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No Child Left Behind Act 20011
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Showing 151 to 165 of 1,079 results Save | Export
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Zachor, Ditza A.; Itzchak, E. Ben – Research in Developmental Disabilities: A Multidisciplinary Journal, 2011
Epidemiologic studies on maternal and pregnancy risk factors for autism spectrum disorder (ASD), including use of assisted reproductive technology (ART), found conflicting results. This study included the following aims: to assess frequencies of ART in a large ASD group; to examine confounding birth and familial risk factors in the ASD with ART…
Descriptors: Body Weight, Autism, Pregnancy, Risk
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Menez, Steven; Cheskin, Lawrence; Geller, Gail – Health Education & Behavior, 2013
Objective: To determine and compare the perspectives of the general public and health care providers (HCPs) on obesity and its treatment in rural West Virginia (WV) and Baltimore, MD. Method: Surveys were completed in both locations by the general public (WV: "n" = 200; Baltimore: "n" = 171) and HCPs (WV: "n" = 25;…
Descriptors: Obesity, Health Personnel, Public Opinion, Body Composition
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Greenwald, Brian H. – Sign Language Studies, 2009
Historian Brian Greenwald offers a revisionist interpretation of Bell. He reviews Bell's role and influence within the American eugenics movement and shows that Bell had the respect of the most prominent American eugenicists. His intimate knowledge of deafness, from personal experience with his mother and wife and from his studies of deaf people…
Descriptors: United States History, Time Perspective, Genetics, Improvement
Donthu, Ravikiran – ProQuest LLC, 2009
The goal of my dissertation was to fine map the milk yield and composition quantitative trait loci (QTL) mapped to cattle chromosome 3 (BTA3) by Heyen et al. (1999) and to identify candidate genes affecting these traits. To accomplish this, the region between "BL41" and "TGLA263" was mapped to the cattle genome sequence assembly Btau 3.1 and a…
Descriptors: Genetics, Animals, Food, Agricultural Production
Blumenstyk, Goldie – Chronicle of Higher Education, 2009
Sarah L. Kieweg had her own nice surprise when the University of Central Florida contacted her. She understood quite a bit about her father's pioneering work on artificial intelligence in the 1990s. Still, in 2006, eight years after he died of a heart attack, at age 50, the call from the university came out of the blue: some of James R. Driscoll's…
Descriptors: Intellectual Property, Technology Transfer, Artificial Intelligence, College Faculty
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Wozniak, Robert H. – American Psychologist, 2009
James Mark Baldwin is one of the most important and least known early American scientific psychologists. Drawing inspiration from Charles Darwin and other evolutionists of the period, Baldwin developed a biosocial theory of psychological development that influenced both Jean Piaget and Lev S. Vygotsky; and he proposed a mechanism relating learned…
Descriptors: Heredity, Psychologists, Piagetian Theory, Developmental Psychology
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Denny, Kevin – Intelligence, 2008
In a recent paper, [Kanazawa S. & Kovar J.L. (2004). Why beautiful people are more intelligent, "Intelligence," 32, 227-243] assert that given certain empirical regularities about assortative mating and the heritability of intelligence and beauty, that it logically follows that more intelligent people are more beautiful. It is argued here that…
Descriptors: Intelligence, Evidence, Correlation, Aesthetics
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Lynskey, Michael T.; Agrawal, Arpana; Heath, Andrew C. – Journal of the American Academy of Child & Adolescent Psychiatry, 2010
Objective: To provide an overview of the genetic epidemiology of substance use and misuse in adolescents. Method: A selective review of genetically informative research strategies, their limitations, and key findings examining issues related to the heritability of substance use and substance use disorders in children and adolescents is presented.…
Descriptors: Literature Reviews, Children, Heredity, Twins
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Hettinger, Joe A.; Liu, Xudong; Holden, Jeanette Jeltje Anne – Journal of Autism and Developmental Disorders, 2008
Inborn errors of purine metabolism have been implicated as a cause for some cases of autism. This hypothesis is supported by the finding of decreased adenosine deaminase (ADA) activity in the sera of some children with autism and reports of an association of the A allele of the ADA G22A (Asp8Asn) polymorphism in individuals with autism of…
Descriptors: Autism, North Americans, Genetics, Ethnicity
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Park, Soonhye; Chen, Ying-Chih – Journal of Research in Science Teaching, 2012
This study explored the nature of the integration of the five components of pedagogical content knowledge (PCK): (a) Orientations toward Teaching Science, (b) Knowledge of Student Understanding, (c) Knowledge of Instructional Strategies and Representations, (d) Knowledge of Science Curriculum, and (e) Knowledge of Assessment of Science Learning.…
Descriptors: Pedagogical Content Knowledge, Science Instruction, Biology, Heredity
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Ashida, Sato; Hadley, Donald W.; Goergen, Andrea F.; Skapinsky, Kaley F.; Devlin, Hillary C.; Koehly, Laura M. – Gerontologist, 2011
Purpose: This study evaluates the role of older family members as providers of social resources within familial network systems affected by an inherited cancer susceptibility syndrome. Design and Methods: Respondents who previously participated in a study that involved genetic counseling and testing for Lynch syndrome and their family network…
Descriptors: Social Support Groups, Cancer, Genetics, Parent Child Relationship
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Luciano, Michelle; Batty, G. David; McGilchrist, Mark; Linksted, Pamela; Fitzpatrick, Bridie; Jackson, Cathy; Pattie, Alison; Dominiczak, Anna F.; Morris, Andrew D.; Smith, Blair H.; Porteous, David; Deary, Ian J. – Intelligence, 2010
People with higher general cognitive ability in early life have more favourable levels of cardiovascular disease (CVD) risk factors in adulthood and CVD itself. The mechanism of these associations is not known. Here we examine whether general cognitive ability and CVD risk factors share genetic and/or environmental aetiology. In this large,…
Descriptors: Diseases, At Risk Persons, Epidemiology, Genetics
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Bamford, Nigel S.; White, Klane K.; Robinett, Stephanie A.; Otto, Randolph K.; Gospe, Sidney M., Jr. – Developmental Medicine & Child Neurology, 2009
Charcot-Marie-Tooth disease (CMT) is one of the most common inherited neurological disorders, affecting 36 in 100,000 people. CMT type 1A (hereditary motor and sensory neuropathy) is the most frequent form of this disease, affecting 60 to 80% of the CMT population, but its diagnosis may be delayed because of inconsistent clinical signs and…
Descriptors: Neurological Impairments, Heredity, Genetic Disorders, Clinical Diagnosis
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van Gent, Tiejo; Goedhart, Arnold W.; Treffers, Philip D. A. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2012
In this study socio-demographic, deafness-related and diagnostic characteristics of hearing impaired children and adolescents referred to a national mental health service for deaf and hard of hearing children and adolescents were examined. Socio-demographic and diagnostic characteristics were compared to corresponding characteristics of hearing…
Descriptors: Hearing Impairments, Deafness, Mental Health, Health Services
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Dairianathan, Anne; Subramaniam, R. – International Journal of Science Education, 2011
The purpose of this study was to investigate primary students' learning through participation in an out-of-school enrichment programme, held in a science centre, which focused on DNA and genes and whether participation in the programme led to an increased understanding of inheritance as well as promoted interest in the topic. The sample consisted…
Descriptors: Student Interests, Multiple Choice Tests, Surveys, Student Attitudes
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