Osman Demırhan

1.1k total citations
72 papers, 662 citations indexed

About

Osman Demırhan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Osman Demırhan has authored 72 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 22 papers in Pediatrics, Perinatology and Child Health and 19 papers in Molecular Biology. Recurrent topics in Osman Demırhan's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (19 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Osman Demırhan is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (19 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Osman Demırhan collaborates with scholars based in Türkiye, United States and Germany. Osman Demırhan's co-authors include Yaşar Sertdemır, Nilgün Tanrıverdi, Sali̇h Çeti̇ner, Tamer İnal, Ali İrfan Güzel, Seval Türkmen, Stefan Mundlos, Nicholas Humphrey, Karl‐Titus Hoffmann and Richard J. Smith and has published in prestigious journals such as SHILAP Revista de lepidopterología, Fertility and Sterility and American Journal of Tropical Medicine and Hygiene.

In The Last Decade

Osman Demırhan

63 papers receiving 628 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Osman Demırhan Türkiye 14 235 222 139 138 76 72 662
Marina Ciullo Italy 16 220 0.9× 291 1.3× 34 0.2× 41 0.3× 74 1.0× 34 738
Va Lip United States 12 367 1.6× 474 2.1× 439 3.2× 171 1.2× 18 0.2× 17 883
B.J. Otten Netherlands 26 594 2.5× 987 4.4× 288 2.1× 102 0.7× 97 1.3× 55 1.7k
Teresa Nutile Italy 14 128 0.5× 159 0.7× 29 0.2× 34 0.2× 33 0.4× 23 505
Joy B. Redman United States 17 203 0.9× 301 1.4× 71 0.5× 21 0.2× 39 0.5× 27 781
Rogelio H.A. Ruvalcaba United States 18 472 2.0× 393 1.8× 131 0.9× 47 0.3× 34 0.4× 42 888
S Takahashi Japan 15 318 1.4× 216 1.0× 22 0.2× 34 0.2× 100 1.3× 33 868
Igor Medica Slovenia 11 50 0.2× 148 0.7× 67 0.5× 34 0.2× 70 0.9× 28 359
Pedro Moreira Portugal 17 168 0.7× 341 1.5× 258 1.9× 457 3.3× 48 0.6× 37 1.0k
Fengxiao Bu China 12 167 0.7× 164 0.7× 15 0.1× 42 0.3× 389 5.1× 31 834

Countries citing papers authored by Osman Demırhan

Since Specialization
Citations

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

Fields of papers citing papers by Osman Demırhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Osman Demırhan

This figure shows the co-authorship network connecting the top 25 collaborators of Osman Demırhan. A scholar is included among the top collaborators of Osman Demırhan 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 Osman Demırhan. Osman Demırhan 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.
2.
Demırhan, Osman, et al.. (2019). Effect of fetal microchimeric cells on the development of postnatal depression. 3(2). 1 indexed citations
3.
Istıflı, Erman Salih, et al.. (2018). In vitro cytogenotoxic evaluation of sertraline. Interdisciplinary Toxicology. 11(3). 181–188. 6 indexed citations
4.
5.
Demırhan, Osman, et al.. (2018). Constitutional chromosome 16q mosaicism: inheritance and phenotypic effects. SHILAP Revista de lepidopterología. 43(4). 1023–1027. 1 indexed citations
6.
Demırhan, Osman, et al.. (2017). Chromosomal findings and sequence analysis of target exons of calcium-sensingreceptor (CaSR) gene in patients with Sagliker syndrome. TURKISH JOURNAL OF MEDICAL SCIENCES. 47(1). 13–21. 7 indexed citations
7.
Demırhan, Osman, et al.. (2016). Chromosomal Aberrations in Turkish Infertile Couples with Reproductive Problems. 1(1). 6–10. 3 indexed citations
8.
Demırhan, Osman, Ahmet Arslan, Sercan Ergün, et al.. (2016). MP386MULTIPLE GENE MUTATIONS IN GNAS1, FGF23 AND FGFR3 GENES IN CKD PATIENTS WITH SH SAGLIKER SYNDROME. Nephrology Dialysis Transplantation. 31(suppl_1). i468–i468. 1 indexed citations
9.
Demırhan, Osman, et al.. (2015). The Frequency and Types of Chromosomal Aberrations in the Patients with Hypogonadism. 5(1). 2 indexed citations
10.
Demırhan, Osman, et al.. (2014). Frequency and Types of Chromosomal Abnormalities in Turkish Women with Amenorrhea. Journal of Pediatric and Adolescent Gynecology. 27(5). 274–277. 6 indexed citations
11.
Hakverdi, Sibel, et al.. (2013). Chromosome Imbalances and Alterations in the p53 Gene in Uterine Myomas from the Same Family Members: Familial Leiomyomatosis in Turkey. Asian Pacific Journal of Cancer Prevention. 14(2). 651–658. 1 indexed citations
12.
Demırhan, Osman, et al.. (2013). There is no Significant Association Between Death Receptor 4 (DR4) Gene Polymorphisms and Lung Cancer in Turkish Population. Pathology & Oncology Research. 19(4). 779–784. 7 indexed citations
13.
Hanta, İsmail, et al.. (2012). Association of the Nramp1 gene polymorphisms and clinical forms in patients with tuberculosis. Bratislavské lekárske listy/Bratislava medical journal. 113(11). 657–660. 4 indexed citations
14.
Demırhan, Osman, Ali İrfan Güzel, Mehmet Bertan Yılmaz, et al.. (2011). The Reliability of Maternal Serum Triple Test in Prenatal Diagnosis of Fetal Chromosomal Abnormalities of Pregnant Turkish Women. Genetic Testing and Molecular Biomarkers. 15(10). 701–707. 3 indexed citations
15.
Demırhan, Osman, et al.. (2011). Applications of Fluorescence in Situ Hybridization (FISH) for Detecting Genetic Changes in Hematological Malignancies. Journal of Cancer Therapy. 2(2). 125–134. 1 indexed citations
16.
Güzel, Ali İrfan, et al.. (2009). Detection of Parental Origin and Cell Stage Errors of a Double Nondisjunction in a Fetus by QF-PCR. Genetic Testing and Molecular Biomarkers. 13(1). 73–77. 11 indexed citations
17.
Demırhan, Osman, et al.. (2008). Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling.. PubMed. 29(7). 946–51. 22 indexed citations
18.
Coucke, Paul, Peter Van Hauwe, Lorraine A. Everett, et al.. (1999). Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome. Journal of Medical Genetics. 36(6). 475–477. 40 indexed citations
19.
Coucke, Paul, Guy Van Camp, Osman Demırhan, et al.. (1997). The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q. Genomics. 40(1). 48–54. 24 indexed citations
20.
Demırhan, Osman, et al.. (1995). Bloodfeeding behavior of Anopheles sacharovi in Turkey.. PubMed. 11(1). 11–4. 4 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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