Yonatan Perez
Impact in
- Neurology top 5%
- Neuroinflammation and Neurodegeneration Mechanisms
- Developmental Neuroscience top 10%
- Neurogenesis and neuroplasticity mechanisms
Papers in
-
- Single-cell and spatial transcriptomics 3
- RNA Research and Splicing 3
- Ion channel regulation and function 3
- RNA modifications and cancer 3
- Congenital heart defects research 2
- Epigenetics and DNA Methylation 2
- Retinal Development and Disorders 2
- Co-authors
- Arnold R. Kriegstein (4 shared papers)Simone Mayer (2 shared papers)Lucas Schirmer (2 shared papers)David H. Rowitch (1 shared paper)Maximilian Haeussler (2 shared papers)Aparna Bhaduri (1 shared paper)Ohad S. Birk (23 shared papers)Rotem Kadir (17 shared papers)
- Journals
- Brain (3 papers)European Journal of Human Genetics (3 papers)Journal of Medical Genetics (3 papers)Nature Communications (2 papers)Science (2 papers)
- Partner nations
- IsraelUnited StatesUnited Kingdom
In The Last Decade
Yonatan Perez
26 papers receiving 1.1k citations
Yonatan Perez's Hit Papers
Peers
Comparison fields: 5 of 95
- Neurology 148
- Developmental Neuroscience 58
- Biological Psychiatry 25
- Molecular Biology 692
- Cognitive Neuroscience 156
Countries citing papers authored by Yonatan Perez
This map shows the geographic impact of Yonatan Perez'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 Yonatan Perez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yonatan Perez more than expected).
Fields of papers citing papers by Yonatan Perez
This network shows the impact of papers produced by Yonatan Perez. 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 Yonatan Perez. The network helps show where Yonatan Perez may publish in the future.
Co-authors
The 25 scholars most cited alongside Yonatan Perez, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Single-cell genomics identifies cell type–specific molecular changes in autism Hit paper breakdown → | 2019 | 538 |
| 2 | 2023 | 82 | |
| 3 | 2017 | 73 | |
| 4 | 2016 | 64 | |
| 5 | 2013 | 46 | |
| 6 | 2013 | 38 | |
| 7 | 2015 | 37 | |
| 8 | 2019 | 31 | |
| 9 | 2019 | 30 | |
| 10 | 2018 | 29 | |
| 11 | 2023 | 28 | |
| 12 | 2021 | 24 | |
| 13 | 2018 | 21 | |
| 14 | 2018 | 16 | |
| 15 | 2017 | 13 | |
| 16 | 2017 | 13 | |
| 17 | 2016 | 13 | |
| 18 | 2015 | 12 | |
| 19 | 2022 | 11 | |
| 20 | 2017 | 11 |
About Yonatan Perez
Yonatan Perez is a scholar working on Molecular Biology, Epidemiology, Cell Biology, Cellular and Molecular Neuroscience and Genetics, having authored 27 papers that have together received 1.2k indexed citations. Recurring topics across this work include Single-cell and spatial transcriptomics (3 papers), RNA Research and Splicing (3 papers), Ion channel regulation and function (3 papers), RNA modifications and cancer (3 papers), Congenital heart defects research (2 papers), melanin and skin pigmentation (2 papers), Epigenetics and DNA Methylation (2 papers) and Retinal Development and Disorders (2 papers). The work is most often cited by research in Neurology (148 citations), Developmental Neuroscience (58 citations), Biological Psychiatry (25 citations), Molecular Biology (692 citations) and Cognitive Neuroscience (156 citations). Yonatan Perez has collaborated with scholars based in Israel, United States and United Kingdom. Frequent co-authors include Arnold R. Kriegstein, Simone Mayer, Lucas Schirmer, David H. Rowitch, Maximilian Haeussler, Aparna Bhaduri, Ohad S. Birk, Rotem Kadir, Michael Volodarsky and Ohad Wormser. Their work appears in journals such as Brain, European Journal of Human Genetics, Journal of Medical Genetics, Nature Communications and Science.
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.