Publication Date
| In 2026 | 0 |
| Since 2025 | 125 |
| Since 2022 (last 5 years) | 730 |
| Since 2017 (last 10 years) | 1904 |
| Since 2007 (last 20 years) | 5252 |
Descriptor
| Genetics | 7193 |
| Biology | 1558 |
| Genetic Disorders | 1423 |
| Science Instruction | 1337 |
| Foreign Countries | 1289 |
| Children | 1008 |
| Science Education | 991 |
| Teaching Methods | 942 |
| Environmental Influences | 930 |
| Correlation | 776 |
| Autism | 739 |
| More ▼ | |
Source
Author
Publication Type
Education Level
Audience
| Teachers | 424 |
| Practitioners | 348 |
| Researchers | 145 |
| Students | 48 |
| Policymakers | 26 |
| Parents | 24 |
| Administrators | 10 |
| Community | 10 |
| Counselors | 9 |
| Media Staff | 2 |
| Support Staff | 1 |
| More ▼ | |
Location
| United Kingdom | 148 |
| Australia | 128 |
| United States | 83 |
| Sweden | 72 |
| Turkey | 66 |
| Canada | 65 |
| Netherlands | 65 |
| Germany | 58 |
| United Kingdom (England) | 58 |
| Spain | 45 |
| California | 42 |
| More ▼ | |
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Peer reviewedWadsworth, Sally J.; Knopik, Valerie S.; DeFries, J. C. – Reading and Writing: An Interdisciplinary Journal, 2000
Analyzes composition reading performance data from identical and fraternal twin pairs in order to test the hypothesis that genetic influences are more important as a cause of reading disability in girls than in boys. Provides little or no evidence for the hypothesis of greater genetic influence on reading difficulties in girls than in boys. (SC)
Descriptors: Elementary Education, Genetics, Heredity, Reading Difficulties
Peer reviewedSolot, Cynthia B.; Knightly, Carol; Handler, Steven D.; Gerdes, Marsha; McDonald-McGinn, Donna M.; Moss, Edward; Wang, Paul; Cohen, Marilyn; Randall, Peter; Larossa, Don; Driscoll, Deborah; Emanuel, Beverly S.; Zackai, Elaine H. – Journal of Communication Disorders, 2000
The 22q11.2 microdeletion syndrome is a genetic disorder in children with many concomitant medical and developmental problems. Communication disorders are among the most common features of this syndrome and include articulation, language, resonance, and voice problems. Awareness of these features and a multidisciplinary approach are necessary for…
Descriptors: Clinical Diagnosis, Communication Disorders, Congenital Impairments, Genetics
Peer reviewedJensen, Arthur R. – Intelligence, 1997
Data from a previous adoption study using the Wechsler Intelligence Scale for Children-Revised show that the genetic effect is reflected by psychometric "g" (general intelligence) to a greater degree than is the environmental effect. This finding is consistent with the hypothesis that "g" largely reflects the genetic component…
Descriptors: Adoption, Biological Influences, Genetics, Intelligence
Belser, Richard C.; Sudhalter, Vicki – American Journal on Mental Retardation, 2001
Comparison of the production of repetitive speech during conversations in 30 people with either fragile X syndrome, autistic disorder, or mental retardation not caused by fragile X found repetitive speech more prevalent among those with fragile X. Results support the hypothesis that such speech dysfluency reflects the effects of physiological…
Descriptors: Autism, Children, Congenital Impairments, Etiology
Peer reviewedPetrill, Stephen A.; Saudino, Kimberly S.; Wilkerson, Bessie; Plomin, Robert – Intelligence, 2001
Investigated genetic and environmental influences on the similarity and differences among five tests of cognitive abilities in 1,958 pairs of same-sex twins born in 1994 in the United Kingdom. Results suggest a developmental trend from modularity to molarity when considered in relation to multivariate genetic results later in life that show that…
Descriptors: Child Development, Cognitive Ability, Cognitive Tests, Foreign Countries
Peer reviewedFaraone, Stephen V.; Biederman, Joseph – Developmental Review, 2000
Comments on Joseph's review of the genetics of attention deficit disorder, demonstrating errors of scientific logic and oversight of relevant research in Joseph's argument. Argues for the validity of twin studies in supporting a genetic link for ADHD and for the complementary role of nature and nurture in the etiology of the disorder. (JPB)
Descriptors: Attention Deficit Disorders, Genetics, Heredity, Hyperactivity
Peer reviewedJoseph, Jay – Developmental Review, 2000
Answers the most important criticisms by Faraone and Biederman in their critique of Joseph's analysis of evidence supporting a genetic basis of attention deficit hyperactivity disorder. Argues that possible genetic and environmental influences in ADHD twin studies are confounded, obscuring inferences about genetic factors. (JPB)
Descriptors: Attention Deficit Disorders, Genetics, Heredity, Hyperactivity
Jungck, John R.; Soderberg, Patti – Bioscene, 1995
Presents a series of elementary mathematical tools for re-representing pedigrees, pedigree generators, pedigree-driven database management systems, and case studies for exploring genetic relationships. (MKR)
Descriptors: Case Studies, Computer Software, Genetics, Higher Education
Peer reviewedCavallo, Ann M. L. – Journal of Research in Science Teaching, 1996
Explores relationships among school students' (n=189) meaningful learning orientation, reasoning ability and acquisition of meaningful understandings of genetics topics, and ability to solve genetics problems. Results indicate that meaningful learning orientation best predicted students' understanding of genetics interrelationships while reasoning…
Descriptors: Academic Achievement, Genetics, Problem Solving, Scientific Concepts
Peer reviewedLeamnson, Robert – Change, 2000
Recent research suggests that thinking of learning as an activity of the brain will lead to greater understanding of how and why students learn and how faculty can better facilitate learning. Discusses: genetic contributions; epigenetic growth; the synapse; stabilizing synapses; pedagogy; the role of emotions; kinds of learning; active learning;…
Descriptors: Active Learning, Brain, Elementary Secondary Education, Genetics
Peer reviewedClark, Deborah C.; Mathis, Philip M. – American Biology Teacher, 2000
Presents an activity that uses chenille stems, colored yarn, plastic straws, and ingenuity to make a low-cost manipulative kit for modeling mitosis and meiosis. (ASK)
Descriptors: Biology, Genetics, Science Activities, Science Instruction
Peer reviewedCosta, Frances T. – American Biology Teacher, 2000
Describes a method for working with Coomassie Blue to analyze banding patterns of purified eukaryotic cell membrane proteins. (SAH)
Descriptors: Biology, DNA, Genetics, Higher Education
Peer reviewedDale, Philip S.; Ginette, Dionne; Eley, Thalia C.; Plomin, Robert – Journal of Child Language, 2000
Assessed the language development of 2,898 pairs of 2-year-old twins born in England and Wales using the MacArthur Communicative language Development Inventory, which assesses vocabulary and grammar. Moderate heritabilities were found for both. (Author/VWL)
Descriptors: Foreign Countries, Genetics, Grammar, Language Acquisition
Peer reviewedClements, Lee Ann J.; Jackson, Karen E. – American Biology Teacher, 1998
Describes an interactive game designed to help students see and understand the dynamic relationship between DNA, RNA, and proteins. Appropriate for either a class or laboratory setting, following a lecture session about protein synthesis. (DDR)
Descriptors: Biology, DNA, Educational Games, Genetics
Peer reviewedHeim, Werner G. – American Biology Teacher, 2002
Describes a card game that illustrates natural selection acting on random mutations with or without cumulative selection. (YDS)
Descriptors: Active Learning, Biology, Creationism, Evolution


