Thomas Voit

12.9k citations

160 papers · 10.5k · h-index 59

Impact in

Genetics top 1%
- Neurogenetic and Muscular Disorders Research
Molecular Biology top 0.5%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Mitochondrial Function and Pathology
- Nuclear Structure and Function

Papers in

Molecular Biology 112
- Muscle Physiology and Disorders 87
- Mitochondrial Function and Pathology 8
- RNA Research and Splicing 8
Cellular and Molecular Neuroscience 23
- Genetic Neurodegenerative Diseases 17

Co-authors: Volker W. Straub (24 shared papers)Francesco Muntoni (6 shared papers)Francesco Muntoni (16 shared papers)Ralf Herrmann (10 shared papers)S. Brown (5 shared papers)Norma Beatriz Romero (8 shared papers)Caroline A. Sewry (8 shared papers)Martin Brockington (8 shared papers)
Journals: Neuromuscular Disorders (31 papers)Neurology (8 papers)Annals of Neurology (6 papers)The American Journal of Human Genetics (6 papers)European Journal of Pediatrics (6 papers)
Partner nations: Germany United Kingdom France

In The Last Decade

Thomas Voit

156 papers receiving 10.1k citations

Peers

Countries citing papers authored by Thomas Voit

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Voit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Thomas Voit, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Thomas Voit Line = papers co-authored together Thomas Voit links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 160 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1 Developmental Cell ·Aruto Yoshida, Kazuhiro Kobayashi, Hiroshi Manya, Kiyomi Taniguchi, Hiroki Kano, Mamoru Mizuno, Toshiyuki Inazu, Hideyo Mitsuhashi	2001	611
2	Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan The American Journal of Human Genetics ·Martin Brockington, Derek J. Blake, Paola Prandini, S. Brown, Silvia Torelli, Matthew A. Benson, Chris Paul Ponting, Brigitte Estournet	2001	514
3	G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex Science ·Xianhua Piao, R. Sean Hill, Adria Bodell, Bernard S. Chang, Lina Basel‐Vanagaite, Rachel Straussberg, William B. Dobyns, Bassam Qasrawi	2004	447
4	Lack of myostatin results in excessive muscle growth but impaired force generation Proceedings of the National Academy of Sciences ·Helge Amthor, Raymond Macharia, Roberto Navarrete, Markus Schuelke, S. Brown, Anthony Otto, Thomas Voit, Francesco Muntoni	2007	351
5	Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy The American Journal of Human Genetics ·Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi, Pietro Attilio Tonali, Marina Mora, Lucia Ovidia Morandi, Alessandro Romorini, Thomas Voit	2000	330
6	Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies The American Journal of Human Genetics ·Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau, Behzad Moghadaszadeh, Nathalie Goemans, Carsten G. Bönnemann, Heinz Jungbluth, Volker W. Straub	2002	288
7	Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study The Lancet Neurology ·Thomas Voit, Haluk Topaloğlu, Volker W. Straub, Francesco Muntoni, Nicolas Deconinck, G. Campion, Sjef J. de Kimpe, Michelle Eagle	2014	262
8	Phenotypic spectrum associated with mutations in the fukutin‐related protein gene Annals of Neurology ·Eugenio Maria Mercuri, Martin Brockington, Volker W. Straub, Susana Quijano‐Roy, Yeliz Yuva, Ralf Herrmann, S. Brown, Silvia Torelli	2003	202
9	The congenital muscular dystrophies in 2004: a century of exciting progress Neuromuscular Disorders ·Francesco Muntoni, Thomas Voit	2004	199
10	Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy Nature Genetics ·Jan Senderek, Michael J. B. Krieger, Claudia Stendel, Carsten Bergmann, Markus Moser, Nico Breitbach‐Faller, Sabine Rudnik-Schöneborn, Astrid Blaschek	2005	198
11	Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy Nature Communications ·Caroline Le Guiner, Laurent Servais, Marie Montus, Thibaut Larcher, Bodvael Fraysse, Sophie Moullec, Marine Allais, Virginie François	2017	194
12	Combined Enzymatic Complex I and III Deficiency Associated with Mutations in the Nuclear Encoded NDUFS4 Gene Biochemical and Biophysical Research Communications ·Sandy Budde, Lambert P.W.J. van den Heuvel, Antoon J. M. Janssen, Roel Smeets, Carin A. F. Buskens, L. DeMeirleir, Rudy Van Coster, Martina Baethmann	2000	172
13	Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity Nature Genetics ·Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre, France Leturcq, Kemal Azibi, Cherif Beldjord, Alain Carrié, Dominique Récan	1995	169
14	A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Annals of Neurology ·Ana Ferreiro, Nicole Monnier, Norma Beatriz Romero, Jean‐Paul Leroy, Carsten G. Bönnemann, Charles-Antoine Haenggeli, Volker W. Straub, W Voss	2002	168
15	Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial Neuromuscular Disorders ·Lars Klinge, Volker W. Straub, Ulrich Neudorf, Joerg Schaper, T. Bosbach, Klaus Goerlinger, M. Wallot, S. M. Richards	2004	154
16	Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies American Journal Of Pathology ·S. Brown, Silvia Torelli, Martin Brockington, Yeliz Yuva, Cecilia Jimenez-Mallebrera, Lucy Feng, Louise V.B. Anderson, Isabella Ugo	2004	147
17	Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease Neurology ·Bru Cormand, Helena S. Pihko, Mónica Bayés, Leena K. Valanne, Pirkko Santavuori, Beril Talim, Ruth Gershoni‐Baruch, Arsalan Ahmad	2001	143
18	Secondary calpain3 deficiency in 2q-linked muscular dystrophy Neurology ·Henna Haravuori, Anna Vihola, Volker W. Straub, Mari Auranen, Isabelle Richard, Stéphanie Marchand, Thomas Voit, Siegfried Labeit	2001	143
19	Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain – a review European Journal of Pediatrics ·Jörg Klepper, Thomas Voit	2002	143
20	Longterm noninvasive ventilation in children and adolescents with neuromuscular disorders European Respiratory Journal ·Uwe Mellies, Regine Ragette, Christian Schwake, Holger Boehm, Thomas Voit, Helmut Teschler	2003	143

About Thomas Voit

Thomas Voit is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Genetics and Physiology, having authored 160 papers that have together received 10.5k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (87 papers), Cardiomyopathy and Myosin Studies (19 papers), Genetic Neurodegenerative Diseases (17 papers), Neurogenetic and Muscular Disorders Research (14 papers), Tissue Engineering and Regenerative Medicine (12 papers), Virus-based gene therapy research (9 papers), Mitochondrial Function and Pathology (8 papers) and RNA Research and Splicing (8 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (7.4k citations), Cellular and Molecular Neuroscience (1.7k citations), Cell Biology (1.4k citations) and Cardiology and Cardiovascular Medicine (1.4k citations). Thomas Voit has collaborated with scholars based in Germany, United Kingdom and France. Frequent co-authors include Volker W. Straub, Francesco Muntoni, Francesco Muntoni, Ralf Herrmann, S. Brown, Norma Beatriz Romero, Caroline A. Sewry, Martin Brockington, Pascale Guicheney and Eugenio Maria Mercuri. Their work appears in journals such as Neuromuscular Disorders, Neurology, Annals of Neurology, The American Journal of Human Genetics and European Journal of Pediatrics.

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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