Hessa S. Alsaif
Impact in
- Ophthalmology top 10%
-
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
-
- RNA modifications and cancer 4
- Epigenetics and DNA Methylation 3
- Cancer-related gene regulation 2
- RNA Research and Splicing 2
- Genetics 4
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Fowzan S. Alkuraya (17 shared papers)Firdous Abdulwahab (5 shared papers)Niema Ibrahim (5 shared papers)Eissa Faqeih (6 shared papers)Sateesh Maddirevula (5 shared papers)Nisha Patel (4 shared papers)Dragony Fu (1 shared paper)Jenna M. Lentini (1 shared paper)
- Journals
- Human Genetics (5 papers)The American Journal of Human Genetics (3 papers)Genetics in Medicine (2 papers)Clinical Genetics (1 paper)Nature Communications (1 paper)
- Partner nations
- Saudi ArabiaUnited StatesGermany
In The Last Decade
Hessa S. Alsaif
18 papers receiving 421 citations
Peers
Comparison fields: 5 of 56
- Ophthalmology 33
- Genetics 106
- Molecular Biology 227
- Cell Biology 47
- Oncology 59
Countries citing papers authored by Hessa S. Alsaif
This map shows the geographic impact of Hessa S. Alsaif'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 Hessa S. Alsaif with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hessa S. Alsaif more than expected).
Fields of papers citing papers by Hessa S. Alsaif
This network shows the impact of papers produced by Hessa S. Alsaif. 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 Hessa S. Alsaif. The network helps show where Hessa S. Alsaif may publish in the future.
Co-authors
The 25 scholars most cited alongside Hessa S. Alsaif, 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 | 74 | |
| 2 | 2016 | 64 | |
| 3 | 2017 | 63 | |
| 4 | 2020 | 47 | |
| 5 | 2017 | 38 | |
| 6 | 2019 | 37 | |
| 7 | 2018 | 24 | |
| 8 | 2021 | 23 | |
| 9 | 2021 | 12 | |
| 10 | 2021 | 10 | |
| 11 | 2019 | 9 | |
| 12 | 2020 | 9 | |
| 13 | 2020 | 5 | |
| 14 | Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy | 2018 | 4 |
| 15 | 2021 | 4 | |
| 16 | 2022 | 3 | |
| 17 | 2021 | 1 | |
| 18 | 2023 | 1 |
About Hessa S. Alsaif
Hessa S. Alsaif is a scholar working on Molecular Biology, Genetics, Surgery, Oncology and Nutrition and Dietetics, having authored 18 papers that have together received 428 indexed citations. Recurring topics across this work include RNA modifications and cancer (4 papers), Genomics and Rare Diseases (3 papers), Epigenetics and DNA Methylation (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cancer-related Molecular Pathways (2 papers), Trace Elements in Health (2 papers), Cancer-related gene regulation (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Ophthalmology (33 citations), Genetics (106 citations), Molecular Biology (227 citations), Cell Biology (47 citations) and Oncology (59 citations). Hessa S. Alsaif has collaborated with scholars based in Saudi Arabia, United States and Germany. Frequent co-authors include Fowzan S. Alkuraya, Firdous Abdulwahab, Niema Ibrahim, Eissa Faqeih, Sateesh Maddirevula, Nisha Patel, Dragony Fu, Jenna M. Lentini, Stefan T. Arold and Talal Algoufi. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Genetics in Medicine, Clinical Genetics and Nature Communications.
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.