Hakan Ulucan

730 total citations
15 papers, 98 citations indexed

About

Hakan Ulucan is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Hakan Ulucan has authored 15 papers receiving a total of 98 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Hakan Ulucan's work include Hedgehog Signaling Pathway Studies (3 papers), DNA Repair Mechanisms (2 papers) and Digestive system and related health (2 papers). Hakan Ulucan is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), DNA Repair Mechanisms (2 papers) and Digestive system and related health (2 papers). Hakan Ulucan collaborates with scholars based in Türkiye, United States and Serbia. Hakan Ulucan's co-authors include Mehmet Turgut, Mustafa Özen, Jennifer J. Johnston, Davut Gül, Alper Gezdirici, Leslie G. Biesecker, Julie C. Sapp, Erkan Koparir, Mehmet Seven and Adnan Yüksel and has published in prestigious journals such as Gene, Neonatology and Journal of Neurosurgery Pediatrics.

In The Last Decade

Hakan Ulucan

15 papers receiving 97 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hakan Ulucan Türkiye	6	54	44	16	9	9	15	98
Breana Cham Singapore	6	85 1.6×	53 1.2×	12 0.8×	6 0.7×	11 1.2×	12	125
Katherine A. Bosanko United States	7	39 0.7×	42 1.0×	20 1.3×	3 0.3×	7 0.8×	14	88
Nobuhiko Okamoto Japan	4	35 0.6×	34 0.8×	7 0.4×	12 1.3×	7 0.8×	7	68
Houda Karmous‐Benailly France	6	61 1.1×	96 2.2×	19 1.2×	6 0.7×	7 0.8×	11	157
Hugo Hernán Abarca-Barriga Peru	7	86 1.6×	88 2.0×	11 0.7×	13 1.4×	4 0.4×	30	159
Céline Pebrel‐Richard France	7	69 1.3×	91 2.1×	26 1.6×	6 0.7×	6 0.7×	20	138
Irman Forghani United States	6	32 0.6×	44 1.0×	9 0.6×	3 0.3×	6 0.7×	11	75
Fiorenza Soli Italy	6	41 0.8×	33 0.8×	5 0.3×	4 0.4×	3 0.3×	10	72
Andrea Hofmann Germany	4	50 0.9×	75 1.7×	14 0.9×	3 0.3×	2 0.2×	8	133
Hanwei Jiang China	10	133 2.5×	63 1.4×	10 0.6×	41 4.6×	9 1.0×	19	202

Countries citing papers authored by Hakan Ulucan

Since Specialization

Citations

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

Fields of papers citing papers by Hakan Ulucan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hakan Ulucan

This figure shows the co-authorship network connecting the top 25 collaborators of Hakan Ulucan. A scholar is included among the top collaborators of Hakan Ulucan 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 Hakan Ulucan. Hakan Ulucan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Güzel, Esra, et al.. (2021). A novel mutation in FK506 binding protein-like (FKBPL) causes male infertility. Croatian Medical Journal. 62(3). 227–232. 3 indexed citations

Koparır, Asuman, Ömer Faruk Karataş, Bayram Yüksel, et al.. (2015). Whole-exome sequencing revealed two novel mutations in Usher syndrome. Gene. 563(2). 215–218. 4 indexed citations

Koparır, Asuman, Alper Gezdirici, Erkan Koparir, et al.. (2014). Poikiloderma with neutropenia: Genotype‐ethnic origin correlation, expanding phenotype and literature review. American Journal of Medical Genetics Part A. 164(10). 2535–2540. 10 indexed citations

Seven, Mehmet, Alper Gezdirici, Hakan Ulucan, et al.. (2013). A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication. Gene. 527(2). 675–678. 5 indexed citations

Seven, Mehmet, Erkan Koparir, Alper Gezdirici, et al.. (2013). A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve–Melchior–Clausen syndrome. Clinical Dysmorphology. 23(1). 1–7. 7 indexed citations

Ulucan, Hakan, Erkan Koparir, Asuman Koparır, et al.. (2013). Circumferential skin folds and multiple anomalies. Clinical Dysmorphology. 22(2). 87–90. 7 indexed citations

Gezdirici, Alper, Alper Yenigün, Erkan Koparir, et al.. (2012). A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia. Clinical Dysmorphology. 22(1). 33–35. 2 indexed citations

Ulucan, Hakan, et al.. (2008). Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVCgene. BMC Medical Genetics. 9(1). 92–92. 22 indexed citations

Turgut, Mehmet, et al.. (2006). Incomplete Currarino triad as an embryological variant. Journal of Neurosurgery Pediatrics. 105(6). 504–507. 17 indexed citations

10.

Köseoğlu, Vedat, Erol Kısmet, Yasemin Soysal, et al.. (2004). Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G. Pediatrics International. 46(4). 415–418. 3 indexed citations

11.

Ulucan, Hakan, et al.. (2004). Acrocallosal syndrome: report of five Turkish patients. Clinical Dysmorphology. 13(4). 241–246. 3 indexed citations

12.

Dündaröz, Ruşen, et al.. (2003). Analysis of DNA Damage Using the Comet Assay in Infants Fed Cow’s Milk. Neonatology. 84(2). 135–141. 5 indexed citations

13.

Öktenli, Çağatay, Mutlu Sağlam, Şeref Demirbaş, et al.. (2003). A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features. Clinical Dysmorphology. 12(3). 199–201. 1 indexed citations

14.

Dündaröz, Ruşen, et al.. (2002). Preliminary study on DNA damage in non breast‐fed infants. Pediatrics International. 44(2). 127–130. 5 indexed citations

15.

Dündaröz, Ruşen, et al.. (2001). Evaluation of DNA damage using the comet assay in children on long‐term benzathine penicillin for secondary prophylaxis of rheumatic fever. Pediatrics International. 43(3). 276–280. 4 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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