Amy Holt
Impact in
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Retinal Development and Disorders
- Genomics and Phylogenetic Studies
- Epigenetics and DNA Methylation
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- Photoreceptor and optogenetics research
Papers in
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- Genomics and Chromatin Dynamics 7
- Retinal Development and Disorders 5
- RNA and protein synthesis mechanisms 4
- Mitochondrial Function and Pathology 3
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- Photoreceptor and optogenetics research 5
- Neuroscience and Neural Engineering 3
- Genetic Neurodegenerative Diseases 3
- Co-authors
- Edward M. Rubin (9 shared papers)Veena Afzal (9 shared papers)L Pennacchio (9 shared papers)Axel Visel (8 shared papers)Ingrid Plajzer-Frick (8 shared papers)Jennifer A. Akiyama (7 shared papers)Malak Shoukry (7 shared papers)Nadav Ahituv (2 shared papers)
- Journals
- Science (3 papers)Nature Communications (2 papers)Cell (1 paper)Proceedings of the National Academy of Sciences (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Amy Holt
18 papers receiving 2.7k citations
Amy Holt's Hit Papers
Peers
Comparison fields: 5 of 106
- Molecular Biology 2.2k
- Cellular and Molecular Neuroscience 468
- Genetics 662
- Developmental Neuroscience 54
- Cancer Research 189
Countries citing papers authored by Amy Holt
This map shows the geographic impact of Amy Holt'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 Amy Holt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy Holt more than expected).
Fields of papers citing papers by Amy Holt
This network shows the impact of papers produced by Amy Holt. 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 Amy Holt. The network helps show where Amy Holt may publish in the future.
Co-authors
The 25 scholars most cited alongside Amy Holt, 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 | In vivo enhancer analysis of human conserved non-coding sequences Hit paper breakdown → | 2006 | 869 |
| 2 | 2013 | 258 | |
| 3 | 2008 | 248 | |
| 4 | 2007 | 229 | |
| 5 | 2011 | 203 | |
| 6 | 2013 | 171 | |
| 7 | 2019 | 116 | |
| 8 | 2019 | 112 | |
| 9 | 2015 | 108 | |
| 10 | 2014 | 96 | |
| 11 | 2017 | 68 | |
| 12 | 2015 | 66 | |
| 13 | 2005 | 60 | |
| 14 | 2014 | 50 | |
| 15 | 2016 | 48 | |
| 16 | 2009 | 15 | |
| 17 | 2022 | 12 | |
| 18 | 2004 | 2 | |
| 19 | 2024 | 0 |
About Amy Holt
Amy Holt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Infectious Diseases and Astronomy and Astrophysics, having authored 19 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (7 papers), Retinal Development and Disorders (5 papers), Photoreceptor and optogenetics research (5 papers), RNA and protein synthesis mechanisms (4 papers), Neuroscience and Neural Engineering (3 papers), Mitochondrial Function and Pathology (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Animal Genetics and Reproduction (2 papers). The work is most often cited by research in Molecular Biology (2.2k citations), Cellular and Molecular Neuroscience (468 citations), Genetics (662 citations), Developmental Neuroscience (54 citations) and Cancer Research (189 citations). Amy Holt has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Edward M. Rubin, Veena Afzal, L Pennacchio, Axel Visel, Ingrid Plajzer-Frick, Jennifer A. Akiyama, Malak Shoukry, Nadav Ahituv, Shyam Prabhakar and Brian L. Black. Their work appears in journals such as Science, Nature Communications, Cell, Proceedings of the National Academy of Sciences and Human Molecular Genetics.
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.