A 15-Year Study of 63 Teachers at 24 Institutions Reveals: “What the Best College Teachers Do”: Review of: What the Best Teachers Do, by Ken Bain; Harvard University Press (Cambridge, MA); ISBN: 0–6740–1325–5     

Robin L Wright  Aaron Charlson    Carrie F Olson 《CBE life sciences education》2005,4(4):279-280

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Gender Development in Transgender Preschool Children          下载免费PDF全文

Anne A. Fast  Kristina R. Olson 《Child development》2018,89(2):620-637

An increasing number of transgender children—those who express a gender identity that is “opposite” their natal sex—are socially transitioning, or presenting as their gender identity in everyday life. This study asks whether these children differ from gender‐typical peers on basic gender development tasks. Three‐ to 5‐year‐old socially transitioned transgender children (n = 36) did not differ from controls matched on age and expressed gender (n = 36), or siblings of transgender and gender nonconforming children (n = 24) on gender preference, behavior, and belief measures. However, transgender children were less likely than both control groups to believe that their gender at birth matches their current gender, whereas both transgender children and siblings were less likely than controls to believe that other people's gender is stable.  相似文献   

Research Agendas and Computer Technology Visions: The Need for Closely Watched Classrooms     

Larry Miller  John Olson 《Education and Information Technologies》1999,4(1):81-98

There are numerous research methodologies that may be applied to the study of computer technology, and each has the potential to provide insights into its usefulness. The selection of research methodologies should be driven by the nature of the questions under investigation rather than a predetermined idea that some research methods are superior to others. This article focuses on a particular methodology, case studies, and it describes their potential for making a unique contribution to our understanding of computer technology. The special value of case studies lies in helping us understand the complexities found in classrooms, where the multiple variables that influence computer use interact in complex ways. © 1999 IFIP, published by Kluwer Academic Publishers  相似文献   

Systematic Mentoring for New Faculty Teachers and Graduate Teaching Assistants   总被引：3，自引：0，他引：3  

Peg Boyle  Bob Boice 《Innovative Higher Education》1998,22(3):157-179

This study reports on the development and assessment of two mentoring programs, one for new faculty and one for new graduate teaching assistants. The first program was an externally funded, elaborate program; and it suggested the centrality of factors such as sustained, involving relationships for best outcomes with protégés. The second project, with newcomers to graduate study, demonstrated that a simpler program focusing on involvement within the pair and group meetings produces promising results. From both these projects, we developed a replicable model of systematic mentoring; and we obtained a clear picture of the styles and skills of exemplary mentors.Peg Boyle: Graduated from the State University of New York at Stony Brooknow resides in Boone, North Carolina  相似文献   

Spot Reduction of Subcutaneous Adipose Tissue     

Arne L. Olson  Elliott Edelstein 《Research quarterly for exercise and sport》2013,84(3):647-652

Abstract

This study was designed to determine if the skinfold measurements on an exercised arm would decrease as a result of regular weight training with that arm. Thirty-two subjects completed three sets of 7-RM curls and three sets of 7-RM triceps extensions on either a daily or an alternate day schedule for a period of 6 weeks. The nonexercised arm was measured to establish the specificity of the spot reduction on the exercised arm. The results indicate that hard exercise in a specific area of the arm will result in a reduction of the subcutaneous adipose tissue in that area.  相似文献   

The Impact of On-campus Student Growth on First-year Student Engagement and Success     

Steven M. LaNasa  Elizabeth Olson  Natalie Alleman 《Research in higher education》2007,48(8):941-966

During the past two decades institutions of all types have sought to expand and enhance residential facilities. Institutional focus on scale, configuration, amenities, and academic integration has sought to leverage prior research documenting the multiple and often positive impacts of on-campus residence. Although institutional size has been documented to differentially impact student engagement [Kezar, A. J. (2006). NASPA Journal 43(1): 87–114], few studies, however, have directly explored the effect of residential expansion on student engagement. This study, based on a sample of 731 first-time freshmen explores NSSE results before and after the opening of a residential facility that doubled on-campus living at a single, metropolitan institution. Results indicate limited positive differences after opening, and suggest that structure, in the form of size, does not, in and of itself, contribute significantly to shifting engagement. Additionally, these results suggest an alternative method for using NSSE data in institutional analyses.  相似文献   

Confirmatory factor analysis of word recognition and process measures in the Colorado Reading Project     

R. K. Olson  J. J. Gillis  J. P. Rack  J. C. Defries  D. W. Fulker 《Reading and writing》1991,3(3-4):235-248

Measures of word recognition (REC) and two component skills, phonological coding (PHON) and orthographic coding (ORTH), were subjected to multivariate behavioral genetic analysis. Data were obtained from a sample of identical and fraternal twin pairs wherein at least one member of each pair was reading disabled (RD), and from a sample of twins wherein both members of each pair read in the normal range. Confirmatory factor analysis was used to fit the genetic, common environmental, and specific environmental covariance components for REC, PHON, and ORTH within the RD and normal simples. The resulting heritability estimates for REC, PHON, and ORTH were 0.59, 0.41, and 0.05 in the RD sample, and 0.35, 0.52, and 0.20 in the normal sample. After dropping the nonsignificant common environment parameters from the models, the genetic correlations between REC and PHON and between REC and ORTH were respectively 0.81 and 0.45 in the RD sample, and 0.68 and 0.45 in the normal sample. Differences between the genetic correlations were significant in the RD sample (p<0.005), marginally significant in the normal sample (p<0.10), and highly significant in the combined sample (p<0.001), indicating that genetic influences on individual differences in REC are more strongly related to genetic variance in PHON than in ORTH. These results are consistent with previous demonstrations of substantial genetic covariance between the disabled group's deficits in REC and PHON, but not between REC and ORTH (Olson et al., 1989; Olson and Rack, 1990).  相似文献   

Differential genetic etiology of reading disability as a function of IQ   总被引：5，自引：0，他引：5  

Wadsworth SJ  Olson RK  Pennington BF  DeFries JC 《Journal of learning disabilities》2000,33(2):192-199

To test the hypothesis that the genetic etiology of reading disability differs as a function of IQ, composite reading performance data from 223 pairs of identical twins and 169 pairs of same-gender fraternal twins in which at least one member of each pair was classified with reading disability were subjected to multiple regression analysis (DeFries & Fulker, 1985, 1988). In the total sample, heritability of the group deficit in reading performance (h(g)2) was .58 (+/- .08). However, when the basic regression model was fitted separately to data from twin pairs with average Wechsler (1974, 1981) full scale IQ scores below 100 or 100 and above, resulting estimates of h(g)2 were .43 and .72, respectively, a significant difference (p < or = .03, one-tailed). The results of fitting extended regression models to reading performance and continuous IQ data provide evidence that the genetic etiology of reading disability differs as a linear function of IQ (p < or = .007, one-tailed). These results suggest that IQ is relevant for the diagnosis of reading disability and that environmental influences may be more salient as a cause of reading difficulties in children with lower IQ scores.  相似文献   

Learning through experience and learning through media   总被引：1，自引：0，他引：1  

Jerome S. Bruner  David R. Olson 《Prospects》1973,3(1):20-38

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Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene     

Smith SD  Kelley PM  Askew JW  Hoover DM  Deffenbacher KE  Gayán J  Brower AM  Olson RK 《Journal of learning disabilities》2001,34(6):512-519

Linkage analysis has localized a gene influencing specific reading disability (dyslexia) to 6p21.3. The myelin oligodendrocyte glycoprotein (MOG) gene, which maps to this region, was selected as a candidate. Myelin oligodendrocyte glycoprotein is a membrane protein, a member of the immunoglobin superfamily, that is found on the outermost lamellae of mature myelin. Although the exact function of this protein is unknown, its presence in the central nervous system and the hypothesized relationship between dyslexia and temporal processing rate as well as a suggested relationship with intelligence made this gene a candidate for dyslexia. Analysis of the coding exons and adjacent splice sites in a subset of 22 children with dyslexia from 10 sibships found a missense mutation in exon 4 in 2 of the sibships. This change from the published sequence also occurred in 86 of 96 random controls, making it considerably less frequent in this small sample of individuals with dyslexia. Subsequent typing of this single nucleotide polymorphism (SNP) in 74 nuclear families in which at least one child had reading disability showed no significant difference in frequency from the controls, however. Sib-pair linkage analysis with these families did not show significant linkage with the SNP nor with a separate polymorphic dinucleotide repeat marker in the MOG gene (MOG31/32), but association analysis identified two alleles of MOG31/32 that were associated with reading disability phenotypes with a low level of significance. Thus, although alleles in the MOG gene may be in linkage disequilibrium with a locus that contributes to reading disability, it is unlikely that the MOG gene itself is involved.  相似文献