İlgen Şaşmaz

460 citations
18 papers · 200 · h-index 7

Impact in

  • Hematology top 10%
    • Iron Metabolism and Disorders
    • Acute Myeloid Leukemia Research
    • Hemophilia Treatment and Research
    • Platelet Disorders and Treatments
    • Blood Coagulation and Thrombosis Mechanisms
  • Genetics top 10%
    • Hemoglobinopathies and Related Disorders

Papers in

    • Acute Myeloid Leukemia Research 4
    • Iron Metabolism and Disorders 4
    • Hemophilia Treatment and Research 3
    • Platelet Disorders and Treatments 2
    • Hemoglobinopathies and Related Disorders 4

İlgen Şaşmaz

18 papers receiving 187 citations

Peers

İlgen Şaşmaz
Comparison fields: 5 of 45
  • Hematology 109
  • Genetics 84
  • Nephrology 14
  • Pediatrics, Perinatology and Child Health 26
  • Pharmacy 5
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Citations per year

Countries citing papers authored by İlgen Şaşmaz

Since Specialization
Citations

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

Fields of papers citing papers by İlgen Şaşmaz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside İlgen Şaşmaz, 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 İlgen Şaşmaz Line = papers co-authored together İlgen Şaşmaz links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 200089
2 200327
3 201023
4 200311
5 20197
6 20117
7 20137
8 20085
9 20065
10 20164
11
The results of treatment with idarubicin in childhood acute nonlymphoblastic leukemia.
20044
12 20083
13 20183
14 20031
15 20241
16 20081
17 20241
18 20131

About İlgen Şaşmaz

İlgen Şaşmaz is a scholar working on Hematology, Genetics, Molecular Biology, Pulmonary and Respiratory Medicine and Oncology, having authored 18 papers that have together received 200 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (4 papers), Hemoglobinopathies and Related Disorders (4 papers), Iron Metabolism and Disorders (4 papers), Hemophilia Treatment and Research (3 papers), Platelet Disorders and Treatments (2 papers), Acute Lymphoblastic Leukemia research (2 papers), Oral health in cancer treatment (2 papers) and Folate and B Vitamins Research (1 paper). The work is most often cited by research in Hematology (109 citations), Genetics (84 citations), Nephrology (14 citations), Pediatrics, Perinatology and Child Health (26 citations) and Pharmacy (5 citations). İlgen Şaşmaz has collaborated with scholars based in Türkiye and Japan. Frequent co-authors include Yurdanur Kılınç, Bülent Antmen, Aysun Karabay Bayazıt, Aytül Noyan, Ali Anarat, Edip Gali, Rüksan Anarat, Melih Özel, M. Cenk Haytaç and Göksel Leblebisatan. Their work appears in journals such as Journal of Periodontology, Haemophilia, Pediatric Nephrology, Blood and Clinical Transplantation.

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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