Resham Ejaz
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Platelet Disorders and Treatments
Papers in
- Genetics 9
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Craniofacial Disorders and Treatments 2
- Genetics and Neurodevelopmental Disorders 2
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- Fetal and Pediatric Neurological Disorders 3
- Co-authors
- Riyana Babul‐Hirji (1 shared paper)David A. Chitayat (1 shared paper)Yujin Suk (1 shared paper)Robyn Whitney (3 shared papers)Rebecca Barty (1 shared paper)Ishac Nazy (1 shared paper)Na Li (1 shared paper)Susan Blasér (1 shared paper)
- Journals
- Neurology Genetics (2 papers)Neurology (1 paper)npj Genomic Medicine (1 paper)Journal of Thrombosis and Haemostasis (1 paper)Journal of Surgical Oncology (1 paper)
- Partner nations
- CanadaUnited StatesAustralia
In The Last Decade
Resham Ejaz
15 papers receiving 432 citations
Peers
Comparison fields: 5 of 59
- Genetics 253
- Hematology 29
- Pathology and Forensic Medicine 42
- Cancer Research 33
- Molecular Biology 132
Countries citing papers authored by Resham Ejaz
This map shows the geographic impact of Resham Ejaz'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 Resham Ejaz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Resham Ejaz more than expected).
Fields of papers citing papers by Resham Ejaz
This network shows the impact of papers produced by Resham Ejaz. 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 Resham Ejaz. The network helps show where Resham Ejaz may publish in the future.
Co-authors
The 25 scholars most cited alongside Resham Ejaz, 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 | 2016 | 285 | |
| 2 | 2019 | 30 | |
| 3 | 2020 | 29 | |
| 4 | 2024 | 26 | |
| 5 | 2016 | 22 | |
| 6 | 2016 | 14 | |
| 7 | 2018 | 10 | |
| 8 | 2021 | 6 | |
| 9 | 2017 | 5 | |
| 10 | 2016 | 5 | |
| 11 | 2018 | 3 | |
| 12 | 2022 | 3 | |
| 13 | 2023 | 2 | |
| 14 | Selective serotonin reuptake inhibitor discontinuation during pregnancy: at what risk? | 2014 | 1 |
| 15 | 2024 | 1 | |
| 16 | Lateral Meningocele Syndrome | 2016 | 0 |
| 17 | 2025 | 0 | |
| 18 | 2025 | 0 | |
| 19 | 2025 | 0 | |
| 20 | 2024 | 0 |
About Resham Ejaz
Resham Ejaz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Physiology and Public Health, Environmental and Occupational Health, having authored 20 papers that have together received 442 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Tuberous Sclerosis Complex Research (2 papers), Craniofacial Disorders and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Chromatin Remodeling and Cancer (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (253 citations), Hematology (29 citations), Pathology and Forensic Medicine (42 citations), Cancer Research (33 citations) and Molecular Biology (132 citations). Resham Ejaz has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include Riyana Babul‐Hirji, David A. Chitayat, Yujin Suk, Robyn Whitney, Rebecca Barty, Ishac Nazy, Na Li, Susan Blasér, Wen Qin and Donald M. Arnold. Their work appears in journals such as Neurology Genetics, Neurology, npj Genomic Medicine, Journal of Thrombosis and Haemostasis and Journal of Surgical Oncology.
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.