Anja Schirmacher

1.7k citations

35 papers · 923 indexed · h-index 18

Cellular and Molecular Neuroscience top 5%
Molecular Biology
Neurology top 5%
Cognitive Neuroscience top 10%
Experimental and Cognitive Psychology top 10%

Co-authors: Peter Young Gregor Kuhlenbäumer Florian Stögbauer Burkhard Gess Agnes Flöel Matthias Boentert A. Veronica Witte Stefanie Jansen
Topics: Hereditary Neurological Disorders (13 papers)Neurological diseases and metabolism (8 papers)Genetic Neurodegenerative Diseases (6 papers)
Cited by: Neurology Cellular and Molecular Neuroscience Biophysics
Journals: Journal of Neuroscience Neurology Annals of the New York Academy of Sciences
Partner nations: Germany Belgium United States

In The Last Decade

Anja Schirmacher

35 papers receiving 900 citations

Peers

Countries citing papers authored by Anja Schirmacher

Since Specialization

Citations

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

Fields of papers citing papers by Anja Schirmacher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anja Schirmacher

This figure shows the co-authorship network connecting the top 25 collaborators of Anja Schirmacher. A scholar is included among the top collaborators of Anja Schirmacher 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 Anja Schirmacher. Anja Schirmacher 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	A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C 2019 ·NeuroMolecular Medicine ·Saranya Suriyanarayanan,Alaa Othman,Bianca Dräger,Anja Schirmacher,Peter Young,Lejla Mulahasanovic,Konstanze Hörtnagel,Saskia Biskup,Arnold von Eckardstein,Thorsten Hornemann,Museer A. Lone	14
2	SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy 2018 ·Human Genetics ·Katharina Vill,Wolfgang Müller‐Felber,Dieter Gläser,Marius Kuhn,Veronika Teusch,Herbert Schreiber,Joachim Weis,Jörg Klepper,Anja Schirmacher,Astrid Blaschek,(unknown),Tim M. Strom,Bianca Dräger,(unknown),Moritz Tacke,Lucia Gerstl,Peter Young,Rita Horváth,Jan Senderek	15
3	Behr syndrome with homozygous C19ORF12 mutation 2015 ·Journal of the Neurological Sciences ·Ilka Kleffner,(unknown),Burkhard Gess,Catharina Korsukewitz,Thomas Allkemper,Anja Schirmacher,Peter Young,Jan Senderek,Ingo W. Husstedt	15
4	Genetik der Neuropathien 2013 ·Der Nervenarzt ·Burkhard Gess,Anja Schirmacher,Peter Young	3
5	Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population 2013 ·Neuromuscular Disorders ·Burkhard Gess,Anja Schirmacher,Matthias Boentert,Peter Young	53
6	Interaction of BDNF and COMT Polymorphisms on Paired-Associative Stimulation-Induced Cortical Plasticity 2012 ·Journal of Neuroscience ·A. Veronica Witte,(unknown),Stefanie Jansen,Anja Schirmacher,Eva Brand,Jens Sommer,Agnes Flöel	95
7	Enhanced Rapid-Onset Cortical Plasticity in CADASIL as a Possible Mechanism of Preserved Cognition 2011 ·Cerebral Cortex ·Jonathan List,Thomas Duning,Marcus Meinzer,(unknown),Anja Schirmacher,Michael Deppe,Stefan Evers,Peter Young,Agnes Flöel	26
8	REPORT of a novel mutation in the PMP22 gene causing an axonal neuropathy 2011 ·Muscle & Nerve ·Burkhard Gess,Astrid Jeibmann,Anja Schirmacher,Ilka Kleffner,Matthias Schilling,Peter Young	14
9	Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene 2010 ·The American Journal of Human Genetics ·Silke Appenzeller,Anja Schirmacher,Hartmut Halfter,Sebastian Bäumer,Manuela Pendziwiat,Vincent Timmerman,Peter De Jonghe,Klára Fekete,Florian Stögbauer,Peter Lüdemann,(unknown),Elgar Susanne Quabius,E. Bernd Ringelstein,Gregor Kuhlenbäumer	23
10	Specific pattern of early white‐matter changes in pure hereditary spastic paraplegia 2010 ·Movement Disorders ·Thomas Duning,Tobias Warnecke,Anja Schirmacher,Hagen Schiffbauer,Hubertus Lohmann,Siawoosh Mohammadi,Peter Young,Michael Deppe	27
11	COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention 2010 ·Frontiers in Aging Neuroscience ·A. Veronica Witte,Stefanie Jansen,Anja Schirmacher,Peter C. Young,Agnes Flöel	12
12	Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy 2010 ·Journal of Neurology ·Ilka Kleffner,Anja Schirmacher,Burkhard Gess,Matthias Boentert,Peter Young	5
13	Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach–Rott syndrome 2009 ·American Journal of Medical Genetics Part A ·(unknown),Hagit Baris,Gavriel Gal,(unknown),Shlomo Calderon,Marja W. Wessels,Anneke Maat‐Kievit,Björn Menten,Elfride De Baere,Raoul C. M. Hennekam,Anja Schirmacher,Sherri J. Bale,Mordechai Shohat,Patrick J. Willems	4
14	Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women 2004 ·The International Journal of Neuropsychopharmacology ·Katharina Domschke,Christine M. Freitag,Gregor Kuhlenbäumer,Anja Schirmacher,Philipp Sand,Peter Nyhuis,Christian Jacob,Jürgen Fritze,Petra Franke,Marcella Rietschel,Henk Garritsen,Rolf Fimmers,Markus M. Nöthen,Klaus‐Peter Lesch,Florian Stögbauer,Jürgen Deckert	127
15	Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy 2004 ·Muscle & Nerve ·(unknown),Anja Schirmacher,Bernd Ringelstein,Peter Young,Giles D. Watts,Jan Meuleman,Eva Nelis,Phillip F. Chance,Vincent Timmerman,Florian Stögbauer,Gregor Kuhlenbäumer	1
16	Norepinephrine transporter (NET) promoter and 5′-UTR polymorphisms: association analysis in panic disorder 2004 ·Neuroscience Letters ·(unknown),Christa Hohoff,Katharina Domschke,Philipp Sand,Gregor Kuhlenbäumer,Anja Schirmacher,Christine M. Freitag,Jobst Meyer,Gerald Stöber,Petra Franke,Markus M. Nöthen,Jürgen Fritze,Rolf Fimmers,Henk Garritsen,Florian Stögbauer,Jürgen Deckert	32
17	Kinetics of 3-[123I]iodo-l-α-methyltyrosine transport in rat C6 glioma cells 1999 ·PubMed ·Burkhard Riemann,Florian Stögbauer,Klaus Kopka,Hartmut Halfter,(unknown),Anja Schirmacher,Torsten Kuwert,Matthias Weckesser,E. Bernd Ringelstein,Otmar Schober	24
18	A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes 1999 ·Genomics ·Gregor Kuhlenbäumer,Anja Schirmacher,Jan Meuleman,Fadel Tissir,Jurgen Del‐Favero,Florian Stögbauer,Peter Young,Bernd Ringelstein,Christine Van Broeckhoven,Vincent Timmerman	14
19	Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate Genes 1999 ·Annals of the New York Academy of Sciences ·Jan Meuleman,Gregor Kuhlenbäumer,Anja Schirmacher,Manfred Wehnert,Peter Young,Florian Stögbauer,E B Ringelstein,Christine Van Broeckhoven,Vincent Timmerman	2
20	Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c‐myb ET‐locus in two families with hereditary neuralgic amyotrophy (HNA) 1998 ·Annals of Human Genetics ·Gregor Kuhlenbäeumer,Jan Meuleman,Anja Schirmacher,(unknown),E B Ringelstein,M Wehnert,Maria Hoeltzenbein,Christine Van Broeckhoven,Vincent Timmerman	8

About Anja Schirmacher

Anja Schirmacher is a scholar working on Neurology, Cellular and Molecular Neuroscience and Developmental Biology, having authored 35 papers that have together received 923 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (13 papers), Neurological diseases and metabolism (8 papers) and Genetic Neurodegenerative Diseases (6 papers). The work is most often cited by research in Neurology (220 citations), Cellular and Molecular Neuroscience (333 citations) and Biophysics (69 citations). Anja Schirmacher has collaborated with scholars based in Germany, Belgium and United States. Frequent co-authors include Peter Young, Gregor Kuhlenbäumer, Florian Stögbauer, Burkhard Gess, Agnes Flöel, Matthias Boentert, A. Veronica Witte, Stefanie Jansen, E. Bernd Ringelstein and Jens Sommer. Their work appears in journals such as Journal of Neuroscience, Neurology and Annals of the New York Academy of Sciences.

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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