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 |
Sohrabi, F., Saeidifard, S., Ghasemi, M., Asadishad, T., Hamidi, S. M., & Hosseini, S. M. (2021). Role of plasmonics in detection of deadliest viruses: a review. The European Physical Journal Plus, 136(6), 1-71. |
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Hartoyo, E., Thalib, I., Sari, P., Maharani, C., Budianto, W. Y., & Suhartono, E. (2017). A different approach to assess oxidative stress in dengue hemorrhagic fever patients through the calculation of oxidative stress index. Journal of Tropical Life Science, 7(3), 237-242. |
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Srilatha, B. (2017). A Review on Genetic Disorders and Syndromes. Biochem Mol Biol Lett, 3(2), 118. |
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Zhao, X., Gazy, I., Hayward, B., Pintado, E., Hwang, Y. H., Tassone, F., & Usdin, K. (2019). Repeat instability in the fragile X-related disorders: lessons from a mouse model. Brain sciences, 9(3), 52. |
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Arun Kumar, R., Kavya Manaswini, R., & Anitha Sri, S. (2016). Innovative approaches in the field of cardiology. Res Rev Biosci, 11(3), 109. |
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Yuan, S. M. (2017). Palliative therapies for congenital heart disease with ductus dependent pulmonary circulation. Zeitschrift für Geburtshilfe und Neonatologie, 221(06), 272-275. |
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Jajoo, A., Donlon, C., Shnayder, S., Levin, M., & McVey, M. (2020). Sertraline induces DNA damage and cellular toxicity in Drosophila that can be ameliorated by antioxidants. Scientific reports, 10(1), 1-12. |
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Lee, J. H., Jayaprakasha, G. K., Enciso, J., Avila, C. A., Crosby, K. M., & Patil, B. S. (2021). Production system influences tomato phenolics and indoleamines in a cultivar-specific manner. Food Research International, 140, 110016. |
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MEHRAEI, M. (2018). A Proposal for Identifying Potential Strategies to Treat Affective Disorders Using Computer Simulations. |
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?ener Taplak, A., & Erdem, E. (2017). A comparison of breast milk and sucrose in reducing neonatal pain during eye exam for retinopathy of prematurity. Breastfeeding Medicine, 12(5), 305-310. |
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Hemasa, A. L., Naumovski, N., Maher, W. A., & Ghanem, A. (2017). Application of carbon nanotubes in chiral and achiral separations of pharmaceuticals, biologics and chemicals. Nanomaterials, 7(7), 186. |
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Ruan, E. S., Wang, L., & Yang, J. Y. Resent progress on ATP Binding Cassette Subfamily D Member. |
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Sheth, H., Pancholi, D., Bhavsar, R., Mannan, A. U., Ganapathy, A., Chaudhari, M., ... & Sheth, J. (2019). Assessing utility of clinical exome sequencing in diagnosis of rare idiopathic neurodevelopmental disorders in Indian population. |
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Wang, J., Zhu, Q., & Liu, H. (2018). A novel mutation in the ABCD1 gene of a Chinese patient with X-linked adrenoleukodystrophy: Case report. Medicine, 97(21). |
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Behnam, B., & Zakeri, M. (2019). Genetics and genomic medicine in Iran. Molecular genetics & genomic medicine, 7(2), e00606. |
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Emamalizadeh, B., Daneshmandpour, Y., Tafakhori, A., Ranji-Burachaloo, S., Shafiee, S., Ghods, E., & Darvish, H. (2019). Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy. Journal of Pediatric Endocrinology and Metabolism, 32(11), 1207-1215. |
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Benjelloun, F. M., Kriouile, Y., Cheillan, D., Daoud-Tetouani, H., & Chabraoui, L. (2017). Management of X-linked adrenoleukodystrophy in Morocco: actual situation. BMC research notes, 10(1), 1-6. |
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Corvino, V., Apisa, P., Malesci, R., Laria, C., Auletta, G., & Franzé, A. (2018). X-linked sensorineural hearing loss: a literature review. Current genomics, 19(5), 327-338. |
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Gong, K., Xia, M., Wang, Y., Wang, N., Liu, Y., Zhang, V. W., ... & Chen, Y. (2021). Autosomal dominant tubulointerstitial kidney disease genotype and phenotype correlation in a Chinese cohort. Scientific reports, 11(1), 1-10. |
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Wang, Y., Liu, H., He, Q., Yi, Z., Li, Y., & Dang, X. (2020). A novel likely pathogenic variant in the UMOD gene in a family with autosomal dominant tubulointerstitial kidney disease: a case report. BMC nephrology, 21(1), 1-5. |
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Molecular and Genetic Medicine received 3919 citations as per Google Scholar report