Beyhan Tüysüz

7.6k citations
139 papers · 2.5k indexed · h-index 24
Topics
Connective tissue disorders research (30 papers)Genomic variations and chromosomal abnormalities (12 papers)Bone health and treatments (11 papers)

In The Last Decade

Beyhan Tüysüz

132 papers receiving 2.4k citations

Peers

Beyhan Tüysüz
Comparison fields: 5 of 113
  • Molecular Biology 1.4k
  • Genetics 988
  • Cell Biology 469
  • Cellular and Molecular Neuroscience 247
  • Oncology 247
Replace Patrick Nitschké with:
Patrick Nitschké France
Aslıhan Tolun Türkiye
Éliane Chouery Lebanon
John Tolmie United Kingdom
Dalil Hamroun France
Mohnish Suri United Kingdom
Stavit A. Shalev Israel
Bertrand Isidor France
Rika Kosaki Japan
Anna Rajab Oman
Beyhan Tüysüz relative to Patrick Nitschké France Patrick Nitschké's profile →
Citations per field
00.5×1.5×
Patrick Nitschké · 1×
Citations per year

Countries citing papers authored by Beyhan Tüysüz

Since Specialization
Citations

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

Fields of papers citing papers by Beyhan Tüysüz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beyhan Tüysüz

This figure shows the co-authorship network connecting the top 25 collaborators of Beyhan Tüysüz. A scholar is included among the top collaborators of Beyhan Tüysüz 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 Beyhan Tüysüz. Beyhan Tüysüz 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
#WorkIndexed citations
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Neuroimaging and clinical characterization of Sotos syndrome.
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Mega sisterna magna ile seyreden bir diyastrofik displazi olgusu
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A new concept of skeletal dysplasias.
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An eleven-year-old female Turkish patient with progressive pseudorheumatoid dysplasia mimicking juvenile idiopathic arthritis.
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Autosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.
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Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2
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About Beyhan Tüysüz

Beyhan Tüysüz is a scholar working on Genetics, Developmental Biology and Rheumatology, having authored 139 papers that have together received 2.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (30 papers), Genomic variations and chromosomal abnormalities (12 papers) and Bone health and treatments (11 papers). The work is most often cited by research in Genetics (988 citations), Cell Biology (469 citations) and Molecular Biology (1.4k citations). Beyhan Tüysüz has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Cengiz Yalçınkaya, P. Landrieu, L Cavalier, Fayçal Hentati, F Blondeau, M. Kœnig, Christiane Ben Hamida, Samir Belal, Pascale Bomont and Haluk Topaloğlu. Their work appears in journals such as Nature Genetics, Scientific Reports and Developmental Cell.

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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