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Autism-Open Access

Autism-Open Access
Open Access

ISSN: 2165-7890

+44 1223 790975

Autism-Open Access : Citations & Metrics Report

Articles published in Autism-Open Access have been cited by esteemed scholars and scientists all around the world. Autism-Open Access has got h-index 16, which means every article in Autism-Open Access has got 16 average citations.

Following are the list of articles that have cited the articles published in Autism-Open Access.

  2021 2020 2019 2018 2017 2016

Year wise published articles

60 20 10 12 25 47

Year wise citations received

171 164 148 116 172 118
Journal total citations count 883
Journal impact factor 2.19
Journal 5 years impact factor 3.60
Journal cite score 4.59
Journal h-index 16
Journal h-index since 2018 13
Important citations (728)

Mosienko v, beis d, alenina n, wöhr m. reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin. mol autism 2015;6:13.

Wohr m. ultrasonic vocalizations in shank mouse models for autism spectrum disorders: detailed spectrographic analyses and developmental profiles. neurosci biobehav rev 2014;43: 199-212.

Ey e, torquet n, le sourd am, leblond cs, boeckers tm, faure p, et al. the autism prosap1/shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations. behav brain res 2013;256: 677-689.

Qiu t, chang c, li y, qian l, xiao cy, xiao t, et al. two years changes in the development of caudate nucleus are involved in restricted repetitive behaviors in 2–5-year-old children with autism spectrum disorder. dev cogn neurosci 2016; 19:137-143.

Seymour v.the human–nature relationship and its impact on health: a critical review. front public health 2016;4.

Katkuri m. a mini review: ethical usage of animals in pharmacological research 2015.

Mason g, wurbel h. what can be learnt from wheel-running by wild mice, and how can we identify when wheel-running is pathological?. proc biol sci 2016;283(1824):20150738.

Bechard ar, cacodcar n, king ma, lewis mh. how does environmental enrichment reduce repetitive motor behaviors? neuronal activation and dendritic morphology in the indirect basal ganglia pathway of a mouse model. behav brain res 2016; 299: 122-131.

Muehlmann am, bliznyuk n, duerr i, lewis mh.repetitive motor behavior: further characterization of development and temporal dynamics. dev psychobiol 2015;57: 201-211.

Gallucci a, patterson kc, weit ar, van der pol wj, dubois lg, percy ak, et al. microbial community changes in a female rat model of rett syndrome. prog neuropsychopharmacol biol psychiatry 2021;109: 110259.

Vermudez sa, gogliotti rg, arthur b, buch a, morales c, moxley y, rajpal h, conn pj, niswender cm. profiling beneficial and potential adverse effects of mecp2 overexpression in a hypomorphic rett syndrome mouse model. genes brain behav 2021.

Mason g, hanno w. what can be learnt from wheel-running by wild mice, and how can we identify when wheel-running is pathological?. proc biol sci 2016; 10(283): 20150738.

Bechard ar, cacodcar n, king ma, lewis mh. how does environmental enrichment reduce repetitive motor behaviors? neuronal activation and dendritic morphology in the indirect basal ganglia pathway of a mouse model. behav brain res 2016; 299: 122-131.

Muehlmann am, bliznyuk n, duerr i, lewis mh. repetitive motor behavior: further characterization of development and temporal dynamics. dev psychobiol 2015; 57: 201-211.

Schafer dp, heller ct, gunner g, heller m, gordon c, hammond t, et al. microglia contribute to circuit defects in mecp2 null mice independent of microglia-specific loss of mecp2 expression. elife 2016; 5: e15224.

Patterson kc, hawkins ve, arps km, mulkey dk, olsen ml. mecp2 deficiency results in robust rett-like behavioural and motor deficits in male and female rats. hum mol genet 2016;25: 3303-3320.

Percy ak. path to treat rett syndrome. science 2013;18;342(6156):318-320.

Adachi m. monteggia lm. decoding transcriptional repressor complexes in the adult central nervous system. neuropharmacology 2014; 80: 45-52.

Phillips m, pozzo-miller l. dendritic spine dysgenesis in autism related disorders. neurosci lett 2015;601: 30-40.

Baj g, patrizio a, montalbano a, sciancalepore m, tongiorgi e. developmental and maintenance defects in rett syndrome neurons identified by a new mouse staging system in vitro. front cell neurosci 2014; 8: 18.

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