Samaneh Farashi

696 total citations
31 papers, 452 citations indexed

About

Samaneh Farashi is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Samaneh Farashi has authored 31 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Hematology and 8 papers in Molecular Biology. Recurrent topics in Samaneh Farashi's work include Hemoglobinopathies and Related Disorders (15 papers), Iron Metabolism and Disorders (11 papers) and Blood groups and transfusion (6 papers). Samaneh Farashi is often cited by papers focused on Hemoglobinopathies and Related Disorders (15 papers), Iron Metabolism and Disorders (11 papers) and Blood groups and transfusion (6 papers). Samaneh Farashi collaborates with scholars based in Iran, Australia and United States. Samaneh Farashi's co-authors include Cornelis L. Harteveld, Hossein Najmabadi, Jyotsna Batra, Thomas Kryza, Judith A. Clements, Azita Azarkeivan, Mehdi Banan, Mehdi Hedayati, Sirous Zeinali and Hadi Bayat and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Samaneh Farashi

29 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samaneh Farashi Iran 9 244 200 149 87 74 31 452
Monika Horváthová Czechia 11 146 0.6× 119 0.6× 140 0.9× 31 0.4× 50 0.7× 35 337
Flávia Roche Moreira Latini Brazil 11 56 0.2× 106 0.5× 101 0.7× 79 0.9× 18 0.2× 34 342
Francesca La Carpia United States 8 48 0.2× 62 0.3× 124 0.8× 63 0.7× 22 0.3× 15 281
Nicholas Williams United Kingdom 8 138 0.6× 175 0.9× 169 1.1× 44 0.5× 31 0.4× 16 430
Milena Batchvarova United States 9 244 1.0× 228 1.1× 105 0.7× 40 0.5× 32 0.4× 15 496
Chantal Humblet Belgium 13 51 0.2× 66 0.3× 149 1.0× 27 0.3× 14 0.2× 35 460
K. Harano Japan 15 457 1.9× 278 1.4× 180 1.2× 68 0.8× 153 2.1× 89 720
Dharmvir S. Verma United States 12 103 0.4× 224 1.1× 80 0.5× 49 0.6× 15 0.2× 19 392
Walid Al‐Achkar Syria 11 160 0.7× 199 1.0× 108 0.7× 56 0.6× 34 0.5× 52 359
G. P. Tamagnini Portugal 11 235 1.0× 232 1.2× 133 0.9× 51 0.6× 83 1.1× 20 457

Countries citing papers authored by Samaneh Farashi

Since Specialization
Citations

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

Fields of papers citing papers by Samaneh Farashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samaneh Farashi

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

All Works

20 of 20 papers shown
1.
Farashi, Samaneh, Roberto Bonelli, Victoria E. Jackson, et al.. (2024). Decreased Circulating Very Small Low-Density Lipoprotein is Likely Causal for Age-Related Macular Degeneration. SHILAP Revista de lepidopterología. 4(5). 100535–100535.
2.
Eade, Kevin, Brendan R. E. Ansell, Sarah Giles, et al.. (2023). iPSC–derived retinal pigmented epithelial cells from patients with macular telangiectasia show decreased mitochondrial function. Journal of Clinical Investigation. 133(9). 5 indexed citations
3.
Whatmore, Paul, et al.. (2022). IsomiR-eQTL: A Cancer-Specific Expression Quantitative Trait Loci Database of miRNAs and Their Isoforms. International Journal of Molecular Sciences. 23(20). 12493–12493. 1 indexed citations
4.
Farashi, Samaneh, Brendan R. E. Ansell, Zhichao Wu, et al.. (2022). Genetics of reticular pseudodrusen in age-related macular degeneration. Trends in Genetics. 38(4). 312–316. 3 indexed citations
5.
6.
Bonelli, Roberto, Victoria E. Jackson, Aravind Prasad, et al.. (2021). Author Correction: Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. Communications Biology. 4(1). 473–473. 1 indexed citations
7.
Bonelli, Roberto, Victoria E. Jackson, Aravind Prasad, et al.. (2021). Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. Communications Biology. 4(1). 274–274. 22 indexed citations
8.
Farashi, Samaneh, Thomas Kryza, Judith A. Clements, & Jyotsna Batra. (2018). Post-GWAS in prostate cancer: from genetic association to biological contribution. Nature reviews. Cancer. 19(1). 46–59. 66 indexed citations
9.
Farashi, Samaneh & Cornelis L. Harteveld. (2017). Molecular basis of α-thalassemia. Blood Cells Molecules and Diseases. 70. 43–53. 149 indexed citations
10.
Farashi, Samaneh, et al.. (2016). First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain. Hemoglobin. 40(2). 102–107. 4 indexed citations
11.
Farashi, Samaneh, et al.. (2015). Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on theHBA1Gene. Hemoglobin. 40(1). 38–43. 3 indexed citations
12.
Farashi, Samaneh, Mina Ohadi, Saman Hosseinkhani, Hossein Darvish, & Arash Mirabzadeh. (2015). Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder. Cognitive Neurodynamics. 10(3). 269–274. 2 indexed citations
13.
Farashi, Samaneh, et al.. (2015). Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology. 9(1). 107–113. 6 indexed citations
14.
15.
Farashi, Samaneh, et al.. (2015). Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma. Tumor Biology. 36(7). 5225–5231. 22 indexed citations
16.
Farashi, Samaneh, et al.. (2015). Interaction of anα-Globin Gene Triplication withβ-Globin Gene Mutations in Iranian Patients withβ-Thalassemia Intermedia. Hemoglobin. 39(3). 201–206. 26 indexed citations
17.
Farashi, Samaneh, et al.. (2015). Hb Dartmouth ( HBA2 : c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient. Hemoglobin. 39(3). 152–155. 5 indexed citations
18.
Farashi, Samaneh, et al.. (2013). Novel Mutations Responsible for α-Thalassemia in Iranian Families. Hemoglobin. 37(2). 148–159. 9 indexed citations
19.
Banan, Mehdi, Hadi Bayat, Azita Azarkeivan, et al.. (2012). The XmnI andBCL11ASingle Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients. Hemoglobin. 36(4). 371–380. 33 indexed citations
20.
Heidari, Asieh, Ziba Nariman‐Saleh‐Fam, Mehdi Banan, et al.. (2011). Core promoter STRs: Novel mechanism for inter-individual variation in gene expression in humans. Gene. 492(1). 195–198. 23 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Monika Horváthová Breakdown of academic impact, for papers by Flávia Roche Moreira Latini Breakdown of academic impact, for papers by Francesca La Carpia Breakdown of academic impact, for papers by Nicholas Williams Breakdown of academic impact, for papers by Milena Batchvarova Breakdown of academic impact, for papers by Chantal Humblet Breakdown of academic impact, for papers by K. Harano Breakdown of academic impact, for papers by Dharmvir S. Verma Breakdown of academic impact, for papers by Walid Al‐Achkar Breakdown of academic impact, for papers by G. P. Tamagnini
Rankless by CCL
2026