Necat İmirzalıoğlu

615 total citations
31 papers, 429 citations indexed

About

Necat İmirzalıoğlu is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Necat İmirzalıoğlu has authored 31 papers receiving a total of 429 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Hematology. Recurrent topics in Necat İmirzalıoğlu's work include Blood Coagulation and Thrombosis Mechanisms (4 papers), Prenatal Screening and Diagnostics (4 papers) and Inflammasome and immune disorders (4 papers). Necat İmirzalıoğlu is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (4 papers), Prenatal Screening and Diagnostics (4 papers) and Inflammasome and immune disorders (4 papers). Necat İmirzalıoğlu collaborates with scholars based in Türkiye, Serbia and Germany. Necat İmirzalıoğlu's co-authors include Yasemin Soysal, Semra Kahraman, Muhterem Bahçe, M. Cengiz Yakıcıer, Ahmet Dursun, Bora Tastan, A. Coskun Samli, Mustafa Solak, Elif Ağaçayak and Mehmet Kahraman and has published in prestigious journals such as Human Reproduction, International Journal of Clinical Practice and Prenatal Diagnosis.

In The Last Decade

Necat İmirzalıoğlu

29 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Necat İmirzalıoğlu Türkiye 11 159 146 128 64 60 31 429
Kyoko Kumagai Japan 17 64 0.4× 90 0.6× 27 0.2× 97 1.5× 65 1.1× 35 696
Anne Miller United Kingdom 12 35 0.2× 27 0.2× 84 0.7× 124 1.9× 48 0.8× 28 539
P. Wieacker Germany 12 198 1.2× 109 0.7× 177 1.4× 73 1.1× 54 0.9× 43 455
John Tziotis Greece 11 88 0.6× 90 0.6× 29 0.2× 63 1.0× 54 0.9× 17 329
Heidi A. Trau United States 9 119 0.7× 47 0.3× 40 0.3× 73 1.1× 45 0.8× 12 340
Manish Jain India 11 126 0.8× 39 0.3× 88 0.7× 12 0.2× 8 0.1× 45 337
Augusta M.A. Lachmeijer Netherlands 13 180 1.1× 494 3.4× 172 1.3× 57 0.9× 166 2.8× 16 849
Hitomi Arahori Japan 11 139 0.9× 190 1.3× 80 0.6× 62 1.0× 18 0.3× 19 642
Ivan Šubrt Czechia 16 190 1.2× 122 0.8× 366 2.9× 31 0.5× 55 0.9× 52 641
Prapai Dejkhamron Thailand 11 93 0.6× 38 0.3× 79 0.6× 37 0.6× 17 0.3× 36 314

Countries citing papers authored by Necat İmirzalıoğlu

Since Specialization
Citations

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

Fields of papers citing papers by Necat İmirzalıoğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Necat İmirzalıoğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Necat İmirzalıoğlu. A scholar is included among the top collaborators of Necat İmirzalıoğlu 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 Necat İmirzalıoğlu. Necat İmirzalıoğlu 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.
Yıldırım, Engin, Mehmet Kahraman, Murat Bozkurt, et al.. (2018). Human Papilloma Viruses and Their Genotype Distribution in Women with High Socioeconomic Status in Central Anatolia, Turkey: A Pilot Study. Medical Science Monitor. 24. 58–66. 8 indexed citations
2.
Soysal, Yasemin, et al.. (2013). Prothrombotic Gene Polymorphisms in Young Patients with Cerebrovascular Accident. The Annals of Clinical and Analytical Medicine. 4(4). 2 indexed citations
3.
Soysal, Yasemin, Ümit Ubeyt İnan, Tuncay Küsbeci, & Necat İmirzalıoğlu. (2011). Age-Related Macular Degeneration and Association of CFH Y402H and LOC387715 A69S Polymorphisms in a Turkish Population. DNA and Cell Biology. 31(3). 323–330. 16 indexed citations
4.
Soysal, Yasemin, et al.. (2011). Modulator Effects of the Methylenetetrahydrofolate Reductase C677T Polymorphism on Response to Vitamin B12 Therapy and Homocysteine Metabolism. DNA and Cell Biology. 31(5). 820–825. 3 indexed citations
5.
Soysal, Yasemin, et al.. (2011). Case Report Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech. Genetics and Molecular Research. 10(3). 2148–2154. 4 indexed citations
6.
Bozkurt, Mehmet, Yalçın Külahçi, Fatih Zor, et al.. (2011). [Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases].. PubMed. 20(4). 200–4.
7.
Soysal, Yasemin, et al.. (2009). Analysis of PTEN Gene Mutations in a Turkish Patient with Cowden Syndrome. Genetic Testing and Molecular Biomarkers. 13(4). 547–551. 1 indexed citations
8.
Emmıler, Mustafa, et al.. (2009). A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders. Genetics and Molecular Research. 8(2). 426–434. 3 indexed citations
9.
Soysal, Yasemin, Sevim Balcı, Thomas Liehr, et al.. (2009). Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. American Journal of Medical Genetics Part A. 149A(12). 2782–2787. 13 indexed citations
10.
Özel, Melih, Levent Demırtürk, Aydoğan Aydoğdu, et al.. (2007). Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever. International Journal of Clinical Practice. 62(5). 754–761. 14 indexed citations
11.
Karaçay, Şeniz, Işıl Saygun, Yaşar Meriç Tunca, Necat İmirzalıoğlu, & Gülten Güvenç. (2007). Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I. Journal of Indian Society of Pedodontics and Preventive Dentistry. 25(1). 43–43. 9 indexed citations
12.
Samli, A. Coskun, et al.. (2006). GENETIC ANOMALIES DETECTED IN PATIENTS WITH NON-OBSTRUCTIVE AZOOSPERMIA AND OLIGOZOOSPERMIA. Archives of Andrology. 52(4). 263–267. 28 indexed citations
13.
Ergün, Mehmet Ali, Yasemin Soysal, Erol Kısmet, et al.. (2006). Investigating thein vitroeffect of taurine on the infant lymphocytes by sister chromatid exchange. Pediatrics International. 48(3). 284–286. 4 indexed citations
14.
Suer, Funda, et al.. (2005). The vitamin D receptor fokl start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism. Journal of Endocrinological Investigation. 28(11). 810–814. 2 indexed citations
15.
İmirzalıoğlu, Necat, Ahmet Dursun, Bora Tastan, Yasemin Soysal, & M. Cengiz Yakıcıer. (2005). MEFVgene is a probable susceptibility gene for Behçet's disease. Scandinavian Journal of Rheumatology. 34(1). 56–58. 71 indexed citations
16.
Tüzün, Ahmet, Ahmet Dursun, Yüksel Ateş, et al.. (2004). Ailesel Akdeniz ateşi düşünülen 110 vakada sık görülen MEFV gen mutasyonları analiz sonuçları ve klinik bulgularla korelasyonu. 46(3). 238–241. 1 indexed citations
17.
Tunca, Yusuf, et al.. (2003). New heritable fragile site at 15q13 in both members of a nonconsanguineous couple. American Journal of Medical Genetics Part A. 118A(3). 290–292. 8 indexed citations
18.
Solak, Mustafa, et al.. (2003). Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture. Prenatal Diagnosis. 23(10). 847–850. 18 indexed citations
19.
20.
Oğur, Gönül, Samim Özen, Necat İmirzalıoğlu, et al.. (1997). Application of the ‘Apt test’ in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies. Prenatal Diagnosis. 17(9). 879–882. 7 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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