Haluk Akın

491 total citations
39 papers, 361 citations indexed

About

Haluk Akın is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Haluk Akın has authored 39 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Haluk Akın's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Acute Myeloid Leukemia Research (3 papers). Haluk Akın is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Acute Myeloid Leukemia Research (3 papers). Haluk Akın collaborates with scholars based in Türkiye, United States and Germany. Haluk Akın's co-authors include Ferda Özkınay, Hüseyin Önay, Özgür Çoğulu, Ömer Akyol, Hüseyın Özyurt, Burak Durmaz, Hasan Herken, Süleyman Salih Zoroğlu, Haluk A. Savaş and Asude Durmaz and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Annals of Thoracic Surgery and Journal of Clinical Pathology.

In The Last Decade

Haluk Akın

34 papers receiving 353 citations

Peers

Haluk Akın
Yanhui Chen China
Jennifer Su United States
Hamdi Mbarek Netherlands
Yuanyuan Wu China
Hamel Patel United Kingdom
Pascal Bleuzen France
Dóra Török Hungary
Pernilla Stridh Sweden
Camille Alam Canada
Yanhui Chen China
Haluk Akın
Citations per year, relative to Haluk Akın Haluk Akın (= 1×) peers Yanhui Chen

Countries citing papers authored by Haluk Akın

Since Specialization
Citations

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

Fields of papers citing papers by Haluk Akın

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haluk Akın

This figure shows the co-authorship network connecting the top 25 collaborators of Haluk Akın. A scholar is included among the top collaborators of Haluk Akın 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 Haluk Akın. Haluk Akın 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.
Akın, Haluk, et al.. (2025). Determination of Factors Affecting Fever Management of Parents Who Bring Their Children to the Emergency Department with High Fever. SHILAP Revista de lepidopterología. 1 indexed citations
2.
3.
Karaca, Emin, et al.. (2025). A Rare Case of Lhermitte Duclos Disease Associated with Somatic PTEN and Germline SUFU Variants. The Cerebellum. 24(3). 85–85.
4.
Nart, Denız, Yeşim Ertan, Süha Süreyya Özbek, et al.. (2024). Next generation sequence-based targeted somatic mutation analysis in thyroid nodules with pathologically diagnosed as indeterminate cytology. Pathology - Research and Practice. 262. 155566–155566. 1 indexed citations
5.
Akın, Haluk, et al.. (2024). A complex t(15;22;17)(q22;q11.2;q21) variant of APL. Cancer Genetics. 286-287. 48–51. 1 indexed citations
6.
Canda, Ebru, Havva Yazıcı, Yasemin Atik Altınok, et al.. (2024). Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency. Nutrition Metabolism and Cardiovascular Diseases. 34(7). 1798–1806. 4 indexed citations
7.
Hekimgil, Mine, Emin Karaca, Güray Saydam, et al.. (2022). Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study. Journal of Clinical Pathology. 76(4). 244–251. 1 indexed citations
8.
9.
İdiz, Ufuk Oğuz, Hayriye Cankar Dal, Hikmet Can Çubukçu, et al.. (2022). The Effectiveness of Mesenchymal Stem Cell Therapy on COVID-19 Patients at Intensive Care Unit: Case Control Study. Turkish Journal of Hematology. 39(4). 222–229. 1 indexed citations
10.
Durmaz, Burak, Hilmi Bolat, Fuat Akercan, et al.. (2021). 20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey. TURKISH JOURNAL OF MEDICAL SCIENCES. 51(4). 1775–1780. 3 indexed citations
11.
Ünsel‐Bolat, Gül, Hilmi Bolat, Kemal Utku Yazıcı, et al.. (2020). Sluggish Cognitive Tempo and Attention Deficit Hyperactivity Disorder: Similarities and Differences. SHILAP Revista de lepidopterología. 27(3). 170–179. 2 indexed citations
12.
Akısü, Mete, Burak Durmaz, Özge Altun Köroğlu, et al.. (2020). The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model. Pediatric Research. 90(3). 559–564. 5 indexed citations
13.
Karaca, Emin, Asude Durmaz, Burak Durmaz, et al.. (2019). Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure. Reproductive Biology. 20(1). 42–47. 12 indexed citations
14.
Çağırıcı, Ufuk, et al.. (2014). Bilateral Familial Elastofibroma Dorsi: Is Genetic Abnormality Essential?. The Annals of Thoracic Surgery. 98(2). e31–e32. 4 indexed citations
15.
Çoğulu, Özgür, Asude Durmaz, Emin Karaca, et al.. (2011). The Rate of Sex Chromosome Aneuploidies in Prenatal Diagnosis and Subsequent Decisions in Western Turkey. Genetic Testing and Molecular Biomarkers. 16(2). 150–153. 5 indexed citations
16.
Akın, Haluk, et al.. (2011). Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients. Journal of Assisted Reproduction and Genetics. 28(5). 419–423. 20 indexed citations
17.
Önay, Hüseyin, Burak Durmaz, Nuri Bayram, et al.. (2010). Interferon-γ gene and interferon-γ receptor-1 gene polymorphisms in children with tuberculosis from Turkey. Scandinavian Journal of Infectious Diseases. 42(1). 39–42. 12 indexed citations
18.
Durmaz, Asude, Haluk Akın, Hüseyin Önay, et al.. (2009). A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion. Journal of Pediatric Hematology/Oncology. 31(8). 592–594. 17 indexed citations
19.
Gürel, Ahmet, İbrahim Tekedereli, Ömer Akyol, et al.. (2004). The Ala-9Val polymorphism in the mitochondrial targeting sequence (MTS) of the manganese superoxide dismutase gene is not associated with juvenile-onset asthma. Clinical Biochemistry. 37(12). 1117–1120. 10 indexed citations
20.
Özkınay, Ferda, et al.. (1997). Multiple pterygium syndrome. The Indian Journal of Pediatrics. 64(1). 113–116. 3 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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