Journal of Genetic Syndromes & Gene Therapy : Citations & Metrics Report
Articles published in Journal of Genetic Syndromes & Gene Therapy have been cited by esteemed scholars and scientists all around the world. Journal of Genetic Syndromes & Gene Therapy has got h-index 23, which means every article in Journal of Genetic Syndromes & Gene Therapy has got 23 average citations.
Following are the list of articles that have cited the articles published in Journal of Genetic Syndromes & Gene Therapy.
2021 | 2020 | 2019 | 2018 | 2017 | 2016 | |
---|---|---|---|---|---|---|
Year wise published articles |
25 | 8 | 2 | 1 | 8 | 40 |
Year wise citations received |
174 | 175 | 203 | 181 | 251 | 250 |
Journal total citations count | 2102 |
Journal impact factor | 5.89 |
Journal 5 years impact factor | 13.25 |
Journal cite score | 20.22 |
Journal h-index | 23 |
Journal h-index since 2019 | 16 |
Important citations (187)
vilaboa n, boellmann f, voellmy r (2011) gene switches for deliberate regulation of transgene expression: recent advances in system development and uses. j genet syndr gene ther 2: 2. |
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li r, chao h, ko kw, cormier s, dieker c, et al. gene therapy targeting ldl cholesterol but not hdl cholesterol induces regression of advanced atherosclerosis in a mouse model of familial hypercholesterolemia. journal of genetic syndrome & gene therapy 2:106. |
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soto-pantoja dr, isenberg js, roberts dd (2011). therapeutic targeting of cd47 to modulate tissue responses to ischemia and radiation. journal of genetic syndrome & gene therapy 2. |
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moghimi b, zolotukhin i, sack bk, herzog rw, cao o (2011) high efficiency ex vivo gene transfer to primary murine b cells using plasmid or viral vectors. journal of genetic syndrome & gene therapy 2. |
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grant p, lipscomb d (2011) primary amenorrhoea due to ovarian dysgenesis: a previously undescribed chromosome 12 abnormality. bmj case reports bcr0720103201. |
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mcclements me, issa pc, blouin v, maclaren re (2016). a fragmented adeno-associated viral dual vector strategy for treatment of diseases caused by mutations in large genes leads to expression of hybrid transcripts. j genet syndr gene ther 7: 2. |
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esposito g, testa f, zacchia m, crispo aa, di iorio v,et al (2017). genetic characterization of italian patients with bardet-biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants. bmc medical genetics 1:10. |
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