Simon D. Topp
Impact in
Papers in
- Co-authors
- Christopher E. Shaw (12 shared papers)Pablo Irarrázabal (1 shared paper)Craig H. Meyer (1 shared paper)Elfar Adalsteinsson (1 shared paper)Albert Macovski (1 shared paper)Daniel M. Spielman (1 shared paper)Bradley N. Smith (10 shared papers)Sverre Rosenbaum (2 shared papers)
- Journals
- Neurobiology of Aging (7 papers)Neuron (5 papers)Nature Genetics (4 papers)Magnetic Resonance Imaging (3 papers)Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (3 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Simon D. Topp
61 papers receiving 6.9k citations
Simon D. Topp's Hit Papers
Peers
Comparison fields: 5 of 143
- Neurology 3.6k
- Genetics 1.8k
- Neurology 1.0k
- Sensory Systems 207
- Molecular Biology 2.9k
Countries citing papers authored by Simon D. Topp
This map shows the geographic impact of Simon D. Topp'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 Simon D. Topp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon D. Topp more than expected).
Fields of papers citing papers by Simon D. Topp
This network shows the impact of papers produced by Simon D. Topp. 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 Simon D. Topp. The network helps show where Simon D. Topp may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon D. Topp, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS Hit paper breakdown → | 2013 | 1206 |
| 2 | Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways Hit paper breakdown → | 2015 | 801 |
| 3 | Genome-wide Analyses Identify KIF5A as a Novel ALS Gene Hit paper breakdown → | 2018 | 526 |
| 4 | An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People Hit paper breakdown → | 2012 | 518 |
| 5 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis Hit paper breakdown → | 2016 | 453 |
| 6 | Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology Hit paper breakdown → | 2021 | 337 |
| 7 | 2014 | 297 | |
| 8 | 2000 | 270 | |
| 9 | 2016 | 211 | |
| 10 | 2017 | 199 | |
| 11 | 2012 | 195 | |
| 12 | 2016 | 181 | |
| 13 | 1998 | 175 | |
| 14 | 2013 | 114 | |
| 15 | 2019 | 103 | |
| 16 | 2014 | 91 | |
| 17 | 1997 | 88 | |
| 18 | 1998 | 86 | |
| 19 | 2019 | 81 | |
| 20 | 2008 | 79 |
About Simon D. Topp
Simon D. Topp is a scholar working on Neurology, Genetics, Neurology, Molecular Biology and Radiology, Nuclear Medicine and Imaging, having authored 61 papers that have together received 7.0k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (35 papers), Neurogenetic and Muscular Disorders Research (19 papers), Neurological diseases and metabolism (10 papers), Parkinson's Disease Mechanisms and Treatments (7 papers), Advanced MRI Techniques and Applications (7 papers), RNA Research and Splicing (5 papers), Prion Diseases and Protein Misfolding (4 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Neurology (3.6k citations), Genetics (1.8k citations), Neurology (1.0k citations), Sensory Systems (207 citations) and Molecular Biology (2.9k citations). Simon D. Topp has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Christopher E. Shaw, Pablo Irarrázabal, Craig H. Meyer, Elfar Adalsteinsson, Albert Macovski, Daniel M. Spielman, Bradley N. Smith, Sverre Rosenbaum, Claire Troakes and Ammar Al‐Chalabi. Their work appears in journals such as Neurobiology of Aging, Neuron, Nature Genetics, Magnetic Resonance Imaging and Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.
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.