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 |
Nur, Muhammad, Fajriani Fajriani, Tenriware Tenriware, Charles PH Simanjuntak, Adiara Firdhita Alam Nasyrah, Neri Kautsari, and Syainullah Wahana. "Fish fauna of the Batetangnga River, West Sulawesi, Indonesia." In E3S Web of Conferences, vol. 322, p. 01026. EDP Sciences, 2021. |
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Saki, Nader, Mojtaba Jahani, Alireza Samarbaf, Gholam Abbas Kaydani, Soheila Nikakhlagh, Malek Kenani, and Sasan Mogehi. "Correlation between tympanosclerosis and Helicobacter pylori." Jundishapur journal of microbiology 8, no. 10 (2015). |
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Saki, Nader, Ali Reza Samarbaf Zadeh, Reza Sheikhpour Jonaky, Seyed Mahdi Noori, Gholam Abbas Kayedani, and Soheila Nikakhlagh. "The prevalence rate of Helicobacter pylori infection in, chronic otitis media with effusion patients." Jundishapur journal of microbiology 7, no. 3 (2014). |
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González, Juan R., Carlos Ruiz-Arenas, Alejandro Cáceres, Ignasi Morán, Marcos López, Lorena Alonso, Ignacio Tolosana et al. "Polymorphic inversions underlie the shared genetic susceptibility to prevalent common diseases." bioRxiv (2019): 859280. |
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González, Juan R., Carlos Ruiz-Arenas, Alejandro Cáceres, Ignasi Morán, Marcos López-Sánchez, Lorena Alonso, Ignacio Tolosana et al. "Polymorphic inversions underlie the shared genetic susceptibility of obesity-related diseases." The American Journal of Human Genetics 106, no. 6 (2020): 846-858. |
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Shwan, Nzar AA, Sandra Louzada, Fengtang Yang, and John AL Armour. "Recurrent rearrangements of human amylase genes create multiple independent CNV series." Human mutation 38, no. 5 (2017): 532-539. |
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Akash, Muhammad Sajid Hamid, Kanwal Rehman, Muhammad Tariq, and Shuqing Chen. "Development of therapeutic proteins: advances and challenges." Turkish Journal of Biology 39, no. 3 (2015): 343-358. |
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Nazarenko, Maria S., Aleksei A. Sleptcov, Igor N. Lebedev, Nikolay A. Skryabin, Anton V. Markov, Maria V. Golubenko, Iuliia A. Koroleva, Anton N. Kazancev, Olga L. Barbarash, and Valery P. Puzyrev. "Genomic structural variations for cardiovascular and metabolic comorbidity." Scientific reports 7, no. 1 (2017): 1-9. |
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Carpenter, Danielle, Sugandha Dhar, Laura M. Mitchell, Beiyuan Fu, Jess Tyson, Nzar AA Shwan, Fengtang Yang, Mark G. Thomas, and John AL Armour. "Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes." Human molecular genetics 24, no. 12 (2015): 3472-3480. |
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Usher, Christina L., Robert E. Handsaker, Tõnu Esko, Marcus A. Tuke, Michael N. Weedon, Alex R. Hastie, Han Cao et al. "Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity." Nature genetics 47, no. 8 (2015): 921-925. |
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Singh, Anudeep, Mahindra Nagar, and Anil Kumar. "Research and Reviews: Journal of Medical and Health Sciences." |
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Wang, Cuihua, Edmund Keliher, Matthias WG Zeller, Gregory R. Wojtkiewicz, Aaron D. Aguirre, Leonard Buckbinder, Hye-Yeong Kim et al. "An activatable PET imaging radioprobe is a dynamic reporter of myeloperoxidase activity in vivo." Proceedings of the National Academy of Sciences 116, no. 24 (2019): 11966-11971. |
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Healing, Ischemic Wound. "DISCOVERY EXPRESS." |
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Boshtam, Maryam, and Hamed Mirzaei. "Plasminogen activator inhibitor type-1 as a regulator of fibrosis." |
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Chen, Yan?Shan, Ling Shen, Rui?Qin Mai, and Ying Wang. "Levels of microRNA?181b and plasminogen activator inhibitor?1 are associated with hypertensive disorders complicating pregnancy." Experimental and therapeutic medicine 8, no. 5 (2014): 1523-1527. |
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Simone, T. M., Longmate, W. M., Law, B. K., & Higgins, P. J. (2015). Targeted inhibition of PAI-1 activity impairs epithelial migration and wound closure following cutaneous injury. Advances in wound care, 4(6), 321-328. |
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Rabieian, Reyhaneh, Maryam Boshtam, Mahshid Zareei, Shirin Kouhpayeh, Aria Masoudifar, and Hamed Mirzaei. "Plasminogen activator inhibitor type?1 as a regulator of fibrosis." Journal of cellular biochemistry 119, no. 1 (2018): 17-27. |
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Marson, Fernando Augusto Lima, Carmen Sílvia Bertuzzo, Tânia Kawasaki de Araujo, Taís Daiene Russo Hortencio, Antônio Fernando Ribeiro, and José Dirceu Ribeiro. "Pancreatic insufficiency in cystic fibrosis: influence of inflammatory response genes." Pancreas 47, no. 1 (2018): 99-109. |
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Baldan, Alessandro, Anna Rita Lo Presti, Francesca Belpinati, Carlo Castellani, Maria Demelza Bettin, Luciano Xumerle, Pier Franco Pignatti, Giovanni Malerba, and Cristina Bombieri. "IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients." Rhinology 53, no. 4 (2015): 359-364. |
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Coutinho, C. A., Marson, F. A., Marcelino, A. R., Bonadia, L. C., Carlin, M. P., Ribeiro, A. F., ... & Bertuzzo, C. S. (2014). TNF-alpha polymorphisms as a potential modifier gene in the cystic fibrosis. International journal of molecular epidemiology and genetics, 5(2), 87. |
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Molecular and Genetic Medicine received 3919 citations as per Google Scholar report