Farideh Mirzayans

1.2k total citations
18 papers, 918 citations indexed

About

Farideh Mirzayans is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Farideh Mirzayans has authored 18 papers receiving a total of 918 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Ophthalmology. Recurrent topics in Farideh Mirzayans's work include Developmental Biology and Gene Regulation (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Hedgehog Signaling Pathway Studies (4 papers). Farideh Mirzayans is often cited by papers focused on Developmental Biology and Gene Regulation (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Hedgehog Signaling Pathway Studies (4 papers). Farideh Mirzayans collaborates with scholars based in Canada, United States and United Kingdom. Farideh Mirzayans's co-authors include Michael A. Walter, W G Pearce, Fred B. Berry, Alan J. Mears, Ian M. MacDonald, Douglas B. Gould, Vincent Raymond, Sharon R. Roberts, Jutta K. Preiksaitis and Francisco Díaz‐Mitoma and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and The Journal of Infectious Diseases.

In The Last Decade

Farideh Mirzayans

16 papers receiving 894 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Farideh Mirzayans Canada 12 625 260 236 163 142 18 918
Hardeep Singh United States 14 444 0.7× 122 0.5× 277 1.2× 74 0.5× 151 1.1× 26 719
Christel Kockx Netherlands 20 1.3k 2.0× 227 0.9× 168 0.7× 53 0.3× 150 1.1× 28 1.7k
Carmen Ramos Spain 15 450 0.7× 268 1.0× 125 0.5× 66 0.4× 39 0.3× 32 720
Danielle Martinet Switzerland 18 767 1.2× 342 1.3× 43 0.2× 83 0.5× 143 1.0× 27 1.1k
Faith H. Barnett United States 11 369 0.6× 304 1.2× 50 0.2× 48 0.3× 126 0.9× 13 665
H. Allen Gardner Canada 14 456 0.7× 193 0.7× 65 0.3× 33 0.2× 129 0.9× 32 745
Muhammad Imran Khan Netherlands 20 663 1.1× 242 0.9× 496 2.1× 151 0.9× 18 0.1× 66 1.0k
Jacques Zaneveld United States 10 450 0.7× 114 0.4× 101 0.4× 21 0.1× 49 0.3× 13 749
Geoffrey J. Maher United Kingdom 14 801 1.3× 326 1.3× 111 0.5× 29 0.2× 43 0.3× 26 1.2k
Uli Schmidt Germany 12 524 0.8× 93 0.4× 62 0.3× 42 0.3× 109 0.8× 38 716

Countries citing papers authored by Farideh Mirzayans

Since Specialization
Citations

This map shows the geographic impact of Farideh Mirzayans'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 Farideh Mirzayans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Farideh Mirzayans more than expected).

Fields of papers citing papers by Farideh Mirzayans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Farideh Mirzayans. 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 Farideh Mirzayans. The network helps show where Farideh Mirzayans may publish in the future.

Co-authorship network of co-authors of Farideh Mirzayans

This figure shows the co-authorship network connecting the top 25 collaborators of Farideh Mirzayans. A scholar is included among the top collaborators of Farideh Mirzayans 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 Farideh Mirzayans. Farideh Mirzayans is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Mirzayans, Farideh, et al.. (2012). Initiation of Early Osteoblast Differentiation Events through the Direct Transcriptional Regulation of Msx2 by FOXC1. PLoS ONE. 7(11). e49095–e49095. 30 indexed citations
2.
Acharya, Moulinath, et al.. (2012). Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein.. PubMed. 18. 2182–9. 5 indexed citations
3.
Itō, Yoko, Tim Footz, Fred B. Berry, et al.. (2009). Severe Molecular Defects of a NovelFOXC1 W152GMutation Result in Aniridia. Investigative Ophthalmology & Visual Science. 50(8). 3573–3573. 45 indexed citations
4.
Sharan, Sapna, Farideh Mirzayans, Tim Footz, Michael A. Walter, & Alex V. Levin. (2008). Elliptical anterior iris stromal defects associated with PAX6 gene sequence changes. Journal of American Association for Pediatric Ophthalmology and Strabismus. 12(4). 340–343.e2. 8 indexed citations
5.
Berry, Fred B., Jonathan M. Skarie, Farideh Mirzayans, et al.. (2007). FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Human Molecular Genetics. 17(4). 490–505. 85 indexed citations
6.
Berry, Fred B., Farideh Mirzayans, & Michael A. Walter. (2006). Regulation of FOXC1 Stability and Transcriptional Activity by an Epidermal Growth Factor-activated Mitogen-activated Protein Kinase Signaling Cascade. Journal of Biological Chemistry. 281(15). 10098–10104. 47 indexed citations
7.
Ekong, Rosemary, Steve Jeremiah, D J Judah, et al.. (2004). Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray. Human Mutation. 24(1). 76–85. 14 indexed citations
8.
Berry, Fred B., et al.. (2003). FOXC1 Interacts with Components of the Nucleo/cytoskeleton. Investigative Ophthalmology & Visual Science. 44(13). 421–421. 1 indexed citations
9.
Mirzayans, Farideh & Michael A. Walter. (2003). Genomic Mismatch Scanning for the Mapping of Genetic Traits. Humana Press eBooks. 175. 37–46.
10.
Mirzayans, Farideh, Douglas B. Gould, Elise Héon, et al.. (2000). Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25. European Journal of Human Genetics. 8(1). 71–74. 94 indexed citations
11.
Mears, Alan J., Tim Jordan, Farideh Mirzayans, et al.. (1998). Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly. The American Journal of Human Genetics. 63(5). 1316–1328. 267 indexed citations
12.
Mirzayans, Farideh, et al.. (1997). Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning. The American Journal of Human Genetics. 61(1). 111–119. 28 indexed citations
13.
Walter, Michael A., et al.. (1996). Autosomal-dominant Iridogoniodysgenesis and Axenfeld-Rieger Syndrome are Genetically Distinct. Ophthalmology. 103(11). 1907–1915. 26 indexed citations
14.
Mirzayans, Farideh, et al.. (1996). Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.. PubMed. 59(6). 1321–7. 58 indexed citations
15.
Mirzayans, Farideh, W G Pearce, Ian M. MacDonald, & Michael A. Walter. (1995). Mutation of the PAX6 gene in patients with autosomal dominant keratitis.. PubMed. 57(3). 539–48. 110 indexed citations
16.
Preiksaitis, Jutta K., Francisco Díaz‐Mitoma, Farideh Mirzayans, Sharon R. Roberts, & D. Lorne Tyrrell. (1992). Quantitative Oropharyngeal Epstein-Barr Virus Shedding in Renal and Cardiac Transplant Recipients: Relationship to Immunosuppressive Therapy, Serologic Responses, and the Risk of Posttransplant Lymphoproliferative Disorder. The Journal of Infectious Diseases. 166(5). 986–994. 99 indexed citations
17.
Mirzayans, Farideh, James M. Parry, & Razmik Mirzayans. (1992). Application of the standard mutagenesis assay results in underestimation of ethyl methanesulphonate-induced mutations to ouabain-resistance in Chinese hamster cells. Mutation Research Letters. 282(1). 31–37. 1 indexed citations
18.
Mirzayans, Farideh, Peter J. Davies, & James M. Parry. (1982). The cytotoxic and mutagenic effects of 4CMB, BC and 4HMB in V79 Chinese hamster cells. Mutation Research/Genetic Toxicology. 100(1-4). 239–244.

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.

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