80. Needleman, H. L., McFarland, C., Ness, R. B., Fienberg, S. E. & Tobin, M. J., Bone lead levels in adjudicated delinquents: A case control study. Neurotoxicol. Teratol. 24, 711–717 (2002).

81. Needleman, H. L., Riess, J. A., Tobin, M. J., Biesecker, G. E. & Greenhouse, J. B., Bone Lead Le- vels and Delinquent Behavior. JAMA 275, 363–369 (1996).

82. Nevin, R., How Lead Exposure Relates to Temporal Changes in IQ, Violent Crime, and Unwed Pregnancy. Environ. Res. 83, 1–22 (2000).

83. Nevin, R., Understanding international crime trends: The legacy of preschool lead exposure. Environ. Res. 104, 315–336 (2007).

84. Pollmer, U. Umweltgifte – Blei im Blut macht Kinder aggressiv. Deutschlandfunk Kultur Available at: https://www.deutschlandfunkkultur.de/umwelt gifte-blei-im-blut-macht-kinder-aggressiv.993.de. html?dram: article_id=303207. (Accessed: 11th October 2018).

85. Wright, J. P. et al., Association of Prenatal and Childhood Blood Lead Concentrations with Criminal Arrests in Early Adulthood. PLOS Med. 5, e101 (2008).

По ту сторону генов и образования

86. Caudill, M. A., Strupp, B. J., Muscalu, L., Nevins, J. E. H. & Canfield, R. L. Maternal choline supplementation during the third trimester of pregnancy improves infant information processing speed: a randomized, double-blind, controlled feeding study. FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol. 32, 2172–2180 (2018).

87. Cheng, R.-K., MacDonald, C. J., Williams, C. L. & Meck, W. H., Prenatal choline supplementation alters the timing, emotion, and memory performance (TEMP) of adult male and female rats as indexed by differential reinforcement of low-rate schedule behavior. Learn. Mem. 15, 153–162 (2008).

88. Glenn, M. J. et al., Prenatal choline availability modulates hippocampal neurogenesis and neurogenic responses to enriching experiences in adult female rats. Eur. J. Neurosci. 25, 2473–2482 (2007).

89. Polidano, C., Zhu, A. & Bornstein, J. C., The relation between cesarean birth and child cognitive development. Sci. Rep. 7, 11483 (2017).

90. Pyapali, G. K., Turner, D. A., Williams, C. L., Meck, W. H. & Swartzwelder, H. S., Prenatal dietary choline supplementation decreases the threshold for induction of long-term potentiation in young adult rats. J. Neurophysiol. 79, 1790–1796 (1998).

91. Rohrer, J. M., Egloff, B. & Schmukle, S. C., Examining the effects of birth order on personality. Proc. Natl. Acad. Sci. U. S. A. 112, 14224–14229 (2015).

Эффект Флинна

92. Amelang, M. et al., Differentielle Psychologie und Persönlichkeitsforschung (Kohlhammer, 2006).

93. Flynn, J. R., Are we getting smarter? Rising IQ in the twenty-first century (Cambridge University Press, 2012).

94. Flynn, J. R., Massive IQ gains in 14 nations: What IQ tests really measure. Psychol. Bull. 101, 171–191 (1987).

95. Maher, B., Poll results: look who’s doping. Nature 452, 674–675 (2008).

96. Maier, L J., Ferris, J. A. & Winstock, A. R., Pharmacological cognitive enhancement among non-ADHD individuals – A cross-sectional study in 15 countries. Int. J. Drug Policy 58, 104–112 (2018).

97. Mingroni, M. A., Resolving the IQ paradox: heterosis as a cause of the Flynn effect and other trends. Psychol. Rev. 114, 806–829 (2007).

98. Mingroni, M. A., The Secular Rise in IQ: Gi- ving Heterosis a Closer Look. Intelligence 32, 65–83 (2004).

99. Nettelbeck, T. & Wilson, C. The Flynn effect: Smarter not faster. Intelligence 32, 85–93 (2004).

100. Pietschnig, J. & Voracek, M. One Century of Global IQ Gains: A Formal Meta-Analysis of the Flynn Effect (1909–2013). Perspect. Psychol. Sci. J. Assoc. Psychol. Sci. 10, 282–306 (2015).

101. Sahakian, B. & Morein-Zamir, S., Professor’s little helper. Nature (2007). doi: 10.1038/4501157a.

102. Trahan, L. H., Stuebing, K. K., Fletcher, J. M. & Hiscock, M., The Flynn effect: a meta-analysis. Psychol. Bull. 140, 1332–1360 (2014).

103. Wongupparaj, P., Kumari, V. & Morris, R. G., A Cross-Temporal Meta-Analysis of Raven’s Progressive Matrices: Age groups and developing versus developed countries. Intelligence 49, 1–9 (2015).

104. Wongupparaj, P., Wongupparaj, R., Kumari, V. & Morris, R. G., The Flynn effect for verbal and visuospatial short-term and working memory: A cross-temporal meta-analysis. Intelligence 64, 71–80 (2017).

«Умные» препараты

105. Bagot, K. S. & Kaminer, Y., Efficacy of stimulants for cognitive enhancement in non-attention deficit hyperactivity disorder youth: a systematic review. Addict. Abingdon Engl. 109, 547–557 (2014).

106. Elliott, R. et al., Effects of methylphenidate on spatial working memory and planning in healthy young adults. Psychopharmacology (Berl.) 131, 196–206 (1997).

107. Killgore, W. D. S., McBride, S. A., Killgore, D. B. & Balkin, T. J., The effects of caffeine, dextroamphetamine, and modafinil on humor appreciation during sleep deprivation. Sleep 29, 841–847 (2006).

Стимуляция мозга магнитным стержнем

108. Bütefisch, C. M., Khurana, V., Kopylev, L. & Cohen, L. G., Enhancing encoding of a motor memory in the primary motor cortex by cortical stimulation. J. Neurophysiol. 91, 2110–2116 (2004).

109. Luber, B. & Lisanby, S. H., Enhancement of human cognitive performance using transcranial magnetic stimulation (TMS). NeuroImage 85 Pt 3, 961–970 (2014).

Энергозатратная вспышка озарения

110. Bikson, M. et al., Safety of Transcranial Direct Current Stimulation: Evidence Based Update 2016. Brain Stimul. Basic Transl. Clin. Res. Neuromodulation 9, 641–661 (2016).

111. Clark, V. P. et al., TDCS Guided using fMRI Significantly Accelerates Learning to Identify Concealed Objects. Neuroimage 59, 117–128 (2012).

112. Coffman, B. A., Clark, V. P. & Parasuraman, R., Battery powered thought: enhancement of attention, learning, and memory in healthy adults using transcranial direct current stimulation. NeuroImage 85 Pt 3, 895–908 (2014).

113. Gooneratne, I. K. et al., Comparing neurostimulation technologies in refractory focal-onset epilepsy. J. Neurol. Neurosurg. Psychiatry 87, 1174–1182 (2016).

114. Kuo, M.-F. & Nitsche, M. A., Exploring prefrontal cortex functions in healthy humans by transcranial electrical stimulation. Neurosci. Bull. 31, 198–206 (2015).

115. Matsumoto, H. & Ugawa, Y., Adverse events of tDCS and tACS: A review. Clin.

116. Neurophysiol. Pract. 2, 19–25 (2017). Steenbergen, L. et al., ›Unfocus‹ on foc.us: commercial tDCS headset impairs working memory. Exp. Brain Res. 234, 637–643 (2016).

117. Tanaka, S., Hanakawa, T., Honda, M. & Watanabe, K., Enhancement of pinch force in the lower leg by anodal transcranial direct current stimulation. Exp.

118. Brain Res. Exp. Hirnforsch. Exp. Cerebrale 196, 459–465 (2009).

Красный свет для всезнаек

119. Barrett, D. W. & Gonzalez-Lima, F., Transcranial infrared laser stimulation produces beneficial cognitive and emotional effects in humans. Neuroscience 230, 13–23 (2013).

120. Gonzalez-Lima, F. & Barrett, D. W., Augmentation of cognitive brain functions with transcranial lasers. Front. Syst. Neurosci. 8, (2014).

121. Hamblin, M. R. & Demidova, T. N., Mechanisms of