Bernd Rautenstrauß

3.4k citations

90 papers · 1.8k indexed · h-index 26

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 2%
Ophthalmology top 1%
Neurology top 2%
Cell Biology top 5%

Co-authors: Thomas Liehr André Reis Karin Michels-Rautenstrauss Kathrin Huehne Gabriela Chavarría‐Soley Francesca Pasutto H. Grehl Christian Y. Mardin
Topics: Hereditary Neurological Disorders (47 papers)Neurological diseases and metabolism (18 papers)Genetic Neurodegenerative Diseases (15 papers)
Cited by: Ophthalmology Neurology Cellular and Molecular Neuroscience
Journals: SHILAP Revista de lepidopterologíaBrain Neurology
Partner nations: Germany United States Belgium

In The Last Decade

Bernd Rautenstrauß

88 papers receiving 1.8k citations

Peers

Countries citing papers authored by Bernd Rautenstrauß

Since Specialization

Citations

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

Fields of papers citing papers by Bernd Rautenstrauß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Rautenstrauß

This figure shows the co-authorship network connecting the top 25 collaborators of Bernd Rautenstrauß. A scholar is included among the top collaborators of Bernd Rautenstrauß 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 Bernd Rautenstrauß. Bernd Rautenstrauß 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	The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy 2015 ·Genetics in Medicine ·Davut Pehli̇van,Christine R. Beck,Yuji Okamoto,Tamar Harel,Zeynep H. Coban Akdemir,Shalini N. Jhangiani,Marjorie Withers,(unknown),Claudia M.B. Carvalho,Dirk Czesnik,Claudia Gonzaga‐Jauregui,Wojciech Wiszniewski,Donna M. Muzny,Richard A. Gibbs,Bernd Rautenstrauß,Michael W. Sereda,James R. Lupski	14
2	The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy 2015 ·NeuroMolecular Medicine ·Saranya Suriyanarayanan,Mari Auranen,Jussi Toppila,Anders Paetau,(unknown),Eino Palin,Wei Yu,(unknown),Beate Schlotter‐Weigel,(unknown),Angela Abicht,Bernd Rautenstrauß,Henna Tyynismaa,Maggie C. Walter,Thorsten Hornemann,Emil Ylikallio	19
3	The instability of the BTB-KELCH protein Gigaxonin causes Giant Axonal Neuropathy and constitutes a new penetrant and specific diagnostic test 2014 ·Acta Neuropathologica Communications ·(unknown),(unknown),Deborah Morrogh,Nancy L. Kuntz,C. Halbert,B. Chabrol,Henry Houlden,Tanya Stojkovic,Brenda A. Schulman,Bernd Rautenstrauß,Pascale Bomont	22
4	Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes 2013 ·BMC Medical Genetics ·(unknown),Peter Schneiderat,Wolfram Kreß,Bernd Rautenstrauß,Jan Senderek,Benedikt Schoser,Maggie C. Walter	17
5	Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I 2011 ·Human Mutation ·Annelies Rotthier,Anke Penno,Bernd Rautenstrauß,Michaela Auer‐Grumbach,Georg M. Stettner,Bob Asselbergh,(unknown),Heinrich Sticht,Nicolas Lévy,Vincent Timmerman,Thorsten Hornemann,Katrien Janssens	32
6	A rat model of Charcot–Marie–Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients 2011 ·Brain ·Robert Fledrich,Beate Schlotter‐Weigel,(unknown),Sven P. Wichert,Ruth M. Stassart,Gerd Meyer zu Hörste,(unknown),Bernhard G. Weiss,(unknown),Maggie C. Walter,Bernd Rautenstrauß,Walter Paulus,Moritz J. Rossner,Michael W. Sereda	36
7	Phenotypic variability in giant axonal neuropathy 2009 ·Neuromuscular Disorders ·Mériem Tazir,Sonia Nouioua,Laurent Magy,Kathrin Huehne,Salima Assami,Andoni Urtizberea,Djamel Grid,Tarik Hamadouche,Bernd Rautenstrauß,Jean‐Michel Vallat	40
8	Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis 2008 ·Neuromuscular Disorders ·Kathrin Huehne,Christiane Zweier,K Raab,Sylvie Odent,Martine Bonnaure‐Mallet,(unknown),P. Landrieu,Cyril Goizet,J Sarlangue,Matthias Baumann,Thomas Eggermann,Anita Rauch,(unknown),Georg M. Stettner,Bernd Rautenstrauß	29
9	Heterologous expression of wildtype and mutant myocilin in High Five™ insect cells shows comparable effects to cultivated trabecular meshwork cells 2007 ·Biomolecular Engineering ·(unknown),(unknown),Ursula Schlötzer‐Schrehardt,Arif B. Ekici,Bernd Rautenstrauß	3
10	Novel CYP1B1 and Known PAX6 Mutations in Anterior Segment Dysgenesis (ASD) 2006 ·Journal of Glaucoma ·Gabriela Chavarría‐Soley,Karin Michels-Rautenstrauss,Almuth Caliebe,(unknown),Christian Y. Mardin,Bernd Rautenstrauß	38
11	A novel myosin heavy chain gene in human chromosome 19q13.3 2003 ·Gene ·Alejandro Leal,Sabine Endele,(unknown),Kathrin Huehne,(unknown),Ramiro Barrantes,Andreas Winterpacht,Bernd Rautenstrauß	53
12	Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero ( MPZ , P0 ) gene causes different phenotypes in homozygous and heterozygous carriers within one family 2003 ·Neurogenetics ·Alejandro Leal,(unknown),Martin Berghoff,Gerardo Del Valle,Carlos Contreras,(unknown),(unknown),Ramiro Barrantes,(unknown),(unknown),André Reis,Bernd Rautenstrauß,Dieter Heuß	14
13	Transcriptional startpoints and methylation patterns in the PMP22 promoters of peripheral nerve, leukocytes and tumor cell lines 2001 ·International Journal of Molecular Medicine ·Kathrin Huehne,Bernd Rautenstrauß	9
14	A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3 2001 ·The American Journal of Human Genetics ·Alejandro Leal,Bernal Morera-Brenes,Gerardo Del Valle,Dieter Heuß,(unknown),Martin Berghoff,(unknown),(unknown),María Méndez,Hans Christian Hennies,B. Neundörfer,Ramiro Barrantes,André Reis,Bernd Rautenstrauß	49
15	PMP22 Thr118Met is not a clinically relevant CMT1 marker 2000 ·Journal of Neurology ·Peter Young,Florian Stögbauer,(unknown),Peter De Jonghe,A. Löfgren,Vincent Timmerman,Bernd Rautenstrauß,Konrad Oexle,H. Grehl,Gregor Kuhlenbäumer,Christine Van Broeckhoven,E B Ringelstein,Harald Funke	11
16	Charcot‐Marie‐Tooth 1A: Heterozygous T118M Mutation over a CMT1A Duplication Has No Influence on the Phenotype 1999 ·Annals of the New York Academy of Sciences ·Pavel Seeman,Radim Mazanec,T Maríková,Bernd Rautenstrauß	7
17	Localization of mariner DNA Transposons in the Human Genome by PRINS 1999 ·Genome Research ·Lawrence T. Reiter,Thomas Liehr,Bernd Rautenstrauß,Hugh M. Robertson,James R. Lupski	18
18	A GLClA Gene Gln368Stop Mutation in a Patient with Normal-Tension Open-Angle Glaucoma 1999 ·Journal of Glaucoma ·Christian Y. Mardin,(unknown),(unknown),Bernd Rautenstrauß,Karin Michels-Rautenstrauss	40
19	Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion 1996 ·Human Genetics ·Thomas Liehr,Bernd Rautenstrauß,H. Grehl,(unknown),Arif B. Ekici,Anita Rauch,Hans‐Dieter Rott	33
20	Regional localization of rat myelin protein zero Mpz gene to Chromosome 13q24-25 by means of FISH 1995 ·Mammalian Genome ·Thomas Liehr,Arif B. Ekici,Rainer Hillenbrand,Bernd Rautenstrauß	1

About Bernd Rautenstrauß

Bernd Rautenstrauß is a scholar working on Cellular and Molecular Neuroscience, Neurology and Ophthalmology, having authored 90 papers that have together received 1.8k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (47 papers), Neurological diseases and metabolism (18 papers) and Genetic Neurodegenerative Diseases (15 papers). The work is most often cited by research in Ophthalmology (389 citations), Neurology (330 citations) and Cellular and Molecular Neuroscience (725 citations). Bernd Rautenstrauß has collaborated with scholars based in Germany, United States and Belgium. Frequent co-authors include Thomas Liehr, André Reis, Karin Michels-Rautenstrauss, Kathrin Huehne, Gabriela Chavarría‐Soley, Francesca Pasutto, H. Grehl, Christian Y. Mardin, Heinrich Sticht and Pavel Seeman. Their work appears in journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

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