Alisa Mo
Impact in
- Developmental Neuroscience top 10%
-
- Genetic Neurodegenerative Diseases
Papers in
- Genetics 6
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
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- Genetic Neurodegenerative Diseases 2
- Hereditary Neurological Disorders 2
- Co-authors
- Jeremy Nathans (3 shared papers)Joseph R. Nery (2 shared papers)Gilbert Lee Henry (2 shared papers)Sean R. Eddy (2 shared papers)Chongyuan Luo (2 shared papers)Ryan Lister (2 shared papers)Serge Picard (2 shared papers)Mark A. Urich (2 shared papers)
- Journals
- Neuron (2 papers)Clinical Genetics (2 papers)Neurology Genetics (2 papers)Movement Disorders (2 papers)JAMA Neurology (1 paper)
- Partner nations
- United StatesGermanyAustralia
In The Last Decade
Alisa Mo
17 papers receiving 1.0k citations
Alisa Mo's Hit Papers
Peers
Comparison fields: 5 of 90
- Developmental Neuroscience 54
- Cellular and Molecular Neuroscience 222
- Genetics 284
- Molecular Biology 653
- Biological Psychiatry 20
Countries citing papers authored by Alisa Mo
This map shows the geographic impact of Alisa Mo'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 Alisa Mo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alisa Mo more than expected).
Fields of papers citing papers by Alisa Mo
This network shows the impact of papers produced by Alisa Mo. 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 Alisa Mo. The network helps show where Alisa Mo may publish in the future.
Co-authors
The 25 scholars most cited alongside Alisa Mo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Epigenomic Signatures of Neuronal Diversity in the Mammalian Brain Hit paper breakdown → | 2015 | 530 |
| 2 | 2014 | 166 | |
| 3 | 2016 | 135 | |
| 4 | 2011 | 99 | |
| 5 | 2023 | 16 | |
| 6 | 2022 | 15 | |
| 7 | 2023 | 15 | |
| 8 | 2022 | 11 | |
| 9 | 2008 | 9 | |
| 10 | 2024 | 8 | |
| 11 | 2023 | 6 | |
| 12 | 2021 | 6 | |
| 13 | 2025 | 5 | |
| 14 | 2022 | 3 | |
| 15 | 2023 | 1 | |
| 16 | 2022 | 1 | |
| 17 | 2023 | 1 | |
| 18 | 2025 | 0 |
About Alisa Mo
Alisa Mo is a scholar working on Genetics, Genetics, Cellular and Molecular Neuroscience, Molecular Biology and Neurology, having authored 18 papers that have together received 1.0k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Genomics and Chromatin Dynamics (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Hereditary Neurological Disorders (2 papers). The work is most often cited by research in Developmental Neuroscience (54 citations), Cellular and Molecular Neuroscience (222 citations), Genetics (284 citations), Molecular Biology (653 citations) and Biological Psychiatry (20 citations). Alisa Mo has collaborated with scholars based in United States, Germany and Australia. Frequent co-authors include Jeremy Nathans, Joseph R. Nery, Gilbert Lee Henry, Sean R. Eddy, Chongyuan Luo, Ryan Lister, Serge Picard, Mark A. Urich, Joseph R. Ecker and Eran A. Mukamel. Their work appears in journals such as Neuron, Clinical Genetics, Neurology Genetics, Movement Disorders and JAMA Neurology.
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.