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74 results for “social communication”
Promoting Communication in Minimally Verbal Autistic Children with Social Robot
ClinicalTrials.gov study NCT06805916. IPD Sharing: NO. Countries: 1. Publications: 5.
Data from: Density of antennal sensilla influences efficacy of communication in a social insect
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Data from: Plasticity in social communication and its implications for the colonization of novel habitats
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Fig. 2 in Unusual effect of chemical communication on social aggression in juvenile cichlid fish Cichlasoma paranaense (Cichliformes: Cichlidae)
Fig. 2. Establishment of social rank. Dominance index (mean ± S.E.) by rank before aquarium water changing. Data were collapsed across treatments. Letters compare means between ranks within each observation session. Different letters indicate statistical significance among ranks. Asterisks indicate significant differences within rank between the first and the fourth observation session (Mixed Model ANOVA followed by Fisher's LSD post hoc test).
Fig. 1 in Unusual effect of chemical communication on social aggression in juvenile cichlid fish Cichlasoma paranaense (Cichliformes: Cichlidae)
Fig. 1. Ethogram of the aggressive interactions in Cichlasoma paranaense based on Brandão et al. (2015).
Fig. 3 in Unusual effect of chemical communication on social aggression in juvenile cichlid fish Cichlasoma paranaense (Cichliformes: Cichlidae)
Fig. 3. Number (mean ± S.E.) of a. overt aggression and b. restrained aggression following water renewal in each treatment. Letters indicates a significant difference in relation to observation before water change (baseline) within each treatment. Different letters indicate statistical significance. Asterisk compares the observations between treatments. (Mixed Model ANOVA followed by Fisher's LSD post hoc test).
Data from: Is sociality required for the evolution of communicative complexity? Evidence weighed against alternative hypotheses in diverse taxonomic groups
Complex social communication is expected to evolve whenever animals engage in many and varied social interactions; that is, sociality should promote communicative complexity. Yet informal comparisons among phylogenetically independent taxonomic groups seem to cast doubt on the putative role of social factors in the evolution of complex communication. Here, we provide a formal test of the sociality hypothesis along side alternative explanations for the evolution of communicative complexity. We compiled data documenting variation in signal complexity among closely related species for several case study groups – ants, frogs, lizards and birds – and used new phylogenetic methods to investigate the factors underlying communication evolution. Social factors were only implicated in the evolution of complex visual signals in lizards. Ecology, and to some degree allometry, were most likely explanations for complexity in the vocal signals of frogs (ecology) and birds (ecology and allometry). There was some evidence for adaptive evolution in the pheromone complexity of ants, although no compelling selection pressure was identified. For most taxa, phylogenetic null models were consistently ranked above adaptive models and, for some taxa, signal complexity seems to have accumulated in species via incremental or random changes over long periods of evolutionary time. Becoming social presumably lead to the origin of social communication in animals, but its subsequent influence on the trajectory of signal evolution has been neither clear-cut nor general among taxonomic groups.
Figure 1 from: Seibt J, Vestergaard C (2018) Fair Proxy Communication: Using Social Robots to Modify the Mechanisms of Implicit Social Cognition. Research Ideas and Outcomes 4: e31827. https://doi.org/10.3897/rio.4.e31827
Figure 1 A job interview using FPC, from the perspective of the interviewer. The male interviewer (in the definition: H2) communicates via the Telenoid R4 robot with H1, a female job candidate as shown in Fig. 2.
Figure 2 from: Seibt J, Vestergaard C (2018) Fair Proxy Communication: Using Social Robots to Modify the Mechanisms of Implicit Social Cognition. Research Ideas and Outcomes 4: e31827. https://doi.org/10.3897/rio.4.e31827
Figure 2 A job interview using FPC, from the perspective of the job candidate. A female candidate (in the definition D1-1: H1) operates her robotic proxy, a Telenoid R4 robot, while she communicates with the male interviewer. Her head movements, lip movements and speech are translated directly to the robot, either via a kinetic sensor on a headset or by a facial reading programme; her voice may or may not be morphed to mask gender (see section "Practical Significance" below). The camera that projects the interviewer on to her computer screen is in the eyes of the robot –thus, in contrast to a skype session, she looks into the interviewer's eyes when facing the interviewer.
CISBAR Intervention for Social Communication After ABI
ClinicalTrials.gov study NCT05603117. IPD Sharing: YES. Countries: 1. Publications: 0.
Parent-mediated Social-communication Therapy for Young Children Living in Poverty in Brazil
ClinicalTrials.gov study NCT05011240. IPD Sharing: NO. Countries: 0. Publications: 1.
A New Intervention for Social Communication Skills Following Brain Injury
ClinicalTrials.gov study NCT02211339. IPD Sharing: YES. Countries: 0. Publications: 1.
Data from: Pre-linguistic infants employ complex communicative loops to engage mothers in social exchanges and repair interaction ruptures
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Data for: Sociality and signaling activity modulate information flow in river otter communication networks
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Data from: Is sociality required for the evolution of communicative complexity? Evidence weighed against alternative hypotheses in diverse taxonomic groups
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Epigenetic Profiling of Social Communication Trajectories and Co-occurring Mental Health Problems: A Prospective, Methylome-wide Association Study
<p>While previous studies suggest that both genetic and environmental factors play an important role in the development of autism-related traits, little is known about potential biological mechanisms underlying these associations. Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), we examined prospective associations between DNA methylation (DNAm: N-birth=804, N-age7=877) and trajectories of social communication deficits (8-17 years). Methylomic variation at three loci across the genome (false discovery rate=0.048) differentiated children following high (n=80) versus low (n=724) trajectories of social communication deficits. This differential DNAm was specific to the neonatal period and not observed at age 7. Associations between DNAm and trajectory membership remained robust after controlling for co-occurring mental health problems (i.e., hyperactivity/inattention, conduct problems). The three loci identified at birth were not replicated in the Generation R Study. However, to the best of our knowledge, ALSPAC is the only study to date that is prospective enough to examine DNAm in relation to longitudinal trajectories of social communication deficits from late childhood to late adolescence. Although the present findings might point to potentially novel sites that differentiate between a high versus low trajectory of social communication deficits, the results should be considered tentative until further replicated.</p> <p>This dataset contains summary statistics for the methylome-wide association study using DNAm data collected from individuals at age 7.</p> <p>Upload of this dataset was completed by The EWAS Catalog team. The data can be queried along with hundreds of other EWAS at ewascatalog.org. To upload your EWAS summary statistics and have a zenodo DOI generated for you go to ewascatalog.org/upload</p>
Figure 3 from: Seibt J, Vestergaard C (2018) Fair Proxy Communication: Using Social Robots to Modify the Mechanisms of Implicit Social Cognition. Research Ideas and Outcomes 4: e31827. https://doi.org/10.3897/rio.4.e31827
Figure 3 The Telenoid robot created by Hiroshi Ishiguro, ATR Hiroshi Ishiguro Lab, Japan.
Dentist-Patient Communication on Dental Anxiety Using the Social Media and Timing in Communication
ClinicalTrials.gov study NCT04453696. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Parent-implemented Social Communication Treatment in Preschool Children With Autism Spectrum Disorder
ClinicalTrials.gov study NCT05455411. IPD Sharing: NO. Countries: 1. Publications: 0.
Early Behavioral Intervention to Improve Social Communication Function in Infants With Tuberous Sclerosis Complex
ClinicalTrials.gov study NCT02687633. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.