten Witte, Bodo Grimbacher, Faranaz Atschekzei

Characterization of serum biomarkers and antibody responses against Prevotella spp. in preclinical and new-onset phase of rheumatic diseases

风湿病临床前和新发阶段血清生物标志物和抗普氏菌抗体反应的表征

Lena Amend, Benoît Thomas P Gilbert, Penelope Pelczar, Marius Böttcher, Samuel Huber, Torsten Witte, Axel Finckh, Till Strowig

CTLA-4 Insufficiency due to a Novel CTLA-4 Deletion, Identified through Copy Number Variation Analysis

通过拷贝数变异分析确定 CTLA-4 缺陷是由于新的 CTLA-4 缺失所致

Lisa Olfe, Sandra von Hardenberg, Winfried Hofmann, Bernd Auber, Ulrich Baumann, Rita Beier, Ignatius Ryan Adriawan, Faranaz Atschekzei, Torsten Witte, Georgios Sogkas

Novel aspects of regulatory T cell dysfunction as a therapeutic target in giant cell arteritis

调节性 T 细胞功能障碍作为巨细胞动脉炎治疗靶点的新方面

Ignatius Ryan Adriawan, Faranaz Atschekzei, Oliver Dittrich-Breiholz, Panagiotis Garantziotis, Stefanie Hirsch, Linus Maximillian Risser, Maike Kosanke, Reinhold Ernst Schmidt, Torsten Witte, Georgios Sogkas

Common Variable Immunodeficiency-Associated Cancers: The Role of Clinical Phenotypes, Immunological and Genetic Factors

常见变异型免疫缺陷相关癌症:临床表型、免疫学和遗传因素的作用

Luzia Bruns, Victoria Panagiota, Sandra von Hardenberg, Gunnar Schmidt, Ignatius Ryan Adriawan, Eleni Sogka, Stefanie Hirsch, Gerrit Ahrenstorf, Torsten Witte, Reinhold Ernst Schmidt, Faranaz Atschekzei, Georgios Sogkas

Addressing the clinical unmet needs in primary Sjögren's Syndrome through the sharing, harmonization and federated analysis of 21 European cohorts

通过共享、协调和联合分析21个欧洲队列,解决原发性干燥综合征的临床未满足需求

Pezoulas, Vasileios C; Goules, Andreas; Kalatzis, Fanis; Chatzis, Luke; Kourou, Konstantina D; Venetsanopoulou, Aliki; Exarchos, Themis P; Gandolfo, Saviana; Votis, Konstantinos; Zampeli, Evi; Burmeister, Jan; May, Thorsten; Marcelino Pérez, Manuel; Lishchuk, Iryna; Chondrogiannis, Thymios; Andronikou, Vassiliki; Varvarigou, Theodora; Filipovic, Nenad; Tsiknakis, Manolis; Baldini, Chiara; Bombardieri, Michele; Bootsma, Hendrika; Bowman, Simon J; Soyfoo, Muhammad Shahnawaz; Parisis, Dorian; Delporte, Christine; Devauchelle-Pensec, Valérie; Pers, Jacques-Olivier; Dörner, Thomas; Bartoloni, Elena; Gerli, Roberto; Giacomelli, Roberto; Jonsson, Roland; Ng, Wan-Fai; Priori, Roberta; Ramos-Casals, Manuel; Sivils, Kathy; Skopouli, Fotini; Torsten, Witte; A G van Roon, Joel; Xavier, Mariette; De Vita, Salvatore; Tzioufas, Athanasios G; Fotiadis, Dimitrios I

Natural antibodies and CRP drive anaphylatoxin production by urate crystals

天然抗体和C反应蛋白驱动尿酸盐晶体产生过敏毒素

Anne Kathrin Wessig ,Leonie Hoffmeister ,Annika Klingberg ,Anika Alberts ,Andreas Pich ,Korbinian Brand ,Torsten Witte ,Konstantin Neumann

Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

遗传性GATA2缺陷通过单倍体不足表现为显性遗传,并表现出不完全临床外显率

Carmen Oleaga-Quintas ,Edgar Borges de Oliveira-Júnior # ,Jérémie Rosain # ,Franck Rapaport # ,Caroline Deswarte # ,Antoine Guérin # ,Sairaj Munavar Sajjath # ,Yu Jerry Zhou # ,Stéphane Marot # ,Claire Lozano # ,Lidia Branco ,Nuria Fernández-Hidalgo ,Dukhee Betty Lew ,Anne-Sophie Brunel ,Caroline Thomas ,Elise Launay ,Andrés Augusto Arias ,Alexis Cuffel ,Vanesa Cunill Monjo ,Anna-Lena Neehus ,Laura Marques ,Manon Roynard ,Marcela Moncada-Vélez ,Bengü Gerçeker ,Roger Colobran ,Marie-Gabrielle Vigué ,Gabriela Lopez-Herrera ,Laura Berron-Ruiz ,Nora Hilda Segura Méndez ,Patricia O'Farrill Romanillos ,Tom Le Voyer ,Anne Puel ,Christine Bellanné-Chantelot ,Kacy A Ramirez ,Lazaro Lorenzo-Diaz ,Noé Ramirez Alejo ,Rebeca Pérez de Diego ,Antonio Condino-Neto ,Fethi Mellouli ,Carlos Rodriguez-Gallego ,Torsten Witte ,José Franco Restrepo ,Mariana Jobim ,Stéphanie Boisson-Dupuis ,Eric Jeziorski ,Claire Fieschi ,Guillaume Vogt ,Jean Donadieu ,Marlène Pasquet ,Julia Vasconcelos ,Fatma Omur Ardeniz ,Mónica Martínez-Gallo ,Regis A Campos ,Luiz Fernando Jobim ,Rubén Martínez-Barricarte ,Kang Liu ,Aurélie Cobat # ,Laurent Abel # ,Jean-Laurent Casanova # ,Jacinta Bustamante

Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1

NFKB1 基因出现新型致病错义变异,导致免疫缺陷患者易患脑膜炎球菌病

Manfred Anim, Georgios Sogkas, Gunnar Schmidt, Natalia Dubrowinskaja, Torsten Witte, Reinhold Ernst Schmidt, Faranaz Atschekzei

Impaired proteolysis by SPPL2a causes CD74 fragment accumulation that can be recognized by anti-CD74 autoantibodies in human ankylosing spondylitis

SPPL2a蛋白水解受损会导致CD74片段积累,而这些片段可被人类强直性脊柱炎中的抗CD74自身抗体识别。

Tessa S van Kempen ,Emmerik F A Leijten ,Marthe F S Lindenbergh ,Michel Olde Nordkamp ,Christoph Driessen ,Robert-Jan Lebbink ,Niklas Baerlecken ,Torsten Witte ,Timothy R D J Radstake ,Marianne Boes