Beyhan Tüysüz

7.6k total citations
139 papers, 2.5k citations indexed

About

Beyhan Tüysüz is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Beyhan Tüysüz has authored 139 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Genetics, 65 papers in Molecular Biology and 18 papers in Oncology. Recurrent topics in Beyhan Tüysüz's work include Connective tissue disorders research (30 papers), Genomic variations and chromosomal abnormalities (12 papers) and Bone health and treatments (11 papers). Beyhan Tüysüz is often cited by papers focused on Connective tissue disorders research (30 papers), Genomic variations and chromosomal abnormalities (12 papers) and Bone health and treatments (11 papers). Beyhan Tüysüz collaborates with scholars based in Türkiye, United States and Germany. Beyhan Tüysüz's co-authors include Cengiz Yalçınkaya, Samir Belal, F Blondeau, Haluk Topaloğlu, Fayçal Hentati, Christiane Ben Hamida, Pascale Bomont, P. Landrieu, M. Kœnig and Rudolf Korinthenberg and has published in prestigious journals such as Nature Genetics, Scientific Reports and Developmental Cell.

In The Last Decade

Beyhan Tüysüz

132 papers receiving 2.4k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Beyhan Tüysüz 1.4k 988 469 247 247 139 2.5k
Mohnish Suri 1.2k 0.9× 736 0.7× 260 0.6× 222 0.9× 224 0.9× 82 2.2k
Patrick Nitschké 1.9k 1.4× 1.0k 1.0× 309 0.7× 229 0.9× 275 1.1× 78 3.7k
Diana Baralle 1.8k 1.4× 761 0.8× 426 0.9× 142 0.6× 197 0.8× 84 2.7k
Kaya Bilgüvar 992 0.7× 532 0.5× 284 0.6× 217 0.9× 198 0.8× 78 2.0k
Andreas Winterpacht 2.5k 1.8× 1.4k 1.4× 252 0.5× 166 0.7× 243 1.0× 85 3.7k
Éliane Chouery 1.7k 1.3× 621 0.6× 205 0.4× 277 1.1× 141 0.6× 130 2.8k
Rika Kosaki 1.3k 0.9× 846 0.9× 379 0.8× 100 0.4× 114 0.5× 113 2.3k
John Tolmie 2.1k 1.6× 1.7k 1.7× 463 1.0× 253 1.0× 217 0.9× 108 3.5k
F. Dagna Bricarelli 2.1k 1.6× 1.8k 1.8× 557 1.2× 146 0.6× 235 1.0× 51 4.4k
Dalil Hamroun 2.1k 1.6× 976 1.0× 230 0.5× 361 1.5× 273 1.1× 60 3.5k

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
1.
Uyguner, Zehra Oya, Birsen Karaman, Can Baykal, et al.. (2024). Genotype-Phenotype Correlation in Lipoid Proteinosis: 15 Cases from Turkiye. Molecular Syndromology. 16(4). 327–334.
2.
Güneş, Nilay, et al.. (2023). The Clinical and Molecular Spectrum of Trichorhinophalangeal Syndrome Types I and II in a Turkish Cohort Involving 22 Patients. Turkish Archives of Pediatrics. 58(1). 98–104. 2 indexed citations
3.
Dedeoğlu, Reyhan, et al.. (2023). Congenital Heart Defects and Outcome in a Large Cohort of Down Syndrome: A Single-Center Experience from Turkey. Turkish Archives of Pediatrics. 58(5). 473–479. 4 indexed citations
4.
Güneş, Nilay, et al.. (2023). Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. Turkish Archives of Pediatrics. 58(4). 376–381. 1 indexed citations
5.
Dedeoğlu, Reyhan, et al.. (2023). A Large Turkish Cohort of Williams Syndrome: The Evaluation of Facial, Cardiovascular, and Neuropsychiatric Features. Turkish Archives of Pediatrics. 58(2). 182–188.
6.
Güneş, Nilay, et al.. (2023). Effects of Long-Term Pamidronate Treatment on Bone Density and Fracture Rate in 65 Osteogenesis Imperfecta Patients. Turkish Archives of Pediatrics. 56(5). 474–478. 1 indexed citations
7.
Tüysüz, Beyhan, et al.. (2022). Natural history of clinical features in two brothers with acromesomelic dysplasia related to PRKG2. Clinical Genetics. 103(5). 574–579. 2 indexed citations
8.
Çağlayan, Ahmet Okay, Beyhan Tüysüz, Cengiz Yalçınkaya, et al.. (2022). Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome. Journal of Human Genetics. 67(9). 553–556. 2 indexed citations
9.
Tüysüz, Beyhan, et al.. (2022). Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM. Turkish Archives of Pediatrics. 57(5). 521–525. 2 indexed citations
10.
Canpolat, Nur, Seha Saygılı, Nazlı Kara, et al.. (2021). A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome. Clinical Genetics. 101(3). 346–358. 7 indexed citations
11.
Baş, Firdevs, Zeynep Şıklar, Merih Berberoğlu, et al.. (2021). Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome. Journal of Clinical Research in Pediatric Endocrinology. 13(3). 308–319. 8 indexed citations
12.
Toksoy, Güven, Şahin Avcı, Nilay Güneş, et al.. (2020). Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey. Molecular Syndromology. 11(4). 183–196. 6 indexed citations
13.
Çağlayan, Ahmet Okay, Beyhan Tüysüz, Süleyman Coşkun, et al.. (2016). A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP. Journal of Human Genetics. 61(5). 395–403. 13 indexed citations
14.
Türkmen, Seval, et al.. (2015). Neuroimaging and clinical characterization of Sotos syndrome.. PubMed. 26(1). 1–12. 6 indexed citations
15.
Tüysüz, Beyhan, Saliha Yılmaz, Luis Kolb, et al.. (2013). Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype. American Journal of Medical Genetics Part A. 161(6). 1300–1308. 16 indexed citations
16.
Duran, Rıdvan, Ülfet Vatansever, Nükhet Aladağ Çiftdemir, Betül Acunaş, & Beyhan Tüysüz. (2007). Mega sisterna magna ile seyreden bir diyastrofik displazi olgusu. DergiPark (Istanbul University). 24(2). 158–161.
17.
Tüysüz, Beyhan. (2004). A new concept of skeletal dysplasias.. PubMed. 46(3). 197–203. 7 indexed citations
18.
Balcı, Sibel, Ebru Aypar, Özgür Kasapçopur, Beyhan Tüysüz, & Nı̇l Arısoy. (2002). An eleven-year-old female Turkish patient with progressive pseudorheumatoid dysplasia mimicking juvenile idiopathic arthritis.. PubMed. 19(6). 759–759. 7 indexed citations
19.
Afzal, Ali R., Anna Rajab, Christiane Fenske, et al.. (2000). Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2. Journal of Medical Genetics. 37. 2 indexed citations
20.
Oldridge, Michael, et al.. (2000). Autosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.. The American Journal of Human Genetics. 67. 389–389. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Mohnish Suri Breakdown of academic impact, for papers by Patrick Nitschké Breakdown of academic impact, for papers by Diana Baralle Breakdown of academic impact, for papers by Kaya Bilgüvar Breakdown of academic impact, for papers by Andreas Winterpacht Breakdown of academic impact, for papers by Éliane Chouery Breakdown of academic impact, for papers by Rika Kosaki Breakdown of academic impact, for papers by John Tolmie Breakdown of academic impact, for papers by F. Dagna Bricarelli Breakdown of academic impact, for papers by Dalil Hamroun
Rankless by CCL
2026