Infant cognition is a flourishing and respected field of inquiry, but its practitioners agree that a large share of experiments are underpowered and that replicability is a serious issue (Frank et al., 2017). A consortium consisting of all four babylabs in the Dutch Baby Brain and Cognition Network will replicate two exemplary studies, each fundamental to the core debates in the field. The algebraic rule learning study reported in Science by Marcus, Vijaya, Bandi and Vishton (1999) plays a key role in the debate on (innate) learning mechanisms involved in language acquisition, and whether these are human- and language-specific, while the study on cognitive gains of bilingualism, reported in PNAS by Kovács and Mehler (2004) is of fundamental importance in the debate on whether bilingualism has a positive influence on cognitive flexibility. By replicating each study in all four labs, we will improve statistical power of the studies, and test the robustness of the original results when the experiments are performed in different labs. In our data analyses, we will depart from the traditional frequentist methods used in the original studies. Specifically, a Bayesian sequential testing approach will be used in order to determine when enough evidence is gathered to evaluate the original findings. This approach also allows us to quantify evidence for the null hypothesis in case we cannot replicate the results of the original studies. Summarizing, by increasing statistical power, the aim of the current project - led by the Dutch Baby Brain and Cognition Network - is to solidify the results of two infant studies addressing fundamental questions concerning human cognition and its ontogenesis.
This project's aim is to predict (family risk of) dyslexia based on EEG (ERP) measurements in infants. State-of-the-art machine learning (deep learning) techniques will be employed to find early patterns in ERP data that are characteristic of (risk of) developmental dyslexia. See https://www.esciencecenter.nl/project/epodium
Specific language impairment (SLI) in children is characterized by severe and persistent difficulties in acquiring a native language, unrelated to intellectual disability, physical limitations, or psychosocial deprivation. The etiology of SLI, in particular the role of neurocognitive processes such as learning and information processing, is poorly understood. Progress in this domain is difficult because of the large etiologic and phenotypic heterogeneity of the SLI population. Here, we propose to address this challenge by examining a population with developmental language impairment resulting from a uniform etiology: the 22q11.2 deletion (22q11DS). Children with 22q11DS display delayed language development, and learning- and information processing deficits similar to SLI. The fact that all 22q11DS share the same genetic etiology provides us with a unique opportunity to identify the mechanisms underlying this language disorder.
The first 1001 days of a child’s life, from conception to the age of two, are of vital importance for the development of our complex brain. The brain structure (e.g. different cell types, connections between brain regions) is formed, which will determine a range of skills and cognitive abilities of the child later in life. This project will focus on language development, as an example of an important skill that is dependent on proper brain development. How do stimuli in the first 1001 days influence language acquisition (and disorders)?
The current project will use machine learning techniques to explore if data on speech processing in infancy can predict the occurrence of later literacy difficulties in individual children. We perform a proof of principle study on existing vocabulary and speech discrimination data from infants at risk of DD and low-risk controls.
This study investigates relationships between language abilities and cognitive control in bilingual minority children in the Netherlands. The aim is to better understand the cognitive effects of bilingualism and to disentangle effects of bilingualism and Developmental Language Disorder.