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Articles published in Hereditary Genetics: Current Research have been cited by esteemed scholars and scientists all around the world. Hereditary Genetics: Current Research has got h-index 9, which means every article in Hereditary Genetics: Current Research has got 9 average citations.
Following are the list of articles that have cited the articles published in Hereditary Genetics: Current Research.
| 2022 | 2021 | 2020 | 2019 | 2018 | |
|---|---|---|---|---|---|
Year wise published articles |
30 | 10 | 11 | 2 | 6 |
Year wise citations received |
79 | 58 | 38 | 33 | 44 |
| Journal total citations count | 465 |
| Journal Impact Factor | 1.42 |
| Journal 5 years Impact Factor | 2.34 |
| Journal CiteScore | 6.18 |
| Journal h-index | 9 |
Important citations
Familial Prion Disease: First Indian Kindred with Gerstmann-Sträussler-Scheinker Syndrome
Diagnosis of Prion Diseases
Transmissible Spongiform Encephalopathies
Prion, prionoids and infectious amyloid
Human prion diseases: surgical lessons learned from iatrogenic prion transmission
Mortality attributed to hereditary haemorrhagic telangiectasia and geographical variability in Spain (1981-2016)
Mortalidad atribuida a telangiectasia hemorrágica hereditaria y variabilidad geográfica en Espana˜ (1981-2016)
Anaesthetic management of a parturient with hereditary haemorrhagic telangiectasia (HHT) and pulmonary haemorrhage requiring urgent caesarean section
A Tale of Two Organ Systems: Imaging Review of Diseases Affecting the Thoracic and Neurological Systems. Part 2
Non-Coding RNAs and Hereditary Hemorrhagic Telangiectasia
Non-Coding RNAs and Hereditary Hemorrhagic Telangiectasia
Non-Coding RNAs and Hereditary Hemorrhagic Telangiectasia
Central nervous system manganese induced lesions and clinical consequences in patients with hereditary hemorrhagic telangiectasia
Prevalence of the MEFV gene mutations and their clinical correlations in Azeri Turkish patients with childhood Henoch-Schonlein purpura: The role of M680I and E148Q mutations
Chemokine MCP1/CCL2 gene polymorphism influences Henoch–Schönlein purpura susceptibility in Iranian Azeri–Turkish patients
Human Embryos Genetically Modified: A Review
Evaluation of Immuno-Rolling Circle Amplification for Multiplex Detection and Profiling of Antigen-Specific Antibody Isotypes
Evaluation of Immuno-Rolling Circle Amplification for Multiplex Detection and Profiling of Antigen-Specific Antibody Isotypes
Human Embryos Genetically Modified: A Review
Formation and Resolution of Pial Microvascular Thrombosis in a Mouse Model of Thrombotic Thrombocytopenic Purpura