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Published on: August 12, 2019
A conceptual contribution to battles in the brain
1Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
Imbalanced genomic imprinting in the brain may explain autism and schizophrenia. This study critiques that model and proposes alternative avenues focusing on imprinted genes and social behavior development.
Area of Science:
- Neurogenetics
- Developmental Psychology
- Psychiatric Genetics
Background:
- The Badcock and Crespi hypothesis proposes that imbalanced genomic imprinting, specifically an unequal expression of paternal and maternal genes in the brain, underlies autism and schizophrenia.
- This hypothesis suggests an extreme paternal gene expression leads to an "autistic" brain, while an extreme maternal expression results in a "schizophrenic" brain.
Purpose of the Study:
- To critically evaluate the conceptual framework of the Badcock and Crespi imprinting hypothesis.
- To propose an alternative model for investigating the role of imprinted genes in social behavior development.
- To identify specific developmental behaviors as potential research areas for understanding imprinting effects.
Main Methods:
- Conceptual analysis and critique of the existing hypothesis.
- Development of an alternative theoretical model.
- Literature review focusing on imprinted genes and social behavior.
Main Results:
- The Badcock and Crespi model is criticized for its reliance on a problematic distinction between physical and mental phenomena.
- An alternative model is presented, offering a potentially more robust framework for research.
- The development of crying, reactive crying, and collaborative behaviors are highlighted as promising research avenues.
Conclusions:
- The original imprinting hypothesis for autism and schizophrenia faces significant conceptual challenges.
- A revised approach focusing on imprinted genes and the development of social behaviors may yield more fruitful insights.
- Investigating early social behaviors like crying offers a promising pathway to understanding the neurodevelopmental impact of genomic imprinting.
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