Maryam Rafati

502 total citations
22 papers, 90 citations indexed

About

Maryam Rafati is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Maryam Rafati has authored 22 papers receiving a total of 90 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Genetics. Recurrent topics in Maryam Rafati's work include Prenatal Screening and Diagnostics (3 papers), Telomeres, Telomerase, and Senescence (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Maryam Rafati is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Telomeres, Telomerase, and Senescence (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Maryam Rafati collaborates with scholars based in Iran, United States and Sweden. Maryam Rafati's co-authors include Saeed Reza Ghaffari, Shirin Moossavi, Mohammad Reza Eshraghian, Danial Roshandel, Hamid Ahmadieh, Yaser Heshmati, Mohammad Reza Sadeghi, Mohammad Mehdi Akhondi, Jia Liu and Tao Wang and has published in prestigious journals such as British Journal of Haematology, European Journal of Human Genetics and Biology of Blood and Marrow Transplantation.

In The Last Decade

Maryam Rafati

19 papers receiving 84 citations

Peers

Maryam Rafati

GENET

PPCH

ONCOL

RNMI

Victor Enciso-Mora United Kingdom

Hüseyin Aslan Türkiye

Nelson Gaburo Brazil

Ilana Fox-Fisher Israel

Noa Ruhrman‐Shahar Israel

Constance Wells France

Mette Jorgensen United Kingdom

Anne‐Sophie Jourdain France

Charoula Matalliotaki Greece

Guillaume Hypolite France

Victor Enciso-Mora United Kingdom

Maryam Rafati

51 ×1.1

12 ×0.7

GENET

24 ×1.5

PPCH

20 ×1.4

ONCOL

9 ×0.6

RNMI

Citations per year, relative to Maryam Rafati Maryam Rafati (= 1×) peers Victor Enciso-Mora

Countries citing papers authored by Maryam Rafati

Since Specialization

Citations

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

Fields of papers citing papers by Maryam Rafati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maryam Rafati

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

All Works

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20 of 20 papers shown

Flórez-Vargas, Oscar, Marena R. Niewisch, Neelam Giri, et al.. (2025). Detailed assessment of rare and common TERT variation in a family with a telomere biology disorder. Human Genetics and Genomics Advances. 7(1). 100536–100536.

Rafati, Maryam, Lisa J. McReynolds, Youjin Wang, et al.. (2024). Hemophagocytic Lymphohistiocytosis Gene Variants in Severe Aplastic Anemia and Their Impact on Hematopoietic Cell Transplantation Outcomes. Transplantation and Cellular Therapy. 30(8). 770.e1–770.e10. 1 indexed citations

Kvarnung, Malin, Maria Pettersson, Maryam Rafati, et al.. (2024). Identification of biallelic POLA2 variants in two families with an autosomal recessive telomere biology disorder. European Journal of Human Genetics. 33(5). 580–587. 2 indexed citations

Brown, Derek W., Weiyin Zhou, Casey Dagnall, et al.. (2024). Telomere length and clonal chromosomal alterations in peripheral blood of patients with severe aplastic anaemia. British Journal of Haematology. 205(3). 1180–1187. 1 indexed citations

Motavaf, Mahsa, et al.. (2023). Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosis. Archives of Dermatological Research. 316(1). 24–24. 1 indexed citations

Soltanghoraee, Haleh, Arash Mohazzab, Mitra Tavakoli, et al.. (2022). Histological Evaluation of Products of Conception, Who Benefits from It?. Fetal and Pediatric Pathology. 42(1). 30–43.

Rafati, Maryam, et al.. (2021). Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature review. BMC Endocrine Disorders. 21(1). 220–220.

Ghaffari, Saeed Reza, et al.. (2020). Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in GUSB Gene.. PubMed. 14(2). 101–106. 4 indexed citations

Roshandel, Danial, et al.. (2019). Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa. International Ophthalmology. 39(11). 2523–2531. 9 indexed citations

10.

Rafati, Maryam, et al.. (2018). Preimplantation High-Resolution HLA Sequencing Using Next Generation Sequencing. Biology of Blood and Marrow Transplantation. 24(8). 1575–1580. 7 indexed citations

11.

Rafati, Maryam, et al.. (2018). Identification of a novel ALMS1 pathogenic variant in a family with Cone-Rod Dystrophy using whole exome sequencing, followed by prenatal diagnosis. Meta Gene. 17. 167–171. 1 indexed citations

12.

Rafati, Maryam, et al.. (2017). Primary ovarian insufficiency with t(5;13): a case report and literature review on disrupted genes. Climacteric. 20(5). 498–502. 3 indexed citations

13.

Rafati, Maryam, et al.. (2016). A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia. European Journal of Medical Genetics. 59(6-7). 330–336. 8 indexed citations

14.

Rafati, Maryam, et al.. (2016). Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing. Fetal and Pediatric Pathology. 35(4). 282–285. 6 indexed citations

15.

Rafati, Maryam, et al.. (2012). "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements. Molecular Cytogenetics. 5(1). 4–4. 3 indexed citations

16.

Rafati, Maryam, et al.. (2012). "Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes. Molecular Cytogenetics. 5(1). 9–9. 5 indexed citations

17.

Rafati, Maryam, et al.. (2012). Familial Williams–Beuren syndrome ascertained by screening rather than targeted diagnosis. Clinical Dysmorphology. 21(3). 118–123. 3 indexed citations

18.

Rafati, Maryam, et al.. (2012). Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophy. Molecular Biology Reports. 40(1). 67–72. 5 indexed citations

19.

Ghaffari, Saeed Reza, et al.. (2011). Her2 amplification status in Iranian breast cancer patients: comparison of immunohistochemistry (IHC) and fluorescence in situ hybridisation (FISH).. PubMed. 12(4). 1031–4. 12 indexed citations

20.

Ghaffari, Saeed Reza, et al.. (2010). A novel truncating mutation in the E-cadherin gene in the first Iranian family with hereditary diffuse gastric cancer. European Journal of Surgical Oncology. 36(6). 559–562. 16 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.

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