Simon E. Fisher
Impact in
- Developmental Biology top 0.1%
-
- Language Development and Disorders
- Reading and Literacy Development
Papers in
- Genetics 156
- Genetics and Neurodevelopmental Disorders 109
- Genetic Associations and Epidemiology 29
- Genomic variations and chromosomal abnormalities 23
-
- Language Development and Disorders 59
- Reading and Literacy Development 30
- Co-authors
- Anthony P. Monaco (36 shared papers)Cecilia S. L. Lai (6 shared papers)Clyde Francks (62 shared papers)Faraneh Vargha‐Khadem (4 shared papers)Jane A. Hurst (2 shared papers)Sonja C. Vernes (19 shared papers)Constance Scharff (4 shared papers)Gary F. Marcus (2 shared papers)
- Journals
- The American Journal of Human Genetics (20 papers)Molecular Psychiatry (18 papers)European Journal of Human Genetics (12 papers)Genes Brain & Behavior (12 papers)Nature Communications (11 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
Simon E. Fisher
308 papers receiving 23.0k citations
Simon E. Fisher's Hit Papers
Peers
Comparison fields: 5 of 199
- Developmental Biology 1.2k
- Developmental and Educational Psychology 5.2k
- Cognitive Neuroscience 7.5k
- Genetics 7.8k
- Developmental Neuroscience 604
Countries citing papers authored by Simon E. Fisher
This map shows the geographic impact of Simon E. Fisher'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 E. Fisher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon E. Fisher more than expected).
Fields of papers citing papers by Simon E. Fisher
This network shows the impact of papers produced by Simon E. Fisher. 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 E. Fisher. The network helps show where Simon E. Fisher may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon E. Fisher, 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 321 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A forkhead-domain gene is mutated in a severe speech and language disorder Hit paper breakdown → | 2001 | 1481 |
| 2 | Molecular evolution of FOXP2, a gene involved in speech and language Hit paper breakdown → | 2002 | 1077 |
| 3 | Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations Hit paper breakdown → | 2011 | 959 |
| 4 | Common genetic variants influence human subcortical brain structures Hit paper breakdown → | 2015 | 669 |
| 5 | A common molecular basis for three inherited kidney stone diseases Hit paper breakdown → | 1996 | 636 |
| 6 | The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data Hit paper breakdown → | 2014 | 627 |
| 7 | The genetic architecture of the human cerebral cortex Hit paper breakdown → | 2020 | 581 |
| 8 | A Functional Genetic Link between Distinct Developmental Language Disorders Hit paper breakdown → | 2008 | 534 |
| 9 | ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries Hit paper breakdown → | 2020 | 432 |
| 10 | 2009 | 427 | |
| 11 | 2009 | 407 | |
| 12 | 1998 | 380 | |
| 13 | 2005 | 325 | |
| 14 | Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium Hit paper breakdown → | 2018 | 296 |
| 15 | 2002 | 292 | |
| 16 | 2007 | 280 | |
| 17 | 2005 | 258 | |
| 18 | 2014 | 246 | |
| 19 | 2002 | 237 | |
| 20 | 2007 | 236 |
About Simon E. Fisher
Simon E. Fisher is a scholar working on Genetics, Developmental and Educational Psychology, Cognitive Neuroscience, Molecular Biology and Developmental Biology, having authored 321 papers that have together received 24.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (109 papers), Language Development and Disorders (59 papers), Congenital heart defects research (50 papers), Hemispheric Asymmetry in Neuroscience (30 papers), Reading and Literacy Development (30 papers), Genetic Associations and Epidemiology (29 papers), Autism Spectrum Disorder Research (28 papers) and Genomic variations and chromosomal abnormalities (23 papers). The work is most often cited by research in Developmental Biology (1.2k citations), Developmental and Educational Psychology (5.2k citations), Cognitive Neuroscience (7.5k citations), Genetics (7.8k citations) and Developmental Neuroscience (604 citations). Simon E. Fisher has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Anthony P. Monaco, Cecilia S. L. Lai, Clyde Francks, Faraneh Vargha‐Khadem, Jane A. Hurst, Sonja C. Vernes, Constance Scharff, Gary F. Marcus, John C. DeFries and Dianne F. Newbury. Their work appears in journals such as The American Journal of Human Genetics, Molecular Psychiatry, European Journal of Human Genetics, Genes Brain & Behavior and Nature Communications.
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.