Can Koşukçu

544 total citations
31 papers, 337 citations indexed

About

Can Koşukçu is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Can Koşukçu has authored 31 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Immunology. Recurrent topics in Can Koşukçu's work include Genomics and Rare Diseases (3 papers), Cancer-related gene regulation (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Can Koşukçu is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cancer-related gene regulation (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Can Koşukçu collaborates with scholars based in Türkiye, Japan and United States. Can Koşukçu's co-authors include Ekim Z. Taşkıran, Mehmet Alikaşifoğlu, Pelin Özlem Şimşek‐Kiper, Koray Boduroğlu, Gülen Eda Ütine, Özlem Akgün Doğan, Ezgi Deniz Batu, Yelda Bilginer, Seza Özen and Erbil Ünsal and has published in prestigious journals such as Journal of the American Society of Nephrology, Lara D. Veeken and Food Control.

In The Last Decade

Can Koşukçu

29 papers receiving 333 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Can Koşukçu Türkiye 12 156 123 72 49 40 31 337
Jose‐Ezequiel Martín Spain 13 133 0.9× 85 0.7× 68 0.9× 31 0.6× 38 0.9× 35 338
Petra J. Neufing Australia 12 160 1.0× 96 0.8× 54 0.8× 141 2.9× 35 0.9× 15 398
Ephrem Chin United States 10 256 1.6× 155 1.3× 49 0.7× 22 0.4× 18 0.5× 16 431
Marjolaine Willems France 13 204 1.3× 156 1.3× 61 0.8× 81 1.7× 85 2.1× 39 531
Hannah Titheradge United Kingdom 9 297 1.9× 80 0.7× 158 2.2× 20 0.4× 28 0.7× 19 433
Diana Alcantara United Kingdom 9 274 1.8× 192 1.6× 54 0.8× 15 0.3× 21 0.5× 11 426
Pietro Sirleto Italy 12 221 1.4× 137 1.1× 28 0.4× 31 0.6× 13 0.3× 25 399
Christophe Battail France 13 419 2.7× 63 0.5× 62 0.9× 50 1.0× 11 0.3× 26 592
Nina Bögershausen Germany 11 280 1.8× 234 1.9× 32 0.4× 34 0.7× 16 0.4× 13 444
D’Juan T. Farmer United States 9 189 1.2× 80 0.7× 23 0.3× 13 0.3× 26 0.7× 15 317

Countries citing papers authored by Can Koşukçu

Since Specialization
Citations

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

Fields of papers citing papers by Can Koşukçu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Can Koşukçu

This figure shows the co-authorship network connecting the top 25 collaborators of Can Koşukçu. A scholar is included among the top collaborators of Can Koşukçu 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 Can Koşukçu. Can Koşukçu 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.
Yalnızoğlu, Dilek, Ali Dursun, Rıza Köksal Özgül, et al.. (2025). Phenotypic diversity in NAXE mutations. Neurological Sciences. 46(6). 2819–2828.
2.
Gülbakan, Basri, Rıza Köksal Özgül, Rahşan Göçmen, et al.. (2024). Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10. American Journal of Medical Genetics Part A. 194(9). e63645–e63645.
3.
Saygılı, Seha, Can Koşukçu, Turgut Baştuğ, et al.. (2023). A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract ( CAKUT ). Clinical Genetics. 104(6). 679–685. 3 indexed citations
4.
Özkök, Aslı, et al.. (2023). Comparing the melissopalynological and next generation sequencing (NGS) methods for the determining of botanical origin of honey. Food Control. 148. 109630–109630. 7 indexed citations
5.
Koşukçu, Can, et al.. (2023). New cases of recently described Thauvin‐Robinet‐Faivre syndrome with a novel homozygous FIBP gene variant. American Journal of Medical Genetics Part A. 194(3). e63449–e63449. 1 indexed citations
6.
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
7.
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
8.
Dursun, Ali, Dilek Yalnızoğlu, Kader Karlı Oğuz, et al.. (2021). Biallelic mutations in ELFN1 gene associated with developmental and epileptic encephalopathy and joint laxity. European Journal of Medical Genetics. 64(11). 104340–104340. 7 indexed citations
9.
Bekircan‐Kurt, Can Ebru, Arda Çetinkaya, Rahşan Göçmen, et al.. (2021). One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family. Journal of Stroke and Cerebrovascular Diseases. 30(9). 105997–105997. 4 indexed citations
10.
Yıldız, Yılmaz, Can Koşukçu, Meltem Akçaboy, et al.. (2021). Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis‐plus syndrome in two siblings. Clinical Genetics. 100(3). 308–317. 13 indexed citations
11.
Özgül, Rıza Köksal, Can Koşukçu, Ali Dursun, et al.. (2021). Clinical and molecular characteristics of carnitineacylcarnitine translocase deficiency with c.270delC and a novel c.408C>A variant. The Turkish Journal of Pediatrics. 63(4). 691–696. 5 indexed citations
12.
Kılıç, Mustafa, Bekir Ergüner, Can Koşukçu, & Rıza Köksal Özgül. (2020). Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population. The Turkish Journal of Pediatrics. 62(1). 19–23. 2 indexed citations
13.
Çetinkaya, Pınar Gür, et al.. (2020). Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study. Journal of Clinical Immunology. 40(3). 494–502. 5 indexed citations
14.
Vurallı, Doğuş, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2020). Hyperinsulinemic Hypoglycemia in a Patient with Costello Syndrome: An Etiology to Consider in Hypoglycemia. Molecular Syndromology. 11(4). 207–216. 5 indexed citations
15.
Koşukçu, Can, Ekim Z. Taşkıran, Ezgi Deniz Batu, et al.. (2020). Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?. Lara D. Veeken. 60(2). 607–616. 11 indexed citations
16.
Taşkıran, Ekim Z., Hafize Emine Sönmez, Can Koşukçu, et al.. (2019). A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease. Journal of Clinical Immunology. 39(1). 99–105. 8 indexed citations
17.
Doğan, Özlem Akgün, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2018). Hyperphosphatasia with mental retardation syndrome type 4 In two siblings-expanding the phenotypic and mutational spectrum. European Journal of Medical Genetics. 62(6). 103535–103535. 5 indexed citations
18.
Şimşek‐Kiper, Pelin Özlem, Can Koşukçu, Özlem Akgün Doğan, et al.. (2018). A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate. European Journal of Medical Genetics. 62(1). 21–26. 3 indexed citations
19.
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
20.
Taşkıran, Ekim Z., Emine Korkmaz, Şafak Güçer, et al.. (2014). Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD. Journal of the American Society of Nephrology. 25(8). 1653–1661. 31 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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Rankless by CCL
2026