Fatma Sılan

1.2k total citations
78 papers, 759 citations indexed

About

Fatma Sılan is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Fatma Sılan has authored 78 papers receiving a total of 759 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Immunology. Recurrent topics in Fatma Sılan's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (6 papers). Fatma Sılan is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (6 papers). Fatma Sılan collaborates with scholars based in Türkiye, Serbia and United Kingdom. Fatma Sılan's co-authors include Öztürk Özdemir, Ahmet Uludağ, Meryem Çam, Aysel Güven, Filiz Özen, Özlem Yavuz, Enver Şimşek, Neslihan Bukan, Semra Özdemir and Murat Alper and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Fatma Sılan

70 papers receiving 733 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatma Sılan Türkiye 15 269 105 100 97 97 78 759
Jakob Triebel Germany 15 184 0.7× 46 0.4× 84 0.8× 76 0.8× 136 1.4× 50 770
Gilles Kauffenstein France 24 420 1.6× 274 2.6× 135 1.4× 132 1.4× 119 1.2× 49 1.4k
Alexey Savov Bulgaria 14 172 0.6× 148 1.4× 56 0.6× 88 0.9× 47 0.5× 63 602
Yutaka Harita Japan 19 427 1.6× 156 1.5× 87 0.9× 124 1.3× 43 0.4× 66 934
Bibiana Moreno-Carranza Mexico 12 151 0.6× 55 0.5× 39 0.4× 32 0.3× 56 0.6× 18 457
Ioanna Mosialou United States 12 552 2.1× 83 0.8× 166 1.7× 114 1.2× 53 0.5× 17 1.3k
Claudia Weidler Germany 12 141 0.5× 77 0.7× 208 2.1× 41 0.4× 141 1.5× 14 692
Bin Cai China 18 316 1.2× 261 2.5× 119 1.2× 101 1.0× 30 0.3× 54 944
Wanda E. Filipiak United States 8 407 1.5× 234 2.2× 77 0.8× 85 0.9× 23 0.2× 11 906
Beatrice B. Yaroslavskiy United States 15 681 2.5× 234 2.2× 114 1.1× 61 0.6× 53 0.5× 21 1.3k

Countries citing papers authored by Fatma Sılan

Since Specialization
Citations

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

Fields of papers citing papers by Fatma Sılan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatma Sılan

This figure shows the co-authorship network connecting the top 25 collaborators of Fatma Sılan. A scholar is included among the top collaborators of Fatma Sılan 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 Fatma Sılan. Fatma Sılan 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.
Sılan, Fatma, et al.. (2025). Exploring and Expanding Secondary Findings Through Exome Sequencing in the Turkish Population. Annals of Human Genetics. 89(2-3). 106–113. 1 indexed citations
2.
Ji, Weizhen, Saquib A. Lakhani, Fatma Sılan, et al.. (2024). CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life Science Alliance. 7(10). e202402708–e202402708. 2 indexed citations
3.
4.
Sılan, Fatma, et al.. (2022). A new entity in the NARS2 variant: the first reported case of type 1 diabetes mellitus associated with the phenotype. Journal of Tropical Pediatrics. 69(1). 6 indexed citations
5.
Paşa, Semir, et al.. (2020). Evaluation inflammatory markers of hemogram parameters in primary ovarian insufficiency. Journal of Turkish Society of Obstetric and Gynecology. 17(1). 9–14. 2 indexed citations
6.
Sılan, Fatma, et al.. (2020). Tedaviyi Etkileyen Tarama Testleri. 5(1). 16–24.
7.
Özdemir, Semra, et al.. (2019). Comparison of SUV<sub>max</sub> Values Obtained from F-18 FDG PET/CT and Cell-free DNA Levels Measured from Plasma in Oncology Patients. Molecular Imaging and Radionuclide Therapy. 28(2). 46–52. 2 indexed citations
8.
Sılan, Fatma, et al.. (2018). Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation. SHILAP Revista de lepidopterología. 3(1). 23–27. 1 indexed citations
9.
Sılan, Fatma, et al.. (2016). Vitamin D Receptor Gene BSMI, FOKI, APAI, and TAQI Polymorphisms and the Risk of Atopic Dermatitis. Journal of Investigational Allergology and Clinical Immunology. 26(2). 106–110. 33 indexed citations
10.
Özkan, Adile, et al.. (2015). Tumour necrosis factor alpha, ınterleukin 10 and ınterleukin 6 gene polymorphisms of ıschemic stroke patients ın south Marmara region of Turkey.. PubMed. 8(10). 13500–4. 12 indexed citations
11.
Sılan, Fatma, et al.. (2014). Fetal Vegf Genotype is More Important for Abortion Risk than Mother Genotype.. PubMed. 3(2). 88–94. 10 indexed citations
12.
13.
Özen, Filiz, et al.. (2013). The Proto-Oncogene KRAS and BRAF Profiles and Some Clinical Characteristics in Colorectal Cancer in the Turkish Population. Genetic Testing and Molecular Biomarkers. 17(2). 135–139. 12 indexed citations
14.
Uludağ, Ahmet, et al.. (2013). Relationship Between Response to Colchicine Treatment and MDR1 Polymorphism in Familial Mediterranean Fever Patients. Genetic Testing and Molecular Biomarkers. 18(2). 73–76. 11 indexed citations
15.
Özdemir, Semra, et al.. (2012). Increased T-Allele Frequency of 677 C>T Polymorphism in the Methylenetetrahydrofolate Reductase Gene in Differentiated Thyroid Carcinoma. Genetic Testing and Molecular Biomarkers. 16(7). 780–784. 15 indexed citations
16.
Sılan, Fatma, et al.. (2011). Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas. Molecular Biology Reports. 39(2). 1595–1599. 13 indexed citations
17.
18.
Özdemir, Öztürk, et al.. (2011). Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations. Genetic Testing and Molecular Biomarkers. 16(4). 279–286. 58 indexed citations
19.
Lehmann, Katarina, Petra Seemann, Fatma Sılan, et al.. (2007). A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN. The American Journal of Human Genetics. 81(2). 388–396. 84 indexed citations
20.
Özdemir, İsmail, Enver Şimşek, Fatma Sılan, & Fati̇h Demi̇rci̇. (2005). Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha-fetoprotein. Prenatal Diagnosis. 25(8). 687–689. 19 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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