Journal of Genetic Syndromes & Gene Therapy
Open Access

ISSN: ISSN: 2157-7412

Journal of Genetic Syndromes & Gene Therapy : Citations & Metrics Report

Articles published in Journal of Genetic Syndromes & Gene Therapy have been cited by esteemed scholars and scientists all around the world. Journal of Genetic Syndromes & Gene Therapy has got h-index 23, which means every article in Journal of Genetic Syndromes & Gene Therapy has got 23 average citations.

Following are the list of articles that have cited the articles published in Journal of Genetic Syndromes & Gene Therapy.

	2024	2023	2022	2021	2020	2019	2018	2017	2016	2015	2014	2013	2012	2011
Total published articles	31	32	31	25	8	2	1	8	40	28	44	99	43	14
Research, Review articles and Editorials	1	0	3	13	3	1	1	6	20	21	33	69	21	13
Research communications, Review communications, Editorial communications, Case reports and Commentary	14	32	27	9	4	1	0	2	16	7	11	22	4	1
Conference proceedings	0	0	0	0	0	0	61	64	56	0	0	0	52	0
Citations received as per Google Scholar, other indexing platforms and portals	118	167	197	209	211	248	217	322	324	339	198	122	53	21

Journal total citations count	2102
Journal impact factor	5.89
Journal 5 years impact factor	13.25
Journal cite score	20.22
Journal h-index	23
Journal h-index since 2019	16

Important citations (187)

doerfler pa, nayak s, corti m, morel l, herzog rw, et al. (2016) targeted approaches to induce immune tolerance for pompe disease therapy. molecular therapy-methods & clinical development 3: 15053. View at Publisher View at Google Scholar
qu w, wang m, wu y, xu r (2015) scalable downstream strategies for purification of recombinant adeno-associated virus vectors in light of the properties. current pharmaceutical biotechnology 16: 684-95. View at Publisher View at Google Scholar
liu cl, ye p, lin j, butts cl, miao ch (2015) anti-cd20 as the b-cell targeting agent in a combined therapy to modulate anti-factor viii immune responses in hemophilia a inhibitor mice. immune responses to aav vectors, from bench to bedside 30: 70. View at Publisher View at Google Scholar
sherman a, schlachterman a, cooper m, merricks ep, raymer ra, et al. () portal vein delivery of viral vectors for gene therapy for hemophilia. gene correction: methods and protocols 2014: 413-426. View at Publisher View at Google Scholar
zolotukhin i, luo d, gorbatyuk os, hoffman be, warrington jr kh, et al. (2013) improved adeno-associated viral gene transfer to murine glioma. journal of genetic syndrome & gene therapy 4. View at Publisher View at Google Scholar
mitchell am, samulski rj (2013) mechanistic insights into the enhancement of adeno-associated virus transduction by proteasome inhibitors. journal of virology. 87: 13035-13041. View at Publisher View at Google Scholar
rogers gl, herzog rw (2015) gene therapy for hemophilia. frontiers in bioscience (landmark edition) 20: 556. View at Publisher View at Google Scholar
wang d, zhong l, nahid ma, gao g (2014) the potential of adeno-associated viral vectors for gene delivery to muscle tissue. expert opinion on drug delivery 11: 345-64. View at Publisher View at Google Scholar
aleksejeva i (2013) use of genetically modified organisms in food production and future challenges. ineconomic science for rural development conference proceedings. View at Publisher View at Google Scholar
stueber d, marvasti-sitterly m, fitch k (2012) cost benefit analysis of gmo corn in nepal. View at Publisher View at Google Scholar
kienle ec secrets to finding the ideal mate: new insights into parameters that govern successful adeno-associated virus (aav) vector evolution (doctoral dissertation). View at Publisher View at Google Scholar
pankajakshan d, agrawal dk (2013) clinical and translational challenges in gene therapy of cardiovascular diseases. intech open access publisher. View at Publisher View at Google Scholar
fuller td, spracklen cn, ryckman kk, knake la, busch td,et al. accepted article preview: published ahead of advance online publication. View at Publisher View at Google Scholar
anderson cd, moisyadi s, avelar a, walton cb, shohet rv (20163). ultrasound-targeted hepatic delivery of factor ix in hemophiliac mice. gene therapy. View at Publisher View at Google Scholar
george la, fogarty pf (2016). gene therapy for hemophilia: past, present and future. inseminars in hematology 53: 46-54. View at Publisher View at Google Scholar
scott dw (2014) inhibitors–cellular aspects and novel approaches for tolerance. haemophilia. 20: 80-6. View at Publisher View at Google Scholar
rogers gl, herzog rw (2015) gene therapy for hemophilia. frontiers in bioscience (landmark edition). 20: 556. View at Publisher View at Google Scholar
scott dw, pratt kp, miao ch (2013) progress toward inducing immunologic tolerance to factor viii. blood 121: 4449-56. View at Publisher View at Google Scholar
high kh, nathwani a, spencer t, lillicrap d (2014. current status of haemophilia gene therapy. haemophilia 20: 43-9. View at Publisher View at Google Scholar
mingozzi f, high ka (2013) immune responses to aav vectors: overcoming barriers to successful gene therapy. blood 122: 23-36. View at Publisher View at Google Scholar
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