Edith Said
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- RNA modifications and cancer
- RNA regulation and disease
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 4
- Genetic and Kidney Cyst Diseases 2
- Genomic variations and chromosomal abnormalities 2
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- Congenital heart defects research 2
- Co-authors
- Roberto Galea (1 shared paper)Doriette Soler (1 shared paper)Caroline A. Sewry (1 shared paper)J. P. Fryns (1 shared paper)A. Cuschieri (2 shared papers)Joris Vermeesch (1 shared paper)Renzo Guerrini (1 shared paper)Klaus Mayer (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)European Journal of Surgical Oncology (1 paper)European Journal of Medical Genetics (1 paper)American Journal of Medical Genetics Part A (4 papers)BMC Medical Genetics (1 paper)
- Partner nations
- MaltaUnited StatesGermany
In The Last Decade
Edith Said
12 papers receiving 118 citations
Peers
Comparison fields: 5 of 43
- Genetics 44
- Molecular Biology 67
- Genetics 9
- Cell Biology 13
- Aging 1
Countries citing papers authored by Edith Said
This map shows the geographic impact of Edith Said'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 Edith Said with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edith Said more than expected).
Fields of papers citing papers by Edith Said
This network shows the impact of papers produced by Edith Said. 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 Edith Said. The network helps show where Edith Said may publish in the future.
Co-authors
The 25 scholars most cited alongside Edith Said, 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 | 22 | |
| 2 | 2011 | 21 | |
| 3 | 2011 | 18 | |
| 4 | 2021 | 15 | |
| 5 | 2006 | 13 | |
| 6 | 2019 | 12 | |
| 7 | 2017 | 8 | |
| 8 | 2015 | 7 | |
| 9 | 2004 | 2 | |
| 10 | 2024 | 2 | |
| 11 | 2019 | 1 | |
| 12 | DiGeorge phenotype in the absence of 22q11 deletion - a case report. | 2017 | 1 |
| 13 | 2024 | 0 |
About Edith Said
Edith Said is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Surgery, having authored 13 papers that have together received 122 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (4 papers), Prenatal Screening and Diagnostics (3 papers), Metabolism and Genetic Disorders (2 papers), Genetic and Kidney Cyst Diseases (2 papers), Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Intestinal Malrotation and Obstruction Disorders (1 paper). The work is most often cited by research in Genetics (44 citations), Molecular Biology (67 citations), Genetics (9 citations), Cell Biology (13 citations) and Aging (1 citation). Edith Said has collaborated with scholars based in Malta, United States and Germany. Frequent co-authors include Roberto Galea, Doriette Soler, Caroline A. Sewry, J. P. Fryns, A. Cuschieri, Joris Vermeesch, Renzo Guerrini, Klaus Mayer, Davor Lessel and Bryn D. Webb. Their work appears in journals such as European Journal of Human Genetics, European Journal of Surgical Oncology, European Journal of Medical Genetics, American Journal of Medical Genetics Part A and BMC Medical 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.