Line H.G. Larsen - Concepedia

Author

Line H.G. Larsen

University of Southern Denmark

Also Known As

G. Huiskamp, Larsen, L. H. G., Larsen, Line, Line H. G. Larsen, Line H.G. Larsen, Line HG Larsen, Line Larsen

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

University of Southern Denmark King's College London Evelina London Children's Healthcare Paracelsus Medical University University of Copenhagen

About

Line H.G. Larsen is an author at University of Southern Denmark specializing in medicine, developmental biology, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	106
2	Engineering	1	1	26
3	Health Sciences	1	1	27
4	Public Health	1	1	36
5	Biomedical Engineering	1	1	26

Line H.G. Larsen

Publications

985

Citations

H-Index

Page 1

	Year	Citations
Benign infantile seizures and paroxysmal dyskinesia caused by an <i>SCN8A</i> mutation Elena Gardella, Felicitas Becker, Rikke S. Møller, Annals of Neurology	2015	187
Germline and somatic mutations in the <i>MTOR</i> gene in focal cortical dysplasia and epilepsy Rikke S. Møller, Sarah Weckhuysen, Mathilde Chipaux, Neurology Genetics	2016	154
Mutations in <i><scp>KCNT</scp>1</i> cause a spectrum of focal epilepsies Rikke S. Møller, Sarah E. Heron, Line H.G. Larsen, Epilepsia	2015	147
Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies Rikke S. Møller, Line H.G. Larsen, Katrine M. Johannesen, Molecular Syndromology	2016	126
Utility of genetic testing for therapeutic decision‐making in adults with epilepsy Katrine M. Johannesen, Natalya Nikanorova, Dragan Marjanović, Epilepsia	2020	78
Incorporating epilepsy genetics into clinical practice: a 360°evaluation Stephanie Oates, Shan Tang, Richard Rosch, npj Genomic Medicine	2018	65
Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center Hannes Hoelz, Christian Herdl, Lucia Gerstl, Clinical EEG and Neuroscience	2019	42
Parental mosaicism in epilepsies due to alleged de novo variants Rikke S. Møller, Nora Liebmann, Line H.G. Larsen, Epilepsia Developmental AnomalyGenetic TestingDevelopmental BiologyGenetic DisorderMedicine	2019	36
Clinical Phenotype of De Novo <i>GNAO1</i> Mutation Inga Talvik, Rikke S. Møller, Merilin Vaher, Child Neurology Open	2015	29
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics Allan Bayat, Alexej Knaus, Annika Wollenberg Juul, Genetics in Medicine Clinical DisordersAutoimmune DiseaseInherited Metabolic DiseaseImmunologyHematology	2019	27

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