Articles published in Molecular and Genetic Medicine have been cited by esteemed scholars and scientists all around the world.
Molecular and Genetic Medicine has got h-index 29, which means every article in Molecular and Genetic Medicine has got 29 average citations.
Following are the list of articles that have cited the articles published in Molecular and Genetic Medicine.
2024 | 2023 | 2022 | 2021 | 2020 | 2019 | 2018 | |
---|---|---|---|---|---|---|---|
Total published articles |
40 | 53 | 61 | 59 | 33 | 62 | 69 |
Research, Review articles and Editorials |
1 | 8 | 7 | 12 | 21 | 38 | 42 |
Research communications, Review communications, Editorial communications, Case reports and Commentary |
39 | 45 | 54 | 47 | 12 | 24 | 27 |
Conference proceedings |
0 | 0 | 13 | 14 | 0 | 36 | 162 |
Citations received as per Google Scholar, other indexing platforms and portals |
4125 | 3135 | 348 | 369 | 376 | 335 | 318 |
Journal total citations count | 3919 |
Journal impact factor | 4.4 |
Journal 5 years impact factor | 6.21 |
Journal cite score | 6.74 |
Journal h-index | 29 |
Journal h-index since 2019 | 19 |
Ayoade, S. (2017). Thalassemias validate germ terrain duality of Malaria. Health Science Journal, 11(3), 1. |
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Zou, W., Slone, J., Cao, Y., & Huang, T. (2020). Mitochondria and their role in human reproduction. DNA and cell biology, 39(8), 1370-1378. |
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Salas, A., Schönherr, S., Bandelt, H. J., Gómez-Carballa, A., & Weissensteiner, H. (2019). Extraordinary claims require extraordinary evidence in the case of asserted mtDNA biparental inheritance. bioRxiv, 585752. |
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Salas, A., Schönherr, S., Bandelt, H. J., Gómez-Carballa, A., & Weissensteiner, H. (2020). Extraordinary claims require extraordinary evidence in asserted mtDNA biparental inheritance. Forensic Science International: Genetics, 47, 102274. |
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Li, H., Slone, J., Fei, L., & Huang, T. (2019). Mitochondrial DNA variants and common diseases: a mathematical model for the diversity of age-related mtDNA mutations. Cells, 8(6), 608. |
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Wallace, D. C. (2018). Mitochondrial genetic medicine. Nature genetics, 50(12), 1642-1649. |
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Singh, R. K., Gupta, A., Bhargava, V., Gupta, A., Tiwari, V., Malik, M., ... & Jain, M. (2020). Effect of De novo donor-specific antibodies on graft function in renal allograft recipients. Indian Journal of Transplantation, 14(2), 130. |
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Srilatha, B. (2017). A Review on Gene cloning and Genome Organization. Biochem Mol Biol Lett, 3(2), 122. |
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Michele, C. A., Teresa, M., Armando, M., Giovanni, M., & Angelo, B. (2021). A Short Review on Circulating Micro-RNAs in Diabetic Patients. Highlights on Medicine and Medical Science Vol. 15, 51-63. |
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Khan, R., Kadamkode, V., Kesharwani, D., Purkayastha, S., Banerjee, G., & Datta, M. (2020). Circulatory miR-98-5p levels are deregulated during diabetes and it inhibits proliferation and promotes apoptosis by targeting PPP1R15B in keratinocytes. RNA biology, 17(2), 188-201. |
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Nath, D., & Bais, P. S. To study the effect of age and blood sugar on the levels of magnesium and glycated hemoglobin in Bundelkhand region: A case control analysis. |
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Hanna, H. H., & Rania, H. (2018). Effect of chromium piclonate versus L-carnitine on high fat diet induced in rats. Life Sci J, 15. |
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Kankana, D. (2017). Study Variation of Anthropometric Variables at Time of Puberty. J Gen Pract (Los Angel), 5(296), 2. |
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Majumdar, R., & Sikdar, D. P. (2017). Use of ICT in building up Women Health Awareness among Tribal Students in India. International Journal of Research in Social Sciences, 7(9), 236-246. |
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Sorapipatcharoen, K., Tim-Aroon, T., Mahachoklertwattana, P., Chantratita, W., Iemwimangsa, N., Sensorn, I., ... & Poomthavorn, P. (2020). DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients. Endocrine Connections, 9(11), 1121-1134. |
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Martín, M., & Nicola, J. P. (2021). Impact of the mutational landscape of the sodium/iodide symporter in congenital hypothyroidism. Thyroid, (ja). |
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Oron, T., Lazar, L., Ben-Yishai, S., Tenenbaum, A., Yackobovitch-Gavan, M., Meyerovitch, J., ... & Lebenthal, Y. (2018). Permanent vs transient congenital hypothyroidism: assessment of predictive variables. The Journal of Clinical Endocrinology & Metabolism, 103(12), 4428-4436. |
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Sasmita, A. O. (2019). Modification of the gut microbiome to combat neurodegeneration. Reviews in the Neurosciences, 30(8), 795-805. |
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Dhara, B., Maity, A., Mondal, P., & Mitra, A. K. (2020). First report of Exserohilum leaf spot: a unique halophilic pathogen in Cucumis sativus in the South Bengal area of India. Australasian Plant Pathology, 49(3), 257-266. |
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Sherman, R. M., & Salzberg, S. L. (2020). Pan-genomics in the human genome era. Nature Reviews Genetics, 21(4), 243-254. |
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Molecular and Genetic Medicine received 3919 citations as per Google Scholar report