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Heinrichs, N.

Publications and source records attributed to Heinrichs, N..

2 recordsLinked to original sources

SingleBehavior Lab: behavioral sequencing and phenotyping with lightweight task specific adaptation

Understanding behavioral differences between experimental groups and quantifying action structure in behavioral experiments remains challenging. Currently, most approaches rely on pose estimation followed by downstream classification, resulting in assay specific pipelines with substantial annotation requirements. Here we present SingleBehavior Lab (SBL), a framework for modeling behavior across experimental contexts using a standardized graphical interface. SBL leverages spatiotemporal embeddings from large video foundation models and combines them with lightweight contrastive adapters, a multi-head attention pooling (MAP) module and a temporal decoder to enable behavior sequencing and task-specific refinement. The framework supports few-shot learning, allowing small models trained on pretrained embeddings to improve action segmentation and classification with limited labeled data, without fine-tuning the underlying video model. In parallel, a large segmentation model with motion-aware memory is used to extract object-centered representations that, together with shared spatiotemporal embeddings, enable unsupervised clustering of behavioral states and analysis of their structure, including cluster prioritization, transition dynamics and attention-based interpretability. Across multiple assays and species, SBL supports identification of group-level differences and rare behaviors, and provides a basis for integrating behavioral representations across experimental contexts.

neuroscience↗

Caregiving quality modulates neuroendocrine and immunological markers in young children in foster care who have experienced early adversity

BackgroundEarly adversity is believed to alter the bodys stress response systems, putting children at increased risk for somatic and mental health problems. However, it remains unclear whether such alterations normalize under improved caregiving experiences. Thus, the goal of the present study was to investigate i) whether children in foster care show endocrine and immunological alterations relative to children living with their biological families, ii) whether these alterations change over time spent with the foster family and iii) whether the alterations are modulated by current caregiving experiences. MethodsA total of 94 children in foster care and 157 biological children, aged two to seven years, took part in a longitudinal study with three assessments conducted over a 12-month study period. At the initial assessment, children lived for an average of 18 months with their current foster families. Childrens cortisol, dehydroepiandrosterone (DHEA) and progesterone concentrations and cortisol/DHEA ratios were measured in scalp hair and childrens secretory immunoglobulin A (sIgA) levels in saliva. Caregiving quality was assessed based on caregiver-reports and observational measures of caregiver-child interactions. ResultsChildren in foster care had lower cortisol/DHEA ratios and higher progesterone concentrations than biological children, while no group differences were found for cortisol, DHEA or sIgA. Time spent with the current foster family did not significantly influence the childs endocrine or immunological markers. Importantly, caregiving quality modulated cortisol/DHEA ratios and sIgA concentrations: children in foster care of lower caregiving quality had lower cortisol/DHEA ratios than children in foster care of higher caregiving quality and showed decreasing, rather than increasing, sIgA concentrations across the study period. ConclusionsOur results indicate that caregiving quality in the foster family may have an important modulating effect on selected indicators of the childs stress response and could thereby mitigate the possible consequences of early childhood adversity.

physiology↗