Mohammad Doosti

738 total citations
18 papers, 137 citations indexed

About

Mohammad Doosti is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Mohammad Doosti has authored 18 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Oncology. Recurrent topics in Mohammad Doosti's work include BRCA gene mutations in cancer (2 papers), Connective tissue disorders research (2 papers) and Pregnancy and preeclampsia studies (1 paper). Mohammad Doosti is often cited by papers focused on BRCA gene mutations in cancer (2 papers), Connective tissue disorders research (2 papers) and Pregnancy and preeclampsia studies (1 paper). Mohammad Doosti collaborates with scholars based in Iran, United Kingdom and United States. Mohammad Doosti's co-authors include Mohammadreza Nassiri, Mohammad Mahdi Kooshyar, Najmeh Ahangari, Ehsan Ghayoor Karimiani, Ali Javadmanesh, Gordon A. Ferns, Nima K. Emami, Majid Ghayour‐Mobarhan, Hassan Kermanshahi and Amirhossein Sahebkar and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Annals of Medicine.

In The Last Decade

Mohammad Doosti

17 papers receiving 135 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammad Doosti Iran 6 40 31 25 19 17 18 137
C.J. Quintans Argentina 11 71 1.8× 33 1.1× 12 0.5× 2 0.1× 26 1.5× 25 396
S Macheiner Austria 4 67 1.7× 27 0.9× 5 0.2× 4 0.2× 45 2.6× 4 200
Maryam Pirhoushiaran Iran 10 82 2.0× 23 0.7× 11 0.4× 4 0.2× 3 0.2× 23 267
Man 7 65 1.6× 21 0.7× 32 1.3× 3 0.2× 54 3.2× 38 206
Yoshimitsu Kitajima Japan 11 62 1.6× 17 0.5× 7 0.3× 2 0.1× 23 1.4× 14 335
Sakshi Gera United States 7 37 0.9× 14 0.5× 10 0.4× 2 0.1× 16 0.9× 12 114
Jennifer Phun United States 3 102 2.5× 11 0.4× 13 0.5× 3 0.2× 21 1.2× 4 187
Yingwen Zhang China 9 117 2.9× 18 0.6× 6 0.2× 6 0.3× 29 1.7× 25 196
Marianna Romžová Czechia 7 59 1.5× 17 0.5× 12 0.5× 16 0.9× 14 148
Andrea Vogel Austria 7 63 1.6× 3 0.1× 9 0.4× 3 0.2× 26 1.5× 15 192

Countries citing papers authored by Mohammad Doosti

Since Specialization
Citations

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

Fields of papers citing papers by Mohammad Doosti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammad Doosti

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Doosti. A scholar is included among the top collaborators of Mohammad Doosti 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 Mohammad Doosti. Mohammad Doosti 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.
Ahangari, Najmeh, et al.. (2023). Limb-Girdle Muscular Dystrophy Type 2B (LGMD2B) Caused by Pathogenic Splice and Missense Variants of DYSF Gene Among Iranians with Muscular Dystrophy. SHILAP Revista de lepidopterología. 12(1). 150–150. 1 indexed citations
2.
Doosti, Mohammad, et al.. (2023). ECEL1 novel mutation in arthrogryposis type 5D: A molecular dynamic simulation study. Molecular Genetics & Genomic Medicine. 11(6). e2153–e2153. 5 indexed citations
3.
Ahangari, Najmeh, et al.. (2022). A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report. SHILAP Revista de lepidopterología.
4.
Rad, Abolfazl, Maryam Najafi, Soheila Abedini, et al.. (2022). Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome. Orphanet Journal of Rare Diseases. 17(1). 97–97. 5 indexed citations
5.
Vona, Barbara, Sara Lewis, Mehran Beiraghi Toosi, et al.. (2022). Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss. Journal of the European Academy of Dermatology and Venereology. 36(9). 1606–1611. 4 indexed citations
6.
Safarchi, Azadeh, et al.. (2021). VEGF-C and p53 Gene Expression in the Normal and Neoplastic Mammary Gland of Canines: A Pilot Study. SHILAP Revista de lepidopterología. 1 indexed citations
7.
Pagnamenta, Alistair T., Francisca Díaz, Matteo P. Ferla, et al.. (2021). Variable skeletal phenotypes associated with biallelic variants in PRKG2. Journal of Medical Genetics. 59(10). 947–950. 5 indexed citations
8.
Ahangari, Najmeh, Mohammad Doosti, Majid Ghayour‐Mobarhan, et al.. (2020). Personalised medicine in hypercholesterolaemia: the role of pharmacogenetics in statin therapy. Annals of Medicine. 52(8). 462–470. 15 indexed citations
9.
Doosti, Mohammad, et al.. (2019). Immunogenic evaluation of FMD virus immuno-dominant epitopes coupled with IL-2/FcIgG in BALB/c mice. Microbial Pathogenesis. 132. 30–37. 4 indexed citations
10.
Ahangari, Najmeh, et al.. (2019). Hereditary thrombophilia genetic variants in recurrent pregnancy loss. Archives of Gynecology and Obstetrics. 300(3). 777–782. 25 indexed citations
11.
Rahmati, Farhad, Mohammad Doosti, & Maryam Bahreini. (2019). The Cost Analysis of Patients with Traffic Traumatic Injuries Presenting to Emergency Department; a Cross-sectional Study.. SHILAP Revista de lepidopterología. 3(1). e2–e2. 4 indexed citations
12.
Nassiri, Mohammadreza, et al.. (2017). Evaluation of different statistical methods using SAS software: an in silico approach for analysis of real-time PCR data. Journal of Applied Statistics. 45(2). 306–319. 3 indexed citations
13.
Kooshyar, Mohammad Mahdi, et al.. (2015). Chromosomal analysis and BRCA2*617delT/88delTG and BRIP1 (c.2392C>T) mutations of Fanconi anemia in Iranian family, and its correlation to breast cancer susceptibility. Journal of chemical and pharmaceutical research. 7. 1 indexed citations
14.
Kermanshahi, Hassan, et al.. (2015). Effect of in ovo injection of threonine on Mucin2 gene expression and digestive enzyme activity in Japanese quail (Coturnix japonica). Research in Veterinary Science. 100. 257–262. 21 indexed citations
15.
Kahkhaie, Kolsoum Rezaie, et al.. (2015). The Effect of a Human Antibacterial Neuropeptide SL-21 on the Expression of Pro-inflammatory Factors in Airway Epithelial Cells. International Journal of Peptide Research and Therapeutics. 21(4). 403–409. 1 indexed citations
16.
Kooshyar, Mohammad Mahdi, et al.. (2013). Identification of Germline BRCA1 Mutations among Breast Cancer Families in Northeastern Iran. Asian Pacific Journal of Cancer Prevention. 14(7). 4339–4345. 18 indexed citations
17.
Nassiri, Mohammadreza, et al.. (2013). Genes and SNPs Associated with Non-hereditary and Hereditary Colorectal Cancer. Asian Pacific Journal of Cancer Prevention. 14(10). 5609–5614. 23 indexed citations
18.
Doosti, Mohammad, et al.. (2007). Mitochondrial DNA (mtDNA) structure of Anopheles superpictus populations in IRAN. SHILAP Revista de lepidopterología. 1 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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