Dennis Lal

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

55h-index9.5kcitations244works3.82yr avg
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Research Topics

Genomics and Rare Diseases(129), Genetics and Neurodevelopmental Disorders(95), Epilepsy research and treatment(57), Genomic variations and chromosomal abnormalities(56), Ion channel regulation and function(20)

Publications233 total

Long‐term seizure reduction with vagus nerve stimulation in Dravet syndrome
Developmental Medicine & Child Neurology·2026
Bridging Genomic Insight and Clinical Care in Chromosome 8p Disorders Through a Registry-Driven Passport
2025Open Access
Cognitive stagnation and executive function deficits in young children with <scp> <i>SCN1A</i> </scp> + Dravet syndrome: Detailed characterization of onset, progression, and impact in the <scp>ENVISION</scp> natural history study
Epilepsia·2025· 1 citedOpen Access
Impact of Structured Bodyweight Training on Obesity-Related Parameters in School-Aged Children: A Randomized Controlled Study
International Journal of Physical Education Sports and Health·2025Open Access
Insights Into <i>DEPDC5</i> -Related Epilepsy From 586 People
Neurology·2025· 3 cited
Underutilization of Syndrome-Specific ICD-10 Codes for Genetic Epilepsies: Implications for Precision Medicine
2025Open Access
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients
Biological Psychiatry Global Open Science·2025Open Access
A research roadmap for SCN8A-related disorders: addressing knowledge gaps and aligning research priorities across stakeholders
Orphanet Journal of Rare Diseases·2025· 4 citedOpen Access
Large-scale copy number variant analysis in genes linked to Parkinson´s disease
npj Parkinson s Disease·2025· 4 citedOpen Access
Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes
Genome biology·2025· 2 citedOpen Access
Novel Deep Learning Methods for Identifying Human Emotions: A Comprehensive Review
Journal of Science Engineering Technology and Management Sciences·2025Open Access
<i>SCN9A</i> should not be considered an epilepsy gene; Refuting a gene–disease association
Epilepsia·2025· 2 citedOpen Access
Epilepsy at Precision Medicine Crossroads—Disease Modification, Presymptomatic Treatment, and Early Screening
JAMA Neurology·2025· 3 cited
Ontology accelerates few-shot learning capability of large language model: A study in extraction of drug efficacy in a rare pediatric epilepsy
International Journal of Medical Informatics·2025· 1 citedOpen Access
Genome-wide association meta-analyses of drug-resistant epilepsy
EBioMedicine·2025· 8 citedOpen Access
Human brain tissue with MOGHE carrying somatic SLC35A2 variants reveal aberrant protein expression and protein loss in the white matter
Acta Neuropathologica·2025· 2 citedOpen Access
Enhancing Rare Disease Education through AI-Driven Podcast Generation
2025· 3 citedOpen Access
Harnessing Mondo and the ILAE Classification for Curation and Analysis of 71,942 epilepsy patient variants
2025Open Access
Long-Term Seizure Reduction Associated with Vagal Nerve Stimulation in Dravet Syndrome
2025Open Access
Advancements in Urban Flood Modeling: A Comprehensive Review of Models and Capabilities
˜The œurban book series·2025
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Frequent Co-authors

Rikke S. Møller(20), Holger Lerche(18), Peter Nürnberg(17), Ingo Helbig(16), Sarah Weckhuysen(16), Eduardo Pérez‐Palma(15), Bernd A. Neubauer(14), Peter De Jonghe(13), Patrick May(13), Hiltrud Muhle(13), Yvonne Weber(12), Fritz Zimprich(11), Renzo Guerrini(10), Henrike Heyne(10), Martha Feucht(9), Bobby P.C. Koeleman(9), Wolfram S. Kunz(9), Costin Leu(9), Johannes R. Lemke(9), Eva M. Reinthaler(8)