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E

Elena Gardella

Danish Epilepsy Center

43H-index
246Paper Count
7.1KCitation Count
Published Papers 81
Publication Date
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Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep: Pathophysiological insights and treatment options
errEpilepsia
IF6.6
err2026-04-28
err0
PREAI
errNicola Specchio; Stéphane Auvin; Andreas Brunklaus; Valentina De Giorgis; Valentina Di Micco; Elena Gardella; Floor E. Jansen; Rima Nabbout; Chiara Pepi; Guido Rubboli; Marina Trivisano; Paolo Curatolo
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Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies
errEpilepsia
IF6.6
err2026-04-02
err0
errOAAI
errSopio Gverdtsiteli; Sebastian Ortiz; Tobias Brünger; Francesca Furia; Carmen Barba; Trine Bjørg-Hammer; Ingo Borggraefe; Roberto Caraballo; Sebahattin Cirak; Alberto Espeche; Walid Fazeli; Renzo Guerrini; Matias Juanes; Karin Kassahn; Maria Kinali; Johannes Krämer; Judith Kröll; Maria Concepción Miranda Herrero; Renske Oegema; Katrin Ounap; Oscar Peñuela; Konrad Platzer; Asuri Narayan Prasad; Aurora Pujol; Karit Reinson; Alfonso Represa; Eugenia Roza; Gabriela Reyes Valenzuela; Agustí Rodríguez-Palmero; Suzanne Sallevelt; Maria Iciar Sanchez-Albiusa; Ingrid E. Scheffer; Cory Smid; Carl E. Stafstrom; Eva-Lena Stattin; Jen R. Suarez; Steffen Syrbe; Kette D. Valente; Matias Wagner; Saskia Wortmann; Elena Gardella; Dennis Lal; Andreas Brunklaus; Rikke S. Møller
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Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants
errEpilepsia
IF0
err2026-01-28
err0
errOAAI
errSebastian Ortiz; Leonardo Affronte; Chiara Bagliani; Serene El-Kamand; Anthony Sze Hon Kan; Isabel T. Kristoffersen; Rebekka S. Dahl; Anne F. Højte; Stéphane Auvin; Arjan Bouman; Shimriet Zeidler; Gerhard Kluger; Gaetan Lesca; Nicolas Chatron; Zeynep Goke-Samar; Maria T. Papadopoulou; Matthildi Athina Papathanasiou Terzi; Elise Schaefer; Anne de Saint Martin; Sarah Baer; Mohammed Al Owain; Saud Takroni; Hesham Al-Dhalaan; Paolo Bonanni; Alessandra Rossi; Nicoletta Zanotta; Marina Trivisano; Nicola Specchio; Angela de Dominicis; Pasquale Striano; Alessandro Orsini; Maria Margherita Mancardi; Sebastian Neuens; Melanie Jennesson-Lyver; Ira Benkel-Herrenbrueck; David Genevieve; Richard Sidlow; Kamer Tezcan; Ilona Krey; Johannes R. Lemke; Konrad Platzer; Damien Lederer; Inga Talvik; Ulvi Vaher; Kees P. J. Braun; Anne-Marie Guerrot; Rebecca More; Matthias De Wachter; Sarah Weckhuysen; Evelina Carapancea; Maria Roberta Cilio; Julia Jacobs; Katalin Sterbova; Simona Balestrini; Renzo Guerrini; Giulio Peroni; Inger-Lise Mero; Walaa ElNaggar; Nour Elkhateeb; Ariane Schmetz; Denise L. Chan; Ghayda M. Mirzaa; Boris Chaumette; Adrien Legrand; Amy McTague; Tommy Stödberg; Rebekah V. Harris; Samuel F. Berkovic; Ingrid E. Scheffer; Mary Chebib; Elena Gardella; Philip K. Ahring; Nathan L. Absalom; Rikke S. Møller
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Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans
errNature Communications
IF15.7
err2026-01-13
err0
errOAAI
errClaudia M. Bonardi; Rikke S. Møller; Nuria Ruiz-Reig; Guoliang Chai; Camilla G. Madsen; Allan Bayat; Trine B. Hammer; Christina D. Fenger; Elena Gardella; Pawel Gawlinski; Mateusz Dawidziuk; Wojciech Wiszniewski; Monika Bekiesinska-Figatowska; Sara Cabet; Massimiliano Rossi; Gaetan Lesca; Evan Gouy; Birgit Jepsen; Tomasz S. Mieszczanek; Rossana Sanchez Russo; Eileen E. Barr; Katrin Õunap; Pilvi Ilves; Monica H. Wojcik; Mohamed Aittaleb; Klaus Brusgaard; Fadel Tissir; Guido Rubboli
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Differential outcomes in familial and sporadic SCN8A self-limited infantile epilepsies: Insights from a large international registry
errEpilepsia
IF6.6
err2025-08-18
err0
PREAI
errFrancesca Furia; Sopio Gverdtsiteli; Wibke Janzarik; Christian Korff; Gaetan Lesca; Maria Margherita Mancardi; Martino Montomoli; Marina Nikanorova; Romina Romaniello; Guido Rubboli; Steffen Syrbe; Federico Vigevano; Rikke S. Møller; Elena Gardella
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Unmasking the role of the occipital lobe in epilepsy with eyelid myoclonia
errEpilepsia
IF6.6
err2025-06-13
err0
errOAAI
errEmilia Ricci; Tomasz Stanislaw Mieszczanek; Monica Zilmer; Katarzyna Cebula; Stefan Juhl; Marina Nikanorova; Katarzyna Maria Mieszczanek; Marianne Søndergaard Khinchi; Britta Inga Ulfsdotter Hesslow; Kristin Siølie Thygesen; Charlotte Reinhardt Pedersen; Kern Olofsson; Stephan Wüstenhagen; Rikke S Møller; Guido Rubboli; Sándor Beniczky; Elena Gardella
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Variants in ATP6V0C are associated with Dravet-like developmental and epileptic encephalopathy
errEpilepsia
IF6.6
err2025-03-14
err0
errOAAI
errMarlene Rong; Paula T. Marques; Quratulain Zulfiqar Ali; Ricardo Morcos; Ilakkiah Chandran; Farah Qaiser; Rikke S. Møller; Allan Bayat; Guido Rubboli; Elena Gardella
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errSave
The epilepsy-autism phenotype associated with developmental and epileptic encephalopathies: New mechanism-based therapeutic options
errEPILEPSIA
IF6.6
err2025-02-22
err0
PREAI
errSpecchio, Nicola; Di Micco, Valentina; Aronica, Eleonora; Auvin, Stephane; Balestrini, Simona; Brunklaus, Andreas; Gardella, Elena; Scheper, Mirte; Taglialatela, Maurizio; Trivisano, Marina; Curatolo, Paolo
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Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy
errEPILEPSIA
IF6.6
err2025-01-15
err0
PREAI
errGjerulfsen, Cathrine E.; Oudin, Madeleine J.; Furia, Francesca; Gverdtsiteli, Sopio; Landmark, Cecilie Johannessen; Trivisano, Marina; Balestrini, Simona; Guerrini, Renzo; Aledo-Serrano, Angel; Morcos, Ricardo; Previtali, Roberto; Veggiotti, Pierangelo; Ricci, Emilia; Rubboli, Guido; Gardella, Elena; Moller, Rikke S.
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Quantitative EEG biomarkers for STXBP1-related disorders
errEPILEPSIA
IF6.6
err2024-10-28
err0
errOAAI
errCossu, Alberto; Furia, Francesca; Proietti, Jacopo; Ancora, Caterina; Reale, Chiara; Darra, Francesca; Previtali, Roberto; Bernardina, Bernardo Dalla; Rubboli, Guido; Beniczky, Sandor; Moller, Rikke S.; Cantalupo, Gaetano; Gardella, Elena
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Epilepsy as a Novel Phenotype of BPTF-Related Disorders
errPEDIATRIC NEUROLOGY
IF2.1
err2024-09-01
err2
PREAI
errFerretti, Alessandro; Furlan, Margherita; Glinton, Kevin E.; Fenger, Christina D.; Boschann, Felix; Amlie-Wolf, Louise; Zeidler, Shimriet; Moretti, Raffaella; Stoltenburg, Corinna; Tarquinio, Daniel C.; Furia, Francesca; Parisi, Pasquale; Rubboli, Guido; Devinsky, Orrin; Mignot, Cyril; Gripp, Karen W.; Moller, Rikke S.; Yang, Yaping; Stankiewicz, Pawel; Gardella, Elena
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errSave
Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy
errANNALS OF NEUROLOGY
IF7.7
err2024-08-23
err0
errOAAI
errQuiros, Vincent Moya; Adham, Ahmed; Convers, Philippe; Lesca, Gaetan; Mauguiere, Francois; Soulier, Hugo; Arzimanoglou, Alexis; Bayat, Allan; Braakman, Hilde; Camdessanche, Jean-Philippe; Casenave, Philippe; Chaton, Laurence; Chaix, Yves; Chochoi, Maxime; Depienne, Christel; Desportes, Vincent; De Ridder, Jessie; Dinkelacker, Vera; Gardella, Elena; Kluger, Gerhard J.; Jung, Julien; Martin, Martine Lemesle; Mancardi, Maria Margherita; Mueller, Markus; Poulat, Anne-Lise; Platzer, Konrad; Roubertie, Agathe; Stokman, Marijn F.; Vulto-van Silfhout, Anneke T.; Wiegand, Gert; Mazzola, Laure
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Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants
errEPILEPSIA
IF6.6
err2024-07-02
err1
PREAI
errCuccurullo, Claudia; Irelli, Emanuele Cerulli; Ugga, Lorenzo; Riva, Antonella; D'Amico, Alessandra; Cabet, Sara; Lesca, Gaetan; Bilo, Leonilda; Zara, Federico; Iliescu, Catrinel; Barca, Diana; Fung, France; Helbig, Katherine; Ortiz-Gonzalez, Xilma; Schelhaas, Helenius J.; Willemsen, Marjolein H.; van der Linden, Inge; Canafoglia, Laura; Courage, Carolina; Gommaraschi, Samuele; Gonzalez-Alegre, Pedro; Bardakjian, Tanya; Syrbe, Steffen; Schuler, Elisabeth; Lemke, Johannes R.; Vari, Stella; Roende, Gitte; Bak, Mads; Huq, Mahbulul; Powis, Zoe; Johannesen, Katrine M.; Hammer, Trine Bjorg; Moller, Rikke S.; Rabin, Rachel; Pappas, John; Zupanc, Mary L.; Zadeh, Neda; Cohen, Julie; Naidu, Sakkubai; Krey, Ilona; Saneto, Russell; Thies, Jenny; Licchetta, Laura; Tinuper, Paolo; Bisulli, Francesca; Minardi, Raffaella; Bayat, Allan; Villeneuve, Nathalie; Molinari, Florence; Dafsari, Hormos Salimi; Moller, Birk; Le Roux, Marie; Houdayer, Clara; Vecchi, Marilena; Mammi, Isabella; Fiorini, Elena; Proietti, Jacopo; Ferri, Sofia; Cantalupo, Gaetano; Battaglia, Domenica Immacolata; Gambardella, Maria Luigia; Contaldo, Ilaria; Brogna, Claudia; Trivisano, Marina; De Dominicis, Angela; Bova, Stefania Maria; Gardella, Elena; Striano, Pasquale; Coppola, Antonietta
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Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A-related epilepsy and/or neurodevelopmental disorders
errEPILEPSIA
IF6.6
err2024-05-27
err4
errOAAI
errConecker, Gabrielle; Xia, Maya Y.; Hecker, JayEtta; Achkar, Christelle; Cukiert, Cristine; Devries, Seth; Donner, Elizabeth; Fitzgerald, Mark P.; Gardella, Elena; Hammer, Michael; Hegde, Anaita; Hu, Chunhui; Kato, Mitsuhiro; Luo, Tian; Schreiber, John M.; Wang, Yi; Kooistra, Tammy; Oudin, Madeleine; Waldrop, Kayla; Youngquist, J. Tyler; Zhang, Dennis; Wirrell, Elaine; Perry, M. Scott
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errSave
Global modified-Delphi consensus on comorbidities and prognosis of SCN8A-related epilepsy and/or neurodevelopmental disorders
errEPILEPSIA
IF6.6
err2024-05-27
err6
errOAAI
errConecker, Gabrielle; Xia, Maya Y.; Hecker, JayEtta; Achkar, Christelle; Cukiert, Cristine; Devries, Seth; Donner, Elizabeth; Fitzgerald, Mark; Gardella, Elena; Hammer, Michael; Hegde, Anaita; Hu, Chunhui; Kato, Mitsuhiro; Luo, Tian; Schreiber, John M.; Wang, Yi; Kooistra, Tammy; Oudin, Madeleine; Waldrop, Kayla; Youngquist, J. Tyler; Zhang, Dennis; Wirrell, Elaine; Perry, M. Scott
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errSave
Developmental epileptic encephalopathy in DLG4-related synaptopathy
errEPILEPSIA
IF6.6
err2024-02-29
err1
errOAAI
errKassabian, Benedetta; Levy, Amanda M.; Gardella, Elena; Aledo-Serrano, Angel; Ananth, Amitha L.; Brea-Fernandez, Alejandro J.; Caumes, Roseline; Chatron, Nicolas; Dainelli, Alice; De Wachter, Matthias; Denomme-Pichon, Anne-Sophie; Dye, Thomas J.; Fazzi, Elisa; Felt, Roxanne; Fernandez-Jaen, Alberto; Fernandez-Prieto, Montse; Gantz, Emily; Gasperowicz, Piotr; Gil-Nagel, Antonio; Gomez-Andres, David; Greiner, Hansel M.; Guerrini, Renzo; Haanpaeae, Maria K.; Helin, Minttu; Hoyer, Juliane; Hurst, Anna C. E.; Kallish, Staci; Karkare, Shefali N.; Khan, Amjad; Kleinendorst, Lotte; Koch, Johannes; Kothare, Sanjeev V.; Koudijs, Suzanna M.; Lagae, Lieven; Lakeman, Phillis; Leppig, Kathleen A.; Lesca, Gaetan; Lopergolo, Diego; Lusk, Laina; Mackenzie, Alex; Mei, Davide; Moller, Rikke S.; Pereira, Elaine M.; Platzer, Konrad; Quelin, Chloe; Revah-Politi, Anya; Rheims, Sylvain; Rodriguez-Palmero, Agusti; Rossi, Andrea; Santorelli, Filippo; Seinfeld, Syndi; Sell, Erick; Stephenson, Donna; Szczaluba, Krzysztof; Trinka, Eugen; Umair, Muhammad; Van Esch, Hilde; van Haelst, Mieke M.; Veenma, Danielle C. M.; Weber, Sacha; Weckhuysen, Sarah; Zacher, Pia; Tuemer, Zeynep; Rubboli, Guido
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Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
errEBIOMEDICINE
IF10.8
err2023-12-01
err5
errOAAI
errLyu, Hang; Bosselmann, Christian M.; Johannesen, Katrine M.; Koko, Mahmoud; Ortigoza-Escobar, Juan Dario; Aguilera-Albesa, Sergio; Nunez, Deyanira Garcia -Navas; Linnankivi, Tarja; Gaily, Eija; Ruiten, Henriette J. A. van; Richardson, Ruth; Betzler, Cornelia; Horvath, Gabriella; Brilstra, Eva; Geerdink, Niels; Orsucci, Daniele; Tessa, Alessandra; Gardella, Elena; Fleszar, Zofia; Schoels, Ludger; Lerche, Holger; Moller, Rikke S.; Liu, Yuanyuan
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GABRA1-Related Disorders: From Genetic to Functional Pathways
errANNALS OF NEUROLOGY
IF7.7
err2023-10-20
err7
errOAAI
errMusto, Elisa; Liao, Vivian W. Y.; Johannesen, Katrine M.; Fenger, Christina D.; Lederer, Damien; Kothur, Kavitha; Fisk, Katrina; Bennetts, Bruce; Vrielynck, Pascal; Delaby, Delphine; Ceulemans, Berten; Weckhuysen, Sarah; Sparber, Peter; Bouman, Arjan; Ardern-Holmes, Simone; Troedson, Christopher; Battaglia, Domenica I.; Goel, Himanshu; Feyma, Timothy; Bakhtiari, Somayeh; Tjoa, Linda; Boxill, Martin; Demina, Nina; Shchagina, Olga; Dadali, Elena; Kruer, Michael; Cantalupo, Gaetano; Contaldo, Ilaria; Polster, Tilman; Isidor, Bertrand; Bova, Stefania M.; Fazeli, Walid; Wouters, Leen; Miranda, Maria J.; Darra, Francesca; Pede, Elisa; Le Duc, Diana; Jamra, Rami Abou; Kury, Sebastien; Proietti, Jacopo; Mcsweeney, Niamh; Brokamp, Elly; Andrews, Peter Ian; Gouray Garcia, Marie; Chebib, Mary; Moller, Rikke S.; Ahring, Philip K.; Gardella, Elena
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Vinpocetine improved neuropsychiatric and epileptic outcomes in a patient with a GABRA1 loss-of-function variant
errANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
IF3.9
err2023-07-11
err4
errOAAI
errGjerulfsen, Cathrine E.; Mieszczanek, Tomasz S.; Johannesen, Katrine M.; Liao, Vivian W. Y.; Chebib, Mary; Norby, Helene A. J.; Gardella, Elena; Rubboli, Guido; Ahring, Philip; Moller, Rikke S.
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IRF2BPL as a novel causative gene for progressive myoclonus epilepsy
errEPILEPSIA
IF6.6
err2023-06-08
err7
errOAAI
errGardella, Elena; Michelucci, Roberto; Christensen, Hanne M.; Fenger, Christina D.; Reale, Chiara; Riguzzi, Patrizia; Pasini, Elena; Albini-Riccioli, Luca; Papa, Valentina; Foschini, Maria Pia; Cenacchi, Giovanna; Furia, Francesca; Marjanovic, Dragan; Hammer, Trine B.; Moller, Rikke S.; Rubboli, Guido
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Research Directions

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Co-authors
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