Koray Boduroğlu

3.1k total citations
109 papers, 1.0k citations indexed

About

Koray Boduroğlu is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Koray Boduroğlu has authored 109 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Genetics, 43 papers in Molecular Biology and 18 papers in Surgery. Recurrent topics in Koray Boduroğlu's work include Genomic variations and chromosomal abnormalities (22 papers), Connective tissue disorders research (16 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Koray Boduroğlu is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Connective tissue disorders research (16 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Koray Boduroğlu collaborates with scholars based in Türkiye, United States and Germany. Koray Boduroğlu's co-authors include Yasemin Alanay, Gülen Eda Ütine, Pelin Özlem Şimşek‐Kiper, Mehmet Alikaşifoğlu, Ergül Tunçbılek, E Tunçbilek, Ekim Z. Taşkıran, Dilek Aktaş, Müjgan Alikaşifoğlu and Can Koşukçu and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

Koray Boduroğlu

105 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Koray Boduroğlu Türkiye 20 457 421 231 176 171 109 1.0k
Solaf M. Elsayed Egypt 15 548 1.2× 471 1.1× 146 0.6× 109 0.6× 72 0.4× 63 1.1k
Young Bae Sohn South Korea 19 293 0.6× 382 0.9× 204 0.9× 119 0.7× 88 0.5× 93 1.1k
Jung Min Ko South Korea 22 767 1.7× 677 1.6× 123 0.5× 184 1.0× 167 1.0× 156 1.6k
Frans A. Hol Netherlands 21 1.0k 2.2× 407 1.0× 285 1.2× 216 1.2× 221 1.3× 41 1.6k
Christel Thauvin‐Robinet France 21 762 1.7× 532 1.3× 115 0.5× 116 0.7× 166 1.0× 80 1.4k
Encarna Guillén‐Navarro Spain 23 899 2.0× 696 1.7× 127 0.5× 179 1.0× 114 0.7× 120 1.5k
Sung Yoon Cho South Korea 19 260 0.6× 322 0.8× 177 0.8× 86 0.5× 129 0.8× 105 939
Erawati V. Bawle United States 17 562 1.2× 442 1.0× 108 0.5× 229 1.3× 91 0.5× 38 1.1k
Séverine Drunat France 21 581 1.3× 443 1.1× 93 0.4× 144 0.8× 150 0.9× 57 1.1k
Yunping Lei United States 18 580 1.3× 253 0.6× 193 0.8× 231 1.3× 133 0.8× 56 964

Countries citing papers authored by Koray Boduroğlu

Since Specialization
Citations

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

Fields of papers citing papers by Koray Boduroğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Koray Boduroğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Koray Boduroğlu. A scholar is included among the top collaborators of Koray Boduroğlu 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 Koray Boduroğlu. Koray Boduroğlu 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.
Şimşek‐Kiper, Pelin Özlem, et al.. (2024). Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families. Molecular Syndromology. 15(3). 175–184. 1 indexed citations
2.
Şimşek‐Kiper, Pelin Özlem, et al.. (2023). A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American Journal of Medical Genetics Part A. 191(4). 1119–1127. 5 indexed citations
3.
Donkervoort, Sandra, Pelin Özlem Şimşek‐Kiper, Rahşan Göçmen, et al.. (2022). A Life-Threatening Complication in a Patient with Ehlers-Danlos Syndrome Musculocontractural Type. SHILAP Revista de lepidopterología. 9(3). 297–301. 1 indexed citations
4.
Taşkıran, Ekim Z., Pelin Özlem Şimşek‐Kiper, Eda Ütine, et al.. (2021). Spondyloepimetaphyseal dysplasia EXTL3‐deficient type: Long‐term follow‐up and review of the literature. American Journal of Medical Genetics Part A. 185(10). 3104–3110. 5 indexed citations
5.
Koşukçu, Can, Ekim Z. Taşkıran, Pelin Özlem Şimşek‐Kiper, et al.. (2021). Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum. The Cleft Palate-Craniofacial Journal. 59(9). 1114–1124. 4 indexed citations
6.
Şimşek‐Kiper, Pelin Özlem, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2021). Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features. American Journal of Medical Genetics Part A. 185(6). 1888–1896. 12 indexed citations
7.
Şimşek‐Kiper, Pelin Özlem, et al.. (2021). Natural history of TRPV4-Related disorders: From skeletal dysplasia to neuromuscular phenotype. European Journal of Paediatric Neurology. 32. 46–55. 6 indexed citations
8.
Tural, Dilber Ademhan, Sevilay Karahan, Nagehan Emiralioğlu, et al.. (2021). Obstructive sleep apnea in children with Down syndrome: is it possible to predict severe apnea?. European Journal of Pediatrics. 181(2). 735–743. 9 indexed citations
9.
Şimşek‐Kiper, Pelin Özlem, Ekim Z. Taşkıran, Ümüt Arslan, et al.. (2020). Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience. Journal of Human Genetics. 66(6). 585–596. 3 indexed citations
10.
Gönç, E. Nazlı, Ekim Z. Taşkıran, Gülen Eda Ütine, et al.. (2020). Genetic IGF1R defects: new cases expand the spectrum of clinical features. Journal of Endocrinological Investigation. 43(12). 1739–1748. 4 indexed citations
11.
Ütine, Gülen Eda, Ekim Z. Taşkıran, Can Koşukçu, et al.. (2017). HERC1 mutations in idiopathic intellectual disability. European Journal of Medical Genetics. 60(5). 279–283. 38 indexed citations
12.
Şimşek‐Kiper, Pelin Özlem, et al.. (2015). Experience of a skeletal dysplasia registry in Turkey: A five‐years retrospective analysis. American Journal of Medical Genetics Part A. 167(9). 2065–2074. 12 indexed citations
13.
Şimşek‐Kiper, Pelin Özlem, Esra Dikoglu, Belinda Campos‐Xavier, et al.. (2014). Positive effects of an angiotensin II type 1 receptor antagonist in Camurati–Engelmann disease: A single case observation. American Journal of Medical Genetics Part A. 164(10). 2667–2671. 19 indexed citations
14.
Takçı, Şahin, Ayşe Korkmaz, Pelin Özlem Şimşek‐Kiper, et al.. (2013). Congenital partial arhinia: a rare malformation of the nose coexisting with holoprosencephaly.. PubMed. 54(4). 440–3. 4 indexed citations
15.
Takçı, Şahin, Şule Yiğit, Mithat Haliloğlu, Koray Boduroğlu, & Nural Ki̇per. (2013). Pulmonary agenesis and pulmonary sling anomaly in an infant with Down syndrome.. PubMed. 24(3). 337–41. 1 indexed citations
16.
Ütine, Gülen Eda, et al.. (2013). A case of Sotos syndrome with 5q35 microdeletion and novel clinical findings.. PubMed. 55(2). 207–9. 3 indexed citations
17.
Dikoglu, Esra, Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, et al.. (2013). Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome. American Journal of Medical Genetics Part A. 161(12). 3161–3165. 11 indexed citations
18.
Tunçbilek, E, Koray Boduroğlu, & Mehmet Alikaşifoğlu. (2000). Results of the Turkish congenital malformation survey.. PubMed. 41(3). 287–97. 22 indexed citations
19.
Boduroğlu, Koray, et al.. (1998). Infantile Galactosialidosis Associated With Vitamin D Deficiency Rickets. DergiPark (Istanbul University). 1 indexed citations
20.
Olcay, Lale, Fatma Gümrük, Koray Boduroğlu, Turgay Coşkun, & E Tunçbilek. (1998). Anaemia and thrombocytopenia due to haemophagocytosis in a 7‐month‐old boy with galactosialidosis. Journal of Inherited Metabolic Disease. 21(6). 679–680. 13 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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