G.W. Padberg
Impact in
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 10%
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Muscle Physiology and Disorders 11
- Mitochondrial Function and Pathology 3
-
- Genetic Neurodegenerative Diseases 3
- Co-authors
- Peter Lunt (2 shared papers)Rune R. Frants (7 shared papers)Manuela C. Koch (1 shared paper)Michel Fardeau (1 shared paper)Egbert Bakker (5 shared papers)Oebele F. Brouwer (2 shared papers)Cisca Wijmenga (2 shared papers)Lodewijk A. Sandkuijl (2 shared papers)
- Journals
- Journal of Medical Genetics (4 papers)Neurology (2 papers)Annals of Neurology (2 papers)Journal of Neurology Neurosurgery & Psychiatry (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- NetherlandsUnited StatesFrance
In The Last Decade
G.W. Padberg
22 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 69
- Sensory Systems 147
- Genetics 130
- Molecular Biology 744
- Cellular and Molecular Neuroscience 172
- Cardiology and Cardiovascular Medicine 185
Countries citing papers authored by G.W. Padberg
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
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-authors
The 25 scholars most cited alongside G.W. Padberg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 176 | |
| 2 | 2010 | 118 | |
| 3 | 1994 | 102 | |
| 4 | 1995 | 95 | |
| 5 | 1995 | 80 | |
| 6 | 1996 | 67 | |
| 7 | Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas. | 1997 | 60 |
| 8 | 1997 | 54 | |
| 9 | 1998 | 47 | |
| 10 | 2007 | 43 | |
| 11 | 1996 | 36 | |
| 12 | 1999 | 31 | |
| 13 | 2009 | 26 | |
| 14 | 1993 | 25 | |
| 15 | Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy. | 2010 | 18 |
| 16 | 1989 | 15 | |
| 17 | 1998 | 10 | |
| 18 | 1987 | 10 | |
| 19 | 1997 | 4 | |
| 20 | 2004 | 4 |
About G.W. Padberg
G.W. Padberg is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Genetics and Neurology, having authored 22 papers that have together received 1.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (11 papers), Cardiomyopathy and Myosin Studies (5 papers), Genetic Neurodegenerative Diseases (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Mitochondrial Function and Pathology (3 papers), BRCA gene mutations in cancer (2 papers), Neurological diseases and metabolism (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). The work is most often cited by research in Sensory Systems (147 citations), Genetics (130 citations), Molecular Biology (744 citations), Cellular and Molecular Neuroscience (172 citations) and Cardiology and Cardiovascular Medicine (185 citations). G.W. Padberg has collaborated with scholars based in Netherlands, United States and France. Frequent co-authors include Peter Lunt, Rune R. Frants, Manuela C. Koch, Michel Fardeau, Egbert Bakker, Oebele F. Brouwer, Cisca Wijmenga, Lodewijk A. Sandkuijl, Baziel G.M. van Engelen and Guy Van Camp. Their work appears in journals such as Journal of Medical Genetics, Neurology, Annals of Neurology, Journal of Neurology Neurosurgery & Psychiatry and Neuromuscular Disorders.
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.