Mustafa Solak

906 total citations
54 papers, 708 citations indexed

About

Mustafa Solak is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mustafa Solak has authored 54 papers receiving a total of 708 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Genetics and 8 papers in Surgery. Recurrent topics in Mustafa Solak's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Congenital limb and hand anomalies (5 papers) and Prenatal Screening and Diagnostics (4 papers). Mustafa Solak is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Congenital limb and hand anomalies (5 papers) and Prenatal Screening and Diagnostics (4 papers). Mustafa Solak collaborates with scholars based in Türkiye, United States and United Kingdom. Mustafa Solak's co-authors include Müjgan Özdemir Erdoğan, Ömer Faruk Karataş, Mustafa Özen, Michael Ittmann, A. Coskun Samli, Olcay Eser, Esra Güzel, Asiye Durmaz Akyol, Ahmet Şenel and Alpay Haktanır and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal Of Hand Surgery and Head & Neck.

In The Last Decade

Mustafa Solak

48 papers receiving 681 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mustafa Solak Türkiye 16 325 154 124 119 102 54 708
Volkmar Heidecke Germany 22 156 0.5× 507 3.3× 382 3.1× 55 0.5× 80 0.8× 42 1.3k
Manuel Pombo‐Suárez Spain 14 226 0.7× 151 1.0× 51 0.4× 102 0.9× 80 0.8× 28 809
W. Burkert Germany 20 111 0.3× 429 2.8× 288 2.3× 44 0.4× 63 0.6× 48 1.1k
Kyoichi Obata Japan 15 198 0.6× 89 0.6× 46 0.4× 28 0.2× 124 1.2× 57 543
E. K. Weir United States 15 315 1.0× 243 1.6× 44 0.4× 48 0.4× 134 1.3× 33 1.1k
Ramakrishnan Rajagopalan United States 17 240 0.7× 252 1.6× 33 0.3× 50 0.4× 202 2.0× 27 814
Changlong Guo China 12 791 2.4× 131 0.9× 35 0.3× 67 0.6× 163 1.6× 31 1.1k
Jan Walter Germany 16 158 0.5× 450 2.9× 258 2.1× 94 0.8× 30 0.3× 42 863
Michael Möllmann Germany 17 187 0.6× 315 2.0× 158 1.3× 26 0.2× 22 0.2× 66 875
Ingrid Arvidsson Sweden 14 105 0.3× 175 1.1× 179 1.4× 37 0.3× 59 0.6× 24 889

Countries citing papers authored by Mustafa Solak

Since Specialization
Citations

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

Fields of papers citing papers by Mustafa Solak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mustafa Solak

This figure shows the co-authorship network connecting the top 25 collaborators of Mustafa Solak. A scholar is included among the top collaborators of Mustafa Solak 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 Mustafa Solak. Mustafa Solak 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.
Varol, Nuray, et al.. (2023). Relationship between expression levels of TDRD7 and CRYBB3 and development of age-related cortico-nuclear cataracts. SHILAP Revista de lepidopterología. 24(1). 1 indexed citations
2.
3.
Elmas, Muhsin, et al.. (2021). Neurodevelopment and Genetic Evaluation of Sotos Syndrome Cases with a Novel Mutation: a Single-Center Experience. Journal of Molecular Neuroscience. 72(1). 149–157. 4 indexed citations
4.
Solak, Mustafa, et al.. (2020). Investigation of the expression levels of CPEB4, APC, TRIP13, EIF2S3, EIF4A1, IFNg, PIK3CA and CTNNB1 genes in different stage colorectal tumors. TURKISH JOURNAL OF MEDICAL SCIENCES. 51(2). 661–674. 8 indexed citations
5.
Yıldız, Mustafa, Hakan Terzi, Nuray Varol, et al.. (2020). Proteomic analysis of the anticancer effect of various extracts of endemicThermopsisturcica in human cervical cancer cells. TURKISH JOURNAL OF MEDICAL SCIENCES. 50(8). 1993–2004. 1 indexed citations
6.
Ağaoğlu, Nihat Buğra, et al.. (2019). Relationship between SIRT1 gene expression level and disease in age-related cataract cases. TURKISH JOURNAL OF MEDICAL SCIENCES. 49(4). 1068–1072. 7 indexed citations
7.
Erdoğan, Müjgan Özdemir, et al.. (2016). Lack of association between the methylenetetrahydropholate reductase gene A1298C polymorphism and neural tube defects in a Turkish study group. Genetics and Molecular Research. 15(2). 6 indexed citations
8.
Özen, Mustafa, Ömer Faruk Karataş, Şükrü Güllüoğlu, et al.. (2015). Overexpression of miR-145–5p Inhibits Proliferation of Prostate Cancer Cells and Reduces SOX2 Expression. Cancer Investigation. 33(6). 251–258. 80 indexed citations
9.
Solak, Mustafa, et al.. (2014). Association of obesity with rs1421085 and rs9939609 polymorphisms of FTO gene. Molecular Biology Reports. 41(11). 7381–7386. 17 indexed citations
10.
Güzel, Esra, Ömer Faruk Karataş, Mehmet Buğrahan Düz, et al.. (2014). Differential expression of stem cell markers and ABCG2 in recurrent prostate cancer. The Prostate. 74(15). 1498–1505. 44 indexed citations
11.
Berdelı, Afig, Sevgı Mır, Necil Kütükçüler, et al.. (2011). Comprehensive Analysis of a Large-Scale Screen for MEFV Gene Mutations: Do They Truly Provide a “Heterozygote Advantage” in Turkey?. Genetic Testing and Molecular Biomarkers. 15(7-8). 475–482. 11 indexed citations
12.
Eser, Olcay, et al.. (2011). Short aggrecan gene repetitive alleles associated with lumbar degenerative disc disease in Turkish patients. Genetics and Molecular Research. 10(3). 1923–1930. 15 indexed citations
13.
Eser, Olcay, et al.. (2010). Association of the Polymorphisms of Vitamin D Receptor and Aggrecan Genes with Degenerative Disc Disease. Genetic Testing and Molecular Biomarkers. 14(3). 313–317. 75 indexed citations
14.
Solak, Mustafa, et al.. (2008). Analysis of Familial Mediterranean Fever Gene Mutations in 202 Patients with Familial Mediterranean Fever. Genetic Testing. 12(3). 341–344. 34 indexed citations
15.
Çam, Fethi Sırrı, et al.. (2008). Analysis of the dermatoglyphics in Turkish patients with Klinefelter's syndrome. Hereditas. 145(4). 163–166. 3 indexed citations
16.
Gürkan, Yavuz, Tülay Hoşten, Mustafa Solak, & Kamíl Toker. (2007). Lateral sagittal infraclavicular block: clinical experience in 380 patients. Acta Anaesthesiologica Scandinavica. 52(2). 262–266. 28 indexed citations
17.
Kuru, İlhami, et al.. (2006). Synpolydactyly of the Foot in Homozygotes. Journal of the American Podiatric Medical Association. 96(4). 297–304. 2 indexed citations
18.
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
19.
Samli, A. Coskun, et al.. (2006). Y CHROMOSOME MICRODELETION IN A CASE WITH KLINEFELTER'S SYNDROME. Archives of Andrology. 52(6). 427–431. 5 indexed citations
20.
Yücel, Aylin, et al.. (2005). Radiographic evaluation and unusual bone formations in different genetic patterns in synpolydactyly. Skeletal Radiology. 34(8). 468–476. 9 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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