Munis Dündar

3.0k total citations
211 papers, 1.8k citations indexed

About

Munis Dündar is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Munis Dündar has authored 211 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 57 papers in Genetics and 20 papers in Oncology. Recurrent topics in Munis Dündar's work include Prenatal Screening and Diagnostics (13 papers), Sexual Differentiation and Disorders (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Munis Dündar is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Sexual Differentiation and Disorders (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Munis Dündar collaborates with scholars based in Türkiye, Italy and United Kingdom. Munis Dündar's co-authors include Ahmet Okay Çağlayan, Yusuf Özkul, Tommaso Beccari, Serpil Taheri, Matteo Bertelli, Mevlüt Başkol, Astrit Dautaj, Andreas Janecke, Thomas Müller and Julia Vodopiutz and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Biological Psychiatry.

In The Last Decade

Munis Dündar

187 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Munis Dündar Türkiye 20 800 431 200 179 139 211 1.8k
Luis E. Figuera Mexico 23 637 0.8× 622 1.4× 302 1.5× 140 0.8× 159 1.1× 134 1.8k
Justine A. Ellis Australia 31 598 0.7× 485 1.1× 236 1.2× 221 1.2× 359 2.6× 93 2.6k
Carlos Alberto Moreira‐Filho Brazil 28 1.0k 1.3× 622 1.4× 90 0.5× 172 1.0× 218 1.6× 113 2.4k
Jason Yang United States 26 885 1.1× 886 2.1× 185 0.9× 300 1.7× 206 1.5× 82 2.7k
Weikuan Gu United States 33 1.8k 2.3× 674 1.6× 215 1.1× 230 1.3× 263 1.9× 164 3.8k
Pankaj Gupta United States 30 811 1.0× 307 0.7× 347 1.7× 323 1.8× 289 2.1× 121 3.1k
Xinyi Xia China 23 803 1.0× 361 0.8× 49 0.2× 120 0.7× 107 0.8× 181 2.1k
Osama Alsmadi Kuwait 22 623 0.8× 462 1.1× 52 0.3× 103 0.6× 204 1.5× 74 1.6k
Rinaldo Wellerson Pereira Brazil 23 920 1.1× 485 1.1× 139 0.7× 68 0.4× 238 1.7× 88 2.1k
Bowang Chen Germany 23 734 0.9× 400 0.9× 57 0.3× 190 1.1× 94 0.7× 70 1.9k

Countries citing papers authored by Munis Dündar

Since Specialization
Citations

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

Fields of papers citing papers by Munis Dündar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Munis Dündar

This figure shows the co-authorship network connecting the top 25 collaborators of Munis Dündar. A scholar is included among the top collaborators of Munis Dündar 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 Munis Dündar. Munis Dündar 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.
Erdoğan, Murat, Hakan Gümüş, Ahmet Sami Güven, et al.. (2025). A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis. Neurogenetics. 26(1). 47–47.
2.
Özcan, Alper, Ebru Yılmaz, Atıl Bişgin, et al.. (2025). Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders. Research and Practice in Thrombosis and Haemostasis. 9(4). 102873–102873.
3.
Turan, Tayfun, et al.. (2025). Oxytocin receptor gene single nucleotide polymorphisms in patients with bipolar disorder. International Journal of Psychiatry in Clinical Practice. 29(1). 18–24. 1 indexed citations
4.
Bonetti, Graziella, Gary T. Henehan, Richard E. Brown, et al.. (2024). Promoting International Scientific Cooperation: the Role of Scientific Societies. The EuroBiotech Journal. 8(3). 115–121.
5.
6.
Ayaz‐Güner, Şerife, et al.. (2024). Mesenchymal stem cells from adipose tissue prone to lose their stemness associated markers in obesity related stress conditions. Scientific Reports. 14(1). 19702–19702. 6 indexed citations
7.
8.
Yılmaz, M. Tuğrul, et al.. (2023). Impacts of Biotechnologically Developed Microorganisms on Ecosystems. The EuroBiotech Journal. 7(4). 196–205.
9.
Zararsız, Gökmen, Vahap Eldem, Osman Başpınar, et al.. (2023). Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing. Genes and Immunity. 25(1). 14–42. 1 indexed citations
10.
Michelini, Sandro, Bruno Amato, Stefano Gentileschi, et al.. (2021). CDH5 , a Possible New Candidate Gene for Genetic Testing of Lymphedema. Lymphatic Research and Biology. 20(5). 496–506. 2 indexed citations
11.
Michelini, Sandro, Syed Hussain Basha, Juraj Krajčovič, et al.. (2020). TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema. International Journal of Molecular Sciences. 21(18). 6780–6780. 12 indexed citations
12.
Michelini, Sandro, Bruno Amato, Elena Manara, et al.. (2020). Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema. Genes. 11(11). 1361–1361. 4 indexed citations
13.
Compagna, Rita, Bruno Amato, Syed Hussain Basha, et al.. (2020). Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes. International Journal of Genomics. 2020. 1–9.
14.
İsmailoğulları, Sevda, et al.. (2020). Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift. Sleep Medicine. 73. 101–105. 10 indexed citations
15.
Baydilli, Numan, et al.. (2018). The frequencies of Y chromosome microdeletions in infertile males. SHILAP Revista de lepidopterología. 44(5). 389–392. 19 indexed citations
16.
Bruson, Alice, et al.. (2017). Genetic testing for non syndromic retinitis pigmentosa. The EuroBiotech Journal. 1(s1). 92–95. 3 indexed citations
17.
Alikaşifoğlu, Ayfer, Nurgün Kandemir, Munis Dündar, et al.. (2016). A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria. 86. 1 indexed citations
18.
Diri, Halit, et al.. (2014). Etiopathogenesis of Sheehan’s Syndrome: Roles of Coagulation Factors and TNF-Alpha. International Journal of Endocrinology. 2014. 1–6. 5 indexed citations
19.
Dündar, Munis, et al.. (2010). Rare disease and orphan drugs in Turkey; medical and social problem.. 32(3). 195–200. 2 indexed citations
20.
Eşel, Ertuğrul, et al.. (2001). Albright's Hereditary Osteodystrophy and dementia: a case report. Klinik Psikofarmakoloji Bülteni-Bulletin of Clinical Psychopharmacology. 11(3). 183–186. 1 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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