Maggie C. Walter

9.0k citations

122 papers · 2.9k indexed · h-index 32

Molecular Biology top 5%
Genetics top 1%
Cellular and Molecular Neuroscience top 5%
Epidemiology top 10%
Physiology top 5%

Co-authors: Hanns Lochmüller Peter Reilich Benedikt Schoser Wolfgang Müller‐Felber D. Pongratz Sabine Krause Simone Thiele Beate Schlotter‐Weigel
Topics: Muscle Physiology and Disorders (61 papers)Neurogenetic and Muscular Disorders Research (29 papers)Cardiomyopathy and Myosin Studies (24 papers)
Cited by: Genetics Cellular and Molecular Neuroscience Molecular Biology
Journals: Proceedings of the National Academy of Sciences PLoS ONE Brain
Partner nations: Germany United Kingdom United States

In The Last Decade

Maggie C. Walter

117 papers receiving 2.9k citations

Peers

Countries citing papers authored by Maggie C. Walter

Since Specialization

Citations

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

Fields of papers citing papers by Maggie C. Walter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maggie C. Walter. 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 Maggie C. Walter. The network helps show where Maggie C. Walter may publish in the future.

Co-authorship network of co-authors of Maggie C. Walter

This figure shows the co-authorship network connecting the top 25 collaborators of Maggie C. Walter. A scholar is included among the top collaborators of Maggie C. Walter 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 Maggie C. Walter. Maggie C. Walter 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	Patient-Reported Health-Related Quality of Life, Anxiety and Depression in Patients with Inclusion Body Myositis: A Register-Based Cross-Sectional Study in Germany 2023 ·Journal of Clinical Medicine ·(unknown),Simone Thiele,(unknown),Maggie C. Walter,Klaus Nagels	6
2	Systemic deletion of DMD exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking DMD exon 52 2023 ·Proceedings of the National Academy of Sciences ·(unknown),(unknown),Andreas Blutke,Elisabeth Kemter,Andreas Lange,(unknown),(unknown),(unknown),Mayuko Kurome,Barbara Keßler,Valeri Zakhartchenko,Andrea Bähr,Nikolai Klymiuk,Hiroshi Nagashima,Maggie C. Walter,Wolfgang Wurst,Christian Kupatt,Thomas Fröhlich,Eckhard Wolf	9
3	Congenital myopathy and epidermolysis bullosa due to PLEC variant 2021 ·Neuromuscular Disorders ·Maggie C. Walter,Peter Reilich,Sabine Krause,(unknown),(unknown),Hans H. Goebel,Benedikt Schoser,Angela Abicht	3
4	A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A 2021 ·Orphanet Journal of Rare Diseases ·Shahram Attarian,Peter Young,Thomas H. Brannagan,David Adams,Philip Van Damme,Florian P. Thomas,(unknown),(unknown),Céline Tard,Maggie C. Walter,Yann Péréon,David Walk,Amro Stino,Marianne de Visser,Camiel Verhamme,Anthony A. Amato,Gregory Carter,Laurent Magy,Jeffrey Statland,Kevin J. Felice	31
5	Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study 2019 ·Journal of Neuromuscular Diseases ·Maggie C. Walter,Stephan Wenninger,Simone Thiele,Julia M. Stauber,Miriam Hiebeler,(unknown),Kristina Ståhl,Astrid Pechmann,Hanns Lochmüller,Janbernd Kirschner,Benedikt Schoser	125
6	The multifaceted clinical presentation of VCP-proteinopathy in a Greek family. 2017 ·PubMed ·George K. Papadimas,George P. Paraskevas,Thomas Zambelis,(unknown),Mara Bourbouli,Anastasia Bougea,Maggie C. Walter,(unknown),Sabine Krause,Elisabeth Kapaki	13
7	Spinale Muskelatrophie: Zeit für das Neugeborenenscreening? 2017 ·Der Nervenarzt ·Katharina Vill,Astrid Blaschek,Ulrike Schara,Heike Kölbel,Katharina Hohenfellner,(unknown),B. Olgemöller,Maggie C. Walter,Wolfgang Müller‐Felber	3
8	216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15–17, 2016 Naarden, The Netherlands 2016 ·Neuromuscular Disorders ·Isabelle Richard,(unknown),Sebahattin Çirak,John Vissing,S. Brown,Kevin P. Campbell,Evelyne Gicquel,Jean‐Yves Hogrel,(unknown),(unknown),(unknown),Katherine D. Mathews,Francesco Muntoni,Susana Quijano‐Roy,Agata Robertson,(unknown),Tanya Stojkovic,Volker Straub,Haluk Topaloğlu,Jiri Vajsar,Maggie C. Walter	13
9	Disease burden of spinal muscular atrophy in Germany 2016 ·Orphanet Journal of Rare Diseases ·(unknown),Olivia Schreiber‐Katz,Simone Thiele,(unknown),(unknown),Peter Reilich,Maggie C. Walter,Klaus Nagels	87
10	An Integrated Diagnosis Strategy for Congenital Myopathies 2013 ·PLoS ONE ·Johann Böhm,Nasim Vasli,Edoardo Malfatti,Stéphanie Le Gras,Claire Feger,Bernard Jost,Nicole Monnier,Julie Brocard,Hatice Karasoy,Marion Gérard,Maggie C. Walter,Peter Reilich,Valérie Biancalana,Christine Kretz,Nadia Messaddeq,Isabelle Marty,Joël Lunardi,Norma B. Romero,Jocelyn Laporte	43
11	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
12	Flow Cytometry for the Analysis of α-Dystroglycan Glycosylation in Fibroblasts from Patients with Dystroglycanopathies 2013 ·PLoS ONE ·Elizabeth Stevens,Silvia Torelli,Lucy Feng,Rahul Phadke,Maggie C. Walter,Peter Schneiderat,Ayad Eddaoudi,Caroline A. Sewry,Francesco Muntoni	13
13	The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy 2010 ·Neuromuscular Disorders ·Peter Reilich,Benedikt Schoser,Nicolai Schramm,Sabine Krause,Joachim Schessl,Wolfram Kreß,Josef Müller‐Höcker,Maggie C. Walter,Hanns Lochmüller	67
14	In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes 2009 ·Human Molecular Genetics ·Stefanie Bulst,Angela Abicht,Elke Holinski‐Feder,(unknown),Udo Koehler,Christian Thirion,Maggie C. Walter,Joanna D. Stewart,Patrick F. Chinnery,Hanns Lochmüller,Rita Horváth	44
15	Lower Limb Radiology of Distal Myopathy due to the S60F Myotilin Mutation 2009 ·European Neurology ·Alisdair McNeill,Daniel Birchall,Volker Straub,Lev G. Goldfarb,Peter Reilich,Maggie C. Walter,Nicolai Schramm,Hanns Lochmüller,Patrick F. Chinnery	11
16	Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies 2008 ·Neuromuscular Disorders ·Katharina Strach,Torsten Sommer,(unknown),Carsten H. Meyer,Dirk Fischer,Maggie C. Walter,Matthias Vorgerd,Peter Reilich,Harald Bär,Jens Reimann,Ulrike Reuner,Alfried Germing,Hans H. Goebel,Hanns Lochmüller,Bernd J. Wintersperger,Rolf Schröder	31
17	Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy 2006 ·Neuromuscular Disorders ·Juliane S. Müller,Henriett Pikó,Benedikt Schoser,Beate Schlotter‐Weigel,Peter Reilich,(unknown),Christine Born,Veronika Karcagi,D. Pongratz,Hanns Lochmüller,Maggie C. Walter	19
18	125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23–25 April 2004, Naarden, The Netherlands 2004 ·Neuromuscular Disorders ·Luba Kalaydjieva,Hanns Lochmüller,Ivailo Tournev,Frank Baas,Judit Béres,J. Colomer,Velina Guergueltcheva,Ralf Herrmann,Veronika Karcagi,R. H. M. King,Toshiyuki Miyata,Andrea Müllner-Eidenböck,Tomohiko Okuda,Vedrana Milić Rašić,(unknown),Beril Talim,Juan J. Vílchez,Maggie C. Walter,Andoni Urtizberea,Luciano Merlini	22
19	A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation 2003 ·Neuromuscular Disorders ·Sabine Krause,Beate Schlotter‐Weigel,Maggie C. Walter,Hossein Najmabadi,Heinz Wiendl,Josef Müller‐Höcker,Wolfgang Müller‐Felber,D. Pongratz,Hanns Lochmüller	56
20	Genetic identity of Marinesco–Sjogren/myoglobinuria and CCFDN syndromes 2002 ·Neurology ·Luciano Merlini,Rebecca Gooding,Hanns Lochmüller,Wolfgang Müller‐Felber,Maggie C. Walter,Dora Angelicheva,Beril Talim,Joachim Hallmayer,Luba Kalaydjieva	25

About Maggie C. Walter

Maggie C. Walter is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience, having authored 122 papers that have together received 2.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (61 papers), Neurogenetic and Muscular Disorders Research (29 papers) and Cardiomyopathy and Myosin Studies (24 papers). The work is most often cited by research in Genetics (718 citations), Cellular and Molecular Neuroscience (558 citations) and Molecular Biology (1.8k citations). Maggie C. Walter has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Hanns Lochmüller, Peter Reilich, Benedikt Schoser, Wolfgang Müller‐Felber, D. Pongratz, Sabine Krause, Simone Thiele, Beate Schlotter‐Weigel, Rita Horváth and Chris Andersen. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Brain.

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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