Haluk Akın
Haluk Akın publishes mostly in Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health, on topics such as Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities.
- World rank
- #7,660,814 of 7,710,434 ranked researchers
- Rank in Türkiye
- #115,884 of 117,622
- Works
- 81
- Citations
- 520
- Citations per work
- 6.4
What does Haluk Akın research?
Haluk Akın's work is mostly in Biochemistry, Genetics and Molecular Biology (32%), Medicine (22%).
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
- Everything else3746.0%
- Life Sciences2632.3%
- Health Sciences1821.7%
- Medicine1821.7%
- 1Molecular Biology16% of their works
- 2Genetics16% of their works
- 3Pediatrics, Perinatology and Child Health9% of their works
- 4Hematology4% of their works
- 5Endocrinology, Diabetes and Metabolism4% of their works
- 6Reproductive Medicine4% of their works
Research topics
- Prenatal Screening and Diagnostics
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Sexual Differentiation and Disorders
- Genetics and Neurodevelopmental Disorders
- Nutrition, Genetics, and Disease
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Which keywords describe Haluk Akın's research?
The keywords of their largest research topics: Aneuploidy Screening, Prenatal Diagnosis, Genetic Variants, Copy Number Variation, Genomic Rearrangements, Congenital Adrenal Hyperplasia, Sex Determination and Steroid 21-Hydroxylase Deficiency.
- Personalized Nutrition
- Nutrigenomics
- Clinical Genomics
- Fragile X Syndrome
- Steroid 21-Hydroxylase Deficiency
- Congenital Adrenal Hyperplasia
- Copy Number Variation
- Prenatal Diagnosis
- Aneuploidy Screening
- Genetic Variants
- Genomic Rearrangements
- Sex Determination
- X Chromosome Inactivation
- Rett Syndrome
- Genomic Imprinting
- Parental Influence
- Sequence Interpretation
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 17 words, with their numbers
- Aneuploidy Screening111 topic
- Prenatal Diagnosis111 topic
- Genetic Variants102 topics
- Copy Number Variation81 topic
- Genomic Rearrangements81 topic
- Congenital Adrenal Hyperplasia71 topic
- Sex Determination71 topic
- Steroid 21-Hydroxylase Deficiency71 topic
- X Chromosome Inactivation71 topic
- Fragile X Syndrome51 topic
- Rett Syndrome51 topic
- Clinical Genomics31 topic
- Genomic Imprinting31 topic
- Nutrigenomics31 topic
- Parental Influence31 topic
- Personalized Nutrition31 topic
- Sequence Interpretation31 topic
Where does Haluk Akın work?
Haluk Akın's main affiliation in the publication record is Ege University, Türkiye.
How many publications and citations does Haluk Akın have?
OpenAlex counts 81 works and 520 citations for Haluk Akın, an h-index of 12, ranking #7,660,814 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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