M. Sarfarazi
- Molecular Biology top 5%
- Genetics top 2%
- Cellular and Molecular Neuroscience top 5%
- Ophthalmology top 1%
- Genetics top 5%
- Co-authors
- Peter S. HarperI. StoilovJohn B. SchenkmanP. PearsonMarianne JanssonKay E. DaviesJeffrey MurrayR. Williamson
- Topics
- Muscle Physiology and Disorders (13 papers)Genetic Neurodegenerative Diseases (12 papers)Connective tissue disorders research (8 papers)
- Journals
- New England Journal of MedicineProceedings of the National Academy of SciencesNucleic Acids Research
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
M. Sarfarazi
67 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 111
- Molecular Biology 1.7k
- Genetics 819
- Cellular and Molecular Neuroscience 435
- Ophthalmology 415
- Genetics 330
Countries citing papers authored by M. Sarfarazi
This map shows the geographic impact of M. Sarfarazi'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 M. Sarfarazi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Sarfarazi more than expected).
Fields of papers citing papers by M. Sarfarazi
This network shows the impact of papers produced by M. Sarfarazi. 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 M. Sarfarazi. The network helps show where M. Sarfarazi may publish in the future.
Co-authorship network of co-authors of M. Sarfarazi
This figure shows the co-authorship network connecting the top 25 collaborators of M. Sarfarazi. A scholar is included among the top collaborators of M. Sarfarazi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Sarfarazi. M. Sarfarazi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Genome Scan of Two Large Families with Adult-Onset Primary Open Angle Glaucoma (POAG) Suggests a Probable Locus on 5q33-q35 | 3 |
| 2 | 198 | |
| 3 | 84 | |
| 4 | The Third Genetic Locus (GLC3C) for Primary Congenital Glaucoma (PCG) Maps to Chromosome 14q24.3 | 48 |
| 5 | Identification of an OPA1 truncating mutation in a family with Optic Atrophy | 1 |
| 6 | 194 | |
| 7 | 70 | |
| 8 | 222 | |
| 9 | 64 | |
| 10 | 138 | |
| 11 | 26 | |
| 12 | 1 | |
| 13 | 5 | |
| 14 | 3 | |
| 15 | 3 | |
| 16 | 17 | |
| 17 | 36 | |
| 18 | 34 | |
| 19 | 60 | |
| 20 | 10 |
About M. Sarfarazi
M. Sarfarazi is a scholar working on Developmental Biology, Cellular and Molecular Neuroscience and Genetics, having authored 67 papers that have together received 3.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (13 papers), Genetic Neurodegenerative Diseases (12 papers) and Connective tissue disorders research (8 papers). The work is most often cited by research in Ophthalmology (415 citations), Developmental Biology (76 citations) and Genetics (330 citations). M. Sarfarazi has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Peter S. Harper, I. Stoilov, John B. Schenkman, P. Pearson, Marianne Jansson, Kay E. Davies, Jeffrey Murray, R. Williamson, T O'Brien and Nick Thomas. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.
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.