Alexander Zimprich

15.7k total citations
76 papers, 3.3k citations indexed

About

Alexander Zimprich is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alexander Zimprich has authored 76 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Neurology, 31 papers in Molecular Biology and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alexander Zimprich's work include Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological diseases and metabolism (10 papers) and Neuropeptides and Animal Physiology (10 papers). Alexander Zimprich is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological diseases and metabolism (10 papers) and Neuropeptides and Animal Physiology (10 papers). Alexander Zimprich collaborates with scholars based in Austria, Germany and United States. Alexander Zimprich's co-authors include Thomas Gasser, Volker Höllt, Fritz Zimprich, Elisabeth Stögmann, Thomas Meitinger, Daniela Berg, Tatiana Simon, Tim M. Strom, Friedrich Asmus and Peter Lichtner and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Alexander Zimprich

71 papers receiving 3.2k citations

Peers

Countries citing papers authored by Alexander Zimprich

Since Specialization

Citations

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

Fields of papers citing papers by Alexander Zimprich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Zimprich

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Zimprich. A scholar is included among the top collaborators of Alexander Zimprich 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 Alexander Zimprich. Alexander Zimprich 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	Abatacept Induces Long-Term Reconstitution of the B-Cell Niche in a Patient With CTLA-4 Haploinsufficiency 2024 ·Neurology Neuroimmunology & Neuroinflammation ·Steffen Pfeuffer, (unknown), Marc Pawlitzki, Tobias Ruck, Christina B. Schroeter, Christian Thomas, Guido Kobbe, Sascha Dietrich, Alexander Zimprich, Heinz Wiendl, Sven G. Meuth	0
2	Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation 2024 ·Annals of Clinical and Translational Neurology ·(unknown), Sigrid Klotz, (unknown), (unknown), (unknown), Theresa König, Lukas Haider, Tatjana Traub‐Weidinger, Matias Wagner, Theresa Brunet, Melanie Brügger, Alexander Zimprich, Jakob Rath, Elisabeth Stögmann, Ellen Gelpí, Hakan Çetin	1
3	Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes 2023 ·Human Genomics ·(unknown), Theresa König, Raphael Wurm, (unknown), Evelyn Berger–Sieczkowski, (unknown), Christoph Hotzy, Matias Wagner, Riccardo Berutti, Esther Sammler, Elisabeth Stögmann, Alexander Zimprich	1
4	No Association of Multiple Sclerosis with C9orf72 Hexanucleotide Repeat Size in an Austrian Cohort 2023 ·International Journal of Molecular Sciences ·Theresa König, Fritz Leutmezer, Thomas Berger, Alexander Zimprich, (unknown), Elisabeth Stögmann, Tobias Zrzavy	0
5	C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients 2022 ·Neurobiology of Disease ·Theresa König, Raphael Wurm, (unknown), (unknown), Christoph Hotzy, Hakan Çetin, Sigrid Klotz, Ellen Gelpí, C. Bancher, Thomas Benke, Peter Dal‐Bianco, Michaela Defrancesco, Peter Fischer, Josef Marksteiner, Hedwig Sutterlüty, Gerhard Ransmayr, Reinhold Schmidt, Alexander Zimprich, Elisabeth Stögmann	6
6	Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2 2013 ·Brain ·Elisabeth Stögmann, Eva M. Reinthaler, Salwa El Tawil, (unknown), (unknown), Nevine El Nahas, (unknown), (unknown), Sherif Edris, Anna Benet‐Pagès, Sebastian Eck, Ekaterina Pataraia, Davide Mei, Alexis Brice, (unknown), Renzo Guerrini, Fritz Zimprich, Tim M. Strom, Alexander Zimprich	51
7	Lack of Association Between ABCC2 Gene Variants and Treatment Response in Epilepsy 2012 ·Pharmacogenomics ·Eva Hilger, Eva M. Reinthaler, Elisabeth Stögmann, Christoph Hotzy, Ekaterina Pataraia, Christoph Baumgartner, Alexander Zimprich, Fritz Zimprich	32
8	A novel mutation in the VCP gene (G157R) in a german family with inclusion‐body myopathy with paget disease of bone and frontotemporal dementia 2009 ·Muscle & Nerve ·Atbin Djamshidian, Jochen Schaefer, Dietrich Haubenberger, Elisabeth Stögmann, Fritz Zimprich, Eduard Auff, Alexander Zimprich	51
9	Analysis of the prodynorphin promoter polymorphism in atopic dermatitis and disease-related pruritus 2009 ·Clinical and Experimental Dermatology ·Elli K. Greisenegger, Alexander Zimprich, Fritz Zimprich, Georg Stingl, Tamara Kopp	4
10	Role of LINGO1 polymorphisms in Parkinson's disease 2009 ·Movement Disorders ·Dietrich Haubenberger, Christoph Hotzy, Walter Pirker, Regina Katzenschlager, Thomas Brücke, Fritz Zimprich, Eduard Auff, Alexander Zimprich	22
11	A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis 2008 ·Neurogenetics ·Elisabeth Stögmann, Shadi Tawil, Janine Wagenstaller, Ahmed Gaber, Sherif Edris, (unknown), Eva Assem‐Hilger, Fritz Leutmezer, Silvia Bonelli, Christian Baumgärtner, Fritz Zimprich, Tim M. Strom, Alexander Zimprich	28
12	Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease 2005 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·María Martínez, Alexis Brice, Jenny Vaughan, Alexander Zimprich, Monique M.B. Breteler, G. Meco, Alessandro Filla, Matthew J. Farrer, Christine Bétard, Andrew Singleton, John Hardy, Giuseppe De Michele, Vincenzo Bonifati, Ben A. Oostra, Thomas Gasser, Nicholas Wood, Alexandra Dürr, (unknown)	28
13	Multiple regions of α‐synuclein are associated with Parkinson's disease 2005 ·Annals of Neurology ·Jakob C. Mueller, Julia Fuchs, Anne Höfer, Alexander Zimprich, Peter Lichtner, Thomas Illig, Daniela Berg, Ullrich Wüllner, Thomas Meitinger, Thomas Gasser	183
14	PARK11 is not linked with Parkinson's disease in European families 2004 ·European Journal of Human Genetics ·Jürgen Prestel, Manu Sharma, Petra Leitner, Alexander Zimprich, Jenny Vaughan, Alexandra Dürr, Vincenzo Bonifati, Giuseppe De Michele, Haşmet Hanağası, Matthew J. Farrer, Anne Höfer, Friedrich Asmus, Giampiero Volpe, G. Meco, Alexis Brice, Nicholas Wood, Bertram Müller-Myhsok, Thomas Gasser	18
15	A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy 2002 ·Annals of Neurology ·Elisabeth Stögmann, Alexander Zimprich, Christoph Baumgartner, Susanne Aull‐Watschinger, Volker Höllt, Fritz Zimprich	79
16	Myoclonus–dystonia syndrome: ε‐sarcoglycan mutations and phenotype 2002 ·Annals of Neurology ·Friedrich Asmus, Alexander Zimprich, Sophie Tézenas du Montcel, Christian Kabus, Günther Deuschl, Andreas Kupsch, Ulf Ziemann, Mirna Castro, Andrea A. Kühn, Tim M. Strom, Marie Vidailhet, Kailash P. Bhatia, Alexandra Dürr, Nicholas Wood, Alexis Brice, Thomas Gasser	97
17	Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families 2001 ·Annals of Neurology ·Friedrich Asmus, Alexander Zimprich, Markus Naumann, Daniela Berg, Markus Bertram, Andrés Ceballos-Baumann, (unknown), Christian Kabus, Martin Dichgans, Sigrid Fuchs, (unknown), Thomas Gasser	30
18	Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome 2001 ·Nature Genetics ·Alexander Zimprich, Monika Grabowski, Friedrich Asmus, Markus Naumann, Daniela Berg, Markus Bertram, K H Scheidtmann, Peter Kern, Juliane Winkelmann, Bertram Müller‐Myhsok, (unknown), Matthias Bauer, Tanja R. Müller, Mirna Castro, Thomas Meitinger, Tim M. Strom, Thomas Gasser	309
19	An Allelic Variation in the Human Prodynorphin Gene Promoter Alters Stimulus‐Induced Expression 2000 ·Journal of Neurochemistry ·Alexander Zimprich, Jürgen Kraus, Michael Wöltje, P. Mayer, Elisabeth Rauch, Volker Höllt	90
20	Promoter Region and Alternatively Spliced Exons of the Rat μ‐Opioid Receptor Gene 1996 ·Journal of Neurochemistry ·P. Mayer, S Schulzeck, J. Kraus, Alexander Zimprich, V. Höllt	29

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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