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Sarah Weckhuysen

VIB

70H-index
250Paper Count
1.5WCitation Count
Published Papers 128
Publication Date
Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal cultures
err2026-04-09
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errNina Dirkx; Bob Asselbergh; Peter Verstraelen; Jonas Van Lent; Els De Vriendt; Vincent Timmerman; Winnok H. De Vos; Sarah Weckhuysen
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Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
err2026-01-07
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errJohannes R. Lemke; Andrea Eoli; Ilona Krey; Bernt Popp; Vincent Strehlow; Dirk A. Wittekind; Anna-Leena Vuorinen; Hesham M. Aldhalaan; Sarah Baer; Anne de Saint Martin; Trine B. Hammer; Isabella Herman; Frauke Hornemann; Trine Ingebrigtsen; Damien Lederer; Gaetan Lesca; Dana Marafie; Mikael Mathot; Jill A. Rosenfeld; Rikke S. Møller; Helenius J. Schelhaas; Chelsey Stillman; Alessandro Orsini; Anup D. Patel; Juliette Piard; Pierangelo Veggiotti; Danique R. M. Vlaskamp; Sarah Weckhuysen; Stephen F. Traynelis; Tim A. Benke; Henrike O. Heyne; Steffen Syrbe
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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
err2025-11-10
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errGhayda M. Mirzaa; Keqin Yan; Raissa Relator; Mathieu Levesque; Pranisha Jayasinghe; Sara Timpano; Binnaz Yalcin; Stephan Collins; Alban Ziegler; Emily Pao; Nora Oyama; Elise Brischoux-Boucher; Juliette Piard; Kristin G. Monaghan; Maria. J. Guillen Sacoto; William B. Dobyns; Kristen L. Park; Daniel Martin Fernández-Mayoralas; Alberto Fernández-Jaén; Parul Jayakar; María Palomares-Bralo; Fernando Santos-Simarro; Alfredo Brusco; Vincenzo Antona; Elisa Giorgio; Malin Kvarnung; Bertrand Isidor; Solène Conrad; Benjamin Cogné; Wallid Deb; Kyra E. Stuurman; Katalin Štěrbová; Noor Smal; Sarah Weckhuysen; Renske Oegema; A. Micheil Innes; Daniel. C. Koboldt; Tawfeg Ben-Omran; Rebecca C. Yeh; Michael C. Kruer; Somayeh Bakhtiari; Antigone Papavasiliou; Sébastien Moutton; Sophie Nambot; Sirisak Chanprasert; Sarah A. Paolucci; Kait Miller; Barbara Burton; Katherine Kim; Emily O’Heir; Zandre Bruwer; Kirsten. A. Donald; Tjitske Kleefstra; Amy Goldstein; Brad Angle; Kelly Bontempo; Peter Miny; Pascal Joset; Florence Demurger; Emma Hobson; Lewis Pang; Lori Carpenter; Dong Li; Dominique Bonneau; Bekim Sadikovic; David J. Picketts
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Investigating HLA haplotypes as a potential risk factor for nodding syndrome: A case-control study in the Mahenge area, Tanzania
err2025-11-01
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PREAI
errHadermann, Amber; Bhwana, Dan; Mhina, Athanas D.; Amaral, Luis-Jorge; Fodjo, Joseph N. Siewe; Emonds, Marie-Paule; Weckhuysen, Sarah; Mmbando, Bruno P.; Colebunders, Robert
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Imaging brain development in a KCNQ2-developmental and epileptic encephalopathy mouse model: identifying early biomarkers for functional and structural brain changes
err2025-10-25
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errCharissa Millevert; Nicholas Vidas-Guscic; Mohit H. Adhikari; Alan Miranda; Liesbeth Vanherp; Laurent Villard; Elisabeth Jonckers; Philippe Joye; Johan Van Audekerke; Ignace Van Spilbeeck; Els De Vriendt; Marleen Verhoye; Steven Staelens; Daniele Bertoglio; Sarah Weckhuysen
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GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
err2025-10-14
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errJohannes R. Lemke; Andrea Eoli; Ilona Krey; Bernt Popp; Vincent Strehlow; Dirk A. Wittekind; Anna-Leena Vuorinen; Hesham M. Aldhalaan; Sarah Baer; Anne de Saint Martin; Trine B. Hammer; Isabella Herman; Frauke Hornemann; Trine Ingebrigtsen; Damien Lederer; Gaetan Lesca; Dana Marafie; Mikael Mathot; Jill A. Rosenfeld; Rikke S. Møller; Helenius J. Schelhaas; Chelsey Stillman; Alessandro Orsini; Anup D. Patel; Juliette Piard; Pierangelo Veggiotti; Danique R. M. Vlaskamp; Sarah Weckhuysen; Stephen F. Traynelis; Tim A. Benke; Henrike O. Heyne; Steffen Syrbe
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KV7.2 channel dysfunction delays neuronal maturation and undermines early network development in a hiPSC model of KCNQ2-DEE
err2025-09-23
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errFilip Rosa; Stephan Theiss; Susanne Krepp; Heidi Loeffler; Dulini C. Mendis; Stefanie Klingenstein; Stefan Liebau; Sarah Weckhuysen; Michael Alber; Steven Petrou; Holger Lerche; Snezana Maljevic; Thomas V. Wuttke
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Altered cardiac excitability and arrhythmia in models of SCN1B-linked developmental and epileptic encephalopathy
err2025-09-09
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errRamos-Mondragon, Roberto; Wang, Shuyun; Edokobi, Nnamdi; Liu, Qinghua; Qiao, Xiaotan; Shih, Maya; Dang, Louis T.; Tsan, Yao-Chang; Sterbova, Katalin; Helms, Adam S.; Weckhuysen, Sarah; Lopez-Santiago, Luis F.; Parent, Jack M.; Isom, Lori L.
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Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes
err2025-08-26
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PREAI
errCristina T. Vicente; Tejasvi Niranjan; Elise Coopman; Júlia Faura; Sara Alidadiani; Claudia Schrauwen; Billie J. Matchett; Bavo Heeman; Marleen Van den Broeck; Wouter De Coster; Thuy Nguyen; Julie S. Lau; Saurabh Baheti; Tim de Pooter; Peter De Rijk; Mojca Strazisar; Matt Baker; Mariely DeJesus-Hernandez; NiCole A. Finch; Cyril Pottier; Marka van Blitterswijk; Yan Asmann; Melissa E. Murray; Leonard Petrucelli; Andrew King; Claire Troakes; Safa Al-Sarraj; Robert A. Rissman; Annie Hiniker; Margaret Flanagan; Bret M. Evers; Charles L. White; Carlos Cruchaga; Rudolph Castellani; Jeroen G.J. van Rooij; Merel O. Mol; Harro Seelaar; John C. van Swieten; Björn Oskarsson; Robert Ross Reichard; Aivi T. Nguyen; Keith A. Josephs; Ronald C. Petersen; Nilüfer Ertekin-Taner; Bradley F. Boeve; Neill R. Graff-Radford; Sarah Weckhuysen; Dennis W. Dickson; Rosa Rademakers
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SUDEP risk is influenced by longevity genomics: a polygenic risk score study
err2025-07-28
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errHelena Martins; James D. Mills; Susanna Pagni; Medine I. Gulcebi; Angeliki Vakrinou; Patrick B. Moloney; Lisa M. Clayton; Ravishankara Bellampalli; Hannah Stamberger; Sarah Weckhuysen; Pasquale Striano; Federico Zara; Richard D. Bagnall; Rebekah V. Harris; Kate M. Lawrence; Lynette G. Sadleir; Douglas E. Crompton; Daniel Friedman; Juliana Laze; Ling Li; Samuel F. Berkovic; Christopher Semsarian; Ingrid E. Scheffer; Orrin Devinsky; Karoline Kuchenbaecker; Simona Balestrini; Sanjay M. Sisodiya
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The fast-dissociating D2 antagonist antipsychotic JNJ-37822681 is a neuronal Kv7 channel opener: Potential repurposing for epilepsy treatment
err2025-07-23
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errLidia Carotenuto; Oliver Keminer; Giusy Carleo; Andrea Zaliani; Antonio Leo; Rita Citraro; Giovambattista De Sarro; Nina Dirkx; Marcus Kaji; Sarah Weckhuysen; Jeanette Reinshagen; Vincenzo Barrese; Natascia Guida; Carmine Ostacolo; Francesco Miceli; Philip Gribbon; Maurizio Taglialatela
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Budget impact analysis of cenobamate, a novel adjunctive therapy for the treatment of drug resistant focal onset seizures, from the Belgian healthcare payer perspective
err2025-06-27
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errKristl Vonck; Olivier Bodart; Sarah Weckhuysen; Ann Tanghe; Britt Callebaut; Caroline Verdonck; Lynn Van den Bergh; Benjamin Legros
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The genetic and phenotypic spectrum of GABRB1-related disorders
errBrain
IF11.7
err2025-06-05
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errCharissa Millevert; Anthony Sze Hon Kan; Moritz Hanke; Mahmoud Koko; Maryam Erfanian Omidvar; Ulrike B S Hedrich; Thomas V Wuttke; Nina Barišić; Lieven Lagae; Ángel Aledo-Serrano; Eva-Maria Niehoff; Konrad Platzer; Pia Zacher; Tilman Polster; Robertino Dilena; Edoardo Monfrini; David Geneviève; Agathe Roubertie; Ange-Line Bruel; Frederic Tran Mau-Them; Majed Dasouki; Stacey Cohen; Ingo Helbig; Alicia G Harrison; Collin Ellis; Holly A Dubbs; Eric D Marsh; Sébastien Lebon; Na He; Heng Meng; Mary Chebib; Rikke S Møller; Carla Marini; Philip K Ahring; Holger Lerche; Sarah Weckhuysen
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Precision medicine in epilepsy: Clinicians' perspectives from an international qualitative study
err2025-05-24
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PREAI
errMatthias De Wachter; Anne Juul; Annelies Colliers; Berten Ceulemans; Sarah Weckhuysen; Anna C. Jansen; Rikke S. Møller
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Tracking brain maturation in vivo: functional connectivity, white matter integrity, and synaptic density in developing mice
err2025-05-01
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PREAI
errMillevert, Charissa; Vidas-Guscic, Nicholas; Adhikari, Mohit H.; Miranda, Alan; Vanherp, Liesbeth; Jonckers, Elisabeth; Joye, Philippe; Van Audekerke, Johan; Van Spilbeeck, Ignace; Verhoye, Marleen; Staelens, Steven; Bertoglio, Daniele; Weckhuysen, Sarah
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ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias
err2025-05-01
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PREAI
errMoya-Mendez, Mary E.; Bidzimou, Minu-Tshyeto; Muralidharan, Padmapriya; Zhang, Zhushan; Ezekian, Jordan E.; Perelli, Robin M.; Parker, Lauren E.; Prange, Lyndsey; Boggs, April; Kim, Jeffrey J.; Howard, Taylor S.; Word, Tarah A.; Wehrens, Xander H. T.; Reyes Valenzuela, Gabriela; Caraballo, Roberto; Garone, Giacomo; Vigevano, Federico; Weckhuysen, Sarah; Millevert, Charissa; Troncoso, Monica; Matamala, Mario; Sisodiya, Sanjay M.; Poole, Josephine; Zucca, Claudio; Panagiotakaki, Eleni; Tchaicha, Sebile; Zawadzka, Marta; Mazurkiewicz-Beldzinska, Maria; Fons, Carmen; Anticona, Jennifer; De Grandis, Elisa; Cordani, Ramona; Pisciotta, Livia; Groppa, Sergiu; Paryjas, Sandra; Ragona, Francesca; Mangia, Elena; Granata, Tiziana; Megvinov, Andrey; Pavlicek, Mirjana; Ess, Kevin; Simmons, Christine Q.; George Jr, Alfred L.; Vavassori, Rosaria; Mikati, Mohamad A.
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Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study
err2025-02-17
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errDe Wachter, Matthias; Millevert, Charissa; Nicolai, Joost; Cats, Elisabeth; Kluger, Gerhard; Milh, Mathieu; Cloarec, Robin; Syrbe, Steffen; Arts, Katrijn; Jansen, Katrien; Krygier, Magdalena; Smigiel, Robert; Auvin, Stephane; Olofson, Kern; Gjerulfsen, Cathrine Elisabeth; Ceulemans, Berten; Moller, Rikke S.; Bayat, Allan; Weckhuysen, Sarah
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Fibroblast transcriptomics uncovers pathogenic genomic variants in individuals with exome-negative childhood onset epilepsy
err2025-01-29
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PREAI
errSmal, Noor; Millevert, Charissa; De Wachter, Matthias; De Vriendt, Els; Eddafir, Zakaria; Schoonjans, An-Sofie; Bayat, Allan; Moller, Rikke Steensbjerre; Mei, Davide; Balestrini, Simona; Guerrini, Renzo; Meeuwissen, Marije E. C.; Jansen, Anna C.; Weckhuysen, Sarah
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Heterozygous Missense Variants in the ATPase Phospholipid Transporting 9A Gene, ATP9A, Alter Dendritic Spine Maturation and Cause Dominantly Inherited Nonsyndromic Intellectual Disability
err2025-01-01
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errCordovado, Amelie; Herenger, Yvan; Cormier, Coline; Lopez-Martin, Estrella; Stamberger, Hannah; Faivre, Laurence; Denomme-Pichon, Anne-Sophie; Vitobello, Antonio; Abdallah, Hamza Hadj; Barcia, Giulia; Courtin, Thomas; Martinez-Delgado, Beatriz; Bermejo-Sanchez, Eva; Barrero, Maria J.; Gasser, Brooklynn; Bezieau, Stephane; Kury, Sebastien; Weckhuysen, Sarah; Laumonnier, Frederic; Toutain, Annick; Vuillaume, Marie-Laure
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Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2- developmental encephalopathy
err2024-11-27
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PREAI
errNappi, Mario; Alberini, Giulio; Berselli, Alessandro; Roscioni, Agnese; Soldovieri, Maria Virginia; Servettini, Ilenio; Barrese, Vincenzo; Weckhuysen, Sarah; Chiu, Ting-Gee Annie; Scheffer, Ingrid E.; Benfenati, Fabio; Maragliano, Luca; Miceli, Francesco; Taglialatela, Maurizio
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