Coşkun Özdemır

1.8k total citations
17 papers, 502 citations indexed

About

Coşkun Özdemır is a scholar working on Neurology, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Coşkun Özdemır has authored 17 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Neurology, 7 papers in Cardiology and Cardiovascular Medicine and 6 papers in Molecular Biology. Recurrent topics in Coşkun Özdemır's work include Myasthenia Gravis and Thymoma (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Cardiac Valve Diseases and Treatments (3 papers). Coşkun Özdemır is often cited by papers focused on Myasthenia Gravis and Thymoma (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Cardiac Valve Diseases and Treatments (3 papers). Coşkun Özdemır collaborates with scholars based in Türkiye, United States and Cyprus. Coşkun Özdemır's co-authors include Robert R. Young, Darryl C. DeVivo, Rabi Tawil, Audrey S. Penn, Robert C. Griggs, Louis J. Ptáček, Steven G. Pavlakis, Feza Deymeer, Piraye Oflazer and Xin‐Ming Shen and has published in prestigious journals such as Annals of Neurology, Annals of the New York Academy of Sciences and Muscle & Nerve.

In The Last Decade

Coşkun Özdemır

16 papers receiving 464 citations

Peers

Countries citing papers authored by Coşkun Özdemır

Since Specialization

Citations

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

Fields of papers citing papers by Coşkun Özdemır

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Coşkun Özdemır

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Sudden sensorineural hearing loss as the only symptom of multiple sclerosis 2018 ·Indian Journal of Otology ·Hatice Çelik, Coşkun Özdemır	0
2	Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up 2017 ·Neuromuscular Disorders ·Hacer Durmuş, Xin‐Ming Shen, Piraye Oflazer, Bülent Kara, (unknown), Coşkun Özdemır, Joan M. Brengman, Feza Deymeer, Andrew G. Engel	28
3	Use of External Valvular Stenting on Isolated Saphenofemoral Junction Incompetence: Report of 3 Cases 2008 ·eArsiv - Adu (Adnan Menderes University) ·Sami Karapolat, Coşkun Özdemır	2
4	An alternative agent for radial arterial graft spasm: Application of topical iloprost 2006 ·Scandinavian Cardiovascular Journal ·Coşkun Özdemır, (unknown), (unknown), (unknown), Başar Sırmagül	6
5	Decrement pattern in Lambert–Eaton myasthenic syndrome is different from myasthenia gravis 2006 ·Neuromuscular Disorders ·Mehmet Barış Baslo, Feza Deymeer, Piraye Oflazer, Yeşim Parman, Coşkun Özdemır, Marina Cuttini	18
6	Does radial artery harvesting for coronary revascularization cause neurological injury in the forearm and hand? 2005 ·European Journal of Cardio-Thoracic Surgery ·(unknown), Serhat Özkan, (unknown), Coşkun Özdemır, (unknown), (unknown), (unknown), (unknown)	14
7	Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity 2001 ·Neurogenetics ·Kyproula Christodoulou, Feza Deymeer, Piraye Oflazer, Coşkun Özdemır, (unknown), (unknown), Panos Ioannou, (unknown), (unknown), Lefkos Middleton	22
8	Electrical myotonia in heterozygous carriers of recessive myotonia congenita 1999 ·Muscle & Nerve ·Feza Deymeer, Frank Lehmann‐Horn, Piraye Oflazer, (unknown), (unknown), Reinhardt Rüdel, Coşkun Özdemır	1
9	Congenital Myasthenic Syndrome (CMS) Type Ia: Clinical and Genetic Diversity^a 1998 ·Annals of the New York Academy of Sciences ·Lefkos Middleton, Kyproula Christodoulou, (unknown), Piraye Oflazer, Coşkun Özdemır, Abdelkarim A. Al-Qudah, (unknown), Ioannis Mavromatis, Ioannis Mylonas, Amelia Evoli, (unknown), (unknown), (unknown)	2
10	The use of botulinum toxin in localizing neuromyotonia to the terminal branches of the peripheral nerve 1998 ·Muscle & Nerve ·Feza Deymeer, (unknown), Piraye Oflazer, Jale Yazıcı, Coşkun Özdemır, (unknown)	1
11	Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time1This work was presented at the New Challenges in Neuromuscular Disorders, 25–27 September 1996, London, UK.1 1997 ·Neuromuscular Disorders ·Feza Deymeer, Piraye Oflazer, (unknown), (unknown), Tayfun Özçelık, Coşkun Özdemır	19
12	Identification of a one-basepair deletion in exon 6 of the dystrophin gene 1995 ·Human Mutation ·(unknown), Milhan Telatar, Piraye Oflazer, Feza Deymeer, Coşkun Özdemır, Aslıhan Tolun	1
13	Andersen's syndrome: Potassium‐sensitive periodic paralysis, ventricular ectopy, and dysmorphic features 1994 ·Annals of Neurology ·Rabi Tawil, Louis J. Ptáček, Steven G. Pavlakis, Darryl C. DeVivo, Audrey S. Penn, Coşkun Özdemır, Robert C. Griggs	231
14	Emery‐Dreifuss muscular dystrophy with unusual features 1993 ·Muscle & Nerve ·Feza Deymeer, Ali Emre Öge, Çiçek Bayındır, Cıhangır Kaymaz, Yílmaz Nişancí, Kâmil Adalet, John R.W. Yates, Coşkun Özdemır	4
15	DNA analysis in Turkish Duchenne/Becker muscular dystrophy families 1992 ·Human Genetics ·Esra Battaloğlu, Milhan Telatar, Feza Deymeer, Piraye Oflazer, (unknown), Coşkun Özdemır, Memnune Yüksel Apak, Aslıhan Tolun	10
16	THE RESULTS TO BE EXPECTED FROM ELECTRICAL TESTING IN THE DIAGNOSIS OF MYASTHENIA GRAVIS* 1976 ·Annals of the New York Academy of Sciences ·Coşkun Özdemır, Robert R. Young	84
17	ELECTRICAL TESTING IN MYASTHENIA GRAVIS* 1971 ·Annals of the New York Academy of Sciences ·Coşkun Özdemır, Robert R. Young	59

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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