Open Peer Commentary
Genetic explanations of environment explain little
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- 19 May 2011, pp. 395-396
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Have four module and eat it too!
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- 19 May 2011, p. 561
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In what context is latent inhibition relevant to the symptoms of schizophrenia?
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- 19 May 2011, pp. 28-29
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Optimality and constraint
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- 19 May 2011, pp. 222-223
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Types of optimality: Who is the steersman?
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- 19 May 2011, pp. 223-224
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Gestures, persons and communication: Sociocognitive factors in the development and evolution of linguistic abilities
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- 19 May 2011, pp. 562-563
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Novelty value in associative learning
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- 19 May 2011, p. 29
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“Significant and substantial” or minor and unreliable genetic influences on measures of the environment?
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- 19 May 2011, pp. 396-397
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Schizophrenia and stored memories: Left hemisphere dysfunction after all?
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- 19 May 2011, p. 30
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Planning and the brain
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- 19 May 2011, pp. 563-564
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There is indeed no substitute for multivariate genetic and environmental analyses
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- 19 May 2011, p. 397
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Natural science, social science and optimality
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- 19 May 2011, pp. 224-225
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The role of long-term memory (LTM) and monitoring in schizophrenia: Multiple functions
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- 19 May 2011, pp. 30-31
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Obfuscation of interaction
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- 19 May 2011, pp. 397-398
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Why optimality is not worth arguing about
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- 19 May 2011, p. 225
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If you've got it, why not flaunt it? Monkeys with Broca's area but no syntactical structure to their vocal utterances
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- 19 May 2011, p. 564
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Genes and environment: A complicated affair
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- Published online by Cambridge University Press:
- 19 May 2011, p. 398
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The example of psychology: Optimism, not optimality
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- 19 May 2011, pp. 225-226
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A cardinal principle for neuropsychology, with implications for schizophrenia and mania
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- 19 May 2011, pp. 31-32
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Neurobiology and language acquisition: Continuity and identity
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- 19 May 2011, p. 565
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