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Imaging genetics is an interdisciplinary field that integrates neuroimaging and genetic data to improve behavioral prediction and investigate the genetic bases of brain structure and function. It aims to identify associations between genetic markers and brain imaging phenotypes, with a behavioral or clinical trait as the outcome of interest. Since its emergence nearly 30 years ago, the field has advanced substantially, fueled by rapid developments in molecular-genetic and neuroimaging techniques. These advances have opened new avenues for exploring individual differences in cognitive and socio-emotional development and their links to neurodevelopmental disorders. This systematic review examined studies published between 2020 and 2024, focusing on developmental psychopathology. We screened 769 articles from PubMed/MEDLINE and PsycINFO and selected 42 publications that met specific inclusion criteria for review. The studies were categorized into three groups based on the developmental ages in which conditions typically develop: birth/early childhood, late childhood or early adolescence, and late adolescence. Although the field has seen considerable progress, multiple challenges in data acquisition, analysis, and interpretation remain. Larger sample sizes and novel analytical techniques are crucial for the continued advancement of imaging genetics, with animal studies offering potential complementary insights.
The bilingual advantage hypothesis, which associates bilingualism with benefits in executive functioning (EF), has been challenged by studies demonstrating inconsistent results. Considering explicit calls to revise the hypothesis, research has turned toward understanding which specific bilingualism-related aspects might impact bilinguals’ EF. Notably, patterns of everyday language use, referred to as interactional contexts in the adaptive control hypothesis (ACH), have emerged as a prominent factor modulating the association between bilingualism and EF. This scoping review synthesizes findings from 49 studies investigating interactional contexts and bilinguals’ EF. The results indicate that the current literature is highly heterogeneous regarding the operationalization, measurement, experimental manipulations of interactional contexts, the EF tasks employed and sample characteristics. This variability limits definitive conclusions about the adaptation of bilinguals’ EF to the demands of interactional contexts. More studies with comparable research designs and clearer predictions on the associations between EF domains and bilinguals’ language-use patterns are needed.
In this essay, I will briefly sample different instances of the utilization of the concept of resilience, attempting to complement a comprehensive representation of the field in the special issue of Development and Psychopathology inspired by the 42nd Minnesota Symposium on Child Psychology, hosted by the Institute of Child Development at the University of Minnesota and held in October of 2022. Having established the general context of the field, I will zoom in on some of its features, which I consider “low-hanging fruit” and which can be harvested in a systematic way to advance the study of resilience in the context of the future of developmental psychopathology.
This chapter is concerned with prevention, assessment, and intervention for reading disability (dyslexia). The initial section is concerned with the reading wars that have fought over the most appropriate way to teach reading. The development of this debate over the past century is outlined and the current focus upon the highly publicized “science of reading” movement is examined and evaluated. The chapter then considers the prevention of reading disability and the nature and role of screening. In so doing, the chapter highlights the complexities of screening for dyslexia when this latter term is used both as a synonym for reading disability and alternatively as a discrete condition that applies only to some struggling readers. The bulk of the chapter is concerned with an examination of “what works” for struggling readers of different ages and levels of difficulty. The often disappointing effects of what are considered to be the most promising interventions are considered. Findings from other, less scientifically grounded, alternative treatments are reported and critiqued. Finally, the lack of any meaningful relationship between a dyslexia diagnosis and differential intervention is examined. It is noted that programs for struggling readers cannot be meaningfully determined on this basis.
The opening section of this chapter charts the history of the dyslexia construct. The distinction between scientific understandings of dyslexia (a difficulty in accurate and fluent word reading) and reading comprehension is emphasized. Different conceptions of dyslexia exist, however, and these are grouped within four categories, each of which is examined and critiqued in turn. Dyslexia 1 concerns an understanding whereby dyslexia refers to those with the most severe and persistent forms of reading. Dyslexia 2 describes the widely held view that only some struggling readers are dyslexic, and such individuals need to be identified by expert assessors using various cognitive tests. In these cases, the individual’s reading problem is often considered to be unexpected. The role of intelligence, and intelligence/reading discrepancy, as a marker of dyslexia is examined in significant detail. A Dyslexia 3 conception places emphasis on the struggling reader’s difficulty to make significant progress even when provided with high-quality intervention. Dyslexia 4 concerns the understanding that reading difficulties should be considered as only one part of a much broader dyslexic condition that may provide a number of compensatory gifts. The need to eschew unitary explanations in favor of multifactorial understandings of reading disability involving a combination of biology and environment is emphasized.
This chapter considers the neurobiological bases of reading disability (dyslexia). These primarily concern the working of the brain and the nature and role of genetics (heritability). The first part of the chapter considers the development of the “reading brain,” describing key brain areas and their functions. The historical development of brain studies in reading disability from the early role of postmortems to present-day scanning techniques is outlined. The discussion of each of contemporary measurement approaches is split into two parts. Opening with work that focuses upon brain structure, discussion then considers brain functioning, particularly functional magnetic resonance imaging (fMRI). The second part of the chapter focuses upon the contribution of genetics to the dyslexia debate. In so doing, it considers both quantitative and more recent molecular approaches. The significant heritability of reading skill is discussed and the rudimentary knowledge base concerning the genetics of reading is acknowledged. The chapter concludes by noting that, despite significant scientific advances in both fields, neither current brain scanning techniques nor genetic analyses can be used to diagnose reading disability/dyslexia or inform practitioners about appropriate forms of intervention.
This chapter is largely concerned with arguments for and against the use of the dyslexia construct as a diagnosed label. The most commonly voiced arguments for the value of the label put forward in response to the publication of The Dyslexia Debate in 2014 are listed, analyzed, and critiqued. Key arguments for the label are clustered under the following headings: learner empowerment and exculpation, gaining access to finite resources, the perceived failure of teachers, schools and school systems, meeting the needs of adult learners in further and higher education, neurodiversity, disability, and the dyslexic identity, and other arguments offered for retention of the label. Having shown the flaws in each of these arguments, the chapter concludes by reasserting the key message provided throughout the book that there is no need or justification for the continuation of dyslexia diagnoses or labels. Rather, efforts should focus upon ensuring that the needs of all struggling readers are identified and addressed.
This chapter considers the cognitive literature in relation to dyslexia, repeating the message that unitary explanations involving single processes are overly simplistic and multifactorial models are needed. Each of the various processes (deficits) that have been cited in the literature as having a potential causal role in reading disability is examined. Key processes considered in detail are phonological/phonemic awareness, rapid naming, short-term and working memory, executive functioning, auditory processing, visual processing, visual attention, and visual stress (scotopic sensitivity, psycho-motor processing). The educational and clinical implications that result from this body of work are considered.
This final chapter provides a series of conclusions and recommendations for the way forward. In the light of the experience of the past decade, this chapter recommends the continued use of the term dyslexia to describe a severe and persistent difficulty with accurate and fluent reading. However, it is recommended that the use of the term dyslexia as a diagnosed label or category for specific individuals should be discontinued. The importance of removing the existing arbitrary distinction between dyslexic and nondyslexic poor readers and the rejection of the expanded use of the term to incorporate a wide range of cognitive strengths and weaknesses is explained. The implications of these recommendations for the development of teacher expertise and educational practice are outlined.
In every country, and in every language, a significant proportion of children struggle to master the skill of reading. In 2014, The Dyslexia Debate examined the problematic interpretation of the term 'dyslexia' as well as questioning its efficacy as a diagnosis. Ten years on, The Dyslexia Debate Revisited reflects on the changes in dyslexia assessment and treatment over the last decade, including the introduction of dyslexia legislation in many US states. Addressing the critical responses to their original challenge of the dyslexia construct, Julian G. Elliott and Elena L. Grigorenko also consider why, despite scientific critiques, existing dyslexia conceptions and assessment practices continue to be highly attractive to many professionals, individuals, and families. Based on current scientific knowledge, the authors strive to promote a shared understanding of reading difficulties and emphasize the importance of providing timely and appropriate intervention and support to anyone who faces difficulties with learning to read.
The spread of literacy throughout the world made it necessary to develop a systematic (stage-based) and effective (quick and inexpensive) way of teaching reading that could be delivered to many (different) people simultaneously with the use of the ever-changing textures of reading. In this chapter, it will be shown that all of these considerations, when contemplated holistically, define the parameters of the genetic system that is the foundation of literacy in general and (a)typical reading and writing in particular. Yet it is a distal one, with the proximal foundation being the brain. It will be concluded that the genetic bases of (a)typical reading and writing is nothing more than the genetic bases of a brain that, pressured by the demands and opportunities imposed by modern society, has turned itself into a reading and writing (i.e., literate) brain.