Aslıhan Tolun

5.0k total citations
81 papers, 2.3k citations indexed

About

Aslıhan Tolun is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Aslıhan Tolun has authored 81 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 37 papers in Genetics and 11 papers in Cell Biology. Recurrent topics in Aslıhan Tolun's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers) and DNA Repair Mechanisms (6 papers). Aslıhan Tolun is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers) and DNA Repair Mechanisms (6 papers). Aslıhan Tolun collaborates with scholars based in Türkiye, Pakistan and United States. Aslıhan Tolun's co-authors include Sı̇bel Aylı̇n Uğur İşerı̇, Çiğdem Köroğlu, Donald R. Helinski, Ulf Pettersson, Suna Önengüt, Patrick Concannon, Richard A. Gatti, Hatice Karasoy, Sharon N. Teraoka and Peter Aleström and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Aslıhan Tolun

79 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aslıhan Tolun Türkiye 24 1.4k 936 228 224 222 81 2.3k
Israela Lerer Israel 29 1.2k 0.9× 972 1.0× 343 1.5× 108 0.5× 194 0.9× 77 2.5k
Mohnish Suri United Kingdom 24 1.2k 0.9× 736 0.8× 137 0.6× 260 1.2× 222 1.0× 82 2.2k
Patrick Nitschké France 33 1.9k 1.4× 1.0k 1.1× 290 1.3× 309 1.4× 229 1.0× 78 3.7k
Kaya Bilgüvar United States 27 992 0.7× 532 0.6× 168 0.7× 284 1.3× 217 1.0× 78 2.0k
Beyhan Tüysüz Türkiye 24 1.4k 1.0× 988 1.1× 126 0.6× 469 2.1× 247 1.1× 139 2.5k
Ruth Newbury‐Ecob United Kingdom 25 2.0k 1.5× 1.3k 1.4× 181 0.8× 267 1.2× 208 0.9× 64 3.2k
Sabine Fauré France 7 1.9k 1.4× 1.1k 1.2× 95 0.4× 160 0.7× 314 1.4× 10 3.3k
Dvorah Abeliovich Israel 31 1.5k 1.1× 1.4k 1.5× 291 1.3× 98 0.4× 131 0.6× 98 3.0k
Éliane Chouery Lebanon 29 1.7k 1.3× 621 0.7× 87 0.4× 205 0.9× 277 1.2× 130 2.8k
Rika Kosaki Japan 25 1.3k 0.9× 846 0.9× 236 1.0× 379 1.7× 100 0.5× 113 2.3k

Countries citing papers authored by Aslıhan Tolun

Since Specialization
Citations

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

Fields of papers citing papers by Aslıhan Tolun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aslıhan Tolun

This figure shows the co-authorship network connecting the top 25 collaborators of Aslıhan Tolun. A scholar is included among the top collaborators of Aslıhan Tolun 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 Aslıhan Tolun. Aslıhan Tolun 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.
Tolun, Aslıhan, et al.. (2022). A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Genetic Testing and Molecular Biomarkers. 26(1). 37–42. 4 indexed citations
2.
Koprulu, Mine, et al.. (2022). KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies. European Journal of Human Genetics. 30(11). 1292–1296. 2 indexed citations
3.
Koprulu, Mine, et al.. (2021). The first adolescent case of Fraser syndrome 3, with a novel nonsense variant in GRIP1. American Journal of Medical Genetics Part A. 185(6). 1858–1863. 6 indexed citations
4.
Kara, Bülent, et al.. (2019). FAM160B1 deficit associated with microcephaly, severe intellectual disability, ataxia, behavioral abnormalities and speech problems. Clinical Genetics. 96(5). 456–460. 1 indexed citations
5.
Küçükkaya, Reyhan Diz, et al.. (2019). A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing. Turkish Journal of Hematology. 36(1). 29–36. 9 indexed citations
6.
Yıldırım, Yeşerin, et al.. (2018). Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility. European Journal of Human Genetics. 26(6). 876–885. 15 indexed citations
7.
8.
Khan, Amjad, et al.. (2015). RBBP8 syndrome with microcephaly, intellectual disability, short stature and brachydactyly. American Journal of Medical Genetics Part A. 167(12). 3148–3152. 4 indexed citations
9.
Kara, Bülent, et al.. (2014). Adult phenotype and further phenotypic variability in SRD5A3-CDG. BMC Medical Genetics. 15(1). 10–10. 22 indexed citations
10.
Yıldırım, Yeşerin, et al.. (2013). A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family. European Journal of Human Genetics. 22(3). 333–337. 12 indexed citations
11.
Duru, Nadire, et al.. (2010). Early-Onset Progressive Myoclonic Epilepsy With Dystonia Mapping to 16pter-p13.3. Journal of Neurogenetics. 24(4). 207–215. 10 indexed citations
12.
Köroğlu, Çiğdem, et al.. (2009). Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3–q25.1. Neurogenetics. 10(4). 325–331. 32 indexed citations
13.
Kabakuş, Nimet, et al.. (2008). Very‐late‐onset pyridoxine‐dependent seizures not linking to the known 5q31 locus. Pediatrics International. 50(5). 703–705. 5 indexed citations
14.
Önengüt, Suna, Sı̇bel Aylı̇n Uğur İşerı̇, Hatice Karasoy, Nur Yüceyar, & Aslıhan Tolun. (2003). Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2–p21.32. Neuromuscular Disorders. 14(1). 4–9. 19 indexed citations
15.
Önengüt, Suna, et al.. (2000). Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians. Annals of Human Genetics. 64(1). 33–40. 16 indexed citations
16.
Teraoka, Sharon N., Milhan Telatar, Sara Becker-Catania, et al.. (1999). Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences. The American Journal of Human Genetics. 64(6). 1617–1631. 239 indexed citations
17.
Telatar, Milhan, Patrick Concannon, & Aslıhan Tolun. (1994). Dinucleotide repeat polymorphism at the NCAM locus. Human Molecular Genetics. 3(5). 842–842. 7 indexed citations
18.
Goonewardena, P., K. H. Gustavson, Gösta Holmgren, et al.. (1986). Analysis of fragile X‐mental retardation families using flanking polymorphic DNA probes. Clinical Genetics. 30(4). 249–254. 9 indexed citations
19.
Tolun, Aslıhan & U. Pettersson. (1975). Termination sites for adenovirus type 2 DNA replication. Journal of Virology. 16(4). 759–766. 43 indexed citations
20.
Tolun, Aslıhan, et al.. (1974). Repair of Radiation-Induced Strand Breaks as Related to the Inducible Inhibitor of Postirradiation DNA Degradation. Biophysical Journal. 14(9). 691–696. 14 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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