Roya Mostafavi
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetic and Kidney Cyst Diseases
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- Prenatal Screening and Diagnostics
- Childhood Cancer Survivors' Quality of Life
Papers in
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- Chromatin Remodeling and Cancer 3
- Genetics 4
- Genomics and Rare Diseases 3
- BRCA gene mutations in cancer 2
- Genetic Syndromes and Imprinting 1
- Co-authors
- Kim E. Nichols (7 shared papers)Rose B. McGee (4 shared papers)Stephen F. Miller (2 shared papers)Belinda N. Mandrell (2 shared papers)Ajay J. Talati (1 shared paper)Enikö K. Pivnick (3 shared papers)Jewell C. Ward (2 shared papers)Katianne M. Howard Sharp (1 shared paper)
- Journals
- Molecular Case Studies (1 paper)Clinical Cancer Research (1 paper)Neuro-Oncology (1 paper)Cancer Medicine (1 paper)Pediatric Blood & Cancer (1 paper)
- Partner nations
- United StatesNetherlandsAustralia
In The Last Decade
Roya Mostafavi
11 papers receiving 57 citations
Peers
Comparison fields: 5 of 23
- Genetics 30
- Pediatrics, Perinatology and Child Health 13
- Cancer Research 5
- Neurology 4
- Pathology and Forensic Medicine 4
Countries citing papers authored by Roya Mostafavi
This map shows the geographic impact of Roya Mostafavi'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 Roya Mostafavi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roya Mostafavi more than expected).
Fields of papers citing papers by Roya Mostafavi
This network shows the impact of papers produced by Roya Mostafavi. 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 Roya Mostafavi. The network helps show where Roya Mostafavi may publish in the future.
Co-authors
The 25 scholars most cited alongside Roya Mostafavi, 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 | 2021 | 10 | |
| 2 | 2023 | 10 | |
| 3 | 2022 | 10 | |
| 4 | 2024 | 9 | |
| 5 | 2020 | 7 | |
| 6 | 2021 | 4 | |
| 7 | 2023 | 2 | |
| 8 | 2024 | 2 | |
| 9 | 2024 | 1 | |
| 10 | 2018 | 1 | |
| 11 | Long Term Follow-up of Morbidity and Quality of Life Associated with Isolated Gastroschisis | 2012 | 1 |
| 12 | 2023 | 0 | |
| 13 | 2022 | 0 |
About Roya Mostafavi
Roya Mostafavi is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Surgery, having authored 13 papers that have together received 57 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Chromatin Remodeling and Cancer (3 papers), Cancer Mechanisms and Therapy (2 papers), BRCA gene mutations in cancer (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Autism Spectrum Disorder Research (1 paper), Cancer Genomics and Diagnostics (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (30 citations), Pediatrics, Perinatology and Child Health (13 citations), Cancer Research (5 citations), Neurology (4 citations) and Pathology and Forensic Medicine (4 citations). Roya Mostafavi has collaborated with scholars based in United States, Netherlands and Australia. Frequent co-authors include Kim E. Nichols, Rose B. McGee, Stephen F. Miller, Belinda N. Mandrell, Ajay J. Talati, Enikö K. Pivnick, Jewell C. Ward, Katianne M. Howard Sharp, Cheryl Garganta and Julie M. Gastier‐Foster. Their work appears in journals such as Molecular Case Studies, Clinical Cancer Research, Neuro-Oncology, Cancer Medicine and Pediatric Blood & Cancer.
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.