Rahşan Göçmen

1.3k total citations
120 papers, 800 citations indexed

About

Rahşan Göçmen is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Rahşan Göçmen has authored 120 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Neurology, 26 papers in Molecular Biology and 20 papers in Genetics. Recurrent topics in Rahşan Göçmen's work include Peripheral Neuropathies and Disorders (13 papers), Cerebrovascular and Carotid Artery Diseases (12 papers) and Acute Ischemic Stroke Management (12 papers). Rahşan Göçmen is often cited by papers focused on Peripheral Neuropathies and Disorders (13 papers), Cerebrovascular and Carotid Artery Diseases (12 papers) and Acute Ischemic Stroke Management (12 papers). Rahşan Göçmen collaborates with scholars based in Türkiye, United States and Germany. Rahşan Göçmen's co-authors include Kader Karlı Oğuz, Ethem Murat Arsava, Mehmet Akif Topçuoğlu, Atay Vural, Göknur Haliloğlu, Burçe Özgen, Banu Anlar, Erhan Akpınar, Miraç Yıldırım and Bahadır Konuşkan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and PEDIATRICS.

In The Last Decade

Rahşan Göçmen

102 papers receiving 787 citations

Peers

Countries citing papers authored by Rahşan Göçmen

Since Specialization

Citations

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

Fields of papers citing papers by Rahşan Göçmen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rahşan Göçmen

This figure shows the co-authorship network connecting the top 25 collaborators of Rahşan Göçmen. A scholar is included among the top collaborators of Rahşan Göçmen 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 Rahşan Göçmen. Rahşan Göçmen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Ciclosporin-related posterior reversible encephalopathy syndrome in a paediatric haematopoietic stem cell transplant recipient	European Journal of Hospital Pharmacy	Nadir Yalçın, Fatma Visal Okur et al.	0
2	Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype	Neuromuscular Disorders	Göknur Haliloğlu, Ikeoluwa Osei‐Owusu et al.	1
3	Pectoralis major muscle index as an opportunistic predictor of mortality in acute stroke patients treated with intravenous thrombolysis	Neurological Sciences	Ezgi Yılmaz, Rahşan Göçmen et al.	0
4	Tumefactive demyelinating lesions in children	European Journal of Paediatric Neurology	Rahşan Göçmen, Bahadır Konuşkan et al.	0
5	Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10	American Journal of Medical Genetics Part A	Basri Gülbakan, Rıza Köksal Özgül et al.	0
6	Horizontal gaze palsy with progressive scoliosis: Further expanding the ROBO3 spectrum	Annals of Clinical and Translational Neurology	Rahşan Göçmen, Muharrem Yazıcı et al.	4
7	Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency	European Journal of Paediatric Neurology	Yılmaz Yıldız, Didem Ardıçlı et al.	2
8	Delineation of ADPRHL2 Variants: Report of Two New Patients with Review of the Literature	Neuropediatrics	Dilek Yalnızoğlu, Pelin Özlem Şimşek‐Kiper et al.	1
9	Many Faces of Diencephalic-Mesencephalic Junction Dysplasia Syndrome with <i>GSX2</i> and <i>PCDH12</i> Variants	Molecular Syndromology	Rahşan Göçmen, Pelin Özlem Şimşek‐Kiper et al.	2
10	IgG4‐related pachymeningitis—Long term follow up and outcome of six patients	International Journal of Rheumatic Diseases	G. K. Yardimci, Ertuğrul Çağrı Bölek et al.	1
11	A Life-Threatening Complication in a Patient with Ehlers-Danlos Syndrome Musculocontractural Type	SHILAP Revista de lepidopterología	Sandra Donkervoort, Pelin Özlem Şimşek‐Kiper et al.	1
12	Postpartum reversible cerebral vasoconstriction syndrome presenting with reversible splenial lesion		Ethem Murat Arsava, Rahşan Göçmen et al.	0
13	Applying a Unified Model of Fiber Dissection, Tractography, Microscopic Anatomy and Plastination Techniques for Basic Neuroanatomy Education: Hacettepe University Experience	International Journal of Morphology	İlkan Tatar, Rahşan Göçmen et al.	0
14	Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients	European Journal of Medical Genetics	Dıclehan Orhan, Rahşan Göçmen et al.	11
15	Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features	American Journal of Medical Genetics Part A	Pelin Özlem Şimşek‐Kiper, Can Koşukçu et al.	12
16	Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis	Journal of Human Genetics	Jingyi Xue, Pelin Özlem Şimşek‐Kiper et al.	8
17	A RARE INVOLVEMENT OF CENTRAL NERVOUS SYSTEM INVOLVEMENT DUE TO CTLA-4 GENE DEFECT	Nöro Psikiyatri Arşivi	Rahşan Göçmen, İbrahim Barışta et al.	1
18	Myelin oligodendrocyte glycoprotein antibody associated central nervous system demyelinating disease: a tertiary center experience from Turkey	Multiple Sclerosis and Related Disorders	Rahşan Göçmen, Atay Vural et al.	10
19	Reversible transverse sinus collapse in a patient with idiopathic intracranial hypertension	BMJ Case Reports	Halil Önder, Rahşan Göçmen et al.	16
20	A Case of Neurocutaneous Melanosis and Neuroimaging Findings	Journal of Radiology Case Reports	Rahşan Göçmen, Ezgi Güler et al.	11

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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