Anna Hurst
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 21
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 8
- BRCA gene mutations in cancer 5
- Genetic Syndromes and Imprinting 4
- Genetics and Neurodevelopmental Disorders 3
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- Congenital heart defects research 4
- RNA modifications and cancer 3
- 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 (3 shared papers)T. Prescott Atkinson (1 shared paper)Kory R. Johnson (1 shared paper)Joshua D. Bernstock (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Journal of Personalized Medicine (1 paper)European Journal of Human Genetics (1 paper)Journal of Allergy and Clinical Immunology (1 paper)Molecular Cytogenetics (1 paper)
- Partner nations
- United StatesCanadaThailand
In The Last Decade
Anna Hurst
23 papers receiving 173 citations
Peers
Comparison fields: 5 of 59
- Genetics 69
- Pediatrics, Perinatology and Child Health 34
- Neurology 24
- Health Informatics 2
- Rheumatology 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 23 | |
| 2 | 2018 | 23 | |
| 3 | 2021 | 23 | |
| 4 | 2017 | 13 | |
| 5 | 2017 | 11 | |
| 6 | 2022 | 10 | |
| 7 | 2022 | 9 | |
| 8 | 2020 | 9 | |
| 9 | 2018 | 8 | |
| 10 | Disorders of GNAS Inactivation | 2017 | 8 |
| 11 | 2024 | 7 | |
| 12 | 2022 | 6 | |
| 13 | 2020 | 5 | |
| 14 | 2022 | 5 | |
| 15 | 2023 | 4 | |
| 16 | 2017 | 2 | |
| 17 | 2023 | 2 | |
| 18 | 2019 | 2 | |
| 19 | 2019 | 1 | |
| 20 | 2022 | 1 |
About Anna Hurst
Anna Hurst is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cell Biology and Cancer Research, having authored 30 papers that have together received 175 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genomic variations and chromosomal abnormalities (8 papers), BRCA gene mutations in cancer (5 papers), Prenatal Screening and Diagnostics (4 papers), Genetic Syndromes and Imprinting (4 papers), Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (69 citations), Pediatrics, Perinatology and Child Health (34 citations), Neurology (24 citations), Health Informatics (2 citations) and Rheumatology (21 citations). Anna Hurst has collaborated with scholars based in United States, Canada and Thailand. Frequent co-authors include Ambika P. Ashraf, Fady M. Mikhail, Abhimanyu Garg, Savithri Nageswaran, Nathaniel H. Robin, T. Prescott Atkinson, Kory R. Johnson, Joshua D. Bernstock, Abdel G. Elkahloun and Chad Haldeman‐Englert. Their work appears in journals such as Genetics in Medicine, Journal of Personalized Medicine, European Journal of Human Genetics, Journal of Allergy and Clinical Immunology and Molecular Cytogenetics.
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.