Hülya Azaklı

816 total citations
10 papers, 72 citations indexed

About

Hülya Azaklı is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Hülya Azaklı has authored 10 papers receiving a total of 72 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Hülya Azaklı's work include Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Inflammasome and immune disorders (2 papers). Hülya Azaklı is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Inflammasome and immune disorders (2 papers). Hülya Azaklı collaborates with scholars based in Türkiye, India and Singapore. Hülya Azaklı's co-authors include Duran Üstek, Muzaffer Arıkan, Neslihan Abacı, Candan Gürses, Ayşen Gökyiğit, Aris Çakiris, Olcay Kurşun, Yavuz Aras, Bilge Bılgıç and Altay Sencer and has published in prestigious journals such as Annals of the Rheumatic Diseases, Gene and Clinical Genetics.

In The Last Decade

Hülya Azaklı

9 papers receiving 71 citations

Peers

Countries citing papers authored by Hülya Azaklı

Since Specialization

Citations

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

Fields of papers citing papers by Hülya Azaklı

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hülya Azaklı

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Expanding the spectrum of syndromic PPP2R3C ‐related XY gonadal dysgenesis to XX gonadal dysgenesis 2021 ·Clinical Genetics ·Umut Altunoğlu, (unknown), Anju Shukla, Nathalie Escande‐Beillard, Susanne Ledig, Hülya Azaklı, Shalini S. Nayak, Serpil Eraslan, Katta M. Girisha, Ingo Kennerknecht, Hülya Kayserili	5
2	MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever 2020 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·Necatı Çakir, Hülya Azaklı, Duran Üstek, Ömer Uysal, Eren Gözke	1
3	Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings 2018 ·American Journal of Medical Genetics Part A ·Hülya Azaklı, Ayşe Deniz Akkaya, (unknown), Cüyan Demirkesen, Serpil Eraslan, Hülya Kayserili	4
4	Lack of association between increased mitochondrial DNA ⁴⁹⁷⁷ deletion and ATP levels of sputum cells from chronic obstructive pulmonary disease patients versus healthy smokers 2015 ·Mitochondrial DNA Part A ·(unknown), (unknown), Hülya Azaklı, Murat Kara, Duran Üstek, Bülent Tutluoğlu, İlhan Onaran	2
5	Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis 2014 ·Gene ·Candan Gürses, Hülya Azaklı, Ahmet Alptekin, Aris Çakiris, Neslihan Abacı, Muzaffer Arıkan, Olcay Kurşun, Ayşen Gökyiğit, Duran Üstek	20
6	Lack of association between increased mitochondrial DNA 4977 deletion and ATP levels of sputum cells from chronic obstructive pulmonary disease patients versus healthy smokers 2014 ·(unknown), Duran Üstek, (unknown), Bülent Tutluoğlu, Hülya Azaklı, İlhan Onaran	2
7	Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: A case of mesial temporal lobe epilepsy with hippocampal sclerosis 2013 ·Gene ·Hülya Azaklı, Candan Gürses, Muzaffer Arıkan, Aydın Aydöseli, Yavuz Aras, Altay Sencer, Ayşen Gökyiğit, Bilge Bılgıç, Duran Üstek	16
8	A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology 2012 ·Infection Genetics and Evolution ·Duran Üstek, (unknown), (unknown), Muzaffer Arıkan, Aris Çakiris, Neslihan Abacı, (unknown), Zeliha Emrence, Hülya Azaklı, Fulya Coşan, (unknown), Mahmut Parlak, Olcay Kurşun	12
9	The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still’s disease 2012 ·Rheumatology International ·Fulya Coşan, Zeliha Emrence, (unknown), Hülya Azaklı, (unknown), Ayten Yazıcı, (unknown), Neslihan Abacı, Duran Üstek, Ayşe Çefle	10
10	AB0003 XBP1 splicing and reduced XBP1 expression in behçet's disease 2012 ·Annals of the Rheumatic Diseases ·Neslihan Abacı, Fulya Coşan, Hülya Azaklı, (unknown), Zeliha Emrence, Aris Çakiris, Michael J. Ombrello, Duran Üstek, Ahmet Gül	0

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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