Roxana Kariminejad

2.2k total citations
40 papers, 683 citations indexed

About

Roxana Kariminejad is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Roxana Kariminejad has authored 40 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 17 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Roxana Kariminejad's work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (10 papers) and Congenital heart defects research (8 papers). Roxana Kariminejad is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (10 papers) and Congenital heart defects research (8 papers). Roxana Kariminejad collaborates with scholars based in Iran, Germany and Spain. Roxana Kariminejad's co-authors include Hossein Najmabadi, Farhad Sahebjam, Valeh Hadavi, Andreas Tzschach, Kimia Kahrizi, Shahram Teimourian, Solmaz Sahebjam, Farzin Pourfarzad, Naser Amirizadeh and Masoud Garshasbi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Roxana Kariminejad

38 papers receiving 638 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roxana Kariminejad Iran 13 258 244 231 217 136 40 683
Simona Cavani Italy 16 393 1.5× 84 0.3× 313 1.4× 142 0.7× 160 1.2× 31 692
Tomoyasu Higashimoto United States 14 272 1.1× 138 0.6× 425 1.8× 77 0.4× 52 0.4× 25 697
Chris Fisher United Kingdom 14 227 0.9× 715 2.9× 708 3.1× 466 2.1× 235 1.7× 28 1.3k
Eden Haverfield United States 13 277 1.1× 67 0.3× 241 1.0× 40 0.2× 95 0.7× 23 536
Karen Soldano United States 13 57 0.2× 207 0.8× 316 1.4× 134 0.6× 108 0.8× 32 692
John Old United Kingdom 19 177 0.7× 1.0k 4.2× 288 1.2× 797 3.7× 320 2.4× 56 1.3k
Kathryn E. Dickerson United States 10 119 0.5× 49 0.2× 602 2.6× 86 0.4× 25 0.2× 23 786
Josef Davidsson Sweden 11 165 0.6× 55 0.2× 191 0.8× 123 0.6× 82 0.6× 16 442
Carl A. Mitchell United States 8 61 0.2× 52 0.2× 282 1.2× 149 0.7× 21 0.2× 9 521
Sandra M. Suzuka United States 17 64 0.2× 668 2.7× 301 1.3× 423 1.9× 112 0.8× 40 955

Countries citing papers authored by Roxana Kariminejad

Since Specialization
Citations

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

Fields of papers citing papers by Roxana Kariminejad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roxana Kariminejad

This figure shows the co-authorship network connecting the top 25 collaborators of Roxana Kariminejad. A scholar is included among the top collaborators of Roxana Kariminejad 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 Roxana Kariminejad. Roxana Kariminejad 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
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Mahdieh, Nejat, Reza Shervin Badv, Payman Jamali, et al.. (2019). Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.. SHILAP Revista de lepidopterología. 21(3). 337–349. 6 indexed citations
4.
Firouzabadi, Saghar Ghasemi, Roxana Kariminejad, Roshanak Vameghi, et al.. (2016). Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome. Molecular Neurobiology. 54(9). 7019–7027. 19 indexed citations
5.
Rostami, Parvin, Siavash Ghaderi‐Sohi, Navid Almadani, et al.. (2015). Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.. PubMed. 18(5). 296–303. 8 indexed citations
6.
Behjati, Farkhondeh, Saghar Ghasemi Firouzabadi, Kimia Kahrizi, et al.. (2013). Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation. Iranian Red Crescent Medical Journal. 15(10). e8221–e8221. 1 indexed citations
7.
Kariminejad, Roxana, Allan Lind-Thomsen, Zeynep Tümer, et al.. (2011). High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. Human Mutation. 32(12). 1427–1435. 24 indexed citations
8.
Kariminejad, Ariana, Roxana Kariminejad, Stefan Neuenschwander, et al.. (2011). Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18. European Journal of Human Genetics. 19(5). 555–560. 23 indexed citations
9.
Kahrizi, Kimia, Masoud Garshasbi, Seyedeh Sedigheh Abedini, et al.. (2010). Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. European Journal of Human Genetics. 19(1). 115–117. 49 indexed citations
10.
Kariminejad, Ariana, Roxana Kariminejad, Andreas Tzschach, et al.. (2010). 11q14.1‐11q22.1 deletion in a 1‐year‐old male with minor dysmorphic features. American Journal of Medical Genetics Part A. 152A(10). 2651–2655. 4 indexed citations
11.
Kariminejad, Ariana, Roxana Kariminejad, Andreas Tzschach, et al.. (2009). Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis. American Journal of Medical Genetics Part A. 149A(7). 1544–1549. 20 indexed citations
12.
Kahrizi, Kimia, Hossein Najmabadi, Roxana Kariminejad, et al.. (2008). An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4. European Journal of Human Genetics. 17(1). 125–128. 16 indexed citations
13.
Garshasbi, Masoud, Valeh Hadavi, Kimia Kahrizi, et al.. (2008). A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 82(5). 1158–1164. 106 indexed citations
14.
Shafeghati, Yousef, et al.. (2007). Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia. SHILAP Revista de lepidopterología. 2 indexed citations
15.
Hadavi, Valeh, Amir Hossein Taromchi, Mahdi Malekpour, et al.. (2007). Elucidating the spectrum of  -thalassemia mutations in Iran. Haematologica. 92(7). 992–993. 52 indexed citations
16.
Salipante, Stephen J., Kathleen F. Benson, Valeh Hadavi, et al.. (2007). Double de novo mutations ofELA2 in cyclic and severe congenital neutropenia. Human Mutation. 28(9). 874–881. 26 indexed citations
17.
Rezaie, Tayebeh, et al.. (2007). Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family. Ophthalmic Genetics. 28(4). 224–228. 5 indexed citations
18.
Kariminejad, Ariana, et al.. (2006). Comparison of Early and Mid-Trimester Amniocentesis in 1459 Amniotic Fluid Cultures. 4(3). 858–863. 1 indexed citations
19.
Najmabadi, Hossein, Alireza Ghamari, Farhad Sahebjam, et al.. (2006). Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran. Public Health Genomics. 9(2). 93–97. 58 indexed citations
20.
Najmabadi, Hossein, Roxana Kariminejad, Solmaz Sahebjam, et al.. (2001). THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION. Hemoglobin. 25(3). 285–296. 135 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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