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Genetics and intelligence: What's new?
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scholarly article
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title
Genetics and intelligence: What's new?
(English)
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author
Robert Plomin
series ordinal
1
object named as
Robert Plomin
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Stephen Petrill
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2
object named as
Stephen A. Petrill
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publication date
January 1997
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published in
Intelligence
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volume
24
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page(s)
53-77
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issue
1
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cites work
The genetic correlation between intelligence and speed of information processing
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Diet, genetics, and mental retardation interaction between phenylketonuric heterozygous mother and fetus to produce nonspecific diminution of IQ: Evidence in support of the justification hypothesis
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Familial studies of intelligence: a review
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Quantitative trait locus for reading disability on chromosome 6
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Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
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GENETICS AND INTELLIGENCE: A REVIEW.
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Apolipoprotein e4 allele and cognitive decline in elderly men.
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Psychiatric Disorders in Foster Home Reared Children of Schizophrenic Mothers
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Modeling IQ change: evidence from the Texas Adoption Project
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Alzheimer's disease
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Association and linkage: complementary strategies for complex disorders
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The independent prediction of general intelligence by elementary cognitive tasks: genetic and environmental influences
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The genetic and environmental variance underlying elementary cognitive tasks
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Why are children in the same family so different from one another?
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Multivariate behavioral genetic analysis of twin data on scholastic abilities
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DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) Project
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The genetic basis of complex human behaviors
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Variability and stability in cognitive abilities are largely genetic later in life
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Developmental theories for the 1990s: development and individual differences
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Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14
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Survey of expert opinion on intelligence and aptitude testing
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The heritability of memory in the Western Reserve Twin Project
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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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Partitioning environmental and genetic contributions to behavioral development
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DOI
10.1016/S0160-2896(97)90013-1
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