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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.
| 2024 | 2023 | 2022 | 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Total published articles |
10 | 41 | 30 | 10 | 11 | 2 | 6 | 16 | 20 | 27 | 20 | 27 | 17 |
Research, Review articles and Editorials |
0 | 2 | 0 | 1 | 1 | 2 | 6 | 13 | 14 | 12 | 12 | 16 | 12 |
Research communications, Review communications, Editorial communications, Case reports and Commentary |
10 | 39 | 30 | 9 | 10 | 0 | 0 | 3 | 6 | 15 | 8 | 11 | 5 |
Conference proceedings |
0 | 0 | 5 | 8 | 0 | 0 | 58 | 0 | 0 | 0 | 0 | 0 | 0 |
Citations received as per Google Scholar, other indexing platforms and portals |
18 | 33 | 84 | 62 | 43 | 38 | 47 | 48 | 90 | 28 | 17 | 11 | 2 |
| Journal total citations count | 534 |
| Journal impact factor | 1.42 |
| Journal 5 years impact factor | 2.34 |
| Journal cite score | 6.18 |
| Journal h-index | 9 |
Important citations
Human Embryos Genetically Modified: A Review
Spontaneous Appearance and Transmission of Polydactyly in Dexter Cattle
A recessive lethal chondrodysplasia in a miniature zebu family results from an insertion affecting the chondroitin sulfat domain of aggrecan
Germline mutation within COL2A1 associated with lethal chondrodysplasia in a polled Holstein family
Usefulness of Mini-STRs in Analyzing Degraded DNA Samples and Their Forensic Relevance
The genomic ancestry of Jat Sikh population from Northwest India inferred from 15 autosomal STR markers using capillary electrophoresis
Association of ESR? XbaI A >G, ESR? PvuII T > C and ESR? AlwNI T > C Polymorphisms with the Risk of Developing Adolescent Idiopathic Scoliosis: A Systematic Review and Genetic Meta-analysis
From genetics to epigenetics to unravel the etiology of adolescent idiopathic scoliosis
Human Embryos Genetically Modified: A Review
Mutation Spectrum Induced by 8-Bromoguanine, a Base Damaged by Reactive Brominating Species, in Human Cells
NEIL1 p.Gln282Stop variant is predominantly localized in the cytoplasm and exhibits reduced activity in suppressing mutations
MUTYH the base excision repair gene family member associated with colorectal cancer polyposis
Impaired 8-Hydroxyguanine Repair Activity of MUTYH Variant p.Arg109Trp Found in a Japanese Patient with Early-Onset Colorectal Cancer
Human Embryos Genetically Modified: A Review
Comparative Modelling of Huntington Disease
Human Embryos Genetically Modified: A Review
HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association
Coinheritance of Hb D-Punjab and ?-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis
Hemoglobinopathy in India
Amyloidy i prionoidy – czy jest ju? czas, ?eby si? obawia??