Peter C. Sapp
Impact in
Papers in
- Neurology 50
- Amyotrophic Lateral Sclerosis Research 50
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- Paraoxonase enzyme and polymorphisms 2
- Co-authors
- Robert H. Brown (29 shared papers)Diane M. McKenna-Yasek (18 shared papers)Howard Robert Horvitz (15 shared papers)D. McKenna‐Yasek (10 shared papers)Betsy A. Hosler (9 shared papers)John E. Landers (10 shared papers)Jonathan L. Haines (10 shared papers)Daryl A. Bosco (3 shared papers)
- Journals
- Human Molecular Genetics (7 papers)Neurology (6 papers)Neuron (4 papers)Neurogenetics (3 papers)Neurobiology of Aging (3 papers)
- Partner nations
- United StatesUnited KingdomItaly
In The Last Decade
Peter C. Sapp
55 papers receiving 15k citations
Peter C. Sapp's Hit Papers
Peers
Comparison fields: 5 of 128
- Neurology 10.7k
- Aging 149
- Cellular and Molecular Neuroscience 820
- Neurology 358
- Molecular Biology 2.5k
Countries citing papers authored by Peter C. Sapp
This map shows the geographic impact of Peter C. Sapp'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 Peter C. Sapp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter C. Sapp more than expected).
Fields of papers citing papers by Peter C. Sapp
This network shows the impact of papers produced by Peter C. Sapp. 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 Peter C. Sapp. The network helps show where Peter C. Sapp may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter C. Sapp, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis Hit paper breakdown → | 1993 | 6109 |
| 2 | Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis Hit paper breakdown → | 2009 | 2174 |
| 3 | Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways Hit paper breakdown → | 2015 | 807 |
| 4 | Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene Hit paper breakdown → | 2018 | 539 |
| 5 | Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Hit paper breakdown → | 2012 | 498 |
| 6 | 1997 | 445 | |
| 7 | 2010 | 441 | |
| 8 | 2009 | 337 | |
| 9 | 1991 | 312 | |
| 10 | 2006 | 304 | |
| 11 | 2014 | 298 | |
| 12 | 2008 | 238 | |
| 13 | 2015 | 216 | |
| 14 | 2016 | 212 | |
| 15 | 2017 | 201 | |
| 16 | 2012 | 196 | |
| 17 | 2009 | 155 | |
| 18 | 2011 | 147 | |
| 19 | 1994 | 141 | |
| 20 | 1994 | 141 |
About Peter C. Sapp
Peter C. Sapp is a scholar working on Neurology, Clinical Biochemistry, Genetics, Genetics and Cellular and Molecular Neuroscience, having authored 55 papers that have together received 15.5k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (50 papers), Forensic and Genetic Research (2 papers), Paraoxonase enzyme and polymorphisms (2 papers), Muscle Physiology and Disorders (2 papers), Genetic Associations and Epidemiology (2 papers), Epigenetics and DNA Methylation (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Neurology (10.7k citations), Aging (149 citations), Cellular and Molecular Neuroscience (820 citations), Neurology (358 citations) and Molecular Biology (2.5k citations). Peter C. Sapp has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Robert H. Brown, Diane M. McKenna-Yasek, Howard Robert Horvitz, D. McKenna‐Yasek, Betsy A. Hosler, John E. Landers, Jonathan L. Haines, Daryl A. Bosco, Thomas J. Kwiatkowski and Lawrence J. Hayward. Their work appears in journals such as Human Molecular Genetics, Neurology, Neuron, Neurogenetics and Neurobiology of Aging.
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.