Journal of Genetic Syndromes & Gene Therapy

Journal of Genetic Syndromes & Gene Therapy
Open Access

ISSN: ISSN: 2157-7412

+32 28087017

Citations Report

Citations Report - Journal of Genetic Syndromes & Gene Therapy [186 Articles]

The articles published in Journal of Genetic Syndromes & Gene Therapy have been cited 186 times by eminent researchers all around the world. Following is the list of articles that have cited the articles published in Journal of Genetic Syndromes & Gene Therapy.

Sasaki-Honda M, Jonouchi T, Arai M, Hotta A, Mitsuhashi S, Nishino I, Matsuda R, Sakurai H. A patient-derived iPSC model revealed oxidative stress increases facioscapulohumeral muscular dystrophy-causative DUX4. Human molecular genetics. 2018 Aug 9;27(23):4024-35.

DeSimone AM, Pakula A, Lek A, Emerson Jr CP. Facioscapulohumeral muscular dystrophy. Comprehensive Physiology. 2011 Jan 17;7(4):1229-79.

Santosh K. Review on Down Syndrome. Biochem Mol Biol Lett. 2017;3(2):126.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Torres-Carrión PV, González-González CS, Toledo-Delgado PA, Muñoz-Cruz V, Gil-Iranzo R, Reyes-Alonso N, Hernández-Morales S. Improving Cognitive Visual-Motor Abilities in Individuals with Down Syndrome. Sensors. 2019 Jan;19(18):3984.

Srilatha B. A Review on Genetic Disorders and Syndromes. Biochem Mol Biol Lett. 2017;3(2):118.

de Souza MA, Cezarani A, da Silva Lizzi EA, de Queiroz Davoli GB, Mattiello SM, Jones R, Mattiello-Sverzut AC. The use of the gait profile score and gait variable score in individuals with Duchenne Muscular Dystrophy. Journal of biomechanics. 2019 Nov 6:109485.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Momtazi G, Lambrecht BN, Naranjo JR, Schock BC. Regulators of A20 (TNFAIP3): new drug-able targets in inflammation. American Journal of Physiology-Lung Cellular and Molecular Physiology. 2018 Dec 13;316(3):L456-69.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Baid A. ELISA-A mini review. Res. Rev. J. Pharm. Anal. 2016;5:1-8.

Srilatha B. A Review on Genetic Disorders and Syndromes. Biochem Mol Biol Lett. 2017;3(2):118.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Jain SK, Sharma S. Nephronophthisis-A Genetic Cause of Ciliopathy. J Investig Genomics. 2017;4(1):00057.

Bhattacharjee S. Advancement in Genomics: A Review. Biochem Mol Biol Lett. 2017;3(2):117.

Uytingco CR, Green WW, Martens JR. Olfactory loss and dysfunction in ciliopathies: Molecular mechanisms and potential therapies. Current medicinal chemistry. 2019.

Dyka FM, Molday LL, Chiodo VA, Molday RS, Hauswirth WW. Dual ABCA4-AAV Vector Treatment Reduces Pathogenic Retinal A2E Accumulation in a Mouse Model of Autosomal Recessive Stargardt Disease. Human Gene Therapy. 2019 Nov 1;30(11):1361-70.

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