Contents
Open Peer Commentary
Evaluation of gene–environment interaction requires more precise description of both environment and behavior
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- 04 February 2010, pp. 24-25
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Networks with evolutionary potential
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- 04 February 2010, pp. 376-377
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Parapsychology's choice
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- 04 February 2010, pp. 572-573
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Chaos in brains: Fad or insight?
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- 04 February 2010, pp. 180-181
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Connectionist models as neural abstractions
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- 04 February 2010, pp. 181-182
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Ethological invariants: Boxes, rubber bands, and biological processes
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- 04 February 2010, pp. 377-378
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How to dismiss evidence without really trying
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- 04 February 2010, pp. 573-574
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On nonheritable genetic differences
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- 04 February 2010, p. 25
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A cumulative model of within-family differences
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- 04 February 2010, pp. 25-26
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Chaos can be overplayed
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- 04 February 2010, pp. 182-183
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Struggle for reason
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- 04 February 2010, pp. 574-575
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More than meets the eye
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- 04 February 2010, pp. 378-379
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Unconfounding genetic and nonshared environmental effects
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- 04 February 2010, pp. 26-27
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The compleat visual system: From input to output
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- 04 February 2010, pp. 379-380
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Parapsychology on the couch
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- 04 February 2010, pp. 575-576
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Cognition as self–organizing process
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- 04 February 2010, p. 183
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Why parapsychology cannot become a science
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- 04 February 2010, pp. 576-577
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Authors' Response
Physiology: Is there any other game in town?
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- 04 February 2010, pp. 183-195
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Open Peer Commentary
The nervous system/behavior interface: Levels of organization and levels of approach
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- 04 February 2010, pp. 380-381
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Secular change in the relative influence of G, E1, and E2 on cognitive abilities
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- 04 February 2010, pp. 27-28
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