Мартин Модер - Генный апгрейд. Почему мы пользуемся устаревшей моделью тела в новой модели мира и как это исправить

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 low level light therapy – an introduction. Proc SPIE, Vol 6140, art. no. 610011-12 (2006).

122. Karu, T. I., Pyatibrat, L. V., Kolyakov, S. F. & Afanasyeva, N. I., Absorption measurements of a cell monolayer relevant to phototherapy: reduction of cytochrome c oxidase under near IR radiation. J. Photochem. Photobiol. B 81, 98–106 (2005).

123. Michalikova, S., Ennaceur, A., van Rensburg, R. & Chazot, P. L., Emotional responses and memory performance of middle-aged CD1 mice in a 3D maze: effects of low infrared light. Neurobiol. Learn. Mem. 89, 480–488 (2008).

124. Mochizuki-Oda, N. et al., Effects of near-infra-red laser irradiation on adenosine triphosphate and adenosine diphosphate contents of rat brain tissue. Neurosci. Lett. 323, 207–210 (2002).

125. Pastore, D., Greco, M. & Passarella, S., Specific helium-neon laser sensitivity of the purified cytochrome c oxidase. Int. J. Radiat. Biol. 76, 863–870 (2000).

126. Rojas, J. C., Bruchey, A. K. & Gonzalez-Lima, F., Low-level light therapy improves cortical metabolic capacity and memory retention. J. Alzheimers Dis. JAD 32, 741–752 (2012).

127. Uozumi, Y. et al., Targeted increase in cerebral blood flow by transcranial near-infrared laser irradiation. Lasers Surg. Med. 42, 566–576 (2010).

128. Wang, X. et al., Up-regulation of cerebral cytochrome-c-oxidase and hemodynamics by transcranial infrared laser stimulation: A broadband near-infrared spectroscopy study. J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab. 37, 3789–3802 (2017).

129. Wong-Riley, M. T. T. et al., Photobiomodulation directly benefits primary neurons functionally inactivated by toxins: role of cytochrome c oxidase. J. Biol. Chem. 280, 4761–4771 (2005).

ГЛАВА 3. Биология человеческого поведения

130. Brasil-Neto, J. P., Pascual-Leone, A., Valls-Solé, J., Cohen, L. G. & Hallett, M., Focal transcranial magnetic stimulation and response bias in a forced-choice task. J. Neurol. Neurosurg. Psychiatry 55, 964–966 (1992).

131. Libet, B., Unconscious cerebral initiative and the role of conscious will in voluntary action. Behav. Brain Sci. 8, 529–539 (1985).

Чумовой пир на весь мир

Бессознательный страх перед инфекциями

132. Michel, J. F., Parasitological Significance of Bovine Grazing Behaviour. Nature 175, 1088–1089 (1955).

133. Rozin, P., Millman, L. & Nemeroff, C., Operation of the laws of sympathetic magic in disgust and other domains. J. Pers. Soc. Psychol. 50, 703–712 (1986).

Ненависть к чужакам и паразиты

134. Eskine, K. J., Kacinik, N. A. & Prinz, J. J., A bad taste in the mouth: gustatory disgust influences moral judgment. Psychol. Sci. 22, 295–299 (2011).

135. Faulkner, J., Schaller, M., Park, J. H. & Duncan, L. A., Evolved Disease-Avoidance Mechanisms and Contemporary Xenophobic Attitudes. Group Process. Intergroup Relat. 7, 333–353 (2004).

136. Fincher, C. L., Thornhill, R., Murray, D. R. & Schaller, M., Pathogen prevalence predicts human cross-cultural variability in individualism/collectivism. Proc. Biol. Sci. 275, 1279–1285 (2008).

137. Goodall, J., Social rejection, exclusion, and shunning among the Gombe chimpanzees. Ethol. Sociobiol. 7, 227–236 (1986).

138. Horberg, E. J., Oveis, C., Keltner, D. & Cohen, A. B., Disgust and the moralization of purity. J. Pers. Soc. Psychol. 97, 963–976 (2009).

139. Letendre, K., Fincher, C. L. & Thornhill, R., Does infectious disease cause global variation in the frequency of intrastate armed conflict and civil war? Biol. Rev. Camb. Philos. Soc. 85, 669–683 (2010).

140. Markel, H. & Stern, A. M., The Foreignness of Germs: The Persistent Association of Immigrants and Disease in American Society. Milbank Q. 80, 757–788 (2002).

141. Mortensen, C. R., Becker, D. V., Ackerman, J. M., Neuberg, S. L. & Kenrick, D. T., Infection Breeds Reticence: The Effects of Disease Salience on Self-Perceptions of Personality and Behavioral Avoidance Tendencies. Psychol. Sci. 21, 440–447 (2010).