Yeşim Parman

10.4k total citations
98 papers, 1.6k citations indexed

About

Yeşim Parman is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Yeşim Parman has authored 98 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Neurology, 33 papers in Cellular and Molecular Neuroscience and 32 papers in Molecular Biology. Recurrent topics in Yeşim Parman's work include Hereditary Neurological Disorders (26 papers), Myasthenia Gravis and Thymoma (23 papers) and Peripheral Neuropathies and Disorders (19 papers). Yeşim Parman is often cited by papers focused on Hereditary Neurological Disorders (26 papers), Myasthenia Gravis and Thymoma (23 papers) and Peripheral Neuropathies and Disorders (19 papers). Yeşim Parman collaborates with scholars based in Türkiye, United States and Italy. Yeşim Parman's co-authors include Feza Deymeer, Piraye Oflazer, Güher Saruhan‐Direskeneli, Haluk Kulaksızoğlu, Laura Obici, Teresa Coelho, Lucía Galán, Hacer Durmuş, Vuslat Yılmaz and David Adams and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Yeşim Parman

93 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yeşim Parman Türkiye 23 637 580 482 205 200 98 1.6k
Stéphane Mathis France 24 970 1.5× 408 0.7× 655 1.4× 171 0.8× 197 1.0× 126 1.9k
Feza Deymeer Türkiye 25 751 1.2× 659 1.1× 427 0.9× 123 0.6× 77 0.4× 88 1.5k
Piraye Oflazer Türkiye 26 1.0k 1.6× 686 1.2× 372 0.8× 143 0.7× 85 0.4× 100 2.4k
Andrew W. Michell United Kingdom 13 896 1.4× 470 0.8× 294 0.6× 170 0.8× 75 0.4× 24 1.7k
Teresa Sevilla Spain 27 846 1.3× 759 1.3× 1.2k 2.6× 245 1.2× 526 2.6× 102 2.3k
Anna Kostera‐Pruszczyk Poland 22 446 0.7× 613 1.1× 226 0.5× 98 0.5× 72 0.4× 120 1.4k
Eiichiro Uyama Japan 24 499 0.8× 757 1.3× 366 0.8× 185 0.9× 139 0.7× 85 1.8k
J. F. Pellissier France 30 456 0.7× 1.0k 1.8× 445 0.9× 210 1.0× 85 0.4× 91 2.2k
Jean‐Philippe Camdessanché France 25 1.5k 2.3× 300 0.5× 463 1.0× 97 0.5× 104 0.5× 101 2.0k
O. Dubourg France 33 668 1.0× 985 1.7× 910 1.9× 290 1.4× 293 1.5× 70 3.0k

Countries citing papers authored by Yeşim Parman

Since Specialization
Citations

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

Fields of papers citing papers by Yeşim Parman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yeşim Parman

This figure shows the co-authorship network connecting the top 25 collaborators of Yeşim Parman. A scholar is included among the top collaborators of Yeşim Parman 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 Yeşim Parman. Yeşim Parman 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.
Durmuş, Hacer, Arman Çakar, & Yeşim Parman. (2025). Eculizumab as a Rescue Therapy in Prolonged Myasthenic Crisis in the Intensive Care Unit: A Case Series. Neurocritical Care. 42(3). 1099–1101. 2 indexed citations
2.
Çakar, Arman, Reza Maroofian, Yeşim Parman, Mary M. Reilly, & Henry Houlden. (2023). Novel and nano-rare genetic causes of paediatric-onset motor neuronopathies. Brain Communications. 6(1). fcae003–fcae003.
3.
Çakar, Arman, Bedia Samancı, Haşmet Hanağası, & Yeşim Parman. (2023). Botulinum Toxin Treatment in Blepharospasm: Single-center Experience. SHILAP Revista de lepidopterología. 29(3). 204–208. 1 indexed citations
4.
Çakar, Arman, et al.. (2022). Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder. Acta Neurologica Scandinavica. 145(5). 619–626. 2 indexed citations
5.
Ceylaner, Serdar, et al.. (2022). Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study. Neuromuscular Disorders. 32(9). 718–727. 1 indexed citations
6.
Coelho, Teresa, Márcia Waddington‐Cruz, Chi‐Chao Chao, et al.. (2022). Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen. Neurology and Therapy. 12(1). 267–287. 20 indexed citations
7.
Durmuş, Hacer, Heinrich Sticht, Serdar Ceylaner, et al.. (2021). Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3). Neurological Sciences. 42(9). 3871–3878. 8 indexed citations
8.
Durmuş, Hacer, Arman Çakar, Merve Alaylıoğlu, et al.. (2021). An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis. Acta Neurologica Scandinavica. 144(6). 640–646. 7 indexed citations
9.
Guerrero‐Valero, Marta, Silvia Cipriani, Gaëtan Chicanne, et al.. (2021). Dysregulation of myelin synthesis and actomyosin function underlies aberrant myelin in CMT4B1 neuropathy. Proceedings of the National Academy of Sciences. 118(10). 19 indexed citations
10.
Çakar, Arman, Erdi Şahin, Bedia Samancı, et al.. (2021). Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features. Acta Neurologica Belgica. 122(4). 939–945. 2 indexed citations
11.
Bayrak, Ayşe Oytun, Kayıhan Uluç, Necdet Karlı, et al.. (2020). Transthyretin Familial Amyloid Polyneuropathy (TTR-FAP): A Database Analysis (3987). Neurology. 94(15_supplement). 1 indexed citations
12.
Durmuş, Hacer, Fikret Aysal, Behzat Özkan, et al.. (2020). CD4+ T Cells of Myasthenia Gravis Patients Are Characterized by Increased IL-21, IL-4, and IL-17A Productions and Higher Presence of PD-1 and ICOS. Frontiers in Immunology. 11. 809–809. 40 indexed citations
13.
14.
Akçimen, Fulya, Atay Vural, Hacer Durmuş, et al.. (2019). A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID. Journal of Human Genetics. 64(11). 1141–1144. 9 indexed citations
15.
Matur, Zeliha, Arman Çakar, Ümit Hıdır Ulaş, et al.. (2016). Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey. Neuromuscular Disorders. 26(7). 441–446. 19 indexed citations
16.
Okamoto, Yuji, Davut Pehli̇van, Christine R. Beck, et al.. (2013). Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D. Genetics in Medicine. 16(5). 386–394. 29 indexed citations
17.
Borhani‐Haghighi, Afshin, Emel Köseoğlu, Melike Mutlu, et al.. (2012). Association of amyotrophic lateral sclerosis and Behcet’s disease: is there a relationship? A multi-national case series. Clinical Rheumatology. 31(4). 733–738. 6 indexed citations
18.
Deymeer, Feza, et al.. (2007). G.P.13.01 Prevalence of sporadic inclusion body myositis (s-IBM) in Turkey: A muscle biopsy based survey. Neuromuscular Disorders. 17(9-10). 849–849. 4 indexed citations
19.
Parman, Yeşim. (2007). Hereditary neuropathies. Current Opinion in Neurology. 20(5). 542–547. 19 indexed citations
20.
Planté‐Bordeneuve, Violaine, Yeşim Parman, Anne Guiochon‐Mantel, et al.. (2001). The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases. Journal of Neurology. 248(9). 795–803. 28 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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