Marita Munz

1.4k total citations
18 papers, 1.0k citations indexed

About

Marita Munz is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Marita Munz has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Marita Munz's work include Parkinson's Disease Mechanisms and Treatments (5 papers), Neurological diseases and metabolism (4 papers) and Neurological disorders and treatments (4 papers). Marita Munz is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (5 papers), Neurological diseases and metabolism (4 papers) and Neurological disorders and treatments (4 papers). Marita Munz collaborates with scholars based in Germany, Denmark and Austria. Marita Munz's co-authors include Thomas Gasser, Julia Fuchs, Daniela Berg, Jakob C. Mueller, Friedrich Asmus, Saskia Biskup, Owen A. Ross, Christer Nilsson, Elna‐Marie Larsson and Frank A. Middleton and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Marita Munz

18 papers receiving 1000 citations

Peers

Countries citing papers authored by Marita Munz

Since Specialization

Citations

This map shows the geographic impact of Marita Munz'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 Marita Munz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marita Munz more than expected).

Fields of papers citing papers by Marita Munz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marita Munz. 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 Marita Munz. The network helps show where Marita Munz may publish in the future.

Co-authorship network of co-authors of Marita Munz

This figure shows the co-authorship network connecting the top 25 collaborators of Marita Munz. A scholar is included among the top collaborators of Marita Munz 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 Marita Munz. Marita Munz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	The Parkinson’s disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4 2019 ·Scientific Reports ·Natalja Funk, Marita Munz, Thomas Ott, Kathrin Brockmann, Andrea Wenninger-Weinzierl, Ralf Kühn, Daniela M. Vogt Weisenhorn, Florian Giesert, Wolfgang Wurst, Thomas Gasser, Saskia Biskup	20
2	Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort 2016 ·Frontiers in Molecular Neuroscience ·(unknown), Florian Battke, (unknown), Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup	32
3	PCA3 and PSA gene activity correlates with the true tumor cell burden in prostate cancer lymph node metastases 2015 ·Cancer Biomarkers ·Igor Tsaur, Joerg Hennenlotter, Elsie Oppermann, Marita Munz, Ursula Kuehs, Arnulf Stenzl, David Schilling	5
4	GBA‐associated parkinsonism and dementia: beyond α‐synucleinopathies? 2015 ·European Journal of Neurology ·Andrea Pilotto, Claudia Schulte, Ann‐Kathrin Hauser, Saskia Biskup, Marita Munz, Kathrin Brockmann, Eva Schaeffer, Matthis Synofzik, Walter Maetzler, Ulrike Suenkel, Karin Srulijes, Thomas Gasser, Daniela Berg	7
5	Further delineation of the SATB2 phenotype 2013 ·European Journal of Human Genetics ·Dennis Döcker, Max Schubach, Moritz Menzel, Marita Munz, Christiane Spaich, Saskia Biskup, Deborah Bartholdi	68
6	Reliable housekeeping gene combination for quantitative PCR of lymph nodes in patients with prostate cancer. 2013 ·PubMed ·Igor Tsaur, M. Renninger, Joerg Hennenlotter, Elsie Oppermann, Marita Munz, Ursula Kuehs, Arnulf Stenzl, David A. Schilling	16
7	Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype 2012 ·Neurobiology of Aging ·Matthis Synofzik, Walter Maetzler, Torsten Grehl, Johannes Prudlo, Jennifer Müller vom Hagen, Tobias B. Haack, (unknown), Marita Munz, Lüdger Schöls, Saskia Biskup	77
8	Interpretation of the Prostate Cancer Gene 3 in Reference to the Individual Clinical Background: Implications for Daily Practice 2010 ·Urologia Internationalis ·David Schilling, Jörg Hennenlotter, Marita Munz, (unknown), Karl‐Dietrich Sievert, Arnulf Stenzl	17
9	“Jerky” dystonia in children: Spectrum of phenotypes and genetic testing 2008 ·Movement Disorders ·Friedrich Asmus, (unknown), Elaine Eggleston Doherty, (unknown), Marita Munz, Thomas Gasser, Timothy Lynch, Mary D. King	25
10	Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype 2007 ·Brain ·Friedrich Asmus, L. E. Hjermind, E. Dupont, Janine Wagenstaller, Edda Haberlandt, Marita Munz, Tim M. Strom, Thomas Gasser	34
11	Genetic variability in the SNCA gene influences α‐synuclein levels in the blood and brain 2007 ·The FASEB Journal ·Julia Fuchs, Aleš Tichopád, Yulia Golub, Marita Munz, Katherine J. Schweitzer, (unknown), Daniela Berg, Jakob C. Mueller, Thomas Gasser	200
12	The transcription factor PITX3 is associated with sporadic Parkinson's disease 2007 ·Neurobiology of Aging ·Julia Fuchs, Jakob C. Mueller, Peter Lichtner, Claudia Schulte, Marita Munz, Daniela Berg, Ullrich Wüllner, Thomas Illig, Manu Sharma, Thomas Gasser	91
13	Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication 2007 ·Neurology ·Julia Fuchs, Christer Nilsson, Jennifer M. Kachergus, Marita Munz, Elna‐Marie Larsson, Birgitt Schüle, J. William Langston, Frank A. Middleton, Owen A. Ross, Mary Hulihan, Thomas Gasser, Matthew J. Farrer	277
14	Clinical differentiation of genetically proven benign hereditary chorea and myoclonus‐dystonia 2007 ·Movement Disorders ·Friedrich Asmus, Anita Devlin, Marita Munz, Alexander Zimprich, Thomas Gasser, Patrick F. Chinnery	37
15	Myoclonus‐dystonia due to genomic deletions in the epsilon‐sarcoglycan gene 2005 ·Annals of Neurology ·Friedrich Asmus, Farid Salih, Lena E. Hjermind, Karen Østergaard, Marita Munz, Andrea A. Kühn, E. Dupont, Andreas Kupsch, Thomas Gasser	49
16	A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa 2005 ·Neurology ·Friedrich Asmus, Veronka Horber, Joachim Pohlenz, (unknown), Alexander Zimprich, Marita Munz, M. Schöning, Thomas Gasser	58
17	Otitis media and CNS complications. 1992 ·PubMed ·Marita Munz, Jean‐Pierre Farmer, (unknown), (unknown), M D Schloss	7
18	[A retrospective study of 83 cases of children with aseptic meningitis]. 1970 ·PubMed ·Marita Munz, (unknown), Andrew J. Schoenfeld, (unknown)	1

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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