Eva Forman
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Neonatal and fetal brain pathology
Papers in
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- RNA modifications and cancer 2
- Cancer-related gene regulation 2
- Genetics 3
- Genetics and Neurodevelopmental Disorders 2
- Neurogenetic and Muscular Disorders Research 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Mary D. King (5 shared papers)Kathleen M. Gorman (4 shared papers)Afif El‐Khuffash (2 shared papers)Adrienne Foran (2 shared papers)Colm R. Breatnach (2 shared papers)Sally Ann Lynch (5 shared papers)Louise Gallagher (1 shared paper)Jana Šemberová (1 shared paper)
- Journals
- Archives of Disease in Childhood (2 papers)Pediatric Research (1 paper)European Journal of Pediatrics (1 paper)European Journal of Medical Genetics (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- IrelandUnited States
In The Last Decade
Eva Forman
11 papers receiving 128 citations
Peers
Comparison fields: 5 of 41
- Genetics 43
- Pediatrics, Perinatology and Child Health 26
- Clinical Biochemistry 8
- Cognitive Neuroscience 20
- Emergency Medicine 9
Countries citing papers authored by Eva Forman
This map shows the geographic impact of Eva Forman'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 Eva Forman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Forman more than expected).
Fields of papers citing papers by Eva Forman
This network shows the impact of papers produced by Eva Forman. 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 Eva Forman. The network helps show where Eva Forman may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva Forman, 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 | 2018 | 52 | |
| 2 | 2017 | 26 | |
| 3 | 2016 | 20 | |
| 4 | 2013 | 7 | |
| 5 | 2018 | 7 | |
| 6 | 2019 | 5 | |
| 7 | 2018 | 5 | |
| 8 | 2020 | 3 | |
| 9 | 2022 | 1 | |
| 10 | 2017 | 1 | |
| 11 | 2019 | 1 |
About Eva Forman
Eva Forman is a scholar working on Molecular Biology, Genetics, Neurology, Genetics and Pediatrics, Perinatology and Child Health, having authored 11 papers that have together received 128 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA modifications and cancer (2 papers), Cancer-related gene regulation (2 papers), Neonatal Respiratory Health Research (2 papers), Neurological disorders and treatments (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (43 citations), Pediatrics, Perinatology and Child Health (26 citations), Clinical Biochemistry (8 citations), Cognitive Neuroscience (20 citations) and Emergency Medicine (9 citations). Eva Forman has collaborated with scholars based in Ireland and United States. Frequent co-authors include Mary D. King, Kathleen M. Gorman, Afif El‐Khuffash, Adrienne Foran, Colm R. Breatnach, Sally Ann Lynch, Louise Gallagher, Jana Šemberová, Veronica McInerney and Janusz Krawczyk. Their work appears in journals such as Archives of Disease in Childhood, Pediatric Research, European Journal of Pediatrics, European Journal of Medical Genetics and Neuromuscular Disorders.
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.