Halil Atilla Idrısoğlu

502 total citations
26 papers, 328 citations indexed

About

Halil Atilla Idrısoğlu is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Halil Atilla Idrısoğlu has authored 26 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Neurology, 9 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Halil Atilla Idrısoğlu's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Halil Atilla Idrısoğlu is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Halil Atilla Idrısoğlu collaborates with scholars based in Türkiye, United States and United Kingdom. Halil Atilla Idrısoğlu's co-authors include Hakan Gürvıt, Haşmet Hanağası, Murat Emre, Tamer Demıralp, Numan Ermutlu, Saçit Karamürsel, Ali Sazcı, Mehmet Barış Baslo, Emel Ergül and Ali Emre Öge and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurobiology of Aging and Clinical Neurophysiology.

In The Last Decade

Halil Atilla Idrısoğlu

25 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Halil Atilla Idrısoğlu Türkiye 10 148 66 66 61 58 26 328
Yuta Kajiyama Japan 10 115 0.8× 105 1.6× 72 1.1× 37 0.6× 42 0.7× 29 358
Elżbieta Szmidt-Sałkowska Poland 9 107 0.7× 84 1.3× 65 1.0× 70 1.1× 38 0.7× 33 283
François‐Charles Wang Belgium 11 147 1.0× 86 1.3× 29 0.4× 91 1.5× 31 0.5× 41 420
T. Naegele Germany 5 137 0.9× 79 1.2× 37 0.6× 116 1.9× 20 0.3× 6 365
Xiaofeng Huang China 11 104 0.7× 53 0.8× 54 0.8× 25 0.4× 60 1.0× 33 313
Namiko Nishida Japan 12 188 1.3× 86 1.3× 72 1.1× 78 1.3× 18 0.3× 38 465
Mohamad J. Alshikho United States 9 175 1.2× 113 1.7× 73 1.1× 37 0.6× 79 1.4× 21 400
Alessandra Cifra Italy 10 60 0.4× 109 1.7× 29 0.4× 142 2.3× 43 0.7× 10 312
Mihaela Bustuchina ̆ Vlaicu France 7 53 0.4× 114 1.7× 86 1.3× 59 1.0× 30 0.5× 10 394
Carol A. Miller United States 4 59 0.4× 55 0.8× 105 1.6× 32 0.5× 41 0.7× 10 298

Countries citing papers authored by Halil Atilla Idrısoğlu

Since Specialization
Citations

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

Fields of papers citing papers by Halil Atilla Idrısoğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Halil Atilla Idrısoğlu. 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 Halil Atilla Idrısoğlu. The network helps show where Halil Atilla Idrısoğlu may publish in the future.

Co-authorship network of co-authors of Halil Atilla Idrısoğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Halil Atilla Idrısoğlu. A scholar is included among the top collaborators of Halil Atilla Idrısoğlu 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 Halil Atilla Idrısoğlu. Halil Atilla Idrısoğlu 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.
Gautam, Mukesh, et al.. (2025). Exosome Proteomics of SOD1 D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker. Annals of Clinical and Translational Neurology. 13(1). 131–143. 1 indexed citations
2.
Sazcı, Ali, et al.. (2021). Investigation of some variations of superoxide dismutase gene family in Turkish sporadic amyotrophic lateral sclerosis patients. SHILAP Revista de lepidopterología. 3. 100013–100013. 1 indexed citations
3.
Idrısoğlu, Halil Atilla, et al.. (2020). Changes in motor unit bioelectrical activity recorded at two different sites in a muscle. Neurophysiologie Clinique. 50(2). 113–118.
4.
Idrısoğlu, Halil Atilla, et al.. (2020). CIDP and membranous nephropathy: a case with limited electrophysiological findings and a rare association. Neurological Sciences. 42(1). 367–371. 6 indexed citations
5.
Sazcı, Ali & Halil Atilla Idrısoğlu. (2019). Pregnancy in Parkinson's disease with PARK2 mutations. Clinical Parkinsonism & Related Disorders. 1. 52–53. 1 indexed citations
6.
Idrısoğlu, Halil Atilla, et al.. (2019). Electrophysiological Findings of Subclinical Lower Motor Neuron Involvement in Degenerative Upper Motor Neuron Diseases. Nöro Psikiyatri Arşivi. 57(3). 228–233. 1 indexed citations
7.
Orhan, Elif Kocasoy, et al.. (2019). Repeater F-waves in amyotrophic lateral sclerosis: Electrophysiologic indicators of upper or lower motor neuron involvement?. Clinical Neurophysiology. 131(1). 96–105. 10 indexed citations
8.
Orhan, Elif Kocasoy, et al.. (2019). Parameters derived from compound muscle action potential scan for discriminating amyotrophic lateral sclerosis‐related denervation. Muscle & Nerve. 60(4). 400–408. 29 indexed citations
9.
Sazcı, Ali, et al.. (2016). Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk. The Journal of Headache and Pain. 17(1). 93–93. 13 indexed citations
10.
Yalçınkaya, Nazlı, Başar Bılgıç, Özkan Özdemir, et al.. (2016). Expression changes of genes associated with apoptosis and survival processes in Parkinson’s disease. Neuroscience Letters. 615. 72–77. 27 indexed citations
11.
Sazcı, Ali, et al.. (2015). Association of Nicotinamide-N-Methyltransferase Gene rs694539 Variant with Epilepsy. Molecular Neurobiology. 53(6). 4197–4200. 13 indexed citations
12.
Sazcı, Ali, et al.. (2014). Association of rs62063857 Variant of the Saitohin Gene with Parkinson’s Disease. Cellular and Molecular Neurobiology. 35(1). 115–121. 3 indexed citations
13.
Çoban, Arzu, Canan Ulusoy, Murat Giriş, et al.. (2013). Serum anti-neuronal antibodies in amyotrophic lateral sclerosis. International Journal of Neuroscience. 123(8). 557–562. 7 indexed citations
14.
Sazcı, Ali, et al.. (2012). Gender-Specific Association of Methylenetetrahydrofolate Reductase Gene Polymorphisms with Sporadic Amyotrophic Lateral Sclerosis. Genetic Testing and Molecular Biomarkers. 16(7). 716–721. 10 indexed citations
15.
Ergül, Emel, et al.. (2011). TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 32(11). 2107.e1–2107.e2. 4 indexed citations
16.
Kasap, Murat, Gürler Akpınar, Ali Sazcı, Halil Atilla Idrısoğlu, & Haluk Vahaboğlu. (2009). Evidence for the presence of full-length PARK2 mRNA and Parkin protein in human blood. Neuroscience Letters. 460(3). 196–200. 14 indexed citations
17.
Gürses, Candan, Başar Bılgıç, Gülşen Akman‐Demir, et al.. (2007). Clinical and magnetic resonance imaging findings of HIV-Negative patients with neurosyphilis. Journal of Neurology. 254(3). 368–374. 26 indexed citations
18.
Eraksoy, Mefkûre, Murat Kürtüncü, G. Akman‐Demir, et al.. (2003). A whole genome screen for linkage in Turkish multiple sclerosis. Journal of Neuroimmunology. 143(1-2). 17–24. 19 indexed citations
19.
Hanağası, Haşmet, Hakan Gürvıt, Numan Ermutlu, et al.. (2002). Cognitive impairment in amyotrophic lateral sclerosis: evidence from neuropsychological investigation and event-related potentials. Cognitive Brain Research. 14(2). 234–244. 116 indexed citations
20.
İrkeç, Ceyla, et al.. (1989). [The viral etiology of amyotrophic lateral sclerosis].. PubMed. 23(2). 102–9. 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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