Osman Demırhan
Osman Demırhan publishes mostly in Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, on topics such as Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities.
- World rank
- #7,658,732 of 7,710,434 ranked researchers
- Rank in Türkiye
- #115,786 of 117,622
- Works
- 151
- Citations
- 1.1k
- Citations per work
- 7.2
What does Osman Demırhan research?
Osman Demırhan's work is mostly in Biochemistry, Genetics and Molecular Biology (42%), Medicine (19%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences6341.7%
- Everything else5938.9%
- Health Sciences2919.4%
- Medicine2919.4%
- 1Genetics28% of their works
- 2Pediatrics, Perinatology and Child Health12% of their works
- 3Molecular Biology11% of their works
- 4Public Health, Environmental and Occupational Health4% of their works
- 5Nephrology3% of their works
- 6Cancer Research3% of their works
Research topics
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Parathyroid Disorders and Treatments
- Genetic Syndromes and Imprinting
- Sexual Differentiation and Disorders
- Electromagnetic Fields and Biological Effects
Which keywords describe Osman Demırhan's research?
The keywords of their largest research topics: Copy Number Variation, Genomic Rearrangements, Aneuploidy Screening, Prenatal Diagnosis, Sex Determination, X Chromosome Inactivation, Fragile X Syndrome and Rett Syndrome.
- Magnetoreception
- Steroid 21-Hydroxylase Deficiency
- Genomic Imprinting
- phosphate
- Rett Syndrome
- X Chromosome Inactivation
- Prenatal Diagnosis
- Genomic Rearrangements
- Copy Number Variation
- Aneuploidy Screening
- Sex Determination
- Fragile X Syndrome
- FGF23
- Congenital Adrenal Hyperplasia
- Parental Influence
- Electromagnetic Fields
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most.
All 16 words, with their numbers
- Copy Number Variation311 topic
- Genomic Rearrangements311 topic
- Aneuploidy Screening281 topic
- Prenatal Diagnosis281 topic
- Sex Determination231 topic
- X Chromosome Inactivation231 topic
- Fragile X Syndrome161 topic
- Rett Syndrome161 topic
- FGF23111 topic
- phosphate111 topic
- Congenital Adrenal Hyperplasia101 topic
- Genomic Imprinting101 topic
- Parental Influence101 topic
- Steroid 21-Hydroxylase Deficiency101 topic
- Electromagnetic Fields61 topic
- Magnetoreception61 topic
Where does Osman Demırhan work?
Osman Demırhan's main affiliation in the publication record is Cukurova University, Türkiye.
How many publications and citations does Osman Demırhan have?
OpenAlex counts 151 works and 1,081 citations for Osman Demırhan, an h-index of 18, ranking #7,658,732 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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