Turgut Tükel

2.2k citations
18 papers · 1.5k indexed · 1 hit paper · h-index 14
Topics
Neurogenetic and Muscular Disorders Research (3 papers)Hereditary Neurological Disorders (3 papers)Lysosomal Storage Disorders Research (3 papers)

In The Last Decade

Turgut Tükel

18 papers receiving 1.5k citations

Hit Papers

High Incidence of Later-Onset Fabry Disease Revealed by N...20062026201220192006200400600

Peers

Turgut Tükel
Comparison fields: 5 of 78
  • Physiology 730
  • Molecular Biology 510
  • Epidemiology 374
  • Cell Biology 358
  • Rheumatology 236
Replace Eiichiro Uyama with:
Eiichiro Uyama Japan
Beth Levy United States
Haiyan Fu United States
Sumita Danda India
Jessica Bagel United States
Luying Pan United States
Michael Fietz Australia
Mohammed Al‐Owain Saudi Arabia
Sheela Nampoothiri India
Kondi Wong United States
Turgut Tükel relative to Eiichiro Uyama Japan Eiichiro Uyama's profile →
Citations per field
00.5×1.5×2.2×
Eiichiro Uyama · 1×
Citations per year

Countries citing papers authored by Turgut Tükel

Since Specialization
Citations

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

Fields of papers citing papers by Turgut Tükel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Turgut Tükel

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

All Works

18 of 18 papers shown
#WorkIndexed citations
1 50
2
High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening*breakdown →
713
3 15
4 18
5 22
6 47
7 56
8 29
9 37
10 127
11 24
12 60
13 10
14 255
15 3
16
Mutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia.
13
17
Establishment of a Nonradioactive Molecular Diagnosis of Fragile-X Syndrome
3
18 45

About Turgut Tükel

Turgut Tükel is a scholar working on Developmental Biology, Genetics and Neurology, having authored 18 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (3 papers), Hereditary Neurological Disorders (3 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Physiology (730 citations), Cell Biology (358 citations) and Neurology (167 citations). Turgut Tükel has collaborated with scholars based in Türkiye, United States and Tunisia. Frequent co-authors include Robert J. Desnick, Alberto Ponzone, Hitoshi Sakuraba, Geetha Thiagarajan, Marco Spada, Severo Pagliardini, Makiko Yasuda, Memnune Yüksel‐Apak, Hülya Kayserili and Memnune Yüksel Apak. Their work appears in journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

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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