Researcher profile · Semantic Scholar

Line H. G. Larsen

h-index: 14
Works: 19
Citations: 1,074

Most-cited papers

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
E. Gardella, F. Becker, R. Møller, Julian Schubert +24 more
2016Annals of Neurology176 citations
Semantic Scholar
Mutations in KCNT1 cause a spectrum of focal epilepsies
R. Møller, S. Heron, Line H. G. Larsen, Chiao X. Lim +27 more
2015Epilepsia141 citations Open access
Semantic Scholar
Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy
R. Møller, S. Weckhuysen, M. Chipaux, Elise Marsan +17 more
2016Neurology: Genetics136 citations Open access
Semantic Scholar
Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies
R. Møller, Line H. G. Larsen, K. Johannesen, I. Talvik +28 more
2016Molecular Syndromology130 citations Open access
Semantic Scholar
Phenotypic spectrum of GABRA1
K. Johannesen, C. Marini, Siona Pfeffer, R. Møller +42 more
2016Neurology93 citations Open access
Semantic Scholar
Mutations in GABRB3: From febrile seizures to epileptic encephalopathies
R. Møller, T. Wuttke, I. Helbig, C. Marini +38 more
2017Neurology82 citations Open access
Semantic Scholar
Utility of genetic testing for therapeutic decision‐making in adults with epilepsy
Kathrine M. Johannesen, N. Nikanorova, D. Marjanović, Agnieszka Pavbro +3 more
2020Epilepsia76 citations Open access
Semantic Scholar
Incorporating epilepsy genetics into clinical practice: a 360°evaluation
S. Oates, Sha Tang, R. Rosch, Rosalie Lear +7 more
2018npj Genomic Medicine62 citations Open access
Semantic Scholar
Parental mosaicism in epilepsies due to alleged de novo variants
R. Møller, Nora Liebmann, Line H. G. Larsen, Mathias Stiller +9 more
2019Epilepsia37 citations Open access
Semantic Scholar
Impact on Clinical Decision Making of Next-generation Sequencing (NGS) in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center
H. Hölz, Christian Herdl, L. Gerstl, M. Tacke +8 more
2019Neuropediatrics35 citations
Semantic Scholar
Clinical Phenotype of De Novo GNAO1 Mutation
I. Talvik, R. Møller, M. Vaher, U. Vaher +4 more
2015Child Neurology Open30 citations Open access
Semantic Scholar
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics
A. Bayat, A. Knaus, A. Juul, D. Dukic +23 more
2019Genetics in Medicine25 citations Open access
Semantic Scholar
SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders
Victoria Vlachou, Line H. G. Larsen, E. Pavlidou, Naila Ismayilova +4 more
2019Journal Genetika20 citations
Semantic Scholar
Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies
Anna M. Tiefes, T. Hartlieb, M. Tacke, Celina von Stülpnagel-Steinbeis +8 more
2018Clinical EEG and Neuroscience15 citations
Semantic Scholar
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters
Eva-Katharina Willimsky, A. Munzig, K. Mayer, S. Biskup +10 more
2020Neuropediatrics8 citations Open access
Semantic Scholar
Genetic Testing in Adults with Intellectual Disability and Epilepsy
H. A. Dahl, Line H. G. Larsen, K. Olofsson, M. Miranda +18 more
20157 citations Open access
Semantic Scholar
Incorporating epilepsy genetics into clinical practice: a 360°evaluation
S. Oates, Sha Tang, R. Rosch, Rosalie Lear +7 more
2018npj Genomic Medicine1 citations Open access
Semantic Scholar
SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders
Victoria Vlachou, Line H. G. Larsen, E. Pavlidou, Naila Ismayilova +4 more
2019Journal Genetika0 citations
Semantic Scholar
KCNB1 mutations are causing a neurodevelopmental disorder including epilepsy and autism
R. Møller, C. de Kovel, S. Syrbe, Bitten Schönewolf-Greulich +33 more
20170 citations
Semantic Scholar

G. Rubboli

×5

I. Talvik×5

T. Talvik×5

S. Syrbe×4

P. Gellert×4

M. Nikanorova×4

Qin Hao×4

Deb K. Pal×4