Rüstem Yilmaz

674 total citations
13 papers, 143 citations indexed

About

Rüstem Yilmaz is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Rüstem Yilmaz has authored 13 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Neurology. Recurrent topics in Rüstem Yilmaz's work include Neurogenetic and Muscular Disorders Research (4 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Rüstem Yilmaz is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Rüstem Yilmaz collaborates with scholars based in Germany, United States and Pakistan. Rüstem Yilmaz's co-authors include Guntram Borck, Christian Kubisch, Jochen H. Weishaupt, Arne Gennerich, Naseebullah Kakar, Rosanna Parlato, Jonathan D. Glass, Janani Parameswaran, Philipp Koch and Gary J. Bassell and has published in prestigious journals such as EMBO Reports, Human Genetics and Antioxidants.

In The Last Decade

Rüstem Yilmaz

12 papers receiving 140 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rüstem Yilmaz Germany 8 85 53 28 25 20 13 143
Cécile Fourrage France 7 73 0.9× 50 0.9× 15 0.5× 33 1.3× 11 0.6× 12 145
Bekir Ergüner Türkiye 7 78 0.9× 68 1.3× 6 0.2× 18 0.7× 9 0.5× 14 162
Tim M. Strom Germany 3 224 2.6× 62 1.2× 32 1.1× 45 1.8× 8 0.4× 3 293
Volkan Okur United States 9 117 1.4× 112 2.1× 8 0.3× 17 0.7× 13 0.7× 15 205
Lucile Pinson France 6 68 0.8× 34 0.6× 32 1.1× 14 0.6× 7 0.3× 8 116
Caroline Mijnsbergen Netherlands 3 82 1.0× 67 1.3× 21 0.8× 10 0.4× 21 1.1× 3 142
Sebastian Röner Germany 3 84 1.0× 68 1.3× 6 0.2× 11 0.4× 7 0.3× 5 160
Eduardo Calpena Spain 11 153 1.8× 42 0.8× 25 0.9× 39 1.6× 14 0.7× 21 272
Saúl Herranz-Martín United Kingdom 8 109 1.3× 25 0.5× 57 2.0× 37 1.5× 51 2.5× 9 167
Elham Alehabib Iran 9 114 1.3× 51 1.0× 11 0.4× 24 1.0× 4 0.2× 24 181

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-authorship network of co-authors of Rüstem Yilmaz

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

All Works

13 of 13 papers shown
1.
Simon, Malte, Rüstem Yilmaz, Rosanna Parlato, et al.. (2025). Identifying similar populations across independent single cell studies without data integration. NAR Genomics and Bioinformatics. 7(2). lqaf042–lqaf042.
2.
Maros, Máté E., Rüstem Yilmaz, Julian Conrad, et al.. (2023). PSEN1/SLC20A2 double mutation causes early-onset Alzheimer’s disease and primary familial brain calcification co-morbidity. Neurogenetics. 24(3). 209–213. 3 indexed citations
3.
Yilmaz, Rüstem, Torsten Grehl, Dávid Brenner, et al.. (2023). Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 24(5-6). 414–419. 3 indexed citations
4.
Parameswaran, Janani, Lu Rao, Rosanna Parlato, et al.. (2022). ALS ‐linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain‐of‐function. EMBO Reports. 23(8). e54234–e54234. 37 indexed citations
5.
Yilmaz, Rüstem, et al.. (2022). Quadruple genetic variants in a sporadic ALS patient. Molecular Genetics & Genomic Medicine. 10(7). e1953–e1953. 4 indexed citations
6.
Brenner, Dávid, Kathrin Müller, Serena Lattante, et al.. (2021). FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees. Neurogenetics. 23(1). 59–65. 3 indexed citations
7.
Kreiner, Grzegorz, Björn Spittau, Katarzyna Kamińska, et al.. (2021). Targeted Ablation of Primary Cilia in Differentiated Dopaminergic Neurons Reduces Striatal Dopamine and Responsiveness to Metabolic Stress. Antioxidants. 10(8). 1284–1284. 10 indexed citations
8.
Khan, Sher Alam, Muhammad Adnan Khan, Niamat Khan, et al.. (2020). A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family. BMC Medical Genetics. 21(1). 97–97. 8 indexed citations
9.
Hashem, Mais, Rüstem Yilmaz, Muddathir H. Hamad, et al.. (2017). Mutations of PTPN23 in developmental and epileptic encephalopathy. Human Genetics. 136(11-12). 1455–1461. 13 indexed citations
10.
Yilmaz, Rüstem, Katalin Szakszon, Umut Altunoğlu, et al.. (2017). Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients. American Journal of Medical Genetics Part A. 176(1). 187–193. 9 indexed citations
11.
Yilmaz, Rüstem, Ana Beleza‐Meireles, Susan Price, et al.. (2015). A recurrent synonymous KAT6B mutation causes Say‐Barber‐Biesecker/Young‐Simpson syndrome by inducing aberrant splicing. American Journal of Medical Genetics Part A. 167(12). 3006–3010. 9 indexed citations
12.
Basel‐Vanagaite, Lina, Rüstem Yilmaz, Sha Tang, et al.. (2014). Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations. Human Genetics. 133(7). 939–949. 28 indexed citations
13.
Borck, Guntram, Naseebullah Kakar, Katrin Friedrich, et al.. (2011). An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group. Human Genetics. 131(2). 209–216. 16 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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2026