Remi Stevelink
Utrecht University
24 Papers
10 Citations
Remi Stevelink is an academic researcher from Utrecht University. The author has contributed to research in topics: Epilepsy & Medicine. The author has an hindex of 8, co-authored 18 publications. Previous affiliations of Remi Stevelink include University of Michigan.
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Papers
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Bassel Abou-Khalil,Pauls Auce,Andreja Avbersek,Melanie Bahlo,David J. Balding,Thomas Bast,Larry Baum,Albert J. Becker,Felicitas Becker,Bianca Berghuis,Samuel F. Berkovic,Katja E. Boysen,Jonathan P. Bradfield,Lawrence C. Brody,Russell J. Buono,Ellen Campbell,Gregory D. Cascino,Claudia B. Catarino,Gianpiero L. Cavalleri,Stacey S. Cherny,Krishna Chinthapalli,Alison J. Coffey,Alastair Compston,Antonietta Coppola,Patrick Cossette,John Craig,Gerrit-Jan de Haan,Peter De Jonghe,Carolien G.F. de Kovel,Norman Delanty,Chantal Depondt,Orrin Devinsky,Dennis J. Dlugos,Colin P. Doherty,Christian E. Elger,Johan G. Eriksson,Thomas N. Ferraro,Martha Feucht,Ben Francis,Andre Franke,Jacqueline A. French,Saskia Freytag,Verena Gaus,Eric B. Geller,Christian Gieger,Tracy A. Glauser,Simon Glynn,David Goldstein,Hongsheng Gui,Youling Guo,Kevin Haas,Hakon Hakonarson,Kerstin Hallmann,Sheryl R. Haut,Erin L. Heinzen,Ingo Helbig,Christian Hengsbach,Helle Hjalgrim,Michele Iacomino,Andres Ingason,Jennifer Jamnadas-Khoda,Marvin Johnson,Reetta Kälviäinen,Anne-Mari Kantanen,Dalia Kasperaviciute,Dorothée G.A. Kasteleijn-Nolst Trenité,Heidi E. Kirsch,Robert C. Knowlton,Bobby P. C. Koeleman,Roland Krause,Martin Krenn,Wolfram S. Kunz,Ruben Kuzniecky,Patrick Kwan,Dennis Lal,Yu-Lung Lau,Anna-Elina Lehesjoki,Holger Lerche,Costin Leu,Wolfgang Lieb,Dick Lindhout,Warren D. Lo,Iscia Lopes-Cendes,Daniel H. Lowenstein,Alberto Malovini,Anthony G Marson,Thomas U. Mayer,Mark McCormack,James L. Mills,Nasir Mirza,Martina Moerzinger,Rikke S. Møller,Anne M. Molloy,Hiltrud Muhle,Mark R Newton,Ping-Wing Ng,Markus M. Noethen,Peter Nuernberg,Terence J. O'Brien,Karen Oliver,Aarno Palotie,Faith Pangilinan,Sarah Peter,Slavé Petrovski,Annapurna Poduri,Michael Privitera,Rodney A. Radtke,Sarah Rau,Philipp S. Reif,Eva M. Reinthaler,Felix Rosenow,Josemir W. Sander,Thomas Sander,Theresa Scattergood,Steven C. Schachter,Christoph J. Schankin,Ingrid E. Scheffer,Bettina Schmitz,Susanne Schoch,Pak C. Sham,Jerry J. Shih,Graeme J. Sills,Sanjay M. Sisodiya,Lisa Slattery,Alexander R. H. Smith,David F. Smith,Mike Smith,Philip E. M. Smith,Anja C M Sonsma,Doug Speed,Michael R. Sperling,Bernhard J. Steinhoff,Ulrich Stephani,Remi Stevelink,Konstantin Strauch,Pasquale Striano,H. Stroink,Rainer Surges,K. Meng Tan,Liu Lin Thio,G. Neil Thomas,Marian Todaro,Rossana Tozzi,Maria Stella Vari,Eileen P.G. Vining,Frank Visscher,Sarah von Spiczak,Nicole M. Walley,Yvonne G. Weber,Zhi Wei,Judith L.Z. Weisenberg,Christopher D. Whelan,Peter Widdess-Walsh,Markus Wolff,Stefan Wolking,Wanling Yang,Federico Zara,Fritz Zimprich,Int League Against Epilepsy Conso +158 more
TL;DR: The authors perform genome-wide association studies for 3 broad and 7 subtypes of epilepsy and identify 16 loci - 11 novel - that are further annotated by eQTL and partitioned heritability analyses that provide leads for epilepsy therapies based on underlying pathophysiology.
Polygenic burden in focal and generalized epilepsies
Costin Leu,Costin Leu,Costin Leu,Remi Stevelink,Alexander W Smith,Slavina B. Goleva,Masahiro Kanai,Lisa Ferguson,Ciaran Campbell,Yoichiro Kamatani,Yukinori Okada,Sanjay M. Sisodiya,Gianpiero L. Cavalleri,Bobby P. C. Koeleman,Holger Lerche,Lara Jehi,Lea K. Davis,Imad Najm,Aarno Palotie,Aarno Palotie,Mark J. Daly,Mark J. Daly,Mark J. Daly,Robyn M. Busch,Dennis Lal +24 more
TL;DR: Using polygenic risk scores from a genome-wide association study in generalized and focal epilepsy, Leu et al. reveal a significantly higher genetic burden for epilepsy in multiple cohorts of people with epilepsy compared to population controls.
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink,Ciaran Campbell,Siwei Chen,Bassel Abou-Khalil,Oluyomi Modupe Adesoji,Zaid Afawi,Elisabetta Amadori,Alison Anderson,Joseph Anderson,Danielle M. Andrade,Grazia Annesi,P. Auce,Andreja Avbersek,Melanie Bahlo,M. Baker,Ganna Balagura,Simona Balestrini,Carmen Barba,Karen Barboza,Fabrice Bartolomei,Thomas Bast,Larry Baum,Tobias Baumgartner,Betül Baykan,Nerses Bebek,Albert J. Becker,F. Becker,Caitlin A. Bennett,B. Berghuis,Samuel F. Berkovic,Ahmad Beydoun,Claudio Bianchini,Francesca Bisulli,I. Blatt,Dheeraj Reddy Bobbili,Ingo Borggraefe,Christian Boßelmann,Vera Braatz,Jonathan P. Bradfield,Knut Brockmann,Lawrence C. Brody,Russell J. Buono,Robyn M. Busch,Hande Caglayan,Ellen Campbell,Laura Canafoglia,Christina Canavati,Gregory D. Cascino,Barbara Castellotti,Claudia B. Catarino,Gianpiero L. Cavalleri,Felecia Cerrato,Francine Chassoux,Stacey S. Cherny,Ching-Lung Cheung,Krishna Chinthapalli,I-Jun Chou,S. Chung,Claire Churchhouse,Peggy Clark,Andrew J. Cole,Alastair Compston,Antonietta Coppola,Mahgenn Cosico,Patrick Cossette,John Craig,Caroline N. Cusick,Mark J. Daly,Lea K. Davis,G. de Haan,Norman Delanty,Chantal Depondt,Philippe Derambure,Orrin Devinsky,L. Di Vito,Dennis J. Dlugos,Viola Doccini,Colin P. Doherty,Hany El-Naggar,Christian E. Elger,Colin A Ellis,Johan G. Eriksson,Annika Faucon,Yen-Chen A. Feng,Lisa Ferguson,Thomas N. Ferraro,Lorenzo Ferri,Martha Feucht,Mark Richard Fitzgerald,Beata Fonferko-Shadrach,Francesco Fortunato,Silvana Franceschetti,Andre Franke,Jacqueline A. French,Elena Freri,Monica Gagliardi,Antonio Gambardella,E. Geller,Tania Giangregorio,L. Gjerstad,Tracy A. Glauser,Ethan M. Goldberg,Alicia M. Goldman,Tiziana Granata,David A. Greenberg,Renzo Guerrini,Namrata Gupta,Kevin F. Haas,Hakon Hakonarson,Kerstin Hallmann,E. Hassanin,Manu Hegde,Erin L. Heinzen,Ingo Helbig,Christian Hengsbach,Henrike O. Heyne,Shinichi Hirose,E. C. Hirsch,H. Hjalgrim,Daniel P. Howrigan,Donald Hucks,Po-Cheng Hung,Michele Iacomino,Lukas L. Imbach,Yushi Inoue,Atsushi Ishii,J. Jamnadas‐Khoda,Lara Jehi,Michael R. Johnson,Reetta Kälviäinen,Yoichiro Kamatani,Moien Kanaan,Masahiro Kanai,Anne-Mari Kantanen,Bülent Kara,Symon M. Kariuki,Dalia Kasperaviciute,Dorothée G.A. Kasteleijn-Nolst Trenité,Mitsuhiro Kato,Josua Kegele,Yesim Kesim,N. Khoueiry-Zgheib,Chontelle King,Heidi E. Kirsch,Karl Martin Klein,Gerhard Kluger,Susanne Knake,Robert C. Knowlton,Bobby P. C. Koeleman,Amos D. Korczyn,Andreas M. Koupparis,Ioanna Kousiappa,Roland Krause,Martin Krenn,Heinz Eric Krestel,Ilona Krey,Wolfram S. Kunz,Mitja I. Kurki,Gerhard Kurlemann,Ruben Kuzniecky,Patrick Kwan,Angelo Labate,A. Lacey,Dennis Lal,Zied Landoulsi,Yu-Lung Lau,Stephen Lauxmann,Stephanie L. Leech,A. Lehesjoki,Johannes R. Lemke,Holger Lerche,Gaetan Lesca,Costin Leu,Naomi Lewin,David Lewis-Smith,Gloria H.-Y. Li,Qingqin S. Li,Laura Licchetta,Kuang-Lin Lin,D. Lindhout,Tarja Linnankivi,Iscia Lopes-Cendes,Daniel H. Lowenstein,C. Lui,Francesca Madia,Sigurdur Magnusson,Anthony G Marson,Patrick May,Chris M McGraw,Davide Mei,James L. Mills,Raffaella Minardi,Nasir Mirza,Rikke S. Møller,Anne M. Molloy,Martino Montomoli,Barbara Mostacci,Lorenzo Muccioli,Hiltrud Muhle,Karen Müller-Schlüter,Imad Najm,Wassim Nasreddine,Benjamin M. Neale,Bernd A. Neubauer,Charles R. Newton,Markus M. Nöthen,Michael Nothnagel,Peter Nürnberg,Terence J. O'Brien,Yukinori Okada,Elias Olafsson,Karen Oliver,Ciḡdem Özkara,Aarno Palotie,Faith Pangilinan,Savvas S. Papacostas,Elena Parrini,Carlos N. Pato,Michele T. Pato,Manuela Pendziwiat,Slavé Petrovski,William O. Pickrell,Rebecca Pinsky,Tommaso Pippucci,Annapurna Poduri,Federica Pondrelli,Robert Powell,Michael Privitera,Annika Rademacher,Rodney Radtke,Francesca Ragona,S. Rau,Mark I. Rees,Brigid M. Regan,Philipp S. Reif,Sylvain Rhelms,Antonella Riva,Felix Rosenow,Philippe Ryvlin,Anni Saarela,Lynette G. Sadleir,Josemir W. Sander,T. Sander,Marcello Scala,T. Scattergood,Steven C. Schachter,Christoph J. Schankin,Ingrid E. Scheffer,Bettina Schmitz,Susanne Schoch,Susanne Schubert-Bast,Andreas Schulze-Bonhage,Paolo Scudieri,Pak C. Sham,Beth Rosen Sheidley,Jerry J. Shih,Graeme J. Sills,Sanjay M. Sisodiya,Michael C Smith,Pete Smith,Anja C. M. Sonsma,Doug Speed,Michael R. Sperling,Hreinn Stefansson,Kari Stefansson,Bernhard J. Steinhoff,Ulrich Stephani,W. C. Stewart,Carlotta Stipa,Pasquale Striano,H. Stroink,Adam Strzelczyk,Rainer Surges,Toshimitsu Suzuki,K. Meng Tan,R. Taneja,George A. Tanteles,Erik Taubøll,Liu Lin Thio,G. Thomas,Rhys H. Thomas,Oskari Timonen,Paolo Tinuper,Maria Todaro,Pinar Topaloglu,R. Tozzi,M. Tsai,Birute Tumiene,Dilsad Turkdogan,Unnur Unnsteinsdottir,Algirdas Utkus,Priya Vaidiswaran,Luc Valton,Andreas van Baalen,Annalisa Vetro,E. Vining,Frank Visscher,Sophie von Brauchitsch,Randi von Wrede,Ryan G. Wagner,Yvonne G. Weber,Sarah Weckhuysen,Judith L.Z. Weisenberg,Michael Weller,Peter Widdess-Walsh,Markus Wolff,Stefan Wolking,David Wu,Kazuhiro Yamakawa,Wanling Yang,Zuhal Yapici,Emrah Yücesan,Sara Zagaglia,Felix Zahnert,Federico Zara,Fritz Zimprich,Gábor Zsurka,Quratulain Zulfiqar Ali +317 more
TL;DR: A multi-ancestry genome-wide association study including 29,944 cases, stratified into three broad categories and seven subtypes of epilepsy, and 52,538 controls identifies 26 genome- wide significant loci, 19 of which are specific to genetic generalized epilepsy (GGE).
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Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
Remi Stevelink,Dania Al-Toma,Floor E. Jansen,Herm J. Lamberink,Ali A. Asadi-Pooya,Mohsen Farazdaghi,Gonçalo Cação,Sita Jayalakshmi,Anuja Patil,Ciḡdem Özkara,Şenay Aydın,Joanna Gesche,Christoph P. Beier,Linda J. Stephen,Martin J. Brodie,Gopeekrishnan Unnithan,Ashalatha Radhakrishnan,Julia Höfler,Eugen Trinka,Roland Krause,Emanuele Cerulli Irelli,Carlo Di Bonaventura,Jerzy P. Szaflarski,Laura E. Hernández-Vanegas,Monica L. Moya-Alfaro,Yingying Zhang,Dong Zhou,Nicola Pietrafusa,Nicola Specchio,G. Japaridze,Sándor Beniczky,Mubeen Janmohamed,Patrick Kwan,Marte Syvertsen,Kaja Kristine Selmer,Bernd J. Vorderwülbecke,Martin Holtkamp,Lakshminarayanapuram Gopal Viswanathan,Sanjib Sinha,Betül Baykan,Ebru Altindag,Felix von Podewils,Juliane Schulz,Udaya Seneviratne,Alejandro Viloria-Alebesque,Ioannis Karakis,Wendyl D'Souza,Josemir W. Sander,Bobby P. C. Koeleman,Willem M. Otte,Kees P.J. Braun +50 more
TL;DR: This article performed an individual participant data (IPD) meta-analysis based on a systematic search in EMBASE and PubMed, including prospective and retrospective observational studies reporting on treatment outcomes of people diagnosed with juvenile myoclonic epilepsy and available seizure outcome data after a minimum one-year follow-up.
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Possibilities and Pitfalls of Social Media for Translational Medicine.
TL;DR: This perspective article describes how social media can be used for patient engagement, publicity, transparency, sharing of knowledge, and implementing findings in society and warns about the potential pitfalls of social media, which can cause research to be misinterpreted and false beliefs to be spread.