Rüstem Yilmaz

674 citations
13 papers · 143 · h-index 8

Impact in

    • Genetics and Neurodevelopmental Disorders
    • Neurogenetic and Muscular Disorders Research
    • Genomic variations and chromosomal abnormalities
    • Amyotrophic Lateral Sclerosis Research

Papers in

    • RNA and protein synthesis mechanisms 2
    • Single-cell and spatial transcriptomics 1
    • Protein Tyrosine Phosphatases 1
    • Neurogenetic and Muscular Disorders Research 4
    • Genetics and Neurodevelopmental Disorders 2
    • Congenital Ear and Nasal Anomalies 1
    • Genetic and Kidney Cyst Diseases 1

Rüstem Yilmaz

12 papers receiving 140 citations

Peers

Rüstem Yilmaz
Comparison fields: 5 of 43
  • Genetics 53
  • Genetics 20
  • Neurology 28
  • Cell Biology 25
  • Molecular Biology 85
Replace Cécile Fourrage with:
Cécile Fourrage France
Caroline Mijnsbergen Netherlands
Shankaracharya United States
Volkan Okur United States
Leire Abalde-Atristain United States
Saúl Herranz-Martín Spain
Bekir Ergüner Türkiye
Eduardo Calpena Spain
Tim M. Strom Germany
Yasuyoshi Kimura Japan
Rüstem Yilmaz relative to Cécile Fourrage France Cécile Fourrage's profile →
Citations per field
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Cécile Fourrage · 1×
Citations per year

Countries citing papers authored by Rüstem Yilmaz

Since Specialization
Citations

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

Fields of papers citing papers by Rüstem Yilmaz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Rüstem Yilmaz, 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 Rüstem Yilmaz Line = papers co-authored together Rüstem Yilmaz links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 202237
2 201428
3 201116
4 201713
5 202110
6 20179
7 20159
8 20208
9 20224
10 20213
11 20233
12 20233
13 20250

About Rüstem Yilmaz

Rüstem Yilmaz is a scholar working on Molecular Biology, Genetics, Neurology, Genetics and Neurology, having authored 13 papers that have together received 143 indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), RNA and protein synthesis mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Single-cell and spatial transcriptomics (1 paper), Congenital Ear and Nasal Anomalies (1 paper), Genetic and Kidney Cyst Diseases (1 paper) and Protein Tyrosine Phosphatases (1 paper). The work is most often cited by research in Genetics (53 citations), Genetics (20 citations), Neurology (28 citations), Cell Biology (25 citations) and Molecular Biology (85 citations). Rüstem Yilmaz has collaborated with scholars based in Germany, United States and Pakistan. Frequent co-authors include Guntram Borck, Christian Kubisch, Jochen H. Weishaupt, Jonathan D. Glass, Janani Parameswaran, Jie Jiang, Liang Shi, Gary J. Bassell, Naseebullah Kakar and Philipp Koch. Their work appears in journals such as Human Genetics, Neurogenetics, NAR Genomics and Bioinformatics, Antioxidants and EMBO Reports.

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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