Citations Report

Molecular and Genetic Medicine : Citations & Metrics Report

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.

	2022	2021	2020	2019	2018
Year wise published articles	61	59	33	62	69
Year wise citations received	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 2018	19

Important citations

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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
Srilatha, B. (2017). A Review on Genetic Disorders and Syndromes. Biochem Mol Biol Lett, 3(2), 118. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
Arun Kumar, R., Kavya Manaswini, R., & Anitha Sri, S. (2016). Innovative approaches in the field of cardiology. Res Rev Biosci, 11(3), 109. View at Publisher View at Google Scholar View at Indexing
Yuan, S. M. (2017). Palliative therapies for congenital heart disease with ductus dependent pulmonary circulation. Zeitschrift für Geburtshilfe und Neonatologie, 221(06), 272-275. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
MEHRAEI, M. (2018). A Proposal for Identifying Potential Strategies to Treat Affective Disorders Using Computer Simulations. View at Publisher View at Google Scholar View at Indexing
?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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
Ruan, E. S., Wang, L., & Yang, J. Y. Resent progress on ATP Binding Cassette Subfamily D Member. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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). View at Publisher View at Google Scholar View at Indexing
Behnam, B., & Zakeri, M. (2019). Genetics and genomic medicine in Iran. Molecular genetics & genomic medicine, 7(2), e00606. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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. View at Publisher View at Google Scholar View at Indexing
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Google Scholar citation report

Citations: 3919

Molecular and Genetic Medicine received 3919 citations as per Google Scholar report

Molecular and Genetic Medicine peer review process verified at publons

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Molecular and Genetic Medicine