Anna Hurst
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Congenital heart defects research
Papers in
- Genetics 42
- Genomics and Rare Diseases 23
- Genetics and Neurodevelopmental Disorders 14
- Genomic variations and chromosomal abnormalities 8
- BRCA gene mutations in cancer 6
- Connective tissue disorders research 4
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- Epigenetics and DNA Methylation 7
- RNA modifications and cancer 4
- Ubiquitin and proteasome pathways 4
- Co-authors
- Ambika P. Ashraf (3 shared papers)Fady M. Mikhail (5 shared papers)Abhimanyu Garg (1 shared paper)Savithri Nageswaran (1 shared paper)Nathaniel H. Robin (4 shared papers)Abdel G. Elkahloun (1 shared paper)Kory R. Johnson (1 shared paper)Andrew K. Groves (1 shared paper)
- Journals
- Genetics in Medicine (9 papers)The American Journal of Human Genetics (5 papers)Human Genetics and Genomics Advances (3 papers)Nature Communications (3 papers)Genome Medicine (2 papers)
- Partner nations
- United StatesFranceCanada
In The Last Decade
Anna Hurst
64 papers receiving 947 citations
Peers
Comparison fields: 5 of 111
- Genetics 366
- Molecular Biology 369
- Psychiatry and Mental health 59
- Aging 7
- Cancer Research 49
Countries citing papers authored by Anna Hurst
This map shows the geographic impact of Anna Hurst'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 Anna Hurst with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Hurst more than expected).
Fields of papers citing papers by Anna Hurst
This network shows the impact of papers produced by Anna Hurst. 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 Anna Hurst. The network helps show where Anna Hurst may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Hurst, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 80 | |
| 2 | 2019 | 74 | |
| 3 | 2022 | 66 | |
| 4 | 2021 | 48 | |
| 5 | 2021 | 41 | |
| 6 | 2021 | 36 | |
| 7 | 2019 | 34 | |
| 8 | 2019 | 29 | |
| 9 | 2023 | 27 | |
| 10 | 2021 | 27 | |
| 11 | 2018 | 26 | |
| 12 | 2022 | 25 | |
| 13 | 2020 | 24 | |
| 14 | 2018 | 24 | |
| 15 | 2019 | 21 | |
| 16 | 2021 | 20 | |
| 17 | 2021 | 20 | |
| 18 | 2023 | 19 | |
| 19 | 2022 | 17 | |
| 20 | 2021 | 16 |
About Anna Hurst
Anna Hurst is a scholar working on Genetics, Molecular Biology, Cell Biology, Pediatrics, Perinatology and Child Health and Cardiology and Cardiovascular Medicine, having authored 72 papers that have together received 967 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (8 papers), Epigenetics and DNA Methylation (7 papers), BRCA gene mutations in cancer (6 papers), RNA modifications and cancer (4 papers), Ubiquitin and proteasome pathways (4 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (366 citations), Molecular Biology (369 citations), Psychiatry and Mental health (59 citations), Aging (7 citations) and Cancer Research (49 citations). Anna Hurst has collaborated with scholars based in United States, France and Canada. Frequent co-authors include Ambika P. Ashraf, Fady M. Mikhail, Abhimanyu Garg, Savithri Nageswaran, Nathaniel H. Robin, Abdel G. Elkahloun, Kory R. Johnson, Andrew K. Groves, Thomas Prescott Atkinson and Joshua D. Bernstock. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Human Genetics and Genomics Advances, Nature Communications and Genome Medicine.
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.