Hiltrud Muhle

11.9k total citations
67 papers, 2.5k citations indexed

About

Hiltrud Muhle is a scholar working on Psychiatry and Mental health, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Hiltrud Muhle has authored 67 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Psychiatry and Mental health, 23 papers in Genetics and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in Hiltrud Muhle's work include Epilepsy research and treatment (28 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Neuroscience and Neuropharmacology Research (12 papers). Hiltrud Muhle is often cited by papers focused on Epilepsy research and treatment (28 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Neuroscience and Neuropharmacology Research (12 papers). Hiltrud Muhle collaborates with scholars based in Germany, United States and Canada. Hiltrud Muhle's co-authors include Ulrich Stephani, Michael Siniatchkin, Friederike Moeller, Stephan Wolff, Hartwig R. Siebner, Sarah von Spiczak, Oliver Granert, Rainer Boor, Heather C. Mefford and Olav Jansen and has published in prestigious journals such as PLoS ONE, NeuroImage and Brain.

In The Last Decade

Hiltrud Muhle

66 papers receiving 2.4k citations

Peers

Countries citing papers authored by Hiltrud Muhle

Since Specialization

Citations

This map shows the geographic impact of Hiltrud Muhle's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hiltrud Muhle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hiltrud Muhle more than expected).

Fields of papers citing papers by Hiltrud Muhle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hiltrud Muhle. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hiltrud Muhle. The network helps show where Hiltrud Muhle may publish in the future.

Co-authorship network of co-authors of Hiltrud Muhle

This figure shows the co-authorship network connecting the top 25 collaborators of Hiltrud Muhle. A scholar is included among the top collaborators of Hiltrud Muhle based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hiltrud Muhle. Hiltrud Muhle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Impact of Video Distraction on Anxiety During Anesthesia Induction in Pediatric Patients Premedicated With Midazolam: A Randomized Controlled Trial 2025 ·Pediatric Anesthesia ·(unknown), (unknown), Sebastian G. Walter, Hiltrud Muhle, (unknown), (unknown), (unknown), D. Melchior, Amke Caliebe, (unknown), Tobias Becher, Ingmar Lautenschläger	0
2	Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy 2013 ·PLoS ONE ·Dennis Lal, Eva M. Reinthaler, (unknown), Mohammad R. Toliat, Hölger Thiele, (unknown), Holger Lerche, Andreas Hahn, (unknown), Hiltrud Muhle, Thomas Sander, Fritz Zimprich, Bernd A. Neubauer	18
3	The role of SLC2A1 in early onset and childhood absence epilepsies 2013 ·Epilepsy Research ·Hiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, Arvid Suls, Sarah von Spiczak, Laura L. Klitten, Hans A. Dahl, Klaus Brusgaard, Bernd A. Neubauer, Peter De Jonghe, Niels Tommerup, Ulrich Stephani, Helle Hjalgrim, Rikke S. Møller	11
4	Exome sequencing in a family with restless legs syndrome 2012 ·Movement Disorders ·Anne Weißbach, (unknown), Norbert Brüggemann, Alexander Schmidt, Meike Kasten, Irene Pichler, Hiltrud Muhle, Ebba Lohmann, Thora Lohnau, E. Schwinger, Johann Hagenah, Ulrich Stephani, Peter P. Pramstaller, Christine Klein, Katja Lohmann	17
5	Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsy 2011 ·Pharmacogenetics and Genomics ·Mike Ufer, Celina von Stülpnagel, Hiltrud Muhle, Sierk Haenisch, Cornelia Remmler, (unknown), (unknown), Ulrich Stephani, Gerhard Kluger, Ingolf Cascorbi	43
6	A retrospective population‐based study on seizures related to childhood vaccination 2011 ·Epilepsia ·Sarah von Spiczak, Ingo Helbig, (unknown), Hiltrud Muhle, Andreas van Baalen, (unknown), Dick Lindhout, Ingrid E. Scheffer, Samuel F. Berkovic, Ulrich Stephani, Brigitte Keller‐Stanislawski	19
7	Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach 2011 ·Epilepsia ·Sarah von Spiczak, (unknown), Hiltrud Muhle, André Franke, Markus B. Schilhabel, Ulrich Stephani, Ingo Helbig	5
8	Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome 2011 ·Epilepsia ·Hiltrud Muhle, Heather C. Mefford, Tanja Obermeier, Sarah von Spiczak, Evan E. Eichler, Ulrich Stephani, Thomas Sander, Katherine L. Helbig	22
9	Decomposition of Neurological Multivariate Time Series by State Space Modelling 2010 ·Bulletin of Mathematical Biology ·Andreas Galka, Kin Foon Kevin Wong, Tohru Ozaki, Hiltrud Muhle, Ulrich Stephani, Michael Siniatchkin	15
10	Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis 2010 ·Epilepsy Research ·Carolien G. F. de Kovel, Dalila Pinto, Ulrike Tauer, Susanne Lorenz, Hiltrud Muhle, Costin Leu, Bernd A. Neubauer, Anne Hempelmann, Petra M.C. Callenbach, Ingrid E. Scheffer, Samuel F. Berkovic, Gabrielle Rudolf, Pasquale Striano, Auli Sirén, Betül Baykan, T. Sander, Dick Lindhout, (unknown), Ulrich Stephani, Bobby P.C. Koeleman	33
11	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity 2010 ·Genetics in Medicine ·Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, (unknown), Pamela J. Reitnauer, Rosemarie Smith, David W. Stockton, Hiltrud Muhle, Ingo Helbig, Evan E. Eichler, Blake C. Ballif, Jill A. Rosenfeld, Karen D. Tsuchiya	137
12	Non-response to antiepileptic pharmacotherapy is associated with the ABCC2 −24C>T polymorphism in young and adult patients with epilepsy 2009 ·Pharmacogenetics and Genomics ·Mike Ufer, (unknown), Hiltrud Muhle, (unknown), Sierk Haenisch, Robert Häsler, Frank Faltraco, Cornelia Remmler, Sarah von Spiczak, Heyo K. Kroemer, Uwe Runge, Rainer Boor, Ulrich Stephani, Ingolf Cascorbi	83
13	Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-Up 2009 ·Pediatric Neurology ·Hiltrud Muhle, Andreas van Baalen, Felix G. Riepe, Axel Rohr, Ulrich Stephani	13
14	Mapping brain activity on the verge of a photically induced generalized tonic–clonic seizure 2009 ·Epilepsia ·Friederike Moeller, Hartwig R. Siebner, Stephan Wolff, Hiltrud Muhle, Oliver Granert, Olav Jansen, Ulrich Stephani, Michael Siniatchkin	37
15	Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system—a novel entity? 2009 ·European Journal of Pediatrics ·Ingo Helbig, (unknown), Jochen Brasch, Ingrid Haußer, Andreas van Baalen, Hiltrud Muhle, Karsten Alfke, Almuth Caliebe, Ulrich Stephani, Rudolf Happle	3
16	Changes in activity of striato–thalamo–cortical network precede generalized spike wave discharges 2007 ·NeuroImage ·Friederike Moeller, Hartwig R. Siebner, Stephan Wolff, Hiltrud Muhle, Rainer Boor, Oliver Granert, Olav Jansen, Ulrich Stephani, Michael Siniatchkin	155
17	Hemodynamic Responses to Interictal Epileptiform Discharges in Children with Symptomatic Epilepsy 2007 ·Epilepsia ·Julia Jacobs, Eliane Kobayashi, Rainer Boor, Hiltrud Muhle, Stephan Wolff, Colin Hawco, François Dubeau, Olav Jansen, Ulrich Stephani, Jean Gotman, Michael Siniatchkin	73
18	Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy 2007 ·Epilepsy Research ·Anne Hempelmann, Joana Cobilanschi, Armin Heils, Hiltrud Muhle, Ulrich Stephani, Yvonne Weber, Holger Lerche, Thomas Sander	13
19	Association of BRD2 polymorphisms with photoparoxysmal response 2006 ·Neuroscience Letters ·Susanne Lorenz, (unknown), (unknown), Tim Becker, Hiltrud Muhle, (unknown), Ulrike Tauer, Thomas Sander, Ulrich Stephani	44
20	Modulation of MAO Activity by Imidazoline and Guanidine Derivatives 1999 ·Annals of the New York Academy of Sciences ·Walter Raasch, Hiltrud Muhle, Peter Dominiak	24

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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