Yalda Nilipour

1.0k total citations
61 papers, 426 citations indexed

About

Yalda Nilipour is a scholar working on Molecular Biology, Rheumatology and Epidemiology. According to data from OpenAlex, Yalda Nilipour has authored 61 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Rheumatology and 13 papers in Epidemiology. Recurrent topics in Yalda Nilipour's work include Muscle Physiology and Disorders (10 papers), Inflammatory Myopathies and Dermatomyositis (9 papers) and Metabolism and Genetic Disorders (7 papers). Yalda Nilipour is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Inflammatory Myopathies and Dermatomyositis (9 papers) and Metabolism and Genetic Disorders (7 papers). Yalda Nilipour collaborates with scholars based in Iran, United States and Canada. Yalda Nilipour's co-authors include Shahriar Nafissi, Seyed Hassan Tonekaboni, Mahmoud Reza Ashrafi, Alireza Sadeghipour, Maryam Kadivar, Masoud Garshasbi, Morteza Heidari, Zahra Rezaei, Man Amanat and Ali Reza Tavasoli and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the Neurological Sciences and Journal of Magnetic Resonance Imaging.

In The Last Decade

Yalda Nilipour

57 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yalda Nilipour Iran 12 219 90 73 71 70 61 426
Carola Hedberg‐Oldfors Sweden 15 335 1.5× 212 2.4× 47 0.6× 83 1.2× 48 0.7× 42 570
Margherita Verardo Italy 12 316 1.4× 68 0.8× 44 0.6× 62 0.9× 49 0.7× 20 442
Elija Schirwis France 5 466 2.1× 40 0.4× 49 0.7× 135 1.9× 80 1.1× 5 526
Cécile Cauquil France 14 363 1.7× 59 0.7× 67 0.9× 82 1.2× 70 1.0× 40 579
Michael Woloschak United States 14 336 1.5× 44 0.5× 34 0.5× 54 0.8× 105 1.5× 23 848
Jorge Pinto‐Basto Portugal 11 204 0.9× 53 0.6× 115 1.6× 40 0.6× 37 0.5× 25 414
Tomiaki Asai Japan 11 135 0.6× 158 1.8× 83 1.1× 43 0.6× 37 0.5× 20 483
Linlin Wan China 10 144 0.7× 230 2.6× 79 1.1× 32 0.5× 22 0.3× 36 699
Tingjun Dai China 13 194 0.9× 58 0.6× 78 1.1× 30 0.4× 41 0.6× 39 427
Ingrid Brænne Germany 8 142 0.6× 87 1.0× 34 0.5× 16 0.2× 199 2.8× 16 437

Countries citing papers authored by Yalda Nilipour

Since Specialization
Citations

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

Fields of papers citing papers by Yalda Nilipour

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yalda Nilipour

This figure shows the co-authorship network connecting the top 25 collaborators of Yalda Nilipour. A scholar is included among the top collaborators of Yalda Nilipour 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 Yalda Nilipour. Yalda Nilipour 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.
Pour‐Rashidi, Ahmad, et al.. (2025). Concurrent glial tumors in the setting of a nonsyndromic adjacent/colliding meningioma: illustrative cases. Journal of Neurosurgery Case Lessons. 9(14). 1 indexed citations
2.
Kariminejad, Ariana, et al.. (2024). Core myopathy in two siblings with a biallelic variant in the CACNA1S gene—A case series study. SHILAP Revista de lepidopterología. 12(8). e9251–e9251. 1 indexed citations
3.
Javanbakht, Mohammad, et al.. (2024). Effect of recurrent severe insulin-induced hypoglycemia on the cognitive function and brain oxidative status in the rats. Diabetology & Metabolic Syndrome. 16(1). 161–161. 3 indexed citations
4.
Ghadimi, Delaram J., et al.. (2023). Glioma Tumor Grading Using Radiomics on Conventional MRI: A Comparative Study of WHO 2021 and WHO 2016 Classification of Central Nervous Tumors. Journal of Magnetic Resonance Imaging. 60(3). 923–938. 5 indexed citations
5.
Nafissi, Shahriar, Yalda Nilipour, Elham Keshavarz, et al.. (2023). Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report. Molecular Genetics & Genomic Medicine. 11(4). e2131–e2131. 1 indexed citations
6.
Ramezani, Mahtab, Yalda Nilipour, Ali Asghar Okhovat, et al.. (2023). Neutral lipid storage disease with myopathy: clinicopathological and genetic features of nine Iranian patients. Neuromuscular Disorders. 35. 19–24. 3 indexed citations
7.
Nilipour, Yalda, et al.. (2022). Congenital Heart Defects in Hirschsprung's Disease: A Survey in Iranian Population. SHILAP Revista de lepidopterología.
8.
Eshghi, Peyman, Yalda Nilipour, Mohsen Rouzrokh, et al.. (2022). The Iranian Childhood Cancer Biobank. 14(4). 150–156. 1 indexed citations
9.
Lima, Behnam Safarpour, et al.. (2021). Neurological Complications of COVID-19: A Rare Case of Bilateral Blindness. Journal of Emergency Medicine. 61(6). e160–e163. 4 indexed citations
10.
Zamani, Babak, Shahriar Nafissi, Farzaneh Larti, et al.. (2021). Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families. Journal of Neurogenetics. 35(2). 84–94. 9 indexed citations
11.
Fatehi, Farzad, Ali Asghar Okhovat, Yalda Nilipour, et al.. (2020). Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD). European Journal of Neurology. 27(11). 2257–2266. 7 indexed citations
12.
Okhovat, Ali Asghar, Yalda Nilipour, Reza Boostani, et al.. (2020). Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients. Neuromuscular Disorders. 31(1). 29–34. 7 indexed citations
13.
Mohammadi, Hassan Reza, et al.. (2020). Diffuse Multifocal Bilateral Dysembryoplastic Neuroepithelial Tumor: A Very Unusual Case Report. SHILAP Revista de lepidopterología. 7(2). 109–112. 1 indexed citations
14.
Badv, Reza Shervin, et al.. (2019). <p>A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran</p>. International Medical Case Reports Journal. Volume 12. 155–159. 10 indexed citations
15.
Ashtari, Fereshteh, et al.. (2019). Tumefactive rebound of multiple sclerosis after the short-term cessation of fingolimod: A case report. Multiple Sclerosis and Related Disorders. 39. 101883–101883. 10 indexed citations
16.
Almasi‐Dooghaee, Mostafa, et al.. (2017). A Mitochondrial Disorder in a Middle Age Iranian Patient: Report of a Rare Case. Basic and Clinical Neuroscience Journal. 8(4). 337–343. 2 indexed citations
17.
Nilipour, Yalda, et al.. (2016). A novel mutation in alpha sarcoglycan gene in an Iranian family with limb girdle muscular dystrophy 2D. Neurological Research. 38(3). 220–223. 3 indexed citations
18.
Nilipour, Yalda, et al.. (2015). JUVENILE DERMATOMYOSITIS WITHOUT SKIN LESIONS; CLINICAL NOTES. 14(3). 171–173. 2 indexed citations
19.
Karkheiran, Siamak, Catharine E. Krebs, Vladimir Makarov, et al.. (2012). Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome. Human Genetics. 132(3). 275–283. 18 indexed citations
20.
Kadivar, Maryam, Yalda Nilipour, & Alireza Sadeghipour. (2007). Osteoclast-Like Giant-Cell Tumor of the Parotid with Salivary Duct Carcinoma: Case Report and Cytologic, Histologic, and Immunohistochemical Findings. Ear Nose & Throat Journal. 86(10). 628–630. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carola Hedberg‐Oldfors Breakdown of academic impact, for papers by Margherita Verardo Breakdown of academic impact, for papers by Elija Schirwis Breakdown of academic impact, for papers by Cécile Cauquil Breakdown of academic impact, for papers by Michael Woloschak Breakdown of academic impact, for papers by Jorge Pinto‐Basto Breakdown of academic impact, for papers by Tomiaki Asai Breakdown of academic impact, for papers by Linlin Wan Breakdown of academic impact, for papers by Tingjun Dai Breakdown of academic impact, for papers by Ingrid Brænne
Rankless by CCL
2026