Rogier Hintzen

ORCID: 0000-0003-2585-3643
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Multiple Sclerosis Research Studies
  • Peripheral Neuropathies and Disorders
  • Cytokine Signaling Pathways and Interactions
  • T-cell and B-cell Immunology
  • Polyomavirus and related diseases
  • Viral Infections and Immunology Research
  • RNA regulation and disease
  • Species Distribution and Climate Change
  • vaccines and immunoinformatics approaches
  • Ecology and Vegetation Dynamics Studies
  • Immunotherapy and Immune Responses
  • Neurogenesis and neuroplasticity mechanisms
  • Bioinformatics and Genomic Networks
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Protein Tyrosine Phosphatases
  • Animal Ecology and Behavior Studies
  • Skin and Cellular Biology Research
  • Glycosylation and Glycoproteins Research
  • Acute Lymphoblastic Leukemia research
  • Atherosclerosis and Cardiovascular Diseases
  • RNA Research and Splicing
  • Sphingolipid Metabolism and Signaling
  • Systemic Lupus Erythematosus Research
  • Genetic Associations and Epidemiology
  • interferon and immune responses

Imperial College London
2014-2025

Erasmus University Rotterdam
2010-2024

Erasmus MC
2010-2024

BenevolentAI (United Kingdom)
2023

John Wiley & Sons (United States)
2020

Hudson Institute
2020

Birmingham Children's Hospital
2019

Witten/Herdecke University
2019

Garrahan Hospital
2019

Massachusetts General Hospital
2019

Ashley Beecham Nikolaos A. Patsopoulos Dionysia K. Xifara Mary F. Davis Anu Kemppinen and 95 more Chris Cotsapas Tejas Shah Chris C. A. Spencer David J. Booth An Goris Annette Oturai Janna Saarela Bertrand Fontaine Bernhard Hemmer Claes Martin Frauke Zipp Sandra D’Alfonso Filippo Martinelli Boneschi Bruce Taylor Hanne F. Harbo Ingrid Kockum Jan Hillert Tomas Olsson Maria Ban Jorge R. Oksenberg Rogier Hintzen Lisa F. Barcellos Cristina Agliardi Lars Alfredsson Mehdi Alizadeh Carl A. Anderson Robert Andrews Helle Bach Søndergaard Amie Baker Gavin Band Sergio E. Baranzini Nadia Barizzone Jeffrey C. Barrett Céline Bellenguez Laura Bergamaschi Luisa Bernardinelli Achim Berthele Viola Biberacher Thomas M.C. Binder Hannah Blackburn Izaura Lima Bomfim Paola Brambilla Simon Broadley Bruno Brochet Lou Brundin Dorothea Buck Helmut Butzkueven Stacy J. Caillier William Camu Wassila Carpentier Paola Cavalla Elisabeth Gulowsen Celius Irène Coman Gıancarlo Comı Lucia Corrado Leentje Cosemans Isabelle Cournu‐Rebeix Bruce Cree Daniele Cusi Vincent Damotte Gilles Defer Silvia Delgado Panos Deloukas Alessia Di Sapio Alexander Dilthey Peter Donnelly Bénédicte Dubois Martin Duddy Sarah Edkins Irina Elovaara Federica Esposito Nikos Evangelou Barnaby Fiddes Judith Field André Franke Colin Freeman Irene Y. Frohlich Daniela Galimberti Christian Gieger Pierre‐Antoine Gourraud Christiane Graetz Andrew Graham Verena Grummel Clara Guaschino Athena Hadjixenofontos Hákon Hákonarson Christopher Halfpenny Gillian Hall Per Hall Anders Hamsten James Harley Timothy Harrower Clive Hawkins Garrett Hellenthal Charles Hillier

10.1038/ng.2770 article EN Nature Genetics 2013-09-29

Background: There has been tremendous growth in research pediatric multiple sclerosis (MS) and immune mediated central nervous system demyelinating disorders since operational definitions for these conditions were first proposed 2007. Further, the International Pediatric Multiple Sclerosis Study Group (IPMSSG), which criteria, expanded substantially membership its international scope. Objective: The purpose of this review is to revise 2007 order incorporate advances delineating clinical...

10.1177/1352458513484547 article EN Multiple Sclerosis Journal 2013-04-09

<h3>Importance</h3> Myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) are consistently identified in a range of demyelinating disorders adults and children. Current therapeutic strategies largely center specific, no treatments have been formally evaluated. <h3>Objective</h3> To examine the clinical phenotypes, treatment responses, outcomes children with relapsing MOG-Ab–associated disease. <h3>Design, Setting, Participants</h3> This study prospectively collected demographic, clinical,...

10.1001/jamaneurol.2017.4601 article EN JAMA Neurology 2018-01-05
Jens Kühle Giulio Disanto Ruth Dobson Rocco Adiutori Luca Bianchi and 94 more J. Topping JP. Bestwick Ute‐Christiane Meier Mónica Marta Gloria Dalla Costa Tessel F. Runia E. P. Evdoshenko N. Lazareva Éric Thouvenot Pietro Iaffaldano Vita Direnzo Mohsen Khademi Fredrik Piehl Manuel Comabella M.H. Sombekke Joep Killestein Harald Hegen Stefan Rauch Sandra D’Alfonso JC Alvarez-Cermeño Pavlína Kleinová Dana Horáková Romy Roesler Florian Lauda Sara Llufriú Timuçin Avşar Uğur Uygunoğlu Ayşe Altıntaş Sabahattin Saip Til Menge Cecília Rajda Roberto Bergamaschi Natalia Moll Michael Khalil Romain Marignier Irena Dujmović Henrik Larsson Clas Malmeström Elio Scarpini Chiara Fenoglio Stig Wergeland Alice Laroni Viviana Annibali Silvia Romano A. Martinez Adriana Carrá Marco Salvetti Antonio Uccelli Øivind Torkildsen K-M Myhr Daniela Galimberti Konrad Rejdak Jan Lycke Jette Lautrup Frederiksen Jelena Drulović Cyrille B. Confavreux David Brassat Christian Enzinger Siegrid Fuchs Isabel Boscá Jean Pelletier Christophe Picard Elena Colombo D. Franciotta Tobias Derfuß RLP Lindberg Özgür Yaldizli László Vécsei BC Kieseier HP Hartung Pablo Villoslada Aksel Sıva Albert Saiz Hayrettin Tumani Eva Havrdová Luisa María Villar Maurizio Leone Nadia Barizzone Florian Deisenhammer C Teunissen Xavier Montalbán Mar Tintoré Tomas Olsson Maria Trojano Sylvain Lehmann Giovanni Castelnovo С. В. Лапин Rogier Hintzen L Kappos Roberto Furlan V Martinelli Giacomo P. Comi SV Ramagopalan Gavin Giovannoni

Background and objective: We explored which clinical biochemical variables predict conversion from clinically isolated syndrome (CIS) to definite multiple sclerosis (CDMS) in a large international cohort. Methods: Thirty-three centres provided serum samples 1047 CIS cases with at least two years’ follow-up. Age, sex, presentation, T2-hyperintense lesions, cerebrospinal fluid (CSF) oligoclonal bands (OCBs), CSF IgG index, cell count, 25-hydroxyvitamin D3 (25-OH-D), cotinine titres against...

10.1177/1352458514568827 article EN Multiple Sclerosis Journal 2015-02-13

<h3>Objective</h3> Antibodies to cell surface central nervous system proteins help diagnose conditions which often respond immunotherapies. The assessment of antibody assays needs reflect their clinical utility. We report the results a multicentre study aquaporin (AQP) 4 (AQP4-Ab) in neuromyelitis optica spectrum disorders (NMOSD). <h3>Methods</h3> Coded samples from patients with (NMO) or NMOSD (101) and controls (92) were tested at 15 European diagnostic centres using 21 including live...

10.1136/jnnp-2015-312601 article EN cc-by-nc Journal of Neurology Neurosurgery & Psychiatry 2016-04-25
Diego Cadavid Michelle Mellion Raymond Hupperts Keith R. Edwards Peter A. Calabresi and 95 more Jelena Drulović Gavin Giovannoni Hans‐Peter Hartung Douglas L. Arnold Elizabeth Fisher Richard A. Rudick Sha Mi Yi Chai Jie Li Yiwei Zhang Wenting Cheng Lei Xu Bing Zhu Susan M Green Ih Chang Aaron Deykin Sarah Sheikh Eduardo Agüera Abdullatif Al Khedr Radek Ampapa Rafael Arroyo Martin Belkin Robert Bonek Alexey Boyко Ruggero Capra Diego Centonze Pierre Clavelou Marc Debouverie Jelena Drulović Keith R. Edwards Nikos Evangelou E. P. Evdoshenko Óscar Fernández Victoria Fernández Sánchez Mark Freedman Steven Freedman Waldemar Fryze Antonio Garcı́a-Merino Mira Gavric-Kezic Angel Ghezzi Olivier Gout Luigi M.E. Grimaldi Barry Hendin Hanka Hertmanowska Rogier Hintzen Pavel Hradílek Raymond Hupperts Jan Ilkowski Evelina Ivashinenkova Guillermo Izquierdo François Jacques Gábor Jakab Ф. А. Хабиров Gabriela Kłodowska-Duda S. Komoly Smiljana Kostić Ivana Kovářová Marcelo Kremenchuzky Christopher LaGanke Yves Lapierre Maciej Maciejowski Francois Grand’ Maison Girolama Alessandra Marfia Sergio Martínez‐Yélamos Eva Meluzínová Xavier Montalbán Ronald S. Murray Robert T. Naismith Scott D. Newsome Viet Anh Nguyen Delia Oreja Gabriel Pardo Elena S. Pasechnik Francesco Patti Andrzej Potemkowski С. В. Прокопенко Peiqing Qian Alfredo Rodríguez Antigüedad Howard Rossman Csilla Rózsa Fernando Sánchez López Krzysztof Selmaj Eli Silber Adam Stępień Anna Stepniewska Maciej Świat Gordana Tončev Ayman Tourbah Tatyana Trushnikova Antonio Uccelli Marta Vachová Martin Vališ László Vécsei Sandrine Wiertlewski Mauro Zaffaroni

10.1016/s1474-4422(19)30137-1 article EN The Lancet Neurology 2019-07-05

Chitinase 3-like 1 (CHI3L1) has been proposed as a biomarker associated with the conversion to clinically definite multiple sclerosis in patients isolated syndromes, based on finding of increased cerebrospinal fluid CHI3L1 levels syndrome who later converted compared those remained syndrome. Here, we aimed validate prognostic large cohort This is longitudinal study clinical, magnetic resonance imaging, and data prospectively acquired. A total 813 samples from were recruited 15 European...

10.1093/brain/awv017 article EN Brain 2015-02-12

The choice of appropriate control group(s) is critical in cerebrospinal fluid (CSF) biomarker research multiple sclerosis (MS). There a lack definitions and nomenclature different groups rationalized application groups. We here propose consensus for the following groups: healthy controls (HCs), spinal anesthesia subjects (SASs), inflammatory neurological disease (INDCs), peripheral (PINDCs), non-inflammatory (NINDCs), symptomatic (SCs). Furthermore, we discuss these specific study designs,...

10.1177/1352458513488232 article EN Multiple Sclerosis Journal 2013-05-21
Mitja Mitrovič Nikolaos A. Patsopoulos Ashley Beecham Theresa Dankowski An Goris and 95 more Bénédicte Dubois Marie D’hooghe Robin Lemmens Philip Van Damme Helle Bach Søndergaard Finn Sellebjerg Per Soelberg Sorensen Henrik Ullum Lise Wegner Thørner Thomas Werge Janna Saarela Isabelle Cournu‐Rebeix Vincent Damotte Bertrand Fontaine Léna Guillot‐Noël Mark Lathrop Sandra Vukusik Pierre‐Antoine Gourraud Till F. M. Andlauer Viola Pongratz Dorothea Buck Christiane Gasperi Antonios Bayas Christoph Heesen Tania Kümpfel Ralf A. Linker Friedemann Paul Martin Stangel Björn Tackenberg Florian Then Bergh Clemens Warnke Heinz Wiendl Brigitte Wildemann Uwe K. Zettl Ulf Ziemann Hayrettin Tumani Ralf Gold Verena Grummel Bernhard Hemmer Benjamin Knier Christina M. Lill Felix Luessi Efthimios Dardiotis Cristina Agliardi Nadia Barizzone Elisabetta Mascia Luisa Bernardinelli Giancarlo Comi Daniele Cusi Federica Esposito Laura Ferrè Cristoforo Comi Daniela Galimberti Maurizio Leone Melissa Sorosina Julia Mescheriakova Rogier Hintzen Cornelia M. van Duijn Charlotte E. Teunissen Steffan D. Bos Kjell‐Morten Myhr Elisabeth Gulowsen Celius Benedicte A. Lie Anne Spurkland Manuel Comabella Xavier Montalbán Lars Alfredsson Pernilla Stridh Jan Hillert Maja Jagodic Fredrik Piehl Ilijas Jelčić Roland Martinꝉ Mireia Sospedra Maria Ban Clive Hawkins Pirro G. Hysi Seema Kalra Fredrik Karpe Jyoti Khadake Geneviève Lachance Matthew Neville Adam Santaniello Stacy J. Caillier Peter A. Calabresi Bruce Cree Anne H. Cross Mary F. Davis Jonathan L. Haines Paul I. W. de Bakker Silvia Delgado Marieme Dembele Keith R. Edwards Kathryn C. Fitzgerald Hákon Hákonarson

Multiple sclerosis is a complex neurological disease, with ∼20% of risk heritability attributable to common genetic variants, including >230 identified by genome-wide association studies. strands evidence suggest that much the remaining also due additive effects variants rather than epistasis between these or mutations exclusive individual families. Here, we show in 68,379 cases and controls up 5% this explained low-frequency variation gene coding sequence. We identify four novel genes...

10.1016/j.cell.2018.09.049 article EN cc-by Cell 2018-10-18

Remotely sensed data - available at medium to high resolution across global spatial and temporal scales are a valuable resource for ecologists. In particular, products from NASA's MODerate-resolution Imaging Spectroradiometer (MODIS), providing twice-daily coverage, have been widely used ecological applications. We present MODISTools, an R package designed improve the accessing, downloading, processing of remotely MODIS data. MODISTools automates process downloading any number locations,...

10.1002/ece3.1273 article EN cc-by Ecology and Evolution 2014-12-01

About 3—5% of all patients with multiple sclerosis experience the onset their disease under age 16. A significant proportion paediatric develop cognitive disturbances and persistent physical disability. The high relapse rate morbidity in population has triggered use disease-modifying therapies that have been shown to reduce rate, progression decline adult sclerosis. Hard evidence for right treatment its appropriate timing is scarce Nevertheless, expertise this field grown thanks recent...

10.1177/1352458510375568 article EN Multiple Sclerosis Journal 2010-08-04

<h3>Objective</h3> The impetus for this consensus discussion was to recommend clinical trial designs that can deliver high-quality data effective therapies pediatric patients, in a reasonable timeframe, with key focus on short- and long-term safety. <h3>Methods</h3> International Pediatric Multiple Sclerosis Study Group convened meeting of experts review the advances understanding pediatric-onset multiple sclerosis (MS) advent trials population. <h3>Results</h3> In last few years, convincing...

10.1212/wnl.0000000000007572 article EN cc-by Neurology 2019-05-02

A recent genome-wide association study reported five loci for which there was strong, but sub-genome-wide significant evidence with multiple sclerosis risk. The aim of this to evaluate the role these potential risk in a large and independent data set ≈ 20,000 subjects. We tested single nucleotide polymorphisms rs228614 (MANBA), rs630923 (CXCR5), rs2744148 (SOX8), rs180515 (RPS6KB1), rs6062314 (ZBTB46) total 8499 cases sclerosis, 8765 unrelated control subjects 958 trios European descent. In...

10.1093/brain/awt101 article EN Brain 2013-06-01

Conservation biology was founded on the idea that efforts to save nature depend a scientific understanding of how it works. It sought apply ecological principles conservation problems. We investigated whether relationship between these fields has changed over time through machine reading full texts 32,000 research articles published in 16 ecology and journals. examined changes topics both have evolved from 2000 2014. As matured, its focus shifted social political aspects conservation. The 2...

10.1111/cobi.13435 article ES cc-by Conservation Biology 2019-11-08

Abstract Objective Chronic neurotoxicity is a recognized long‐term complication following chemotherapy in range of diseases. Neurotoxicity adversely affects patients' quality life. The objective this study to examine whether there evidence acute neurotoxicity. Methods This prospective included patients with secondary progressive multiple sclerosis (SPMS‐BMT, n = 14) and hematological malignancies (HM‐BMT, 17) receiving as preconditioning for bone marrow transplant. control groups SPMS...

10.1002/ana.22169 article EN Annals of Neurology 2010-12-01

Socially learned signals and behaviors are found throughout the animal kingdom often show striking variation within species over space time. However, extent to which this cultural diversity is generated by demographic factors such as immigration dispersal has proved difficult investigate remains largely untested in a natural setting. Focusing on 14 different local neighborhoods wild population of great tits Parus major, we examined relationship between individual movements 7-year period...

10.1093/beheco/aru047 article EN Behavioral Ecology 2014-01-01

<h3>Objective</h3> A recent large-scale study in multiple sclerosis (MS) using the ImmunoChip platform reported on 11 loci that showed suggestive genetic association with MS. Additional data sufficiently sized and independent sets are needed to assess whether these represent genuine MS risk factors. <h3>Methods</h3> The lead SNPs of all were genotyped 10 796 cases 793 controls from Germany, Spain, France, Netherlands, Austria Russia, previously cohorts. Association analyses performed...

10.1136/jmedgenet-2015-103442 article EN Journal of Medical Genetics 2015-10-16
Coming Soon ...