Saeed Reza Ghaffari

1.2k total citations
33 papers, 694 citations indexed

About

Saeed Reza Ghaffari is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Saeed Reza Ghaffari has authored 33 papers receiving a total of 694 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Saeed Reza Ghaffari's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Glycosylation and Glycoproteins Research (2 papers). Saeed Reza Ghaffari is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Glycosylation and Glycoproteins Research (2 papers). Saeed Reza Ghaffari collaborates with scholars based in Iran, United Kingdom and United States. Saeed Reza Ghaffari's co-authors include Seyed Kamaledin Setarehdan, Fergus Shanahan, Richard J. Smith, Sean V. Tavtigian, Kyle J. Hendricks, Emma Lees, Jamila Gupte, Diana Iliev, Maryam Rafati and Lei Lian and has published in prestigious journals such as SHILAP Revista de lepidopterología, Investigative Ophthalmology & Visual Science and Journal of Medical Genetics.

In The Last Decade

Saeed Reza Ghaffari

32 papers receiving 669 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saeed Reza Ghaffari Iran 12 405 168 147 120 83 33 694
Peter H. Domer United States 16 581 1.4× 151 0.9× 99 0.7× 46 0.4× 27 0.3× 20 951
Noah C. Welker United States 9 546 1.3× 73 0.4× 97 0.7× 28 0.2× 47 0.6× 10 865
Mona S. Legator United States 9 275 0.7× 166 1.0× 53 0.4× 45 0.4× 164 2.0× 11 783
Kaveri Suryanarayan United States 13 247 0.6× 95 0.6× 109 0.7× 26 0.2× 54 0.7× 33 651
Isabel Ferreirós-Vidal Spain 12 227 0.6× 229 1.4× 25 0.2× 101 0.8× 37 0.4× 23 638
Simon V. van Reijmersdal Netherlands 11 363 0.9× 434 2.6× 55 0.4× 35 0.3× 297 3.6× 25 1.1k
Françoise Bonnet France 14 294 0.7× 168 1.0× 194 1.3× 82 0.7× 8 0.1× 31 769
Barbara Adler‐Brecher United States 7 462 1.1× 163 1.0× 26 0.2× 40 0.3× 67 0.8× 9 677
Emma D’Andrea Italy 16 294 0.7× 254 1.5× 130 0.9× 83 0.7× 11 0.1× 37 721
Elena Kolomietz Canada 11 305 0.8× 269 1.6× 77 0.5× 15 0.1× 225 2.7× 23 734

Countries citing papers authored by Saeed Reza Ghaffari

Since Specialization
Citations

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

Fields of papers citing papers by Saeed Reza Ghaffari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Saeed Reza Ghaffari. 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 Saeed Reza Ghaffari. The network helps show where Saeed Reza Ghaffari may publish in the future.

Co-authorship network of co-authors of Saeed Reza Ghaffari

This figure shows the co-authorship network connecting the top 25 collaborators of Saeed Reza Ghaffari. A scholar is included among the top collaborators of Saeed Reza Ghaffari 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 Saeed Reza Ghaffari. Saeed Reza Ghaffari 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.
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
2.
3.
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
4.
Ghaffari, Saeed Reza, et al.. (2016). Applying Hidden Markov Model Baby Cry Signal Recognition Based on Cybernetic Theory. IJEIR. 5(3). 243–247. 4 indexed citations
5.
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
6.
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
7.
Rafati, Maryam, et al.. (2012). "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements. Molecular Cytogenetics. 5(1). 4–4. 3 indexed citations
8.
Bergmann, Carsten, Saeed Reza Ghaffari, Manfred Schürmann, et al.. (2012). Next-generation Sequencing Of All Known Genes For RP And Allied Diseases Identifies The Causative Mutations In The Majority Of Patients. Investigative Ophthalmology & Visual Science. 53(14). 4525–4525. 1 indexed citations
9.
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
10.
Pirjani, Reihaneh, et al.. (2012). Normal Ranges for Fetal Femur and Humerus Diaphysis Length During the Second Trimester in an Iranian Population. Journal of Ultrasound in Medicine. 31(7). 991–995. 11 indexed citations
11.
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
12.
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
13.
Pirjani, Reihaneh, et al.. (2011). Normal ranges of fetal nasal bone length during the second trimester in an Iranian population. Prenatal Diagnosis. 31(4). 401–404. 5 indexed citations
14.
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
15.
Ghaffari, Saeed Reza, et al.. (2009). Application of Molecular Cytogenetic Technique for Rapid Prenatal Diagnosis of Aneuploidies in Iranian Population. SHILAP Revista de lepidopterología. 3(2). 49–52. 2 indexed citations
16.
Aghamohammadi, Asghar, Mostafa Moin, Ali Kouhi, et al.. (2008). Chromosomal radiosensitivity in patients with common variable immunodeficiency. Immunobiology. 213(5). 447–454. 40 indexed citations
17.
Ghaffari, Saeed Reza, Soroush Tahmasebi, Soulmaz Shorakae, et al.. (2007). Combining mammaglobin and carcinoembryonic mRNA markers for early detection of micrometastases from breast cancers--a molecular study of 59 patients.. PubMed. 7(3). 396–8. 6 indexed citations
18.
Setarehdan, Seyed Kamaledin, et al.. (2003). Automatic locating the centromere on human chromosome pictures. 56–61. 32 indexed citations
19.
Wong, Andrew, Fergus Shanahan, Joseph C. Y. Chen, et al.. (2000). BRG1, a component of the SWI-SNF complex, is mutated in multiple human tumor cell lines.. PubMed. 60(21). 6171–7. 286 indexed citations
20.
Ghaffari, Saeed Reza, et al.. (1998). Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.. Journal of Medical Genetics. 35(10). 836–840. 11 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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