Olson RK - Search Results

1

The heritability of general cognitive ability increases linearly from childhood to young adulthood.

Haworth CM, Wright MJ, Luciano M, Martin NG, de Geus EJ, van Beijsterveldt CE, Bartels M, Posthuma D, Boomsma DI, Davis OS, Kovas Y, Corley RP, Defries JC, Hewitt JK, Olson RK, Rhea SA, Wadsworth SJ, Iacono WG, McGue M, Thompson LA, Hart SA, Petrill SA, Lubinski D, Plomin R. Haworth CM, et al. Among authors: olson rk. Mol Psychiatry. 2010 Nov;15(11):1112-20. doi: 10.1038/mp.2009.55. Epub 2009 Jun 2. Mol Psychiatry. 2010. PMID: 19488046 Free PMC article.

2

The external validity of age- versus IQ-discrepancy definitions of reading disability: lessons from a twin study.

Pennington BF, Gilger JW, Olson RK, DeFries JC. Pennington BF, et al. Among authors: olson rk. J Learn Disabil. 1992 Nov;25(9):562-73. doi: 10.1177/002221949202500904. J Learn Disabil. 1992. PMID: 1431540

3

Multivariate behavioral genetic analysis of achievement and cognitive measures in reading-disabled and control twin pairs.

Light JG, Defries JC, Olson RK. Light JG, et al. Among authors: olson rk. Hum Biol. 1998 Apr;70(2):215-37. Hum Biol. 1998. PMID: 9549237

4

Quantitative-trait locus for specific language and reading deficits on chromosome 6p.

Gayán J, Smith SD, Cherny SS, Cardon LR, Fulker DW, Brower AM, Olson RK, Pennington BF, DeFries JC. Gayán J, et al. Among authors: olson rk. Am J Hum Genet. 1999 Jan;64(1):157-64. doi: 10.1086/302191. Am J Hum Genet. 1999. PMID: 9915954 Free PMC article.

5

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, Monaco AP. Fisher SE, et al. Among authors: olson rk. Nat Genet. 2002 Jan;30(1):86-91. doi: 10.1038/ng792. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743577

6

Are RAN- and phonological awareness-deficits additive in children with reading disabilities?

Compton DL, DeFries JC, Olson RK. Compton DL, et al. Among authors: olson rk. Dyslexia. 2001 Jul-Sep;7(3):125-49. doi: 10.1002/dys.198. Dyslexia. 2001. PMID: 11765981

7

Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability.

Davis CJ, Gayán J, Knopik VS, Smith SD, Cardon LR, Pennington BF, Olson RK, DeFries JC. Davis CJ, et al. Among authors: olson rk. Behav Genet. 2001 Nov;31(6):625-35. doi: 10.1023/a:1013305730430. Behav Genet. 2001. PMID: 11838539

8

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP. Francks C, et al. Among authors: olson rk. Psychiatr Genet. 2002 Mar;12(1):35-41. doi: 10.1097/00041444-200203000-00005. Psychiatr Genet. 2002. PMID: 11901358

9

Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder.

Willcutt EG, Pennington BF, Smith SD, Cardon LR, Gayán J, Knopik VS, Olson RK, DeFries JC. Willcutt EG, et al. Among authors: olson rk. Am J Med Genet. 2002 Apr 8;114(3):260-8. doi: 10.1002/ajmg.10205. Am J Med Genet. 2002. PMID: 11920845

10

Evidence for linkage and association with reading disability on 6p21.3-22.

Kaplan DE, Gayán J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR. Kaplan DE, et al. Among authors: olson rk. Am J Hum Genet. 2002 May;70(5):1287-98. doi: 10.1086/340449. Epub 2002 Apr 10. Am J Hum Genet. 2002. PMID: 11951179 Free PMC article.

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