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Molecular and Genetic Medicine

ISSN: 1747-0862

Open Access

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.

  2024 2023 2022 2021 2020 2019 2018

Total published articles

50 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
Important citations

Zafar, Sidra, Khabir Ahmad, Rashid Baig, and Azam Ali. "Systemic Review."

Mohan, S., Satagopan, U., Nagasamy, S., Natarajan, S. and Kumaramanickavel, G., 2019. Genetics and Susceptibility of Retinal Eye Diseases in India. In Advances in Vision Research, Volume II (pp. 147-168). Springer, Singapore.

El-Asrag, M. E. S. M. (2016). Determining the causes of recessive retinal dystrophy (Doctoral dissertation, University of Leeds).

Dev Borman, Arundhati. "A Genotype-Phenotype Study of Childhood Onset Retinal Dystrophies." PhD diss., UCL (University College London), 2016.

Zahid, Sarwar, Kari Branham, Dana Schlegel, Mark E. Pennesi, Michel Michaelides, John Heckenlively, and Thiran Jayasundera. "SPATA7." In Retinal Dystrophy Gene Atlas, pp. 257-258. Springer, Cham, 2018.

Xiao, Xueshan, Wenmin Sun, Shiqiang Li, Xiaoyun Jia, and Qingjiong Zhang. "Spectrum, frequency, and genotype–phenotype of mutations in SPATA7." Molecular vision 25 (2019): 821.

Zafar, Sidra, Khabir Ahmed, Azam Ali, and Rashid Baig. "Retinitis pigmentosa genes implicated in South Asian populations: a systematic review." Journal of the Pakistan Medical Association 67, no. 11 (2017): 1734.

Blond, Frédéric, and Thierry Léveillard. "Functional genomics of the retina to elucidate its construction and deconstruction." International journal of molecular sciences 20, no. 19 (2019): 4922.

Eblimit, A., Agrawal, S. A., Thomas, K., Anastassov, I. A., Abulikemu, T., Mardon, G., & Chen, R. (2018). Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. Experimental eye research, 166, 120-130.

Matsui, R., McGuigan III, D.B., Gruzensky, M.L., Aleman, T.S., Schwartz, S.B., Sumaroka, A., Koenekoop, R.K., Cideciyan, A.V. and Jacobson, S.G., 2016. SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa. Ophthalmic genetics, 37(3), pp.333-338.

Nash, Benjamin M., Dale C. Wright, John R. Grigg, Bruce Bennetts, and Robyn V. Jamieson. "Retinal dystrophies, genomic applications in diagnosis and prospects for therapy." Translational pediatrics 4, no. 2 (2015): 139.

Trianti, Irisa, Saengchai Akeprathumchai, Phenjun Mekvichitsaeng, Sansanalak Rachdawong, and Kanokwan Poomputsa. "Recombinant neuraminidase pseudotyped baculovirus: a dual vector for delivery of Angiotensin II peptides and DNA vaccine." AMB Express 8, no. 1 (2018): 1-9.

Elli, Stefano, Nicola Gambacorta, Timothy R. Rudd, Mikhail Matrosovich, and Marco Guerrini. "MD simulation of the interaction between sialoglycans and the second sialic acid binding site of influenza A virus N1 neuraminidase." Biochemical Journal 478, no. 2 (2021): 423-441.

Votapka, Lane, and Rommie E. Amaro. "Multistructural hot spot characterization with FTProd." Bioinformatics 29, no. 3 (2013): 393-394.

Bruno, Pierangela, Francesco Calimeri, and Aldo Marzullo. "Classification and survival prediction in Diffuse Large B-cell Lymphoma by gene expression profiling." In International Conference on Machine Learning, Optimization, and Data Science, pp. 166-178. Springer, Cham, 2018.

Farhadian, Maryam, Hossein Mahjub, Abbas Moghimbeigi, Jalal Poorolajal, and Muharram Mansoorizadeh. "A Gene Selection Method for Survival Prediction in Diffuse Large B-Cell Lymphomas Patients using 1D Discrete Wavelet Transform." Iranian journal of public health 43, no. 8 (2014): 1091.

Jafarzadeh Kohneloo, Arefa, Jalal Poorolajal, and Hosean Mahjub. "Applied the additive hazard model to predict the survival time of patient with diffuse large B-cell lymphoma and determine the effective genes, using microarray data." ISMJ 18, no. 4 (2015): 711-719.

Tapak, L., Mahjub, H., Sadeghifar, M., Saidijam, M., & Poorolajal, J. (2016). Predicting the survival time for bladder cancer using an additive hazards model in microarray data. Iranian journal of public health, 45(2), 239.

Liu, Pengfei, Wenhua Jiang, Jinkun Zhao, and Huilai Zhang. "Integrated analysis of genome?wide gene expression and DNA methylation microarray of diffuse large B?cell lymphoma with TET mutations." Molecular medicine reports 16, no. 4 (2017): 3777-3782.

Palchaudhuri, S., B. Chatterjee, and A. Palchaudhuri. "Xylitol in Prevention of Dental Caries and Respiratory." Archives of Clinical Microbiology 6, no. 4 (2015).

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

Indexed In

 
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