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

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

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Human Papilloma Viruses and Their Genotype Distribution in Women with High Socioeconomic Status in Central Anatolia, Turkey: A Pilot Study	Medical Science Monitor	Engin Yıldırım, Mehmet Kahraman et al.	8
2	Prothrombotic Gene Polymorphisms in Young Patients with Cerebrovascular Accident	The Annals of Clinical and Analytical Medicine	Yasemin Soysal, Özge Yılmaz Küsbeci et al.	2
3	Age-Related Macular Degeneration and Association of CFH Y402H and LOC387715 A69S Polymorphisms in a Turkish Population	DNA and Cell Biology	Yasemin Soysal, Ümit Ubeyt İnan et al.	16
4	Modulator Effects of the Methylenetetrahydrofolate Reductase C677T Polymorphism on Response to Vitamin B12 Therapy and Homocysteine Metabolism	DNA and Cell Biology	Yasemin Soysal, Ahmet Kahraman et al.	3
5	Case Report Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech	Genetics and Molecular Research	Yasemin Soysal, Joris Vermeesch et al.	4
6	[Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases].	PubMed	Mehmet Bozkurt, Yalçın Külahçi et al.	0
7	Analysis of PTEN Gene Mutations in a Turkish Patient with Cowden Syndrome	Genetic Testing and Molecular Biomarkers	Yasemin Soysal, Genshu Tate et al.	1
8	A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders	Genetics and Molecular Research	Mustafa Emmıler, Necat İmirzalıoğlu et al.	3
9	Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy	American Journal of Medical Genetics Part A	Yasemin Soysal, Sevim Balcı et al.	13
10	Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever	International Journal of Clinical Practice	Melih Özel, Levent Demırtürk et al.	14
11	Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I	Journal of Indian Society of Pedodontics and Preventive Dentistry	Şeniz Karaçay, Işıl Saygun et al.	9
12	GENETIC ANOMALIES DETECTED IN PATIENTS WITH NON-OBSTRUCTIVE AZOOSPERMIA AND OLIGOZOOSPERMIA	Archives of Andrology	A. Coskun Samli, Mustafa Solak et al.	28
13	Investigating thein vitroeffect of taurine on the infant lymphocytes by sister chromatid exchange	Pediatrics International	Mehmet Ali Ergün, Yasemin Soysal et al.	4
14	The vitamin D receptor fokl start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism	Journal of Endocrinological Investigation	Funda Suer, Ferhat Denız et al.	2
15	MEFVgene is a probable susceptibility gene for Behçet's disease	Scandinavian Journal of Rheumatology	Necat İmirzalıoğlu, Ahmet Dursun et al.	71
16	Ailesel Akdeniz ateşi düşünülen 110 vakada sık görülen MEFV gen mutasyonları analiz sonuçları ve klinik bulgularla korelasyonu		Ahmet Tüzün, Ahmet Dursun et al.	1
17	New heritable fragile site at 15q13 in both members of a nonconsanguineous couple	American Journal of Medical Genetics Part A	Yusuf Tunca, Necat İmirzalıoğlu et al.	8
18	Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture	Prenatal Diagnosis	Mustafa Solak, Necat İmirzalıoğlu et al.	18
19	Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure	Human Reproduction	Semra Kahraman, Muhterem Bahçe et al.	109
20	Application of the ‘Apt test’ in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies	Prenatal Diagnosis	Gönül Oğur, Samim Özen et al.	7

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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