G.W. Padberg

2.1k total citations
22 papers, 1.0k citations indexed

About

G.W. Padberg is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, G.W. Padberg has authored 22 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in G.W. Padberg's work include Muscle Physiology and Disorders (11 papers), Cardiomyopathy and Myosin Studies (5 papers) and Neurogenetic and Muscular Disorders Research (4 papers). G.W. Padberg is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Cardiomyopathy and Myosin Studies (5 papers) and Neurogenetic and Muscular Disorders Research (4 papers). G.W. Padberg collaborates with scholars based in Netherlands, United States and France. G.W. Padberg's co-authors include Peter Lunt, Rune R. Frants, Michel Fardeau, Manuela C. Koch, Egbert Bakker, Oebele F. Brouwer, Cisca Wijmenga, Lodewijk A. Sandkuijl, Baziel G.M. van Engelen and Patrick J. Willems and has published in prestigious journals such as New England Journal of Medicine, Brain and Neurology.

In The Last Decade

G.W. Padberg

22 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
G.W. Padberg Netherlands 16 784 247 218 169 150 22 1.0k
Daisuke Furutama Japan 18 743 0.9× 133 0.5× 520 2.4× 165 1.0× 48 0.3× 36 1.2k
Ron F. Hrstka United States 5 1.0k 1.3× 234 0.9× 239 1.1× 51 0.3× 164 1.1× 5 1.2k
Marcella Neri Italy 18 546 0.7× 144 0.6× 197 0.9× 99 0.6× 40 0.3× 37 785
Chester M. Hedgepeth United States 7 650 0.8× 426 1.7× 109 0.5× 26 0.2× 65 0.4× 9 1.2k
Emmanuel Nivet France 17 1.1k 1.4× 49 0.2× 211 1.0× 200 1.2× 152 1.0× 32 1.7k
C.S.M. Straathof Netherlands 18 728 0.9× 213 0.9× 154 0.7× 250 1.5× 14 0.1× 35 1.1k
Humberto Santo Neto Brazil 23 893 1.1× 131 0.5× 221 1.0× 115 0.7× 31 0.2× 71 1.4k
Donatella Biral Italy 24 957 1.2× 262 1.1× 315 1.4× 84 0.5× 21 0.1× 51 1.4k
Eppie M. Yiu Australia 19 686 0.9× 79 0.3× 606 2.8× 199 1.2× 33 0.2× 65 1.3k
Marina Pedemonte Italy 21 1.0k 1.3× 176 0.7× 163 0.7× 243 1.4× 30 0.2× 57 1.3k

Countries citing papers authored by G.W. Padberg

Since Specialization
Citations

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

Fields of papers citing papers by G.W. Padberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G.W. Padberg. 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 G.W. Padberg. The network helps show where G.W. Padberg may publish in the future.

Co-authorship network of co-authors of G.W. Padberg

This figure shows the co-authorship network connecting the top 25 collaborators of G.W. Padberg. A scholar is included among the top collaborators of G.W. Padberg 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 G.W. Padberg. G.W. Padberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Greef, Jessica C. de, Richard J.L.F. Lemmers, Pilar Camaño, et al.. (2010). Clinical features of facioscapulohumeral muscular dystrophy 2. Neurology. 75(17). 1548–1554. 117 indexed citations
2.
Voermans, Nicol C., Maïlys Guillard, Martin Lammens, et al.. (2010). Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy.. Clinical Neuropathology. 29(2). 71–7. 18 indexed citations
3.
Horlings, Corinne G.C., Marten Munneke, J.H.J. Allum, et al.. (2009). Epidemiology and pathophysiology of falls in facioscapulohumeral disease. Journal of Neurology Neurosurgery & Psychiatry. 80(12). 1357–1363. 24 indexed citations
4.
Kooi, Anneke J. van der, P. G. Barth, C Höweler, et al.. (2007). Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families. Neurology. 68(24). 2125–2128. 43 indexed citations
5.
Verzijl, H. T. F. M., Baziel G.M. van Engelen, Gerry Steenbergen, et al.. (1999). Reply. Annals of Neurology. 45(4). 548–548. 1 indexed citations
6.
Ensink, R.J.H., Kristien Verhoeven, Henri A. M. Marres, et al.. (1998). Early-Onset Sensorineural Hearing Loss and Late-Onset Neurologic Complaints Caused by a Mitochondrial Mutation at Position 7472. Archives of Otolaryngology - Head and Neck Surgery. 124(8). 886–886. 10 indexed citations
7.
Verzijl, H. T. F. M., Baziel G.M. van Engelen, Gerry Steenbergen, et al.. (1998). Genetic characteristics of myoadenylate deaminase deficiency. Annals of Neurology. 44(1). 140–143. 47 indexed citations
8.
Kerangueven, F, François Eisinger, Tetsuro Noguchi, et al.. (1997). Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions. Oncogene. 14(3). 339–347. 54 indexed citations
9.
Bruyn, R.P.M., et al.. (1997). Familial spastic paraplegia: evidence for a fourth locus. Clinical Neurology and Neurosurgery. 99(2). 87–90. 4 indexed citations
10.
Marsh, Deborah J., Zimu Zheng, Jan Zedenius, et al.. (1997). Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas.. PubMed. 57(3). 500–3. 60 indexed citations
11.
Kooi, Anneke J. van der, P. G. Barth, H. F. M. Busch, et al.. (1996). The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands. Brain. 119(5). 1471–1480. 67 indexed citations
12.
Ensink, R.J.H., Henri A. M. Marres, Cor W. R. J. Cremers, et al.. (1996). Early onset maternal inherited hearing loss with late onset neurological symptoms present in a three generation Dutch family.. Radboud Repository (Radboud University). 2 indexed citations
13.
Bakker, Egbert, Els Voorhoeve, P.F. Ippel, et al.. (1996). Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.. Journal of Medical Genetics. 33(1). 29–35. 36 indexed citations
14.
Camp, Guy Van, Paul Coucke, Wendy Balemans, et al.. (1995). Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Human Molecular Genetics. 4(11). 2159–2163. 79 indexed citations
15.
Padberg, G.W., Rune R. Frants, Oebele F. Brouwer, et al.. (1995). Facioscapulohumeral muscular dystrophy in the dutch population. Muscle & Nerve. 18(S13). S81–S84. 94 indexed citations
16.
Coucke, Paul, Guy Van Camp, Shelley D. Smith, et al.. (1994). Linkage of Autosomal Dominant Hearing Loss to the Short Arm of Chromosome 1 in Two Families. New England Journal of Medicine. 331(7). 425–431. 102 indexed citations
17.
Brouwer, Oebele F., et al.. (1993). Job perspectives in facioscapulohumeral muscular dystrophy. Disability and Rehabilitation. 15(1). 24–28. 25 indexed citations
18.
Padberg, G.W., Peter Lunt, Manuela C. Koch, & Michel Fardeau. (1991). Diagnostic criteria for facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 1(4). 231–234. 175 indexed citations
19.
Sarfarazi, M., Meena Upadhyaya, G.W. Padberg, et al.. (1989). An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.. Journal of Medical Genetics. 26(8). 481–484. 15 indexed citations
20.
Breedveld, F. C., et al.. (1987). RHEUMATOID ARTHRITIS WITH VERTICAL ATLANTO-AXIAL SUBLUXATION COMPLICATED BY HYDROCEPHALUS. Lara D. Veeken. 26(1). 56–58. 10 indexed citations

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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