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Dennis Lal

cleveland clinic

56H指数
253论文数
9.7K被引数
收录论文 114
发表时间
Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy遗传性全身性癫痫患者中多基因风险评分与临床表型的相关性
err2026-09-10
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errOAAI
errSophie von Brauchitsch; Nils Hartung; Robin A. Karge; Bobby Koeleman; Samuel F. Berkovic; Danielle M. Andrade; Francesca Bisulli; Antonio Gambardella; Renzo Guerrini; Ingrid E. Scheffer; Ingo Helbig; Wolfram S. Kunz; Holger Lerche; Hiltrud Muhle; Christian Boßelmann; Savvas S. Papacostas; Mark I. Rees; Sanjay M. Sisodiya; Pasquale Striano; Lynnette Sadleir; Yvonne Weber; Dennis Lal; Costin Leu; Philipp S. Reif; Stefan Wolking; Felix Rosenow; Karl Martin Klein; for the Epi25 Collaborative
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Accurate prediction of gain- and loss-of-function missense variants in GABAA receptorsGABAA受体中增益和失活功能错义突变的准确预测
err2026-08-03
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errOAAI
errChristian M. Boßelmann; Sebastian Ortiz; Rebekka Dahl; Vivian W.Y. Liao; Serene El-Kamand; Susan X.N. Lin; Anthony Sze Hon Kan; Tobias Brünger; Dennis Lal; Holger Lerche; Jules Kreuer; Nico Pfeifer; Mary Chebib; Nathan L. Absalom; Philip K. Ahring; Rikke S. Møller
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Environmental and treatment-related factors associated with developmental outcomes in genetic epilepsies与遗传性癫痫发育结局相关的环境和治疗相关因素
err2026-07-31
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PREAI
errChristian M. Boßelmann; Natasha N. Ludwig; Calliope Holingue; Andres Jimenez-Gomez; Andrea Ganna; M. Scott Perry; Ana Arenivas; Dennis Lal
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The International Classification of Cognitive Disorders in Epilepsy (IC-CoDE) Portal: An open source resource for neuropsychological research in epilepsy癫痫认知障碍的国际分类(IC-CoDE)门户网站:癫痫神经心理学研究的一个开源资源
err2026-05-07
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errRobyn M. Busch; Tobias Brünger; Kayela Arrotta; Lisa Ferguson; Julie K. Janecek; Sara J. Swanson; Anny Reyes; Brook Hurd; Mark St. John; Carrie R. McDonald; Bruce P. Hermann; Dennis Lal
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Genome-wide association study of copy number variations in Parkinson’s disease帕金森病中全基因组拷贝数变异的关联研究
err2026-04-20
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errOAAI
errZied Landoulsi; Ashwin Ashok Kumar Sreelatha; Nicole Kuznetsov; Claudia Schulte; Dheeraj Reddy Bobbili; Ludovica Montanucci; Costin Leu; Lisa-Marie Niestroj; Emadeldin Hassanin; Cloé Domenighetti; Pierre-Emmanuel Sugier; Milena Radivojkov-Blagojevic; Peter Lichtner; Berta Portugal; Connor Edsall; Jens Krüger; Dena G. Hernandez; Cornelis Blauwendraat; George D. Mellick; Alexander Zimprich; Walter Pirker; Manuela Tan; Ekaterina Rogaeva; Anthony Lang; Sulev Koks; Pille Taba; Suzanne Lesage; Alexis Brice; Jean-Christophe Corvol; Marie-Christine Chartier-Harlin; Eugenie Mutez; Kathrin Brockmann; Angela B. Deutschländer; Georges M. Hadjigeorgiou; Efthimos Dardiotis; Leonidas Stefanis; Athina Maria Simitsi; Enza Maria Valente; Simona Petrucci; Letizia Straniero; Anna Zecchinelli; Gianni Pezzoli; Laura Brighina; Carlo Ferrarese; Grazia Annesi; Andrea Quattrone; Monica Gagliardi; Lena F. Burbulla; Hirotaka Matsuo; Akiyoshi Nakayama; Nobutaka Hattori; Kenya Nishioka; Sun Ju Chung; Yun Joong Kim; Lukas Pavelka; Pierre Kolber; Bart PC van de Warrenburg; Bastiaan R. Bloem; Andrew B. Singleton; Dan Vitale; Mathias Toft; Lasse Pihlstrom; Leonor Correia Guedes; Joaquim J. Ferreira; Soraya Bardien; Jonathan Carr; Eduardo Tolosa; Mario Ezquerra; Pau Pastor; Karin Wirdefeldt; Nancy L. Pedersen; Caroline Ran; Andrea C. Belin; Andreas Puschmann; Carl E. Clarke; Karen E. Morrison; Dimitri Krainc; Matt J. Farrer; Dennis Lal; Alexis Elbaz; Thomas Gasser; Rejko Krüger; Manu Sharma; Patrick May
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Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies新生儿发育性及癫痫性脑病伴运动障碍和关节挛缩:一种在脑表达钠通道病中共享的表型
err2026-04-02
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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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Underutilization of syndrome-specific ICD-10 codes for genetic epilepsies: Implications for precision medicine综合征特异性ICD-10代码在遗传性癫痫中的未充分利用:对精准医学的启示
err2026-03-26
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errOAAI
errÉmile Moura Coelho da Silva; Tobias Brünger; Gary Taylor; Mousumi Sinha; Alison Merket; Anu Cherukara; Sunanjay Bajaj; Jessica Clark; Ludovica Montanucci; Emily A. Huth; Mariana Fauteux; Samden D. Lhatoo; Christian M. Boßelmann; Costin Leu; Rahil A. Tai; Dennis Lal
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Long-term seizure reduction with vagus nerve stimulation in Dravet syndrome在Dravet综合征中通过迷走神经刺激长期减少癫痫发作
err2026-01-11
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PREAI
errSunanjay Bajaj; Alina Ivaniuk; Tobias Bruenger; Manish N. Shah; Andreas Alexopoulos; Samden D. Lhatoo; Elia Pestana Knight; Gretchen Von Allmen; Dennis Lal; SCN1A VNS Study Group
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Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studySCN1A Dravet综合征幼儿的认知停滞和执行功能缺陷: ENVISION自然史研究中的发病,进展和影响的详细特征
err2025-11-01
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errSullivan, Joseph; Perry, M. Scott; Scheffer, Ingrid E.; Wheless, James; Boronat, Susana; Brunklaus, Andreas; Laux, Linda; Patel, Anup D.; Roberts, Colin; Dlugos, Dennis; Holder, Deborah; Knupp, Kelly; Lallas, Matt; Phillips, Steven; Segal, Eric; Lal, Dennis; Wirrell, Elaine; Zuberi, Sameer; Gioia, Gerard; Shaffer, Rebecca; Berl, Madison M.; Wojnaroski, Mary; Christensen, Sarah; King, Alexander; James, Emma S.; Vila, Maria Candida; Huang, Norman; Gofshteyn, Jacqueline S.; Rico, Salvador
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Multi-site, multi-ancestry, genome-wide association study meta-analysis of functional seizure disorder in a hospital sample of 675,680 patients多中心、多祖先背景的医院样本功能性癫痫障碍全基因组关联研究荟萃分析(样本量为675,680例患者)
err2025-09-02
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errSlavina B. Goleva; Costin Leu; Yen-Chen Anne Feng; David Burstein; Sanan Venkatesh; Rebecca Birnbaum; Veera M. Rajagopal; Peter Straub; Jakob Christensen; Jocelyn F. Bautista; Robyn M. Busch; Imad M. Najm; Jakob Grove; Anders D. Børglum; Georgios Voloudakis; Panos Roussos; Jordan Smoller; Dennis Lal; Lea K. Davis
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Large-scale copy number variant analysis in genes linked to Parkinson´s disease与帕金森病相关的基因的大规模拷贝数变异分析
err2025-08-01
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errZied Landoulsi; Katja Lohmann; Eva-Juliane Vollstedt; Emily Wedgwood-Benn; Lisa-Marie Niestroj; Björn-Hergen Laabs; Sebastian Sendel; Alexander Balck; Max Borsche; Dennis Lal; Anne Grünewald; Norbert Brüggemann; Andre Franke; Andrew Hicks; Meike Kasten; Kirsten E. Zeuner; Lara M. Lange; Wolfgang Lieb; Brit Mollenhauer; Heike Pawlack; Peter P. Pramstaller; Amke Caliebe; Inke R. König; Patrick May; Christine Klein
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SCN9A should not be considered an epilepsy gene; Refuting a gene–disease associationSCN9A不应被视为癫痫基因;反驳基因-疾病关联
err2025-06-10
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errIsmael Ghanty; Eduardo Perez-Palma; Camilo Villaman; Daniel Stobo; Joseph Symonds; Sameer Zuberi; Dennis Lal; Andreas Brunklaus
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Ontology accelerates few-shot learning capability of large language model: A study in extraction of drug efficacy in a rare pediatric epilepsy本体论加速了大语言模型的少样本学习能力:一项关于在罕见儿科癫痫中提取药物疗效的研究
err2025-05-23
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errGolnari, Pedram; Prantzalos, Katrina; Hood, Veronica; Meskis, Mary Anne; Isom, Lori L.; Wilcox, Karen; Parent, Jack M.; Lal, Dennis; Lhatoo, Samden D.; Goodkin, Howard P.; Wirrell, Elaine C.; Knupp, Kelly G.; Patel, Manisha; Loeb, Jeffrey A.; Sullivan, Joseph E.; Harte-Hargrove, Lauren; Fureman, Brandy E.; Buchhalter, Jeffrey; Sahoo, Satya S.
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Human brain tissue with MOGHE carrying somatic SLC35A2 variants reveal aberrant protein expression and protein loss in the white matter携带MOGHE的人类脑组织显示体细胞SLC35A2变异导致白质中蛋白表达异常和蛋白缺失。
err2025-03-05
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errCecchini, E; Geffers, S; Coras, R; Schultheis, D; Holtzhausen, C; Karandasheva, K; Herrmann, H; Paulsen, F; Stadelmann, C; Kobow, K; Hartlieb, T; Bien, CG; Lal, D; Blumcke, I; Hoffmann, L
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Polygenic scores contribution to Parkinson's disease comorbidities多基因评分对帕金森病合并症的贡献
err2025-01-01
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errOAAI
errHernandez, Carlos F.; Villaman, Camilo; Tejos, Cristian; Repetto, Gabriela M.; Leu, Costin; Lal, Dennis; Mata, Ignacio F.; Klein, Andres D.; Perez-Palma, Eduardo
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Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFR
err2024-11-30
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errOAAI
errBosselmann, Christian M.; Leu, Costin; Bruenger, Tobias; Hoffmann, Lucas; Baldassari, Sara; Chipaux, Mathilde; Coras, Roland; Kobow, Katja; Hamer, Hajo; Delev, Daniel; Roessler, Karl; Bien, Christian G.; Kalbhenn, Thilo; Pieper, Tom; Hartlieb, Till; Becker, Kerstin; Ferguson, Lisa; Busch, Robyn M.; Baulac, Stephanie; Nuernberg, Peter; Najm, Imad; Bluemcke, Ingmar; Lal, Dennis
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Ligand distances as key predictors of pathogenicity and function in NMDA receptors配体距离是NMDA受体致病性和功能的关键预测因子
err2024-11-13
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errMontanucci, Ludovica; Bruenger, Tobias; Bhattarai, Nisha; Bosselmann, Christian M.; Kim, Sukhan; Allen, James P.; Zhang, Jing; Kloeckner, Chiara; Krey, Ilona; Fariselli, Piero; May, Patrick; Lemke, Johannes R.; Myers, Scott J.; Yuan, Hongjie; Traynelis, Stephen F.; Lal, Dennis
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