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M

Mathijs Willemsen

Maastricht University Medical Centre
H指数:12
被引数:516

个人简介

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工作经历

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荣誉奖项

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Adult patients with autoinflammation of unknown origin partially phenocopy the immune presentation of Still’s disease

成人患者不明原因的自发炎症部分模拟了Still病的免疫表型。

Nature Communications
IF15.7
2026-04-010
OAAI
Rafael Veiga; Leana De Vuyst; Christophe Poulet; Julika Neumann; Leoni Bücken; Teresa Prezzemolo; Mathijs Willemsen; Steven Vanderschueren; Patrick Matthys; Emna Chabaane; Maximilien Fléron; Gaël Cobraiville; Dominique Baiwir; Gabriel Mazzucchelli; Bruno Fautrel; Carine Wouters; Dominique De Seny; Stephanie Humblet-Baron; Adrian Liston
Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipients

系统 vaccinology 识别实体器官移植受者 SARS-CoV-2 疫苗反应的免疫学相关性。

npj Vaccines
IF6.5
2025-07-010
OAAI
Nicolas Gemander; Julika Neumann; Rafael Veiga; Isabelle Etienne; Teresa Prezzemolo; Delphine Kemlin; Pieter Pannus; Stéphanie Depickère; Véronique Olislagers; Inès Vu Duc; Alexandra Waegemans; Margaux Gerbaux; Leoni Bücken; Hafid Dahma; Charlotte Martin; Nicolas Dauby; Maria E. Goossens; Isabelle Desombere; Carlos P. Roca; Mathijs Willemsen; Stanislas Goriely; Alain Le Moine; Arnaud Marchant; Adrian Liston; Stephanie Humblet-Baron
OTULIN haploinsufficiency predisposes to environmentally directed inflammation

OTULIN单倍不足易患环境定向炎症

FRONTIERS IN IMMUNOLOGY
IF5.9
2024-05-210
OAAI
Staels, Frederik; Bucken, Leoni; De Vuyst, Leana; Willemsen, Mathijs; Van Nieuwenhove, Erika; Gerbaux, Margaux; Neumann, Julika; Malviya, Vanshika; Van Meerbeeck, Lize; Haughton, Jeason; Seldeslachts, Laura; Gouwy, Mieke; Martinod, Kimberly; Vande Velde, Greetje; Proost, Paul; Yshii, Lidia; Schlenner, Susan; Schrijvers, Rik; Liston, Adrian; Humblet-Baron, Stephanie
Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome
JOURNAL OF CLINICAL IMMUNOLOGY
IF5.7
2023-12-151
OA
Riestra, Maria Rodrigo; Pillay, Bethany A.; Willemsen, Mathijs; Kienapfel, Verena; Ehlers, Lisa; Delafontaine, Selket; Pinton, Antoine; Wouters, Marjon; Hombrouck, Anneleen; Sauer, Kate; Bossuyt, Xavier; Voet, Arnout; Soenen, Stefaan J.; Conde, Cecilia Dominguez; Bucciol, Giorgia; Boztug, Kaan; Humblet-Baron, Stephanie; Touzart, Aurore; Rieux-Laucat, Frederic; Notarangelo, Luigi D.; Moens, Leen; Meyts, Isabelle
Homozygous DBF4 mutation as a cause of severe congenital neutropenia
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
IF11.2
2023-07-013
OA
Willemsen, Mathijs; Barber, John S.; Van Nieuwenhove, Erika; Staels, Frederik; Gerbaux, Margaux; Neumann, Julika; Prezzemolo, Teresa; Pasciuto, Emanuela; Lagou, Vasiliki; Boeckx, Nancy; Filtjens, Jessica; De Visscher, Amber; Matthys, Patrick; Schrijvers, Rik; Tousseyn, Thomas; O'Driscoll, Mark; Bucciol, Giorgia; Schlenner, Susan; Meyts, Isabelle; Humblet-Baron, Stephanie; Liston, Adrian
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations

由新的杂合NFKB1突变引起的具有异质表型的两个家族的常见可变免疫缺陷

FRONTIERS IN IMMUNOLOGY
IF5.9
2022-09-203
OAAI
Staels, Frederik; De Keukeleere, Kerstin; Kinnunen, Matias; Keskitalo, Salla; Lorenzetti, Flaminia; Vanmeert, Michiel; Prezzemolo, Teresa; Pasciuto, Emanuela; Lescrinier, Eveline; Bossuyt, Xavier; Gerbaux, Margaux; Willemsen, Mathijs; Neumann, Julika; Van Loo, Sien; Corveleyn, Anniek; Willekens, Karen; Stalmans, Ingeborg; Meyts, Isabelle; Liston, Adrian; Humblet-Baron, Stephanie; Seppanen, Mikko; Varjosalo, Markku; Schrijvers, Rik
A disease-associated missense mutation in CYP4F3 affects the metabolism of leukotriene B4 via disruption of electron transfer

CYP4F3中与疾病相关的错义突变通过破坏电子转移影响白三烯B4的代谢

JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE
IF9.1
2022-06-099
OA
Smeets, Elien; Huang, Shengyun; Lee, Xiao Yin; Van Nieuwenhove, Erika; Helsen, Christine; Handle, Florian; Moris, Lisa; El Kharraz, Sarah; Eerlings, Roy; Devlies, Wout; Willemsen, Mathijs; Bucken, Leoni; Prezzemolo, Teresa; Humblet-Baron, Stephanie; Voet, Arnout; Rochtus, Anne; Van Schepdael, Ann; de Zegher, Francis; Claessens, Frank
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
IF11.2
2020-11-0130
OAAI
Van Nieuwenhove, Erika; Barber, John S.; Neumann, Julika; Smeets, Elien; Willemsen, Mathijs; Pasciuto, Emanuela; Prezzemolo, Teresa; Lagou, Vasiliki; Seldeslachts, Laura; Malengier-Devlies, Bert; Metzemaekers, Mieke; Hassdenteufel, Sarah; Kerstens, Axelle; van der Kant, Rob; Rousseau, Frederic; Schymkowitz, Joost; Di Marino, Daniele; Lang, Sven; Zimmermann, Richard; Schlenner, Susan; Munck, Sebastian; Proost, Paul; Matthys, Patrick; Devalck, Christine; Boeckx, Nancy; Claessens, Frank; Wouters, Carine; Humblet-Baron, Stephanie; Meyts, Isabelle; Liston, Adrian

研究方向

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H
Humblet-Baron, Stephanie
H 指数:0论文数:1被引数:24
A
Adrian Liston
H 指数:67论文数:361被引数:1.9万
J
Julika Neumann
H 指数:11论文数:37被引数:413
F
Frederik Staels
H 指数:16论文数:46被引数:819
M
Margaux Gerbaux
H 指数:9论文数:25被引数:278
R
Rik Schrijvers
H 指数:29论文数:329被引数:3,103
I
Isabelle Meyts
H 指数:69论文数:439被引数:2.6万
L
Leoni Bücken
H 指数:4论文数:12被引数:41
T
Teresa Prezzemolo
H 指数:14论文数:45被引数:1,325
E
Emanuela Pasciuto
H 指数:19论文数:52被引数:2,201