William Seltzer
Impact in
- Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
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- Genetic Neurodegenerative Diseases
Papers in
-
- Mitochondrial Function and Pathology 8
- Muscle Physiology and Disorders 6
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- Genetic Neurodegenerative Diseases 12
- Hereditary Neurological Disorders 8
- Co-authors
- Edward R.B. McCabe (16 shared papers)Mary G. Powers (4 shared papers)Margo Anderson (6 shared papers)Shu‐Zhen Huang (1 shared paper)M L Law (1 shared paper)Tetsuo Ashizawa (3 shared papers)Michael A. Boss (3 shared papers)Nicholas T. Potter (2 shared papers)
- Journals
- Neurology (6 papers)International Migration Review (4 papers)Population Studies (4 papers)Neuromuscular Disorders (2 papers)Human Genetics (2 papers)
- Partner nations
- United StatesCanadaItaly
In The Last Decade
William Seltzer
75 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 150
- Neurology 541
- Cellular and Molecular Neuroscience 583
- Genetics 211
- Neurology 149
- Genetics 426
Countries citing papers authored by William Seltzer
This map shows the geographic impact of William Seltzer'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 William Seltzer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William Seltzer more than expected).
Fields of papers citing papers by William Seltzer
This network shows the impact of papers produced by William Seltzer. 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 William Seltzer. The network helps show where William Seltzer may publish in the future.
Co-authors
The 25 scholars most cited alongside William Seltzer, 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 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 216 | |
| 2 | 2012 | 193 | |
| 3 | 2008 | 149 | |
| 4 | 2000 | 147 | |
| 5 | 1987 | 136 | |
| 6 | 1998 | 126 | |
| 7 | 2017 | 113 | |
| 8 | Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions. | 1987 | 78 |
| 9 | 2002 | 67 | |
| 10 | 2004 | 63 | |
| 11 | 2007 | 61 | |
| 12 | 1998 | 56 | |
| 13 | Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy. | 1992 | 53 |
| 14 | 1998 | 52 | |
| 15 | 2000 | 52 | |
| 16 | 1989 | 48 | |
| 17 | The Dark Side of Numbers: The Role of Population Data Systems in Human Rights Abuses | 2001 | 46 |
| 18 | 1994 | 45 | |
| 19 | 1998 | 39 | |
| 20 | Genetic analysis of Hispanic individuals with cystic fibrosis. | 1994 | 38 |
About William Seltzer
William Seltzer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health, General Health Professions and Statistics and Probability, having authored 80 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (12 papers), Hereditary Neurological Disorders (8 papers), Census and Population Estimation (8 papers), Mitochondrial Function and Pathology (8 papers), Muscle Physiology and Disorders (6 papers), Cancer, Hypoxia, and Metabolism (6 papers), Global Maternal and Child Health (5 papers) and Cystic Fibrosis Research Advances (5 papers). The work is most often cited by research in Neurology (541 citations), Cellular and Molecular Neuroscience (583 citations), Genetics (211 citations), Neurology (149 citations) and Genetics (426 citations). William Seltzer has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Edward R.B. McCabe, Mary G. Powers, Margo Anderson, Shu‐Zhen Huang, M L Law, Tetsuo Ashizawa, Michael A. Boss, Nicholas T. Potter, Matthew J. Farrer and Balaji S. Srinivasan. Their work appears in journals such as Neurology, International Migration Review, Population Studies, Neuromuscular Disorders and Human Genetics.
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.