Mutluay Arslan

1.8k citations
42 papers · 1.3k · h-index 15

Impact in

    • Epilepsy research and treatment
  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • Epilepsy research and treatment 7
    • Cerebral Palsy and Movement Disorders 3
    • Genetics and Neurodevelopmental Disorders 9
    • Genomics and Rare Diseases 8
    • Genomic variations and chromosomal abnormalities 5

Mutluay Arslan

39 papers receiving 1.2k citations

Peers

Mutluay Arslan
Comparison fields: 5 of 87
  • Psychiatry and Mental health 348
  • Genetics 539
  • Cellular and Molecular Neuroscience 199
  • Clinical Biochemistry 53
  • Molecular Biology 494
Replace Silvia Masnada with:
Silvia Masnada Italy
Bryan Lynch Ireland
Walid Fazeli Germany
Colin Ellis United States
Dilşad Türkdoğan Türkiye
Seyed Hassan Tonekaboni Iran
Lata Vadlamudi Australia
An‐Sofie Schoonjans Belgium
Scott Demarest United States
Xiu‐Yu Shi China
Mutluay Arslan relative to Silvia Masnada Italy Silvia Masnada's profile →
Citations per field
00.5×2×2.7×
Silvia Masnada · 1×
Citations per year

Countries citing papers authored by Mutluay Arslan

Since Specialization
Citations

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

Fields of papers citing papers by Mutluay Arslan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mutluay Arslan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mutluay Arslan Line = papers co-authored together Mutluay Arslan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2015220
2 2019218
3 2013186
4 2017134
5 201562
6 202056
7 202142
8 201834
9 202332
10 202430
11 201729
12 201724
13 200823
14 201621
15 202015
16 201615
17 202012
18 202112
19 201511
20 201810

About Mutluay Arslan

Mutluay Arslan is a scholar working on Psychiatry and Mental health, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Physiology, having authored 42 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (8 papers), Epilepsy research and treatment (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Ion channel regulation and function (3 papers), Infant Development and Preterm Care (3 papers), Cerebral Palsy and Movement Disorders (3 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Psychiatry and Mental health (348 citations), Genetics (539 citations), Cellular and Molecular Neuroscience (199 citations), Clinical Biochemistry (53 citations) and Molecular Biology (494 citations). Mutluay Arslan has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Bülent Ünay, Onur Akın, Süleyman Tolga Yavuz, Emre Adıgüzel, Dennis J. Matthews, Evren Yaşar, Ian G. Phelps, Charles Marques Lourenço, Jay Shendure and Bülent Hacıhamdioğlu. Their work appears in journals such as The American Journal of Human Genetics, Brain and Development, European Journal of Paediatric Neurology, Brain and Annals of Allergy Asthma & Immunology.

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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