Indian journal of human genetics
Published by CLOCKSS Archive
India · Genomic variations and chromosomal abnormalities
Journal at a glance
- ISSN
- 0971-6866, 1998-362X (electronic)
- Publisher
- CLOCKSS Archive
- Country
- India
- Language
- en
Also known as: Indian J Hum Genet (Abbreviation)
Indexing
Metrics
| Metric | Value | Year | Source |
|---|
| DOIs registered (Crossref) | 475 | 2026 | Crossref |
| DOIs, current year (Crossref) | 0 | 2026 | Crossref |
| Works (OpenAlex) | 496 | 2026 | OpenAlex |
| Citations (OpenAlex) | 5522 | 2026 | OpenAlex |
| h-index (OpenAlex) | 33 | 2026 | OpenAlex |
| i10-index (OpenAlex) | 175 | 2026 | OpenAlex |
| 2-year mean citedness (OpenAlex) | 0 | 2026 | OpenAlex |
Subjects
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Hemoglobinopathies and Related Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Folate and B Vitamins Research
- Blood groups and transfusion
- Genetics and Neurodevelopmental Disorders
Similar journals
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- Clinical Genetics — United Kingdom · — · Same subject: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Same subject: Genetics and Neurodevelopmental Disorders, 4 shared subjects in total
- Molecular Cytogenetics — United Kingdom · Open access · Same subject: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Same subject: Genetics and Neurodevelopmental Disorders, 4 shared subjects in total
- Balkan Journal of Medical Genetics — Bulgaria · Open access · Same subject: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Same subject: Genetics and Neurodevelopmental Disorders, 4 shared subjects in total
- Journal of Sickle Cell Disease — Open access · Same subject: Blood groups and transfusion, Same subject: Folate and B Vitamins Research, 4 shared subjects in total
- Journal of Medical Genetics — United Kingdom · — · Same subject: Genetics and Neurodevelopmental Disorders, Same subject: Genomic variations and chromosomal abnormalities, 3 shared subjects in total
Sources: OpenAlex, NLM Catalog, Crossref · Last verified 2026-09-06
Journal homepage