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Goin-Kochel, Robin P.; Mire, Sarah S.; Dempsey, Allison G. – Journal of Autism and Developmental Disorders, 2015
Current research describes a four-category scheme of Autism Spectrum Disorder (ASD) onset: early, regressive, plateau, delay + regression. To replicate prevalence of different onset types, ASD onset (per the "Autism Diagnostic Interview-Revised") was examined in a large North American sample; for a subset, parents' causal beliefs were…
Descriptors: Autism, Pervasive Developmental Disorders, Questionnaires, Symptoms (Individual Disorders)
Lickliter, Robert – International Journal of Developmental Science, 2013
Psychobiological systems theory is a relational approach to development that challenges the longstanding views that (1) genetic and environmental influences on the phenotype can be meaningfully partitioned and that (2) genes are capable of directly specifying phenotypes. Gilbert Gottlieb's theoretical innovations including the notion of…
Descriptors: Genetics, Biological Sciences, Developmental Psychology, Individual Development
Peters, S. U.; Hundley, R. J.; Wilson, A. K.; Carvalho, C. M. B.; Lupski, J. R.; Ramocki, M. B. – Journal of Autism and Developmental Disorders, 2013
The aim of this study was to determine the frequency, timing, and associated features of developmental regression in "MECP2" duplication syndrome. We also examined whether duplication size was associated with regression. Comprehensive psychological evaluations were used to assess 17 boys with "MECP2" duplication syndrome.…
Descriptors: Genetic Disorders, Males, Child Development, Language Skills
Rigoldi, Chiara; Cimolin, Veronica; Camerota, Filippo; Celletti, Claudia; Albertini, Giorgio; Mainardi, Luca; Galli, Manuela – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
Ligament laxity in Ehlers-Danlos syndrome hypermobility type (EDS-HT) patients can influence the intrinsic information about posture and movement and can have a negative effect on the appropriateness of postural reactions. Several measures have been proposed in literature to describe the planar migration of CoP over the base of support, and the…
Descriptors: Scientific Concepts, Motor Development, Genetic Disorders, Patients
Prada, Carlos E.; Grabowski, Gregory A. – Developmental Disabilities Research Reviews, 2013
Background: The lysosomal--autophagocytic system diseases (LASDs) affect multiple body systems including the central nervous system (CNS). The progressive CNS pathology has its onset at different ages, leading to neurodegeneration and early death. Methods: Literature review provided insight into the current clinical neurological findings,…
Descriptors: Genetic Disorders, Neurological Impairments, Symptoms (Individual Disorders), Pathology
Rieger, Deborah; Auerbach, Sarah; Robinson, Paul; Gropman, Andrea – Developmental Disabilities Research Reviews, 2013
Lipid storage diseases, also known as the lipidoses, are a group of inherited metabolic disorders in which there is lipid accumulation in various cell types, including the central nervous system, because of the deficiency of a variety of enzymes. Over time, excessive storage can cause permanent cellular and tissue damage. The brain is particularly…
Descriptors: Genetic Disorders, Metabolism, Neurological Impairments, Physics
Sobrero, Patricio; Valverde, Claudio – Journal of Biological Education, 2013
A simple and cheap laboratory class is proposed to illustrate the lethal effect of UV radiation on bacteria and the operation of different DNA repair mechanisms. The class is divided into two sessions, an initial 3-hour experimental session and a second 2-hour analytical session. The experimental session involves two separate experiments: one…
Descriptors: Biotechnology, Genetics, Microbiology, Laboratories
Simpson, Eleanor H.; Morud, Julia; Winiger, Vanessa; Biezonski, Dominik; Zhu, Judy P.; Bach, Mary Elizabeth; Malleret, Gael; Polan, H. Jonathan; Ng-Evans, Scott; Phillips, Paul E. M.; Kellendonk, Christoph; Krandel, Eric R. – Learning & Memory, 2014
A common genetic polymorphism that results in increased activity of the dopamine regulating enzyme COMT (the "COMT Val" [superscript 158] allele) has been found to associate with poorer cognitive performance and increased susceptibility to develop psychiatric disorders. It is generally assumed that this increase in COMT activity…
Descriptors: Genetics, Cognitive Ability, Brain Hemisphere Functions, Animals
Barber, Nicola C.; Stark, Louisa A. – CBE - Life Sciences Education, 2014
Cells are bustling factories with diverse and prolific arrays of molecular machinery. Remarkably, this machinery self-organizes to carry out the complex biochemical activities characteristic of life. When Watson and Crick published the structure of DNA, they noted that DNA base pairing creates a double-stranded form that provides a means of…
Descriptors: Science Instruction, Biochemistry, Genetics, Molecular Structure
Albrecht, Björn; Brandeis, Daniel; Uebel-von Sandersleben, Henrik; Valko, Lilian; Heinrich, Hartmut; Xu, Xiaohui; Drechsler, Renate; Heise, Alexander; Kuntsi, Jonna; Müller, Ueli C.; Asherson, Philip; Steinhausen, Hans-Christoph; Rothenberger, Aribert; Banaschewski, Tobias – Journal of Child Psychology and Psychiatry, 2014
Background: Difficulties with performance and brain activity related to attentional orienting (Cue-P3), cognitive or response preparation (Cue-CNV) and inhibitory response control (Nogo-P3) during tasks tapping executive functions are familial in ADHD and may represent endophenotypes. The aim of this study was to clarify the impact of dopamine…
Descriptors: Attention Deficit Hyperactivity Disorder, Genetics, Responses, Inhibition
Maas, Anneke P. H. M.; Didden, Robert; Korzilius, Hubert; Curfs, Leopold M. G. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2012
The prevalence of sleep problems in individuals with intellectual disability (ID) seems to vary between genetic syndromes associated with ID. Different types of sleep disturbances may indicate underlying causes of sleep problems and these types of sleep disturbances may vary between different genetic syndromes. We examined and compared five types…
Descriptors: Genetics, Sleep, Incidence, Mental Retardation
Creer, Sarah; Enderby, Pamela; Judge, Simon; John, Alex – International Journal of Language & Communication Disorders, 2016
Background: Commissioners and providers require information relating to the number of people requiring a service in order to ensure provision is appropriate and equitable for the population they serve. There is little epidemiological evidence available regarding the prevalence of people who could benefit from augmentative and alternative…
Descriptors: Foreign Countries, Augmentative and Alternative Communication, Incidence, Epidemiology
Hoffman, Kathleen; Leupen, Sarah; Dowell, Kathy; Kephart, Kerrie; Leips, Jeff – CBE - Life Sciences Education, 2016
Redesigning undergraduate biology courses to integrate quantitative reasoning and skill development is critical to prepare students for careers in modern medicine and scientific research. In this paper, we report on the development, implementation, and assessment of stand-alone modules that integrate quantitative reasoning into introductory…
Descriptors: Undergraduate Study, College Science, Biology, Thinking Skills
Agbonifoh, Julia Adesua – Journal of Education and Practice, 2016
Against the background of the dangers posed by breast cancer world-wide, and the importance of its early detection and therefore breast self examination (BSE), this study investigated the practice of BSE among female students in tertiary institutions in Edo state. A sample of 723 participants selected through a combination of multi-stage,…
Descriptors: Females, Health Behavior, Health Promotion, Cancer
Reilly, Colin; Murtagh, Lelia; Senior, Joyce – Journal of Research in Special Educational Needs, 2016
Research suggests that genetic syndromes associated with intellectual disability often have specific cognitive and behavioural profiles. It has been suggested that educational approaches need to reflect these profiles. Parents (n = 381) and teachers (n = 204) of children with one of four syndromes, fragile X syndrome, Prader-Willi syndrome,…
Descriptors: Teaching Methods, Best Practices, Intellectual Disability, Genetic Disorders

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