Fatma Sılan

1.3k citations
79 papers · 770 · h-index 15

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 7
    • Genomics and Rare Diseases 4
    • Inflammasome and immune disorders 4

Fatma Sılan

70 papers receiving 744 citations

Peers

Fatma Sılan
Comparison fields: 5 of 80
  • Sensory Systems 35
  • Hematology 70
  • Developmental Biology 14
  • Rheumatology 83
  • Obstetrics and Gynecology 34
Replace David Coman with:
David Coman Australia
Tahir Atık Türkiye
Romina Ficarella Italy
Alexey Savov Bulgaria
Alice Krebsová Czechia
S. Merin Israel
Adel Shalata Israel
Margaret Prechel United States
Tetsuo Morioka Japan
Brendan C. Lanpher United States
Fatma Sılan relative to David Coman Australia David Coman's profile →
Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Fatma Sılan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fatma Sılan Line = papers co-authored together Fatma Sılan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 79 papers — load more, or switch the sort, to bring in the rest.

#Work
1 200785
2 200373
3 201158
4 200356
5 201634
6 201830
7 201124
8 201520
9 201520
10 200320
11 200519
12 201316
13 201215
14 201314
15 200414
16 201113
17 201312
18
Tumour necrosis factor alpha, ınterleukin 10 and ınterleukin 6 gene polymorphisms of ıschemic stroke patients ın south Marmara region of Turkey.
201512
19 201312
20
Fetal Vegf Genotype is More Important for Abortion Risk than Mother Genotype.
201411

About Fatma Sılan

Fatma Sılan is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Pathology and Forensic Medicine, having authored 79 papers that have together received 770 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers), Inflammasome and immune disorders (4 papers), Spondyloarthritis Studies and Treatments (4 papers), Genomics and Rare Diseases (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Vitamin D Research Studies (3 papers). The work is most often cited by research in Sensory Systems (35 citations), Hematology (70 citations), Developmental Biology (14 citations), Rheumatology (83 citations) and Obstetrics and Gynecology (34 citations). Fatma Sılan has collaborated with scholars based in Türkiye, Serbia and United States. Frequent co-authors include Öztürk Özdemir, Ahmet Uludağ, Meryem Çam, Aysel Güven, Filiz Özen, Neslihan Bukan, Enver Şimşek, Özlem Yavuz, Semra Özdemir and Coşkun Sılan. Their work appears in journals such as International Journal of Pediatric Otorhinolaryngology, Prenatal Diagnosis, Renal Failure, Molecular Biology Reports and Clinical Neurology and Neurosurgery.

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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