Anna Hurst
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- BRCA gene mutations in cancer
Papers in
- Genetics 20
- Genomics and Rare Diseases 12
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 3
- Genetics and Neurodevelopmental Disorders 2
- Connective tissue disorders research 2
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- Congenital heart defects research 3
- RNA modifications and cancer 3
- Co-authors
- Ambika P. Ashraf (3 shared papers)Savithri Nageswaran (1 shared paper)Fady M. Mikhail (5 shared papers)Abhimanyu Garg (1 shared paper)Andrew K. Groves (1 shared paper)Joshua D. Bernstock (1 shared paper)Abdel G. Elkahloun (1 shared paper)Kory R. Johnson (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Frontiers in Genetics (1 paper)Genome Medicine (1 paper)Hormone Research in Paediatrics (1 paper)Frontiers in Public Health (1 paper)
- Partner nations
- United StatesCanadaGeorgia
In The Last Decade
Anna Hurst
25 papers receiving 184 citations
Peers
Comparison fields: 5 of 54
- Genetics 64
- Health Informatics 2
- Rheumatology 20
- Neurology 19
- Pediatrics, Perinatology and Child Health 21
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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 26 | |
| 2 | 2021 | 24 | |
| 3 | 2018 | 23 | |
| 4 | 2017 | 13 | |
| 5 | 2022 | 13 | |
| 6 | 2017 | 12 | |
| 7 | Disorders of GNAS Inactivation | 2017 | 10 |
| 8 | 2024 | 9 | |
| 9 | 2022 | 9 | |
| 10 | 2020 | 9 | |
| 11 | 2018 | 8 | |
| 12 | 2022 | 6 | |
| 13 | 2022 | 5 | |
| 14 | 2020 | 5 | |
| 15 | 2023 | 4 | |
| 16 | 2023 | 3 | |
| 17 | 2019 | 2 | |
| 18 | 2017 | 2 | |
| 19 | 2025 | 1 | |
| 20 | 2022 | 1 |
About Anna Hurst
Anna Hurst is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 33 papers that have together received 190 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers), Genetic Syndromes and Imprinting (3 papers), RNA modifications and cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Genetics (64 citations), Health Informatics (2 citations), Rheumatology (20 citations), Neurology (19 citations) and Pediatrics, Perinatology and Child Health (21 citations). Anna Hurst has collaborated with scholars based in United States, Canada and Georgia. Frequent co-authors include Ambika P. Ashraf, Savithri Nageswaran, Fady M. Mikhail, Abhimanyu Garg, Andrew K. Groves, Joshua D. Bernstock, Abdel G. Elkahloun, Kory R. Johnson, Michael A. Levine and T. Prescott Atkinson. Their work appears in journals such as Genetics in Medicine, Frontiers in Genetics, Genome Medicine, Hormone Research in Paediatrics and Frontiers in Public Health.
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.