Gregor Kuhlenbäumer

Author

Gregor Kuhlenbäumer

Also Known As

Christos Krogias, Florian Krismer, G Kuhlenbaumer, G Kuhlenbäumer, G. KUHLENBÄUMER, G. Kuhlenbaumer, G. Kuhlenbäumer, G. KuhlenbÄumer, G. Kuhlenbäumer, G. Kuhlenbäumer

205

Publications

7.1K

Citations

H-Index

140

Concepts

All Affiliations

Christian-Albrechts-Universität zu Kiel University of Münster University of Lübeck University of Antwerp University Hospital Münster

About

Gregor Kuhlenbäumer is an author at Christian-Albrechts-Universität zu Kiel specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	36	2.7K
2	Public Health	5	5	709
3	Health Sciences	3	3	147
4	Education	1	1	45
5	Engineering	1	1	14

Gregor Kuhlenbäumer

Publications

5.1K

Citations

H-Index

Page 1

	Year	Citations
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke Daníel F. Guðbjartsson, Hilma Hólm, Sólveig Grétarsdóttir, Nature Genetics ThrombosisIschemic StrokeCardiovascular DiseaseMedicineCerebrovascular Disease	2009	489
Gut microbiota in Parkinson disease in a northern German cohort Franziska Hopfner, Axel Künstner, Stefanie H. Müller, Brain Research ProbioticDysbiosisMicrobiotaGut MicrobiologyGut Microbiota	2017	326
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke Sólveig Grétarsdóttir, Andrei Manolescu, Unnur Styrkársdóttir, Annals of Neurology	2008	285
Mutations in SEPT9 cause hereditary neuralgic amyotrophy Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceGenetic DisorderGenetics	2005	259
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, The American Journal of Human Genetics Chd2 CauseDravet SyndromeMolecular NeuroscienceNeurobiology Of DiseaseGenetic Disorder	2013	219
Acute Cerebrovascular Disease in the Young Arndt Rolfs, Franz Fazekas, Ulrike Grittner, Stroke	2013	210
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women Katharina Domschke, Christine M. Freitag, Gregor Kuhlenbäumer, The International Journal of Neuropsychopharmacology GeneticsGenetic EpidemiologyHuman PolymorphismPsychologyPanic Disorder	2004	158
Genetic predisposition in anti‐LGI1 and anti‐NMDA receptor encephalitis Stefanie H. Mueller, Anna Färber, Nico Melzer, Annals of Neurology	2018	149
Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules Xiaobo Bai, Jonathan R. Bowen, Tara K. Knox, The Journal of Cell Biology Synaptic TransmissionNeurotransmitterMolecular BiologyCytoskeletonCellular Neurobiology	2013	119
Mild Mechanical Traumas Are Possible Risk Factors for Cervical Artery Dissection Ralf Dittrich, DK Rohsbach, Anna Heidbreder, Cerebrovascular Diseases	2006	111

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