Castles, A., Datta, H., Gayan, J., & Olson,
R.K. (1999). Varieties of developmental reading disorder: Genetic
and environmental influences. Journal of Experimental Child
Psychology, 72, 73-94.
Wise, B.W., Ring, J., & Olson, R.K. (1999).
Training phonological awareness with and without attention to
articulation. Journal of Experimental Child Psychology, 72,
271-304.
Wadsworth, S.J., Olson, R.K., Pennington, B.F.,
& DeFries, J.C. (2000). Differential genetic etiology of
reading disability as a function of IQ. Journal of Learning
Disabilities., 33, 192-199.
Wise, B.W., Ring, J., & Olson, R.K. (2000).
Individual differences in gains from computer-assisted remedial
reading with more emphasis on phonological analysis or accurate
reading in context. Journal of Experimental Child Psychology,
77, 197-235.
Willcutt, E.G., Pennington, B.F., Olson, R.K.,
Boada, R., Ogline, J., Tunick, R., & Chhabildas, N. (2001).
A comparison of the cognitive deficits in reading disability
and attention-deficit/hyperactivity disorder. Journal of Abnormal
Psychology, 110, 157-172.
Smith, S.D., Kelley, P.M., Askew, J.W., Hoover,
D.M., Deffenbacher, K.E., Gayan, J., Brower, A., & Olson,
R.K. (2001). Reading disability and chromosome 6p21.3: Evaluation
of MOG as a candidate gene. Journal of Learning Disabilities,
34, 512-519.
Davis, C.J., Gayan, J., Knopik, V.S., Smith, S.D.,
Cardon, L.R., Pennington, B.F., Olson, R.K., & DeFries,
J.C. (2001). Etiology of reading difficulties and rapid naming:
The Colorado Twin Study of Reading Disability. Behavior Genetics,
31 (6), 625-635.
Gayan, J., & Olson, R.K. (2001). Genetic and
environmental influences on orthographic and phonological skills
in children with reading disabilities. Developmental Neuropsychology,
20 (2), 487-511.
Davis, C.J., Knopik, V.S., Olson, R.K., Wadsworth,
S.J., & DeFries, J.C. (2001). Genetic and environmental
influences on rapid naming and reading ability: A twin study.
Annals of Dyslexia, 51, 241-258.
Cross, R.J., Gayan, J., DeFries, J.C., and Olson,
R.K. (2001). Differential genetic etiology of reading disability
as a function of processing speed. Behavioral Genetics, 31,
450 (Abstract)
Davis, C.J., Gayan, J., Knopic, V.S., Smith, S.D.,
Cardon, L.R., Pennington, B.F., Olson, R.K., DeFries, J.C. (2001).
Reading difficulties and rapid naming: Bivariate twin and genetic
linkage analyses. Behavioral Genetics, 31, 451 (Abstract)
Compton, D.L., DeFries, J.C., & Olson, R.K.
(2001). Are RAN and phonological awareness deficits additive
in children with reading disabilities? Dyslexia, 7, 125-149.
Olson, R.K. & Datta, H. (2002). Visual-temporal
processing in reading-disabled and normal twins. Reading and
Writing, 15, 127-149.
Willcutt, E.G., Pennington, B.F., Smith, S.D.,
Cardon, L.R., Gayan, J., Knopic, V.S., Olson, R.K., & DeFries,
J.C. (2002). Quantitative trait locus for reading disability
on chromosome 6p is pleiotropic for attention-deficit/hyperactivity
disorder. American Journal of Medical Genetics (Neuropsychiatric
Genetics), 114, 260-268.
Fisher, S.E., Francks, C., Marlow, A.J., MacPhie,
L., Williams, D.F., Cardon, Lon R., Ishikawa-Brush, Y., Talcott,
J.B., Richardson, A.J., Gayan, J., Olson, R.K., Pennington,
B.F., Smith, S.D., DeFries, J.C., Stein, J.F., & Monaco,
A.P. (2002). Genome-wide scans in independent samples reveal
strong convergent evidence for a chromosome 18 quantitative-trait
locus influencing developmental dyslexia. Nature Genetics, 30,
86-91.
Franks, C., Fisher, S.E., Olson, R.K., Pennington,
B.F., Smith, S.D., DeFries, J.C., & Monaco, A.P. (2002).
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility
locus: Quantitative association analysis and positional candidate
genes SEMA4F and OTX1. Psychiatric Genetics, 12, 35-41.
Kaplan, D.E., Gayan, J., Ahn, J., Won, T.W., Pauls,
D., Olson, R., DeFries, J.C., Wood, F., Pennington, B., Page,
G., Smith, S.D., & Gruen, J.R. (2002). Evidence for linkage
and association with reading disability on 6P21.3-22. American
Journal of Human Genetics, 70, 1287-1298.
Knopik, V.S., Smith, S.D., Cardon, L., Pennington,
B., Gayan, J., Olson, R.K., & DeFries, J.C. (2002). Differential
genetic etiology of reading component processes as a function
of IQ. Behavior Genetics, 32, 181-198.
Compton, D.L., Olson, R.K., & DeFries, J.C.,
and Pennington, B.F. (2002). Are all RAN created equal? Comparing
the relationships among two different formats of alphanumeric
RAN and various word reading skills in normally achieving and
reading disabled individuals. Scientific Studies of Reading,
6 (4), 343-368.
Boada, R., Willcutt, E.G., Tunick, R.A., Chhabildas,
N.A., Olson, R.K., DeFries, J.C., & Pennington, B.F. (2002).
A twin study of the etiology of high reading ability. Reading
and Writing: An Interdisciplinary Journal, 15, 683-707.
Byrne, B., Delaland, C., Fielding-Barnsley, R.,
Quain, P., Samuelsson, S., Hoien, T., Corley, R., DeFries, J.C.,
Wadsworth, S., Willcutt, E., & Olson, R.K. (2002). Longitudinal
twin study of early reading development in three countries:
Preliminary results. Annals of Dyslexia, 52, 49-74.
Olson, R.K. (2002). Dyslexia: Nature and nurture.
Dyslexia, 8, 143-159.
Cross, R.J., Davis, C.J., Rhee, S., Wadsworth,
S.J., DeFries, J.C. & Olson, R.K. (2002). The effect of
subtype classification methods on estimates of differential
heritability (Abst). Behavior Genetics, 32, 462.
Davis, C.J., Fisher, S.E., Franks, C., MacPhie,
I.L., Gayan, J., Smith, S.D., Cardon, L.R., Pennington, B.F.,
Olson, R.K., Monaco, A.P. & DeFries, J.C. (2002). Bivariate
linkage analyses for reading difficulties and rapid naming (Abst.).
Behavior Genetics, 32, 462.
Fisher, S.E., Franks, C., Marlow, A.F., MacPhie,
I.L., Newbury, D.F., Cardon, L.R., Ishikawa-Brush, Y., Richardson,
A.J., Talcott, J.B., Gayan, J., Olson, R.K., Pennington, B.F.,
Smith, S.D., DeFries, J.C., Stein, J.F., & Monaco, A.P.
(2002). Quantitative trait analysis of the entire genome in
large samples of dyslexia sib-pairs from the UK and US (Abst).
Behavior Genetics, 32, 464.
Gayan, J.D., Kaplan, D.E., Ahn, J., Won, T.W.,
Pauls, D., Olson, R.K., DeFries, J.C., Wood, F., Pennington,
B.F., Page, G.P., Smith, S.D., & Gruen, J.R. (2002). Fine
mapping linkage and association analyses of reading disability
in the 6p21.3-22 region (Abst.). Behavior Genetics, 32, 465-466.
Olson, R.K. (2002). Genetic and environmental
influences on reading and related cognitive skills. Dyslexi,
4, 10-16.
Gayan, J., & Olson, R.K. (in press). Genetic
and environmental influences on individual differences in printed
word recognition. Journal of Experimental Child Psychology.
Recent Chapters:
Olson, R.K., Forsberg, H., Gayan, J., & DeFries, J.C.
(1999). A behavioral-genetic analysis of reading disabilities
and component processes. In R.M. Klein & P.A. McMullen
(Eds.), Converging methods for understanding reading and dyslexia
(pp. 133-153). Cambridge Mass.: MIT Press.
Olson, R.K. (2000). Genes, environment, and learning
disabilities. In R. S. Sternberg and L. Spear-Swerling (Eds.),
Perspectives on learning disabilities. Westview/Harper Collins.
Olson, R.K., & Gayan, J. (2001). Brains, Genes,
and Environment in Reading Development. In S. Newman & D.
Dickinson (Eds.). Handbook of early literacy development (pp.
81-96). New York: Guilford Publications, Inc.
Lyon, G.R., Fletcher, J.M., Shaywitz, S.E., Shaywitz,
B.A., Torgesen, J.K., Wood, F.B., Schulte, A., & Olson,
R.K. (2001). Rethinking learning disabilities. In C.E. Finn,
A.J. Rotherham, & C.R. Hokanson Jr. (Eds.), Rethinking special
education for a new century (pp. 259-287). Progressive Policy
Institute and the Thomas B. Fordham Foundation.
Compton, D.L., Davis, C.J., DeFries, J.C., Gayan,
J., & Olson, R.K. (2001). Genetic and environmental influences
on reading and RAN: An overview of results from the Colorado
Twin Study. In M. Wolf (Ed.), Conference proceedings of the
Dyslexia Research Foundation Conference in Extraordinary Brain
Series: Time, fluency, and developmental dyslexia (pp. 277-303).
Baltimore MD: York Press.
Olson, R.K. (2002). Phoneme awareness and reading,
from the old to the new millenium. In E. Hjelmquist and C. von
Euler (Eds.), Dyslexia and literacy: A tribute to Ingvar Lundberg
(pp. 100-116). London: Whurr Publishers.
Willcutt, E.G., DeFries, J.C., Pennington, B.F.,
Smith, S.D., Cardon, L.R., & Olson, R.K. (2003). Genetic
etiology of comorbid reading difficulties and ADHD. In R. Plomin,
J.C. DeFries, I.W. Craig, & P. McGuffin (Eds.), Behavioral
Genetics in the Postgenomic Era (227-246). Washington D.C.:
American Psychological Association.
Fletcher, J.M., Lyon, R., Barnes, M., Stuebing,
K.K., Francis, D.J., Olson, R.K., Shaywitz, S.E., & Shaywitz,
B.A. (2002). Classification of learning disabilities: An evidence
based evaluation. In R. Bradley, L. Danielson, and D.P. Hallahan
(Eds.), Identification of learning disabilities - research to
practice (pp. 185-250). Mahwah, NJ: Erlbaum.
Olson, R.K. (in press). Genetic?? and environmental
influences on the development of reading and related cognitive
skills. In R.M. Joshi & P.G. Aaron (Eds.), Handbook of Orthography
and Literacy. Mahwah, NJ: Laurence Erlbaum Associates.