Nasim Monfared
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 8
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 2
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- Mitochondrial Function and Pathology 2
- Co-authors
- Robin Z. Hayeems (6 shared papers)Sarah Bowdin (6 shared papers)M. Stephen Meyn (6 shared papers)Cheryl Shuman (4 shared papers)Randi Zlotnik Shaul (3 shared papers)James A. Anderson (3 shared papers)Michael J. Szego (3 shared papers)Ronald D. Cohn (3 shared papers)
- Journals
- Clinical Genetics (2 papers)npj Genomic Medicine (1 paper)Journal of Medical Ethics (1 paper)European Journal of Medical Genetics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- CanadaSwitzerland
In The Last Decade
Nasim Monfared
9 papers receiving 265 citations
Peers
Comparison fields: 5 of 46
- Genetics 162
- Aging 10
- Geriatrics and Gerontology 14
- Pharmacology 26
- Pediatrics, Perinatology and Child Health 44
Countries citing papers authored by Nasim Monfared
This map shows the geographic impact of Nasim Monfared'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 Nasim Monfared with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nasim Monfared more than expected).
Fields of papers citing papers by Nasim Monfared
This network shows the impact of papers produced by Nasim Monfared. 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 Nasim Monfared. The network helps show where Nasim Monfared may publish in the future.
Co-authors
The 25 scholars most cited alongside Nasim Monfared, 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 | 63 | |
| 2 | 2017 | 38 | |
| 3 | 2009 | 38 | |
| 4 | 2014 | 36 | |
| 5 | 2015 | 33 | |
| 6 | 2017 | 27 | |
| 7 | 2018 | 13 | |
| 8 | 2017 | 12 | |
| 9 | 2016 | 12 |
About Nasim Monfared
Nasim Monfared is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Cellular and Molecular Neuroscience, having authored 9 papers that have together received 272 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), BRCA gene mutations in cancer (2 papers), Pharmacogenetics and Drug Metabolism (1 paper) and Ethics and Legal Issues in Pediatric Healthcare (1 paper). The work is most often cited by research in Genetics (162 citations), Aging (10 citations), Geriatrics and Gerontology (14 citations), Pharmacology (26 citations) and Pediatrics, Perinatology and Child Health (44 citations). Nasim Monfared has collaborated with scholars based in Canada and Switzerland. Frequent co-authors include Robin Z. Hayeems, Sarah Bowdin, M. Stephen Meyn, Cheryl Shuman, Randi Zlotnik Shaul, James A. Anderson, Michael J. Szego, Ronald D. Cohn, Stephen W. Scherer and Christian R. Marshall. Their work appears in journals such as Clinical Genetics, npj Genomic Medicine, Journal of Medical Ethics, European Journal of Medical Genetics and European Journal of Human 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.