Laura L. Klitten - Concepedia

Author

Laura L. Klitten

University of Copenhagen

Also Known As

Ha. Dahl, L Klitten, L.L. Klitten, Laura Klitten, Laura L Klitten, Laura L. Klitten, Laura Line Klitten

Publications

802

Citations

H-Index

Concepts

All Affiliations

University of Copenhagen University of Southern Denmark Copenhagen University Hospital Christian-Albrechts-Universität zu Kiel VIB-UAntwerp Center for Molecular Neurology

About

Laura L. Klitten is an author at University of Copenhagen specializing in medicine, neurogenetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	467
2	Social Sciences	2	2	341
3	Arts	1	1	37
4	Communicative Disorders	1	1	37
5	Molecular Medicine	1	1	18

Laura L. Klitten

Publications

786

Citations

H-Index

Page 1

	Year	Citations
Mutations in<i>SYNGAP1</i>Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency Martin H. Berryer, Fadi F. Hamdan, Laura L. Klitten, Human Mutation GeneticsPathologyDisease-causing Point MutationsDisease Gene IdentificationSynaptic Signaling	2012	270
Mutations in<i>NRXN1</i>in a family multiply affected with brain disorders:<i>NRXN1</i>mutations and brain disorders Linh T. Duong, Laura L. Klitten, Rikke S. Møller, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2012	81
Reduction of seizure frequency after epilepsy surgery in a patient with <scp><i>STXBP1</i></scp> encephalopathy and clinical description of six novel mutation carriers Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, Epilepsia Neurological DisorderGeneticsWest SyndromeGenetic EpidemiologyClinical Neurology	2013	71
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy Eva M. Reinthaler, Dennis Lal, Sébastien Lebon, Human Molecular Genetics	2014	69
Exon‐disrupting deletions of <scp><i>NRXN1</i></scp> in idiopathic generalized epilepsy Rikke S. Møller, Yvonne Weber, Laura L. Klitten, Epilepsia	2013	67
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy Mai‐Britt Mosbech, Anne S. Olsen, Ditte Neess, Annals of Clinical and Translational Neurology	2014	59
Localization and regulation of dopamine receptor D4 expression in the adult and developing rat retina Laura L. Klitten, Martin F. Rath, Steven L. Coon, Experimental Eye Research Ganglion CellPhotoreceptor CellDevelopmental BiologyRetinaOphthalmology	2008	55
A balanced translocation disrupts<i>SYNGAP1</i>in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA) Laura L. Klitten, Rikke S. Møller, Marina Nikanorova, Epilepsia Myoclonic AbsencesNeurological DisorderGeneticsDisease Gene IdentificationSynaptic Signaling	2011	37
Atypical Vitamin B<sub>6</sub> Deficiency Anna Baumgart, Sarah von Spiczak, Nanda M. Verhoeven‐Duif, Journal of Child Neurology	2013	18
The role of SLC2A1 in early onset and childhood absence epilepsies Hiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, Epilepsy Research Early OnsetPediatricsChildhood Absence EpilepsiesMolecular MedicineMedicine	2013	18

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