Воля и самоконтроль. Как гены и мозг мешают нам бороться с соблазнами — страница extra из 64

Комментарии

Глава 1

1

Bridgett D. J., Burt N. M., Edwards E. S., Deater-Deckard K. (2015) Intergenerational transmission of self-regulation: A multi-disciplinary review and integrative conceptual framework // Psychological Bulletin. 2015 May; 141 (3): 602-54.

2

Moffitt T. E., Arseneault L., Belsky D., Dickson N., Hancox R. J., Harrington H., Houts R., Poulton R., Roberts B. W., Ross S., Sears M. R., Thomson W. M., Caspi A. A gradient of childhood self-control predicts health, wealth, and public safety // Proceedings of the National Academy of Sciences of the United States of America. 2011 Feb 15; 108 (7): 2693-8.

3

Roberts B. W., Kuncel N. R., Shiner R., Caspi A., Goldberg L. R. The Power of Personality: The Comparative Validity of Personality Traits, Socioeconomic Status, and Cognitive Ability for Predicting Important Life Outcomes // Perspectives on Psychological Science. 2007 Dec; 2 (4): 313-45.

4

Moeller F. G., Barratt E. S., Dougherty D. M., Schmitz J. M., Swann A. C. Psychiatric aspects of impulsivity // The American Journal of Psychiatry. 2001 Nov; 158 (11): 1783-93.

5

Chamorro J., Bernardi S., Potenza M. N., Grant J. E., Marsh R., Wang S., Blanco C. Impulsivity in the general population: a national study // Journal of Psychiatric Research. 2012 Aug; 46 (8): 994-1001.

6

Patton J. H., Stanford M. S., Barratt E. S. Factor structure of the Barratt impulsiveness scale // Journal of Clinical Psychology. 1995 Nov; 51 (6):768-74.

7

Ениколопов С. Н., Медведева Т. И. Апробация русскоязычной версии методики "шкала импульсивности Барратта" (BIS-11). [Электронный ресурс] // Психология и право. 2015 (5). № 3. С. 75–89.

8

Malloy-Diniz L. F. et al. Normative data of the Barratt Impulsiveness Scale 11 (BIS-11) for Brazilian adults // Revista Brasileira De Psiquiatria. 2015 Jul-Sep; 37 (3): 245-8.

9

Spinella M. Normative data and a short form of the Barratt Impulsiveness Scale // International Journal of Neuroscience. 2007 Mar; 117 (3): 359-68.

10

Stanford M. S., Mathias C. W., Dougherty D. M., Lake S. L., Anderson N. E., Patton J. H. Fifty years of the Barratt Impulsiveness Scale: An update and review // Personality and Individual Differences. 2009 Oct; 47 (5): 385-95.

11

Ellouze F., Ghaffari O., Zouari O., Zouari B., M'rad M. F. [Validation of the dialectal Arabic version of Barratt's impulsivity scale, the BIS-11]. [Article in French] // L'Encéphale. 2013 Feb; 39 (1): 13-8.

12

Cyders M. A, Smith G. T. Emotion-based dispositions to rash action: positive and negative urgency // Psychological Bulletin. 2008 Nov; 134 (6): 807-28.

Глава 2

1

Baumeister R. F., Bratslavsky E., Muraven M., Tice D. M. Ego depletion: is the active self a limited resource? // Journal of Personality and Social Psychology. 1998 May; 74 (5): 1252-65.

2

Muraven M., Collins R. L., Nienhaus K. Self-control and alcohol restraint: an initial application of the self-control strength model // Psychology of Addictive Behaviors. 2002 Jun; 16 (2): 113-20.

3

Muraven M., Tice D. M., Baumeister R. F. Self-control as limited resource: regulatory depletion patterns // Journal of Personality and Social Psychology. 1998 Mar; 74 (3): 774-89.

4

Gordijn E. H., Hindriks I., Koomen W., Dijksterhuis A., Van Knippenberg A. Consequences of stereotype suppression and internal suppression motivation: a self-regulation approach // Personality and Social Psychology Bulletin. 2004 Feb; 30 (2): 212-24.

5

Finkel E. J., Campbell W. K. Self-control and accommodation in close relationships: an interdependence analysis // Journal of Personality and Social Psychology. 2001 Aug; 81 (2): 263-77.

6

Vohs K. D., Baumeister R. F., Ciarocco N. J. Self-regulation and self-presentation: regulatory resource depletion impairs impression management and effortful self-presentation depletes regulatory resources // Journal of Personality and Social Psychology. 2005 Apr; 88 (4): 632-57.

7

Carter E. C., McCullough M. E. Publication bias and the limited strength model of self-control: has the evidence for ego depletion been overestimated? // Frontiers in Psychology. 2014 Jul 30; 5: 823.

8

Hagger., M. S. et al. A multilab preregistered replication of the ego-depletion effect // Perspectives on Psychological Science. 2016 Jul 29; 11 (4): 546-73.

9

Berg J. M., Tymoczko J. L., Stryer L. // Biochemistry. 5th edition. New York: W. H. Freeman; 2002.

10

McNay E. C., McCarty R. C., Gold P. E. Fluctuations in brain glucose concentration during behavioral testing: dissociations between brain areas and between brain and blood // Neurobiology of Learning and Memory. 2001 May; 75 (3): 325-37.

11

Scholey A. B., Harper S., Kennedy D. O. Cognitive demand and blood glucose // Physiology amp; Behavior. 73 (2001) 585-92.

12

Manning R. T. The Serial Sevens Test // Archives of Internal Medicine. 1982; 142 (6): 1192.

13

Benton D., Owens D. S., Parker P. Y. Blood glucose influences memory and attention in young adults // Neuropsychologia. 1994 May; 32 (5): 595–607.

14

Smid H. G., Trümper B. G., Pottag G., Wagner K., Lobmann R., Scheich H., Lehnert H., Heinze H. J. Differentiation of hypoglycaemia induced cognitive impairments. An electrophysiological approach // Brain. 1997 Jun; 120 (Pt 6): 1041-56.

15

Danziger S., Levav J., Avnaim-Pesso L. Extraneous factors in judicial decisions // Proceedings of the National Academy of Sciences of the United States of America. 2011 Apr 26; 108 (17): 6889-92.

16

Gailliot M. T., Baumeister R. F., DeWall C. N., Maner J. K., Plant E. A., Tice D. M., Brewer L. E., Schmeichel B. J. Self-control relies on glucose as a limited energy source: willpower is more than a metaphor // Journal of Personality and Social Psychology. 2007 Feb; 92 (2): 325-36.

17

Baumeister R. F., Heatherton T. F., Tice D. M. (1994). Losing control: How and why people fail at self-regulation. San Diego., CA: Academic Press.

18

Donohoe R. T., Benton D. Cognitive functioning is susceptible to the level of blood glucose // Psychopharmacology (Berlin). 1999 Aug; 145 (4): 378-85.

19

Allen J. B., Gross A. M., Aloia M. S., Billingsley C. The effects of glucose on nonmemory cognitive functioning in the elderly // Neuropsychologia. 1996 May; 34 (5): 459-65.

20

Berman S. M., London E. D., Morgan M., Rapkin A. J. Elevated gray matter volume of the emotional cerebellum in women with premenstrual dysphoric disorder // Journal of Affective Disorders. 2013 Apr 5; 146 (2): 266-71.

21

Zarei S., Mosalanejad L., Ghobadifar M. A. Blood glucose levels., insulin concentrations., and insulin resistance in healthy women and women with premenstrual syndrome: a comparative study // International Journal of Clinical and Experimental Medicine. 2013 Jun; 40 (2): 76–82.

Глава 3

1

Olds J., Milner P. Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain // Journal of Comparative Psychology. 1954 Dec; 47 (6): 419-27.

2

Jon H. Kaas. Neocortex in early mammals and its subsequent variations // Annals of the New York Academy of Sciences. 2011 Apr; 1225: 28–36.

3

Fazio R. H., Jackson J. R., Dunton B. C., Williams C. J. Variability in automatic activation as an unobtrusive measure of racial attitudes: a bona fide pipeline? // Journal of Personality and Social Psychology. 1995 Dec; 69 (6): 1013-27.

4

Payne B. K. Prejudice and perception: the role of automatic and controlled processes in misperceiving a weapon // Journal of Personality and Social Psychology. 2001 Aug; 81 (2): 181-92.

5

Amodio D. M., Harmon-Jones E., Devine P. G., Curtin J. J., Hartley S. L., Covert A. E. Neural signals for the detection of unintentional race bias // Psychological Science. 2004 Feb; 15 (2): 88–93.

6

Amodio D. M., Devine P. G., Harmon-Jones E. Individual differences in the regulation of intergroup bias: the role of conflict monitoring and neural signals for control // Journal of Personality and Social Psychology. 2008 Jan; 94 (1): 60–74.

7

Brass M., Haggard P. To do or not to do: the neural signature of self-control // Journal of Neuroscience. 2007 Aug 22; 27 (34): 9141-5.

8

Dreher J. C., Koechlin E., Ali S. O., Grafman J. The roles of timing and task order during task switching // NeuroImage. 2002 Sep; 17 (1): 95-109.

9

Kühn S., Haggard P., Brass M. Intentional inhibition: how the "veto-area" exerts control // Human Brain Mapping. 2009 Sep; 30 (9): 2834-43.

10

Lynn M. T., Muhle-Karbe P. S., Brass M. Controlling the self: the role of the dorsal frontomedian cortex in intentional inhibition // Neuropsychologia. 2014 Dec; 65: 247-54.

11

Boccardi E., Della Sala S., Motto C., Spinnler H. Utilisation behaviour consequent to bilateral SMA softening // Cerebral Cortex. 2002 Jun; 38 (3): 289–308.

12

Wright P., He G., Shapira N. A., Goodman W. K., Liu Y. Disgust and the insula: fMRI responses to pictures of mutilation and contamination // Neuroreport. 2004 Oct 25;15 (15): 2347-51.

13

Wicker B., Keysers C., Plailly J., Royet J. P., Gallese V., Rizzolatti G. Both of us disgusted in My insula: the common neural basis of seeing and feeling disgust // Neuron. 2003 Oct 30; 40 (3): 655-64.

14

Naqvi N. H., Rudrauf D., Damasio H., Bechara A. Damage to the insula disrupts addiction to cigarette smoking // Science. 2007 Jan 26; 315 (5811): 531-4.

15

Damasio A. R., Grabowski T. J., Bechara A., Damasio H., Ponto L. L., Parvizi J., Hichwa R. D. Subcortical and cortical brain activity during the feeling of self-generated emotions // Nature Neuroscience. 2000 Oct; 3 (10): 1049-56.

16

Zhang Y. E., Landback P., Vibranovski M. D., Long M. Accelerated recruitment of new brain development genes into the human genome // PLoS Biology. 2011 Oct; 9 (10): e1001179.

17

Barker A. T., Jalinous R., Freeston I. L. Non-invasive magnetic stimulation of human motor cortex // Lancet. 1985 May 11; 1 (8437): 1106-7.

18

Figner B., Knoch D., Johnson E. J., Krosch A. R., Lisanby S. H., Fehr E., Weber E. U. Lateral prefrontal cortex and self-control in intertemporal choice // Nature Reviews Neurosciene. 2010 May; 13 (5): 538-9.

19

Heatherton T. F. Neuroscience of Self and Self-Regulation // Annual Reviews of Psychology. 2011; 62: 363–390.

20

Saver J. L., Damasio A. R. Preserved access and processing of social knowledge in a patient with acquired sociopathy due to ventromedial frontal damage // Neuropsychologia. 1991; 29 (12): 1241-9.

21

Stuss D. T., Benson D. F. (1986). The frontal lobes. New York: Raven Press.

22

Hare T. A., Camerer C. F., Rangel A. Self-control in decision-making involves modulation of the vmPFC valuation system // Science. 2009 May 1; 324 (5927): 646-8.

23

Ballard I. C., Murty V. P., Carter R. M., MacInnes J. J., Huettel S. A., Adcock R. A. Dorsolateral Prefrontal Cortex Drives Mesolimbic Dopaminergic Regions to Initiate Motivated Behavior // Journal of Neuroscience. 2011 Jul 13; 31 (28): 10340-10346.

24

Wallis J. D., Miller E. K. Neuronal activity in primate dorsolateral and orbital prefrontal cortex during performance of a reward preference task // European Journal of Neuroscience. 2003 Oct; 18 (7): 2069-81.

25

Schiller B., Gianotti L. R., Nash K., Knoch D. Individual differences in inhibitory control-relationship between baseline activation in lateral PFC and an electrophysiological index of response inhibition // Cerebral Cortex. 2014 Sep; 24 (9): 2430-5.

26

Gable P. A., Mechin N. C., Hicks J. A., Adams D. L. Supervisory control system and frontal asymmetry: neurophysiological traits of emotion-based impulsivity // SCAN. 2015; 10 (10): 1310–1315.

27

Krmpotich T. D., Tregellas J. R., Thompson L. L., Banich M. T., Klenk A. M., Tanabe J. L. Resting-state activity in the left executive control network is associated with behavioral approach and is increased in substance dependence // Drug and alcohol dependence. 2013 Apr 1; 129 (1–2): 1–7.

28

Князев Г. Г., Слободская Е. Р., Савостьянов А. Н., Рябиченко Т. И., Шушлебина О. А., Левин Е. А. Активация и торможение поведения как основа индивидуальных различий // Психологический журнал. 2004. 25 (4)., 82–94.

29

Kühn S. et al. The neural basis of video gaming // Translational Psychiatry. 2011 Nov 15; 1: e53.

30

Berridge K. C., Kringelbach M. L. Pleasure systems in the brain // Neuron. 2015 May 6; 86 (3): 646-64.

31

Demos K. E., Kelley W. M., Heatherton T. F. Dietary restraint violations influence reward responses in nucleus accumbens and amygdala // Journal of Cognitive Neuroscience. 2011 Aug; 23 (8): 1952-63.

32

Stoeckel L. E., Weller R. E., Cook E. W. III., Twieg D. B., Knowlton R. C., Cox., J. E. Widespread reward-system activation in obese women in response to pictures of high-calorie foods // NeuroImage. 2008. 41 (2)., 636–647.

33

Finn P. R. Motivation., working memory., and decision making: a cognitive-motivational theory of personality vulnerability to alcoholism // Behavioral and Cognitive Neuroscience Reviews. 2002 Sep; 1 (3): 183–205.

34

Shiv B., Fedorikhin A. Heart and mind in conflict: The interplay of affect and cognition in consumer decision making // Journal of Consumer Research., 1999; 26: 278–292.

35

Методика определения кратковременной памяти // Альманах психологических тестов. М., 1995. С. 88.

36

Методика "Оперативная память" // Там же. С. 89.

37

Klingberg T., Forssberg H., Westerberg H. Training of working memory in children with ADHD // Journal of Clinical and Experimental Neuropsychology. 2002 Sep; 24 (6): 781-91.

38

Johnson M. K., McMahon R. P., Robinson B. M., Harvey A. N., Hahn B., Leonard C. J., Luck S. J., Gold J. M. The relationship between working memory capacity and broad measures of cognitive ability in healthy adults and people with schizophrenia // Neuropsychology. 2013 Mar; 27 (2): 220-9.

39

Alloway T. P., Alloway R. G. Investigating the predictive roles of working memory and IQ in academic attainment // Journal of Experimental Child Psychology. 2010 May; 106 (1): 20-9.

40

Alloway T. P., Gathercole S. E., Kirkwood H., Elliott J. The cognitive and behavioral characteristics of children with low working memory // Child Development. 2009 Mar-Apr; 80 (2): 606-21.

Глава 4

1

Connolly., E. J., amp; Beaver., K. M. Examining the genetic and environmental influences on self-control and delinquency: Results from a genetically informative analysis of sibling pairs // Journal of Interpersonal Violence. 2004 Mar; 29 (4): 707–735.

2

Beaver., K. M., Eagle Schutt., J., Boutwell., B. B., Ratchford., M., Roberts., K., Barnes., J. C. Genetic and environmental influences on levels of self-control and delinquent peer affiliation: Results from a longitudinal sample of adolescent twins // Criminal Justice and Behavior 2008 Oct; 36 (1): 41–60.

3

Strauss., G. P., Frank., M. J., Waltz., J. A., Kasanova., Z., Herbener., E. S., Gold., J. M. Deficits in Positive Reinforcement Learning and Uncertainty-Driven Exploration are Associated with Distinct Aspects of Negative Symptoms in Schizophrenia // Biological Psychiatry 2011 Mar; 69 (5): 424–431.

4

Frank., M. J., Samanta., J., Moustafa., A. A., Sherman., S. J. Hold your horses: impulsivity., deep brain stimulation., and medication in parkinsonism // Science 2007 Nov; 318 (5854): 1309–1312.

5

Hegarty S. V., Sullivan A. M., O'Keeffe G. W. Midbrain dopaminergic neurons: a review of the molecular circuitry that regulates their development // Developmental Biology. 2013 Jul 15; 379 (2): 123-38

6

Berridge K. C., Schulkin J. Palatability shift of a salt-associated incentive during sodium depletion. The Quarterly Journal of Experimental Psychology // 1989 May; 41 (2): 121-38.

7

Schultz W., Apicella P., Ljungberg T. Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task // Journal of Neuroscience. 1993 Mar; 13 (3): 900-13.

8

Knutson B., Fong G. W., Adams C. M., Varner J. L., Hommer D. Dissociation of reward anticipation and outcome with event-related fMRI // NeuroReport. 2001 Dec 4; 12 (17): 3683-7.

9

Berridge K. C., Robinson T. E. What is the role of dopamine in reward: hedonic impact., reward learning., or incentive salience? // Brain Research Reviews. 1998 Dec; 28 (3): 309-69.

10

Hopson J. Behavioral Game Design // Gamasutra.Com. The Art and Business of Making Games. 2001 Apr 27. URL: http://www.gamasutra.com/ view/feature/131494/behavioral_game_design.php.

11

Beaver K. M., Wright J. P., DeLisi M., Walsh A., Vaughn M. G., Boisvert D., Vaske J. A gene x gene interaction between DRD2 and DRD4 is associated with conduct disorder and antisocial behavior in males // Behavioral and Brain Functions. 2007 Jun 22; 3: 30.

12

El-Faddagh M., Laucht M., Maras A., Vöhringer L., Schmidt M. H. Association of dopamine D4 receptor (DRD4) gene with attention-deficit/hyperactivity disorder (ADHD) in a high-risk community sample: a longitudinal study from birth to 11 years of age // Journal of Neural Transmission (Vienna). 2004 Jul; 111 (7): 883-9.

13

Faraone S. V., Doyle A. E., Mick E., Biederman J. Meta-analysis of the association between the 7-repeat allele of the dopamine D (4) receptor gene and attention deficit hyperactivity disorder // American Journal of Psychiatry. 2001 Jul; 158 (7): 1052-7.

14

Duan J., Wainwright M. S., Comeron J. M., Saitou N., Sanders A. R., Gelernter J., Gejman P. V. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor // Human Molecular Genetics. 2003 Feb 1; 12 (3): 205-16.

15

Cerasa A., Gioia M. C., Tarantino P., Labate A., Arabia G., Annesi G., Lanza P., Di Palma G., Blasi V., Quattrone A. The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals // Genes., Brain and Behavior. 2009 Jun; 8 (4): 459-63.

16

Neville M. J., Johnstone E. C., Walton R. T. Identification and characterization of ANKK1: a novel kinase gene closely linked to DRD2 on chromosome band 11q23.1 // Human Mutation. 2004 Jun; 23 (6): 540-5.

17

Pan Y. Q., Qiao L., Xue X. D., Fu J. H. Association between ANKK1 (rs1800497) polymorphism of DRD2 gene and attention deficit hyperactivity disorder: a meta-analysis // Neuroscience Letters. 2015 Mar 17; 590: 101-5.

18

Käenmäki M., Tammimäki A., Myöhänen T., Pakarinen K., Amberg C., Karayiorgou M., Gogos J. A., Männistö P. T. Quantitative role of COMT in dopamine clearance in the prefrontal cortex of freely moving mice // Journal of neurochemistry. 2010 Sep;114 (6): 1745-55.

19

Pap D. et al. Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: relevance for major depression // American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2012 Dec; 159B (8): 928-40.

20

Grace A. A. Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: a hypothesis for the etiology of schizophrenia // Neuroscience. 1991; 41 (1): 1-24.

21

Buckholtz J. W., Treadway M. T., Cowan R. L., Woodward N. D., Li R., Ansari M. S., Baldwin R. M., Schwartzman A. N., Shelby E. S., Smith C. E., Kessler R. M., Zald D. H. Dopaminergic network differences in human impulsivity // Science. 2010 Jul 30; 329 (5991): 532.

22

Шакиров М. Ш. Наркобизнес в России. — М.: Центрполиграф, 1998.

23

Гуртовенко В. М., Шамота А. З., Паронян И. Б., Константинова Н. Я., Вышинский К. В., Коновалова С. Г., Русских Н. Н., Мирошниченко М. Л. Выявление факторов риска., влияющих на потребление наркотических веществ несовершеннолетними., и разработка рекомендаций по противодействию распространению потребления наркотиков. — М., 1999.

24

Li C. Y., Mao X., Wei L. Genes and (common) pathways underlying drug addiction. PLoS Computational Biology. 2008 Jan; 4 (1): e2.

25

Doehring A., Hentig Nv., Graff J., Salamat S., Schmidt M., Geisslinger G., Harder S., Lötsch J. Genetic variants altering dopamine D2 receptor expression or function modulate the risk of opiate addiction and the dosage requirements of methadone substitution // Pharmacogenetics and Genomics. 2009 Jun; 19 (6): 407-14.

26

Lynch W. J., Taylor J. R. Persistent changes in motivation to self-administer cocaine following modulation of cyclic AMP-dependent protein kinase A (PKA) activity in the nucleus accumbens // European Journal of Neuroscience. 2005 Sep; 22 (5): 1214-20.

27

Volkow N. D., Wang G. J., Logan J., Alexoff D., Fowler J. S., Thanos P. K., Wong C., Casado V., Ferre S., Tomasi D. Caffeine increases striatal dopamine D2/D3 receptor availability in the human brain // Translational Psychiatry. 2015 Apr 14; 5: e549.

28

Savitz J. B., Ramesar R. S. Genetic variants implicated in personality: a review of the more promising candidates // American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2004 Nov 15; 131B (1): 20–32.

29

Dulawa S. C., Grandy D. K., Low M. J., Paulus M. P., Geyer M. A. Dopamine D4 receptor-knock-out mice exhibit reduced exploration of novel stimuli // Journal of Neuroscience. 1999 Nov 1; 19 (21): 9550-6.

30

Nöthen., M. M. et al. Human dopamine D4 receptor gene: Frequent occurrence of a null allele and observation of homozygosity // Human Molecular Genetics. 1994 Dec; 3 (12): 2207–2212.

31

Clarke T. K., Weiss A. R., Ferarro T. N., Kampman K. M., Dackis C. A., Pettinati H. M., O'brien C. P., Oslin D. W., Lohoff F. W., Berrettini W. H. The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction // Annals of Human Genetics. 2014 Jan; 78 (1): 33-9.

32

Mayfield R. D., Harris R. A., Schuckit M. A. Genetic factors influencing alcohol dependence // British Journal of Pharmacology. 2008 May; 154 (2): 275-87.

33

Andreasen N. C. Creativity and mental illness: prevalence rates in writers and their first-degree relatives // American Journal of Psychiatry. 1987 Oct; 144 (10): 1288-92.

34

Luo H. R., Wu G. S., Pakstis A. J., Tong L., Oota H., Kidd K. K., Zhang Y. P. Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys // Gene. 2009 Apr 15;435 (1–2): 96-103.

35

Goedde H. W., Agarwal D. P., Harada S., Rothhammer F., Whittaker J. O., Lisker R. Aldehyde dehydrogenase polymorphism in North American., South American., and Mexican Indian populations // American Journal of Human Genetics. 1986 Mar; 38 (3): 395-9.

36

Li., H., et al. Refined geographic distribution of the oriental ALDH2* 504Lys (nee 487Lys) variant // Annals Of Human Genetics. 2009 May; 73 (3): 335–345.

37

Oota H. et al. The evolution and population genetics of the ALDH2 locus: random genetic drift., selection., and low levels of recombination // Annals of Human Genetics. 2004 Mar; 68 (Pt 2): 93-109.

38

Watson R. R., Preedy V. R., Zibadi S. (eds). Alcohol., Nutrition., and Health Consequences. Springer Science+Business Media. New York., 2013.

39

Dasgupta A. Alcohol and Its Biomarkers., 1st Edition. Clinical Aspects and Laboratory Determination. Elsevier 2015.

40

Bosron W. F., Li T. K. Genetic polymorphism of human liver alcohol and aldehyde dehydrogenases., and their relationship to alcohol metabolism and alcoholism // Hepatology. 1986 May-Jun; 6 (3): 502-10.

41

Kim S. G. Gender differences in the genetic risk for alcohol dependence — the results of a pharmacogenetic study in Korean alcoholics // Nihon Arukoru Yakubutsu Igakkai Zasshi (Japanese journal of alcohol studies amp; drug dependence). 2009. Dec; 44 (6): 680-5.

42

Higuchi S., Matsushita S., Imazeki H., Kinoshita T., Takagi S., Kono H. Aldehyde dehydrogenase genotypes in Japanese alcoholics // Lancet. 1994 Mar 19; 343 (8899): 741-2.

43

Bennion L. J., Li T. K. Alcohol metabolism in American Indians and whites. Lack of racial differences in metabolic rate and liver alcohol dehydrogenase // New England Journal of Medicine. 1976 Jan 1; 294 (1): 9-13.

44

Popovici I., French M. T. Does Unemployment Lead to Greater Alcohol Consumption? // Industrial Relations. 2013 Apr; 52 (2): 444–466.

45

D'Souza D. C. et al. Enhanced sensitivity to the euphoric effects of alcohol in schizophrenia // Neuropsychopharmacology. 2006 Dec; 31 (12): 2767-75.

46

Winokur G., Coryell W., Endicott J., Keller M., Akiskal H., Solomon D. Familial alcoholism in manic-depressive (bipolar) disease // American Journal of Medical Genetics. 1996 Apr 9; 67 (2): 197–201.

47

Gorwood P., Ades J., Feingold J. Are genes coding for dopamine receptors implicated in alcoholism? // European Psychiatry. 1994; 9: 63.

48

Diaz J., Pilon C., Le Foll B., Gros C., Triller A., Schwartz J. C., Sokoloff P. Dopamine D3 receptors expressed by all mesencephalic dopamine neurons // Journal of Neuroscience. 2000 Dec 1; 20 (23): 8677-84.

49

Heidbreder C. A., Gardner E. L., Xi Z. X., Thanos P. K., Mugnaini M., Hagan J. J., Ashby C. R. Jr. The role of central dopamine D3 receptors in drug addiction: a review of pharmacological evidence // Brain Research Reviews. 2005 Jul; 49 (1): 77-105.

50

Xi Z. X., Gilbert J., Campos A. C., Kline N., Ashby C. R. Jr., Hagan J. J., Heidbreder C. A., Gardner E. L. Blockade of mesolimbic dopamine D3 receptors inhibits stress-induced reinstatement of cocaine-seeking in rats // Psychopharmacology (Berlin). 2004 Oct; 176 (1): 57–65.

51

Blum K., Noble E. P., Sheridan P. J., Montgomery A., Ritchie T., Jagadeeswaran P., Nogami H., Briggs A. H., Cohn J. B. Allelic association of human dopamine D2 receptor gene in alcoholism // Journal of the American Medical Association (JAMA). 1990 Apr 18; 263 (15): 2055-60.

52

Munafò M. R., Matheson I. J., Flint J. Association of the DRD2 gene Taq1A polymorphism and alcoholism: a meta-analysis of case-control studies and evidence of publication bias // Molecular Psychiatry. 2007 May; 12 (5): 454-61.

53

Erritzoe D. et al. In vivo imaging of cerebral dopamine D3 receptors in alcoholism // Neuropsychopharmacology. 2014 Jun; 39 (7): 1703-12.

54

Mitchell J. M., O'Neil J. P., Janabi M., Marks S. M., Jagust W. J., Fields H. L. Alcohol consumption induces endogenous opioid release in the human orbitofrontal cortex and nucleus accumbens // Science Translational Medicine. 2012 Jan 11; 4 (116): 116ra6.

55

Mick I. et al. Blunted Endogenous Opioid Release Following an Oral Amphetamine Challenge in Pathological Gamblers // Neuropsychopharmacology. 2016 Jun; 41 (7): 1742-50.

56

Creswell K. G., Sayette M. A., Manuck S. B., Ferrell R. E., Hill S. Y., Dimoff J. D. DRD4 polymorphism moderates the effect of alcohol consumption on social bonding // PLoS One. 2012; 7 (2): e28914.

57

Banerjee N. Neurotransmitters in alcoholism: A review of neurobiological and genetic studies // Indian Journal of Human Genetics. 2014 Jan-Mar; 20 (1): 20–31.

58

Wafford K. A., Whiting P. J. Ethanol potentiation of GABAA receptors requires phosphorylation of the alternatively spliced variant of the gamma 2 subunit // FEBS Letters. 1992 Nov 23; 313 (2): 113-7.

59

Zhai J., Stewart R. R., Friedberg M. W., Li C. Phosphorylation of the GABAA receptor gamma2L subunit in rat sensory neurons may not be necessary for ethanol sensitivity // Brain Research. 1998 Sep 14; 805 (1–2): 116-22.

60

Zalocusky K. A., Ramakrishnan C., Lerner T. N., Davidson T. J., Knutson B., Deisseroth K. Nucleus accumbens D2R cells signal prior outcomes and control risky decision-making // Nature. 2016 Mar 31; 531 (7596): 642-6.

61

Teicher M. H., Andersen S. L., Hostetter J. C. Jr. Evidence for dopamine receptor pruning between adolescence and adulthood in striatum but not nucleus accumbens // Developmental Brain Research. 1995 Nov 21; 89 (2): 167-72.

62

Seeman P., Bzowej N. H., Guan H. C., Bergeron C., Becker L. E., Reynolds G. P., Bird E. D., Riederer P., Jellinger K., Watanabe S., et al. Human brain dopamine receptors in children and aging adults // Synapse. 1987; 1 (5): 399–404.

63

Galvan A. Adolescent development of the reward system // Frontiers in Human Neuroscience. 2010 Feb 12; 4: 6.

64

Stunkard A. J., Foch T. T., Hrubec Z. A twin study of human obesity // Journal of the American Medical Association (JAMA). 1986 Jul 4; 256 (1): 51-4.

65

O'Rahilly S., Farooqi I. S. Genetics of obesity // Philosophical Transactions of the Royal Society B: Biological Sciences. 2006 Jul 29; 361 (1471): 1095–1105.

66

Hebert J. R., Patterson R. E., Gorfine M., Ebbeling C. B., St Jeor S. T., Chlebowski R. T. Differences between estimated caloric requirements and self-reported caloric intake in the women's health initiative // Annals of Epidemiology. 2003 Oct; 13 (9): 629-37.

67

Bouchard C., Tremblay A. Genetic effects in human energy expenditure components // International Journal of Obesity. 1990; 14 Suppl 1:49–55; discussion 55-8.

68

Farooqi I. S., Keogh J. M., Yeo G. S., Lank E. J., Cheetham T., O'Rahilly S. Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene // New England Journal of Medicine. 2003 Mar 20; 348 (12): 1085-95.

69

Appelhans B. M., Woolf K., Pagoto S. L., Schneider K. L., Whited M. C., Liebman R. Inhibiting food reward: delay discounting., food reward sensitivity., and palatable food intake in overweight and obese women // Obesity (Silver Spring). 2011 Nov; 19 (11): 2175-82.

70

Small D. M., Jones-Gotman M., Dagher A. Feeding-induced dopamine release in dorsal striatum correlates with meal pleasantness ratings in healthy human volunteers // NeuroImage. 2003 Aug; 19 (4): 1709-15.

71

Wang G. J., Volkow N. D., Logan J., Pappas N. R., Wong C. T., Zhu W., Netusil N., Fowler J. S. Brain dopamine and obesity // Lancet. 2001 Feb 3; 357 (9253): 354-7.

72

Duckworth A. L., Seligman M. E. Self-discipline outdoes IQ in predicting academic performance of adolescents // Psychological Science. 2005 Dec; 16 (12): 939-44.

73

Beaver K., Vaughn M., Wright J., DeLisi M. amp; Howard M. Three dopaminergic polymorphisms are associated with academic achievement in middle and high school // Intelligence. 2010; 38: 596–604.

74

Blum K., Noble E. Handbook of Psychiatric Genetics. CRC Press (29 Oct. 1996): 512 p., ISBN-13: 978-0849344862.

75

Barnard., N. D. et al. D2 dopamine receptor Taq1A polymorphism., body weight., and dietary intake in type 2 diabetes // Nutrition. 2009 Jan; 25 (1): 58–65.

76

Rajeevan H. et al. ALFRED — the ALlele FREquency Database. Update. // Nucleic Acids Research. 2003; 31 (1): 270–271.

77

Thomas., G. N., Critchley., J. A., Tomlinson., B., Cockram., C. S., Chan., J. C. Relationships between the TaqI polymorphism of the dopamine D2 receptor and blood pressure in hyperglycaemic and normoglycaemic Chinese subjects // Clinical endocrinology. 2001; 55 (5): 605–611.

78

Silveira P. P. et al. Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children // Appetite. 2014 Feb;73: 15–22.

79

Sobik L., Hutchison K., Craighead L. Cue-elicited craving for food: a fresh approach to the study of binge eating // Appetite. 2005 Jun; 44 (3): 253-61.

80

Twain M., Smith H. E. Autobiography of Mark Twain., Vol 1. University of California Press., 2012.

81

Li M. D., Cheng R., Ma J. Z., Swan G. E. A meta-analysis of estimated genetic and environmental effects on smoking behaviour in male and female adult twins // Addiction. 2003 Jan; 98 (1): 23–31.

82

Huang W., Payne T. J., Ma J. Z., Li M. D. A functional polymorphism., rs6280., in DRD3 is significantly associated with nicotine dependence in European-American smokers // American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2008 Oct 5; 147B (7): 1109-15.

83

Trinidad., D. R., Pérez-Stable., E. J., Emery., S. L., White., M. M., Grana., R. A., Messer., K. S. Intermittent and light daily smoking across racial/ethnic groups in the United States // Nicotine amp; Tobacco Research. 2009 Feb; 11 (2): 203–210.

84

Novak G., LeBlanc M., Zai C., Shaikh S., Renou J., DeLuca V., Bulgin N., Kennedy J. L., Le Foll B. Association of polymorphisms in the BDNF., DRD1 and DRD3 genes with tobacco smoking in schizophrenia // Annals of Human Genetics. 2010 Jul; 74 (4): 291-8.

85

Khaled M. A., Farid Araki K., Li B., Coen K. M., Marinelli P. W., Varga J., Gaál J., Le Foll B. The selective dopamine D3 receptor antagonist SB 277011-A., but not the partial agonist BP 897., blocks cue-induced reinstatement of nicotine-seeking // International Journal of Neuropsychopharmacology. 2010 Mar; 13 (2): 181-90.

86

Guillin O., Diaz J., Carroll P., Griffon N., Schwartz J. C., Sokoloff P. BDNF controls dopamine D3 receptor expression and triggers behavioural sensitization // Nature. 2001 May 3; 411 (6833): 86-9.

87

Yang J., Wang S., Yang Z., Hodgkinson C. A., Iarikova P., Ma J. Z., Payne T. J., Goldman D., Li M. D. The contribution of rare and common variants in 30 genes to risk nicotine dependence // Molecular Psychiatry. 2015 Nov; 20 (11): 1467-78.

88

Thorgeirsson T. E. et al. A variant associated with nicotine dependence., lung cancer and peripheral arterial disease // Nature. 2008 Apr 3; 452 (7187): 638-42.

89

Brunner H. G., Nelen M., Breakefield X. O., Ropers H. H., van Oost B. A. Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A // Science. 1993 Oct 22; 262 (5133): 578-80.

90

Raine A. From genes to brain to antisocial behaviour // Current Directions in Psychological Science. 2008; 17:323–328.

91

Lei H., Zhang X., Di X., Rao H., Ming Q., Zhang J., Guo X., Jiang Y., Gao Y., Yi J., Zhu X., Yao S. A functional polymorphism of the MAOA gene modulates spontaneous brain activity in pons // BioMed Research International. 2014; 2014: 243280.

92

Tiihonen J., Rautiainen M. R., Ollila H. M., Repo-Tiihonen E., Virkkunen M., Palotie A., Pietiläinen O., Kristiansson K., Joukamaa M., Lauerma H., Saarela J., Tyni S., Vartiainen H., Paananen J., Goldman D., Paunio T. Genetic background of extreme violent behavior // Molecular Psychiatry. 2015 Jun; 20 (6): 786-92.

93

Caspi A., McClay J., Moffitt T. E., Mill J., Martin J., Craig I. W., Taylor A., Poulton R. Role of genotype in the cycle of violence in maltreated children // Science. 2002 Aug 2; 297 (5582): 851-4.

94

van der Vegt E. J., Oostra B. A., Arias-Vásquez A., van der Ende J., Verhulst F. C., Tiemeier H. High activity of monoamine oxidase A is associated with externalizing behaviour in maltreated and nonmaltreated adoptees // Psychiatric Genetics. 2009 Aug; 19 (4): 209-11.

95

Byrd A. L., Manuck S. B. MAOA., childhood maltreatment., and antisocial behavior: meta-analysis of a gene-environment interaction // Biological Psychiatry. 2014 Jan 1;75 (1): 9-17.

96

Ouellet-Morin I., Côté S. M., Vitaro F., Hébert M., Carbonneau R., Lacourse É., Turecki G., Tremblay R. E. Effects of the MAOA gene and levels of exposure to violence on antisocial outcomes // British Journal of Psychiatry. 2016 Jan; 208 (1): 42-8.

97

McDermott R., Tingley D., Cowden J., Frazzetto G., D. P. Johnson D. Monoamine oxidase A gene (MAOA) predicts behavioral aggression following provocation // Proceedings of the National Academy of Sciences of the United States of America. 2009 Feb 17; 106 (7): 2118–2123.

98

Crockett M. J., Clark L., Tabibnia G., Lieberman M. D., Robbins T. W. Serotonin modulates behavioral reactions to unfairness // Science. 2008 Jun 27; 320 (5884): 1739.

99

van Donkelaar E. L., Blokland A., Ferrington L., Kelly P. A., Steinbusch H. W., Prickaerts J. Mechanism of acute tryptophan depletion: is it only serotonin? // Molecular Psychiatry. 2011 Jul; 16 (7): 695–713.

100

Bondy B., Erfurth A., de Jonge S., Krüger M., Meyer H. Possible association of the short allele of the serotonin transporter promoter gene polymorphism (5-HTTLPR) with violent suicide // Molecular Psychiatry. 2000 Mar; 5 (2): 193-5.

101

Носкова Т. Г. и др. Роль гена переносчика серотонина в развитии униполярной депрессии // Материалы Международной конференции "Генетика в России и мире", посвященной 40-летию Института общей генетики им. Н. И. Вавилова РАН, Москва, 28 июня — 2 июля., 2006. М., 2006. С. 142.

102

Hariri A. R., Mattay V. S., Tessitore A., Kolachana B., Fera F., Goldman D., Egan M. F., Weinberger D. R. Serotonin transporter genetic variation and the response of the human amygdala // Science. 2002 Jul 19; 297 (5580): 400-3.

103

Kobiella A., Reimold M., Ulshöfer D. E., Ikonomidou V. N., Vollmert C., Vollstädt-Klein S., Rietschel M., Reischl G., Heinz A., Smolka M. N. How the serotonin transporter 5-HTTLPR polymorphism influences amygdala function: the roles of in vivo serotonin transporter expression and amygdala structure // Translational Psychiatry. 2011 Aug 30; 1: e37.

104

Gallinat J., Bauer M., Heinz A. Genes and neuroimaging: advances in psychiatric research // Neurodegenerative Diseases. 2008; 5 (5): 277-85.

105

Jasinska A. J., Lowry C. A., Burmeister M. Serotonin transporter gene., stress and raphe-raphe interactions: a molecular mechanism of depression // Trends in Neuroscience. 2012 Jul; 35 (7): 395–402.

106

Петровский Е. Д., Савостьянов А. Н. и др. Влияние полиморфизма аллелей серотонинового транспортера на индивидуальные особенности мозговой гемодинамики у людей в условиях экспериментальной парадигмы "стоп-сигнал" // Вавиловский журнал генетики и селекции. 2014. Т. 18. № 4/3: 1281-8.

107

Slof-Op't Landt M. C., Bartels M., Middeldorp C. M., van Beijsterveldt C. E., Slagboom P. E., Boomsma D. I., van Furth E. F., Meulenbelt I. Genetic variation at the TPH2 gene influences impulsivity in addition to eating disorders // Behavior Genetics. 2013 Jan; 43 (1): 24–33.

108

Chung I. W., Kim H., Sribney W., Hong J. B., Lee C. H., Lee K. Y., Nan H. M., Kim Y. S., Manowitz P. Tryptophan hydroxylase polymorphism is associated with age of onset of alcoholism related behaviors // Alcohol. 2005 May; 36 (1): 1–3.

109

Ruocco A. C., Rodrigo A. H., Carcone D., McMain S., Jacobs G., Kennedy J. L. Tryptophan hydroxylase 1 gene polymorphisms alter prefrontal cortex activation during response inhibition // Neuropsychology. 2016 Jan; 30 (1): 18–27.

110

Preuss N., Salehi B., van der Veen J. W., Shen J., Drevets W. C., Hodgkinson C., Goldman D., Hasler G. Associations between prefrontal γ-aminobutyric acid concentration and the tryptophan hydroxylase isoform 2 gene., a panic disorder risk allele in women // International Journal of Neuropsychopharmacology. 2013 Sep; 16 (8): 1707-17.

111

Harris A. D., Singer H. S., Horska A., Kline T., Ryan M., Edden R. A., Mahone E. M. GABA and Glutamate in Children with Primary Complex Motor Stereotypies: An 1H-MRS Study at 7T // American Journal of Neuroradiology. 2016 Mar; 37 (3): 552-7.

112

Silveri M. M., Sneider J. T., Crowley D. J., Covell M. J., Acharya D., Rosso I. M., Jensen J. E. Frontal lobe γ-aminobutyric acid levels during adolescence: associations with impulsivity and response inhibition // Biological Psychiatry. 2013 Aug 15; 74 (4): 296–304.

113

Lee R., Petty F., Coccaro E. F. Cerebrospinal fluid GABA concentration: relationship with impulsivity and history of suicidal behavior., but not aggression., in human subjects // Journal of Psychiatric Research. 2009 Jan; 43 (4): 353-9.

114

Boy F., Evans C. J., Edden R. A., Lawrence A. D., Singh K. D., Husain M., Sumner P. Dorsolateral prefrontal γ-aminobutyric acid in men predicts individual differences in rash impulsivity // Biological Psychiatry. 2011 Nov 1; 70 (9): 866-72.

115

Ke Yet al. Frontal lobe GABA levels in cocaine dependence: a two-dimensional., J-resolved magnetic resonance spectroscopy study // Psychiatry Research. 2004 Apr 30; 130 (3): 283-93.

116

Lane S. D., Tcheremissine O. V., Lieving L. M., Nouvion S., Cherek D. R. Acute effects of alprazolam on risky decision making in humans // Psychopharmacology (Berlin). 2005 Sep; 181 (2): 364-73.

117

Davies M. The role of GABAA receptors in mediating the effects of alcohol in the central nervous system // Journal of Psychiatry amp; Neuroscience. 2003 Jul; 28 (4): 263-74.

118

Kareken D. A., Liang T., Wetherill. L., Dzemidzic M., Bragulat V., Cox C., Talavage T., O'Connor S. J., Foroud T. A polymorphism in GABRA2 is associated with the medial frontal response to alcohol cues in an fMRI study // Alcoholism: Clinical and Experimental Research. 2010 Dec; 34 (12): 2169-78.

119

Hemby S. E., O'connor J. A., Acosta G., Floyd D., Anderson N., McCool B. A., Friedman D., Grant K. A. Ethanol-induced regulation of GABA-A subunit mRNAs in prefrontal fields of cynomolgus monkeys // Alcoholism: Clinical and Experimental Research. 2006 Dec; 30 (12): 1978-85.

120

Dick D. M. et al. The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages // Behavior Genetics. 2006 Jul; 36 (4): 577-90.

121

Villafuerte S., Heitzeg M. M., Foley S., Yau W. Y., Majczenko K., Zubieta J. K., Zucker R. A., Burmeister M. Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism // Molecular Psychiatry. 2012 May; 17 (5): 511-9.

122

Vlachou S., Markou A. GABAB receptors in reward processes // Advances in Pharmacological Sciences. 2010; 58:315-71.

123

Hayes D. J., Jupp B., Sawiak S. J., Merlo E., Caprioli D., Dalley J. W. Brain γ-aminobutyric acid: a neglected role in impulsivity // European Journal of Neuroscience. 2014 Jun; 39 (11): 1921-32.

124

Coccaro E. F., Lee R., Vezina P. Cerebrospinal fluid glutamate concentration correlates with impulsive aggression in human subjects // Journal of Psychiatric Research. 2013 Sep; 47 (9): 1247-53.

125

Hoerst M., Weber-Fahr W., Tunc-Skarka N., Ruf M., Bohus M., Schmahl C., Ende G. Correlation of glutamate levels in the anterior cingulate cortex with self-reported impulsivity in patients with borderline personality disorder and healthy controls // Archives of General Psychiatry. 2010 Sep; 67 (9): 946-54.

126

Smith H., Passik S. (eds). Pain and Chemical Dependency., 1st Edition. Oxford University Press., New York., 2008.

127

Rotberg B., Kronenberg S., Carmel M., Frisch A., Brent D., Zalsman G., Apter A., Weizman A. Additive effects of 5-HTTLPR (serotonin transporter) and tryptophan hydroxylase 2 G-703T gene polymorphisms on the clinical response to citalopram among children and adolescents with depression and anxiety disorders // Journal of child and adolescent psychopharmacology. 2013 Mar; 23(2): 117-22.

Глава 5

1

Mao W., Schuler M. A., Berenbaum M. R. A dietary phytochemical alters caste-associated gene expression in honey bees // Science advances. 2015 Aug 28;1 (7): e1500795.

2

Luckenbach J. A., Borski R. J., Daniels H. V., Godwin J. Sex determination in flatfishes: Mechanisms and environmental influences // Seminars in Cell and Developmental Biology. 2009 May; 20 (3):256-63.

3

Wassenaar C. A., Dong Q., Wei Q., Amos C. I., Spitz M. R., Tyndale R. F. Relationship between CYP2A6 and CHRNA5-CHRNA3-CHRNB4 variation and smoking behaviors and lung cancer risk // The Journal of the National Cancer Institute. 2011 Sep 7; 103 (17): 1342-6.

4

Thorgeirsson T. E. et al. A variant associated with nicotine dependence, lung cancer and peripheral arterial disease // Nature. 2008 Apr 3; 452 (7187): 638-42.

5

Joan Stiles amp; Terry L. Jernigan. The Basics of Brain Development // Neuropsychology Reviews. 2010 Dec; 20 (4): 327–348.

6

Hubel D. H, Wiesel T. N. Receptive fields of single neurones in the cat's striate cortex // The Journal of Physiology. 1959 Oct; 148: 574-91.

7

Markham J. A., Greenough W. T. Experience-driven brain plasticity: beyond the synapse // Neuron Glia Biology. 2004 Nov; 1 (4): 351-63.

8

Lipina S. J., Posner M. I. The impact of poverty on the development of brain networks // Frontiers in Human Neuroscience. 2012; 6: 238.

9

Hebb D. O. The effects of early experience on problem-solving at maturity // American Psychologist. 1947. 2, 306–307.

10

Бадридзе Я. К. Волк. Проблемы, связанные с реинтродукцией крупных хищных млекопитающих. М.: Модерн, Архэ, 2016.

11

Crandall F. M. Hospitalism // Archives of Pediatrics, 1897, June 14 (6): 448–454.

12

Greenough, W. T., amp; Black, J. E. Induction of brain structure by experience: Substrates for cognitive development. In M. R. Gunnar amp; C. A. Nelson (Eds.), Developmental behavioral neuroscience // The Minnesota Parenting and Executive Functioning symposia on child psychology. 1992. Vol. 24, pp. 155–200. Hillsdale, NJ: Erlbaum.

13

Sánchez M. M., Ladd C. O., Plotsky P. M. Early adverse experience as a developmental risk factor for later psychopathology: evidence from rodent and primate models // Development and psychopathology. 2001 Summer; 13 (3): 419-49.

14

Wright J. P., Beaver K. M. Do parents matter in creating self-control in their children? A genetically informed test of Gottfredson and Hirschi's theory of low self-control // Criminology, 2005 Nov; 43 (4): 1169–1202.

15

Bradley R. H., Corwyn R. F. Socioeconomic status and child development // Annual Reviews of Psychology. 2002; 53: 371-99.

16

McLoyd V. C. Socioeconomic disadvantage and child development // American Psychologist. 1998 Feb; 53 (2): 185–204.

17

Kishiyama M. M., Boyce W. T., Jimenez A. M., Perry L. M., Knight R. T. Socioeconomic disparities affect prefrontal function in children // Journal of Cognitive Neuroscience. 2009 Jun; 21 (6): 1106-15.

18

Noble K. G. et al. Family income, parental education and brain structure in children and adolescents // Nature Neuroscience. 2015 May; 18 (5): 773-8.

19

Carson V., Spence J. C., Cutumisu N., Cargill L. Association between neighborhood socioeconomic status and screen time among pre-school children: a cross-sectional study // BMC Public Health. 2010 Jun 24; 10: 367.

20

Tandon P. S., Zhou C., Sallis J. F., Cain K. L., Frank L. D., Saelens B. E. Home environment relationships with children's physical activity, sedentary time, and screen time by socioeconomic status // The International Journal of Behavioral Nutrition and Physical Activity. 2012; 9: 88.

21

Wills T. A., Gibbons F. X., Sargent J. D., Gerrard M., Lee H. R., Dal Cin S. Good self-control moderates the effect of mass media on adolescent tobacco and alcohol use: tests with studies of children and adolescents // Health Psychology. 2010 Sep; 29 (5): 539-49.

22

Harris J. L., Bargh J. A., Brownell K. D. Priming effects of television food advertising on eating behaviour // Health Psychology. 2009 Jul; 28 (4): 404-13.

23

Giese H., König L. M., Tăut D., Ollila H., Băban A., Absetz P., Schupp H., Renner B. Exploring the association between television advertising of healthy and unhealthy foods, self-control, and food intake in three European countries // Applied Psychology: Health and Well-Being. 2015 Mar; 7 (1): 41–62.

24

Selye H. A Syndrome produced by Diverse Nocuous Agents // Nature. 1936 Jul; 138 (3479): 32.

25

Work related Stress, Anxiety and Depression Statistics in Great Britain 2016 // Health and Safety Esecutive. URL: http://www.hse.gov.uk/statistics/causdis/stress/stress.pdf?pdf=stress.

26

Simmons S. P., Simmons J. C. Measuring emotional intelligence. New York: Summit Publishing Group; 1997.

27

Sandi C., Pinelo-Nava T. M. Stress and Memory: Behavioral Effects and Neurobiological Mechanisms // Neural Plasticity. 2007: 78970.

28

Porcelli A. J., Delgado M. R. Acute stress modulates risk taking in financial decision making. // Psychological science. 2009 Mar; 20 (3): 278-83.

29

Tversky A., Kahneman D. The framing of decisions and the psychology of choice // Science. 1981 Jan 30; 211 (4481): 453-8.

30

De Martino B., Camerer C. F., Adolphs R. Amygdala damage eliminates monetary loss aversion // Proceedings of the National Academy of Sciences of the United States of America. 2010 Feb 23; 107 (8): 3788-92.

31

Glass D. C., Siger J. E., Friedman L. N. Psychic cost of adaptation to an environmental stressor // Journal of Personality and Social Psychology. 1969 Jul; 12 (3): 200-10.

32

Sherrod D. R. Crowding, perceived control, and behavioral after- effects // Journal of Applied Social Psychology. 1974; 4: 171–186.

33

White M. J., Lawford B. R., Morris C. P., Young R. M. Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity // Behavior Genetics. 2009 May; 39 (3): 285-95.

34

White M. J., Morris C. P., Lawford B. R., Young R. M. Behavioral phenotypes of impulsivity related to the ANKK1 gene are independent of an acute stressor // Behavioral and Brain Functions. 2008; 4: 54.

35

Rodin J., Langer E. J. Long-term effects of a control-relevant intervention with the institutionalized aged // Journal of Personality and Social Psychology. 1977 Dec; 35 (12): 897–902.

36

Mallers M. H., Claver M., Lares L. A. Perceived control in the lives of older adults: the influence of Langer and Rodin's work on gerontological theory, policy, and practice // Gerontologist. 2014 Feb; 54 (1): 67–74.

37

Cohen S., Evans G. F., Krantz D. S., Stokols D., Kelly S. Aircraft Noise and Children: Longitudinal and Cross-Sectional Evidence on Adaptation to Nose and the Effectiveness of Noise Abatement // Journal of Personality and Social Psychology. 1981; 40 (2): 331–345.

38

Stansfeld S. A. et al. Aircraft and road traffic noise and children's cognition and health: a cross-national study // Lancet. 2005 Jun 4-10; 365 (9475): 1942-9.

39

Sinha R. How does stress increase risk of drug abuse and relapse? // Psychopharmacology (Berlin). 2001 Dec; 158 (4): 343-59.

40

Sinha R. Chronic Stress, Drug Use, and Vulnerability to Addiction // Annals of the New York Academy of Sciences. 2008 Oct; 1141: 105–130.

41

Водопьянова Н. Е. Психодиагностика стресса. СПб.: Питер, 2009.

42

Morgan D. et al. Social dominance in monkeys: dopamine D2 receptors and cocaine self-administration // Nature Neuroscience. 2002 Feb; 5 (2): 169-74.

43

Hall F. S., Wilkinson L. S., Humby T., Inglis W., Kendall D. A., Marsden C. A., Robbins T. W. Isolation rearing in rats: pre- and postsynaptic changes in striatal dopaminergic systems // Pharmacology Biochemistry and Behavior. 1998 Apr; 59 (4): 859-72.

44

Vyas A., Mitra R., Shankaranarayana Rao B. S., Chattarji S. Chronic stress induces contrasting patterns of dendritic remodeling in hippocampal and amygdaloid neurons // Journal of Neuroscience. 2002 Aug 1; 22 (15): 6810-8.

45

Liston C., Miller M. M., Goldwater D. S., Radley J. J., Rocher A. B., Hof P. R., Morrison J. H., McEwen B. S. Stress-induced alterations in prefrontal cortical dendritic morphology predict selective impairments in perceptual attentional set-shifting // Journal of Neuroscience. 2006 Jul 26; 26 (30): 7870-4.

46

Bloss E. B., Janssen W. G., McEwen B. S., Morrison J. H. Interactive effects of stress and aging on structural plasticity in the prefrontal cortex // Journal of Neuroscience. 2010 May 12; 30 (19): 6726-31.

47

Mizoguchi K., Yuzurihara M., Ishige A., Sasaki H., Chui D. H., Tabira T. Chronic stress induces impairment of spatial working memory because of prefrontal dopaminergic dysfunction // Journal of Neuroscience. 2000 Feb 15; 20 (4): 1568-74.

48

Magariños A. M., Verdugo J. M., McEwen B. S. Chronic stress alters synaptic terminal structure in hippocampus // Proceedings of the National Academy of Sciences of the United States of America. 1997 Dec 9; 94 (25): 14002-8.

49

Gianaros P. J., Jennings J. R., Sheu L. K., Greer P. J., Kuller L. H., Matthews K. A. Prospective reports of chronic life stress predict decreased grey matter volume in the hippocampus // NeuroImage. 2007 Apr 1; 35 (2): 795–803.

50

Popoli M., Yan Z., McEwen B. S., Sanacora G. The stressed synapse: the impact of stress and glucocorticoids on glutamate transmission // Nature Reviews Neuroscience. 2011 Nov 30; 13 (1): 22–37.

51

Mizoguchi K., Ishige A., Aburada M., Tabira T. Chronic stress attenuates glucocorticoid negative feedback: involvement of the prefrontal cortex and hippocampus // Neuroscience. 2003; 119 (3): 887-97.

52

Pich E. M., Agnati L. F., Zini I., Marrama P., Carani C. Neuropeptide Y produces anxiolytic effects in spontaneously hypertensive rats // Peptides. 1993 Sep-Oct; 14 (5): 909-12.

53

Clark J. T., Kalra P. S., Crowley W. R., Kalra S. P. Neuropeptide Y and human pancreatic polypeptide stimulate feeding behavior in rats // Endocrinology. 1984 Jul; 115 (1): 427-9.

54

Kuo L. E., Kitlinska J. B., Tilan J. U., Li L., Baker S. B., Johnson M. D., Lee E. W., Burnett M. S., Fricke S. T., Kvetnansky R., Herzog H., Zukowska Z. Neuropeptide Y acts directly in the periphery on fat tissue and mediates stress-induced obesity and metabolic syndrome. // Nature Medicine. 2007 Jul;13 (7): 803-11.

55

Gotlib I. H., Joormann J., Minor K. L., Hallmayer J. HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression // Biological Psychiatry. 2008 May 1; 63 (9): 847-51.

56

Grabe H. J., Lange M., Wolff B., Völzke H., Lucht M., Freyberger H. J., John U., Cascorbi I. Mental and physical distress is modulated by a polymorphism in the 5-HT transporter gene interacting with social stressors and chronic disease burden // Molecular Psychiatry. 2005 Feb; 10 (2): 220-4.

57

Kendler K. S., Kuhn J. W., Vittum J., Prescott C. A., Riley B. The interaction of stressful life events and a serotonin transporter polymorphism in the prediction of episodes of major depression: a replication // Archives of general psychiatry. 2005 May; 62 (5): 529-35.

58

Brummett B. H., Boyle S. H., Siegler I. C., Kuhn C. M., Surwit R. S., Garrett M. E., Collins A., Ashley-Koch A., Williams R. B. HPA axis function in male caregivers: effect of the monoamine oxidase-A gene promoter (MAOA-uVNTR) // Biological Psychology. 2008 Oct; 79 (2): 250-5.

59

Enoch M. A., Hodgkinson C. A., Yuan Q., Shen P. H., Goldman D., Roy A. The Influence of GABRA2, Childhood Trauma and their Interaction on Alcohol, Heroin and Cocaine Dependence // Biological Psychiatry. 2010 Jan 1; 67 (1): 20-7.

60

Villafuerte S., Strumba V., Stoltenberg S. F., Zucker R. A., amp; Burmeister M. Impulsiveness mediates the association between GABRA2 SNPs and lifetime alcohol problems // Genes, brain and behaviour. 2013; 12 (5): 525–531.

61

Bartels M., Van den Berg M., Sluyter F., Boomsma D. I., de Geus E. J. Heritability of cortisol levels: review and simultaneous analysis of twin studies // Psychoneuroendocrinology. 2003 Feb; 28 (2): 121-37.

62

Keller A., Litzelman K., Wisk L. E. et al. Does the Perception that Stress Affects Health Matter? The Association with Health and Mortality // Health Psychology. 2012; 31 (5): 677–684.

63

Samochowiec J., Rybakowski F., Czerski P., Zakrzewska M., Stepień G., Pełka-Wysiecka J., Horodnicki J., Rybakowski J. K., Hauser J. Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationship to temperamental dimensions measured by the Temperament and Character Inventory in healthy volunteers // Neuropsychobiology. 2001; 43 (4): 248-53.

64

Cloninger C. R., Przybeck T. R., Svrakic D. M., Wetzel R. D. The Temperament and Character Inventory (TCI): A guide to its development and use. St. Louis, MO: Center for Psychobiology of Personality. 1994.

65

Melke J., Westberg L., Nilsson S., Landen M., Soderstrom H., Baghaei F., Rosmond R., Holm G., Björntorp P., Nilsson L. G., Adolfsson R., Eriksson E. A polymorphism in the serotonin receptor 3A (HTR3A) gene and its association with harm avoidance in women // Archives of general psychiatry. 2003 Oct; 60 (10): 1017-23.

66

Iidaka T., Ozaki N., Matsumoto A., Nogawa J., Kinoshita Y., Suzuki T., Iwata N., Yamamoto Y., Okada T., Sadato N. A variant C178T in the regulatory region of the serotonin receptor gene HTR3A modulates neural activation in the human amygdala // Journal of Neuroscience. 2005 Jul 6; 25 (27): 6460-6.

67

Cadet R., Pradier P., Dalle M., Delost P. Effects of prenatal maternal stress on the pituitary adrenocortical reactivity in guinea-pig pups // Journal of Developmental Physiology. 1986; 8: 467–475.

68

Koehl M., Darnaudéry M., Dulluc J., Van Reeth O., Le Moal M., Maccari S. Prenatal stress alters circadian activity of hypothalamo-pituitary-adrenal axis and hippocampal corticosteroid receptors in adult rats of both gender // Journal of Neurobiology. 1999 Sep 5; 40 (3): 302-15.

69

Seckl J. R. Glucocorticoids, developmental 'programming' and the risk of affective dysfunction // Progress in Brain Research. 2008; 167: 17–34.

70

Barbazanges A., Piazza P. V., Le Moal M., Maccari S. Maternal glucocorticoid secretion mediates long-term effects of prenatal stress // Journal of Neuroscience. 1996 Jun 15; 16 (12): 3943-9.

71

Cratty M. S., Ward H. E., Johnson E. A., Azzaro A. J., Birkle D. L. Prenatal stress increases corticotropin-releasing factor (CRF) content and release in rat amygdala minces // Brain Research. 1995 Mar 27; 675 (1–2): 297–302.

72

Lupien S. J., McEwen B. S., Gunnar M. R., Heim C. Effects of stress throughout the lifespan on the brain, behaviour and cognition // Nature Reviews Neuroscience. 2009 Jun; 10 (6): 434-45.

73

Henry C., Guegant G., Cador M., Arnauld E., Arsaut J., LeMoal M. et al. Prenatal stress in rats facilitates amphetamine-induced sensitization and induces long-lasting changes in dopamine receptors in the nucleus accumbens // Brain Research. 1995; 685: 179–186.

74

Converse A. K., Moore C. F., Moirano J. M., Ahlers E. O., Larson J. A., Engle J. W., Barnhart T. E., Murali D., Christian B. T., DeJesus O. T., Holden J. E., Nickles R. J., Schneider M. L. Prenatal stress induces increased striatal dopamine transporter binding in adult nonhuman primates // Biological Psychiatry. 2013 Oct 1;74 (7): 502-10.

75

Van den Hove D. L., Lauder J. M., Scheepens A., Prickaerts J., Blanco C. E., Steinbusch H. W. Prenatal stress in the rat alters 5-HT1A receptor binding in the ventral hippocampus // Brain Research. 2006 May 23; 1090 (1): 29–34.

76

Miyagawa K., Tsuji M., Ishii D., Takeda K., Takeda H. Prenatal stress induces vulnerability to stress together with the disruption of central serotonin neurons in mice // Behavioural Brain Research. 2015 Jan 15; 277: 228-36.

77

Talge N. M., Neal C., Glover V. Early Stress, Translational Research and Prevention Science Network: Fetal and Neonatal Experience on Child and Adolescent Mental Health. Antenatal maternal stress and long-term effects on child neurodevelopment: how and why? // Journal of Child Psychology and Psychiatry. 2007 Mar-Apr; 48 (3–4): 245-61.

78

Lou H. C., Hansen D., Nordentoft M., Pryds O., Jensen F., Nim J., Hemmingsen R. Prenatal stressors of human life affect fetal brain development // Developmental Medicine amp; Child Neurology. 1994 Sep; 36 (9): 826-32.

79

Duthie L., Reynolds R. M. Changes in the maternal hypothalamic-pituitary-adrenal axis in pregnancy and postpartum: influences on maternal and fetal outcomes // Neuroendocrinology. 2013; 98 (2): 106-15.

80

Hillhouse E. W., Grammatopoulos D., Milton N. G., Quartero H. W. The identification of a human myometrialcorticotropin-releasing hormone receptor that increases in affinity during pregnancy // The Journal of Clinical Endocrinology amp; Metabolism. 1993 Mar; 76 (3): 736-41.

81

O'Donnell K. J., Bugge Jensen A., Freeman L., Khalife N., O'Connor T. G., Glover V. Maternal prenatal anxiety and downregulation of placental 11β-HSD2 // Psychoneuroendocrinology. 2012 Jun; 37 (6): 818-26.

82

Davis E. P., Glynn L. M., Waffarn F., Sandman C. A. Prenatal maternal stress programs infant stress regulation // Journal of Child Psychology and Psychiatry. 2011 Feb; 52 (2): 119-29.

83

Gutteling B. M., de Weerth C., Buitelaar J. K. Prenatal stress and children's cortisol reaction to the first day of school // Psychoneuroendocrinology. 2005 Jul; 30 (6): 541-9.

84

Pluess M., Velders F. P., Belsky J., van I. Jzendoorn M. H., Bakermans-Kranenburg M. J., Jaddoe V. W., Hofman A., Arp P. P., Verhulst F. C., Tiemeier H. Serotonin transporter polymorphism moderates effects of prenatal maternal anxiety on infant negative emotionality // Biological Psychiatry. 2011 Mar 15; 69 (6): 520-5.

85

Braithwaite E. C., Ramchandani P. G., O'Connor T. G., van Ijzendoorn M. H., Bakermans-Kranenburg M. J., Glover V., Netsi E., Evans J., Meaney M. J., Murphy S. E. No moderating effect of 5-HTTLPR on associations between antenatal anxiety and infant behavior // Journal of the American Academy of Child and Adolescent Psychiatry 2013 May; 52 (5): 519-26.

86

Zohsel K., Buchmann A. F., Blomeyer D., Hohm E., Schmidt M. H., Esser G., Brandeis D., Banaschewski T., Laucht M. Mothers' prenatal stress and their children's antisocial outcomes — a moderating role for the dopamine D4 receptor (DRD4) gene // Journal of Child Psychology and Psychiatry. 2014 Jan; 55 (1): 69–76.

87

Buchmann A. F., Zohsel K., Blomeyer D., Hohm E., Hohmann S., Jennen-Steinmetz C., Treutlein J., Becker K., Banaschewski T., Schmidt M. H., Esser G., Brandeis D., Poustka L., Zimmermann U. S., Laucht M. Interaction between prenatal stress and dopamine D4 receptor genotype in predicting aggression and cortisol levels in young adults // Psychopharmacology (Berlin). 2014 Aug; 231 (16): 3089-97.

88

Conway C. C., Slavich G. M., Hammen C. Daily stress reactivity and serotonin transporter gene (5-HTTLPR) variation: internalizing responses to everyday stress as a possible transdiagnostic phenotype // Biology of Mood amp; Anxiety Disorders. 2014 Jan 24; 4 (1): 2.

89

Jones K. L., Smith R. M., Edwards K. S., Givens B., Tilley M. R., Beversdorf D. Q. Combined effect of maternal serotonin transporter genotype and prenatal stress in modulating offspring social interaction in mice // International Journal of Developmental Neuroscience. 2010 Oct; 28 (6): 529-36.

90

Gentile J. P., Atiq R., Gillig P. M. Adult ADHD: Diagnosis, Differential Diagnosis, and Medication Management // Psychiatry (Edgmont). 2006 Aug; 3 (8): 25–30.

91

Grizenko N., Fortier M. E., Zadorozny C., Thakur G., Schmitz N., Duval R., Joober R. Maternal Stress during Pregnancy, ADHD Symptomatology in Children and Genotype: Gene-Environment Interaction // Journal of the Canadian Academy of Child and Adolescent Psychiatry. 2012 Feb; 21 (1): 9-15.

92

Neuman R. J., Lobos E., Reich W., Henderson C. A., Sun L. W., Todd R. D. Prenatal smoking exposure and dopaminergic genotypes interact to cause a severe ADHD subtype // Biological Psychiatry. 2007 Jun 15; 61 (12): 1320-8.

93

Turner M. G., Livecchi C. M., Beaver K. M., Booth J. Moving beyond the socialization hypothesis: The effects of maternal smoking during pregnancy on the development of self-control // Journal of Criminal Justice. 2011 Mar-Apr; 39 (2): 120-27.

94

Wiebe S. A., Espy K. A., Stopp C., Respass J., Stewart P., Jameson T. R., Gilbert D. G, Huggenvik J. I. Gene-environment interactions across development: Exploring DRD2 genotype and prenatal smoking effects on self-regulation // Developmental Psychology. 2009 Jan; 45 (1): 31–44.

95

Meldrum R. C., Barnes J. C. Prenatal Exposure to Secondhand Smoke and the Development of Self-Control // Journal of Developmental and Life-Course Criminology. 2016. doi:10.1007/s40865-016-0038-1

96

Bublitz M. H., Stroud L. R. Maternal Smoking During Pregnancy and Offspring Brain Structure and Function: Review and Agenda for Future Research. // Nicotine amp; tobacco research: official journal of the Society for Research on Nicotine and Tobacco. 2012 Apr; 14 (4): 388–397.

97

Waddington C. H. Genetic Assimilation of the Bithorax Phenocopy // Evolution. 1956 Mar; 10 (1): 1-13.

98

Lee T. M., Zucker I. Vole infant development is influenced perinatally by maternal photoperiodic history // American Journal of Physiology. 1988 Nov; 255 (5 Pt 2): R831-8.

99

Wang H., Duclot F., Liu Y., Wang Z., Kabbaj M. Histone deacetylase inhibitors facilitate partner preference formation in female prairie voles // Nature Neuroscience. 2013 Jul; 16 (7): 919-24.

100

Weaver I. C., Cervoni N., Champagne F. A., D'Alessio A. C., Sharma S., Seckl J. R., Dymov S., Szyf M., Meaney M. J. Epigenetic programming by maternal behavior // Nature Neurosciences. 2004 Aug; 7 (8): 847-54.

101

Essex M. J., Klein M. H., Cho E., Kalin N. H. Maternal stress beginning in infancy may sensitize children to later stress exposure: effects on cortisol and behavior // Biological Psychiatry. 2002 Oct 15; 52 (8): 776-84.

102

Essex M. J., Boyce W. T., Hertzman C., Lam L. L., Armstrong J. M., Neumann S. M., Kobor M. S. Epigenetic vestiges of early developmental adversity: childhood stress exposure and DNA methylation in adolescence // Child Development. 2013 Jan-Feb; 84 (1): 58–75.

103

Niculescu M. D., Zeisel S. H. Diet, methyl donors and DNA methylation: interactions between dietary folate, methionine and choline // Journal of Nutrition. 2002 Aug; 132 (8 Suppl): 2333S — 2335S.

104

Niwa M., Jaaro-Peled H., Tankou S., Seshadri S., Hikida T., Matsumoto Y., Cascella N. G., Kano S., Ozaki N., Nabeshima T., Sawa A. Adolescent stress-induced epigenetic control of dopaminergic neurons via glucocorticoids // Science. 2013 Jan 18; 339 (6117): 335-9.

105

Duman E. A., Canli T. Influence of life stress, 5-HTTLPR genotype, and SLC6A4 methylation on gene expression and stress response in healthy Caucasian males // Biology of Mood amp; Anxiety Disorders. 2015 May 14; 5: 2.

106

Roth T. L., Lubin F. D., Funk A. J., Sweatt J. D. Lasting epigenetic influence of early-life adversity on the BDNF gene // Biological Psychiatry. 2009 May 1; 65 (9): 760-9.

107

Franklin T. B., Russig H., Weiss I. C., Gräff J., Linder N., Michalon A., Vizi S., Mansuy I. M. Epigenetic transmission of the impact of early stress across generations // Biological Psychiatry. 2010 Sep 1; 68 (5): 408-15.

108

Yehuda R., Daskalakis N. P., Bierer L. M., Bader H. N., Klengel T., Holsboer F., Binder E. B. Holocaust Exposure Induced Intergenerational Effects on FKBP5 Methylation // Biological Psychiatry. 2016 Sep 1; 80 (5): 372-80.

109

Perroud N., Rutembesa E., Paoloni-Giacobino A., Mutabaruka J., Mutesa L., Stenz L., Malafosse A., Karege F. The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis // The World Journal of Biological Psychiatry. 2014 May; 15 (4): 334-45.

110

Donkin I. et al. Obesity and Bariatric Surgery Drive Epigenetic Variation of Spermatozoa in Humans // Cell Metabolism. 2016 Feb 9; 23 (2): 369-78.

111

Taylor S. E., Way B. M., Welch W. T., Hilmert C. J., Lehman B. J., Eisenberger N. I. Early family environment, current adversity, the serotonin transporter promoter polymorphism, and depressive symptomatology // Biological Psychiatry. 2006 Oct 1; 60 (7): 671-6.

112

Koenen K. C., Aiello A. E., Bakshis E., Amstadter A. B., Ruggiero K. J., Acierno R., Kilpatrick D. G., Gelernter J., Galea S. Modification of the association between serotonin transporter genotype and risk of posttraumatic stress disorder in adults by county-level social environment // American Journal of Epidemiology. 2009 Mar 15; 169 (6): 704-11.

113

Belsky J., Jonassaint C., Pluess M., Stanton M., Brummett B., Williams R. Vulnerability genes or plasticity genes? // Molecular Psychiatry. 2009; 14 (8): 746–754.

114

Foley D. L., Eaves L. J., Wormley B., Silberg J. L., Maes H. H., Kuhn J., Riley B. Childhood adversity, monoamine oxidase a genotype, and risk for conduct disorder // Archives of general psychiatry. 2004 Jul; 61 (7): 738-44.

115

Петровский Е. Д., Савостьянов А. Н., Савелов А. А., Науменко В. С., Синякова Н. А., Левин Е. А., Таможников С. С., Тулупов А. А., Мордвинов В. А., Колчанов Н. А., Афтанас Л. И. Влияние полиморфизма аллелей серотонинового транспортера на индивидуальные особенности мозговой гемодинамики у людей в условиях экспериментальной парадигмы "стоп-сигнал" // Вавиловский журнал генетики и селекции. 2014; 18 (4–3): 1281–1288.

116

Савостьянов А. Н., Науменко В. С., Синякова Н. А., Львова М. Н., Левин Е. А., Залешин М. С., Кавай-оол У. Н., Мордвинов В. А., Колчанов Н. А., Афтанас Л. И. Взаимосвязь уровня тревожности с полиморфными вариантами гена серотонинового транспортера у русских и тувинцев // Вавиловский журнал генетики и селекции. 2014. 18 (4–3): 1268–1280.

Глава 6

1

Routh V. H. Glucose Sensing Neurons in the Ventromedial Hypothalamus // Sensors (Basel, Switzerland). 2010; 10 (10), 9002–9025.

2

Symmonds M., Emmanuel J. J., Drew M. E., Batterham R. L., amp; Dolan R. J. Metabolic State Alters Economic Decision Making under Risk in Humans // PLoS ONE. 2010 Jun 16;5 (6): e11090.

3

Gailliot M. T., Baumeister R. F. Self-regulation and sexual restraint: dispositionally and temporarily poor self-regulatory abilities contribute to failures at restraining sexual behavior // Personality amp; social psychology bulletin. 2007 Feb; 33 (2): 173-86.

4

Oaten M. amp; Cheng K. Improved Self-Control: The Benefits of a Regular Program of Academic Study // Basic and Applied Social Psychology. 2006; 28 (1): 1-16.

5

Mischel W. The Marshmallow Test: Mastering Self-Control // Little, Brown and Company. 2014. ISBN 10: 0316230871.

6

Wise P. M., Nattress L., Flammer L. J., Beauchamp G. K. Reduced dietary intake of simple sugars alters perceived sweet taste intensity but not perceived pleasantness // American Journal of Clinical Nutrition. 2016 Jan; 103 (1): 50–60.

7

Gawrilow C., Gollwitzer P. M. amp; Oettingen G. If-Then Plans Benefit Delay of Gratification Performance in Children With and Without ADHD // Cognitive Therapy and Research. 2011; 35: 442–455.

8

Gawrilow C., Gollwitzer P. M. amp; Oettingen G. If-Then Plans Benefit Executive Functions in Children with ADHD // Journal of Social and Clinical Psychology. 2011; 30 (6).

9

Schulteiss O. C. amp; Brunstein J. C. An implicit motive perspective on competence // A. J. Elliot amp; C. Dweck (Eds.), Handbook of competence and motivation (pp. 31–51). 2005, New York: Guilford.

10

Hershfield H. E., Goldstein D. G., Sharpe W. F., Fox J., Yeykelis l., Carstensen l.L. amp; Bailenson J. N. Increasing saving behavior through age-progressed renderings of the future self // Journal of Marketing Research. 2011: 48, S. 23–37.

11

Ersner-Hershfield H., Wimmer G. E., amp; Knutson B. Saving for the future self: Neural measures of future self-continuity predict temporal discounting // Social Cognitive and Affective Neuroscience. 2009: 4 (1), 85–92.

12

Chen K. M. The Effect of Language on Economic Behavior: Evidence from Savings Rates, Health Behaviors, and Retirement Assets. // American Economic Review. 2013; 103 (2): 690–731.

13

Soutschek A., Ruff C. C., Strombach T., Kalenscher T., amp; Tobler P. N. Brain stimulation reveals crucial role of overcoming self-centeredness in self-control // Science Advances. 2016, 2 (10), e1600992.

14

Melby-Lervåg M., Hulme C. Is working memory training effective? A meta-analytic review // Developmental psychology. 2013 Feb; 49 (2): 270-91.

15

Vorhees C. V., amp; Williams M. T. Morris water maze: procedures for assessing spatial and related forms of learning and memory // Nature Protocols. 2006: 1 (2), 848–858.

16

Hamid A. A., Pettibone J. R., Mabrouk O. S., Hetrick V. L., Schmidt R., Vander Weele C. M., Hamid A.A., Pettibone J.R., Mabrouk O.S., Hetrick V.L., Schmidt R., Vander Weele CM., Kennedy R.T., Aragona B.J., Berke J. D. Mesolimbic Dopamine Signals the Value of Work // Nature Neuroscience. 2016: 19 (1), 117–126.

17

Schulteiss O. C. amp; Rohde W. Implicit power motivation predicts men's testosterone changes and implicit learning in a contest situation // Hormones and behavior. 2002 Mar; 41 (2): 195–202.

18

Esch T. amp; Stefano G. B. The neurobiology of pleasure, reward processes, addiction and their health implications // Neuroendocrinology letters. 2004 Aug; 25 (4): 235-51.

19

Barker R. A., Drouin-Ouellet J. amp; Parmar M. Cell-based therapies for Parkinson disease — past insights and future potential // Nature Reviews Neurology. 2015; 11 (9), 492–503.

20

Wessel J. R., Conner C. R., Aron A. R. amp; Tandon N. Chronometric electrical stimulation of right inferior frontal cortex increases motor braking // Journal of Neuroscienceю 2013; 3 (50), 19611-19619.

21

Park D. W. et al. Graphene-based carbon-layered electrode array technology for neural imaging and optogenetic applications // Nature Сommunications. 2014; 5: 5258.

22

Ramirez S., et al. Creating a false memory in the hippocampus // Science. 2013; 341 (6144), 387–391.

23

Choi M., Choi J. W., Kim S., Nizamoglu S., Hahn S. K., Yun S. H. Light-guiding hydrogels for cell-based sensing and optogenetic synthesis in vivo // Nature photonics. 2013; 7 (12), 987–994.

24

Barnett W. S., Kwanghee J., Yarosz D. J., Thomas J., Hornbeck A., Stechuk R., Burns S. Educational effects of the Tools of the Mind curriculum: A randomized trial // Early Childhood Research Quarterly. 2008; 23 (3), 299–313.

25

Diamond A., Barnett W. S., Thomas J., Munro S. Preschool Program Improves Cognitive Control // Science. 2007; 318 (5855), 1387–1388.

26

Wilson S. J., amp; Farran, D. C. (2012). Experimental Evaluation of the Tools of the Mind Preschool Curriculum. Paper presented at the Society for Research on Educational Effectiveness, Washington, DC.

27

Ridaura V. K., Faith J. J., Rey F. E., Cheng J., Duncan A. E., Kau A. L. amp; Muehlbauer, M. J. et al. // Gut microbiota from twins discordant for obesity modulate metabolism in mice. Science. 2013; 341 (6150), 124–214.

28

De Palma G. et al. Microbiota and host determinants of behavioural phenotype in maternally separated mice // Nature communications. 2015; 6: 7735.

29

Ait‐Belgnaoui A., Colom A., Braniste V., Ramalho L., Marrot A., Cartier C.,… amp; Tompkins T. Probiotic gut effect prevents the chronic psychological stress‐induced brain activity abnormality in mice // Neurogastroenterology amp; Motilityю 2014; 26 (4), 510–520.

30

Schüssler P., Kluge M., Yassouridis A., Dresler M., Uhr M., amp; Steiger A. Ghrelin levels increase after pictures showing food // Obesity. 2012; 20 (6), 1212–1217.

31

Ghoniem A., Hofmann W. A neglected spot in self-control — the influence of attitudes towards impulses on self-control // European Health Psychology. 2016, Vol. 18.

32

Brody G. H., Yu T., Chen E., Miller G. E., Kogan S. M., amp; Beach S. R. H. Is Resilience Only Skin Deep? Rural African Americans' Preadolescent Socioeconomic Status-Related Risk and Competence and Age 19 Psychological Adjustment and Allostatic Load // Psychological Science. 2013; 24 (7), 1285–1293.

33

Miller G. E., Yu T., Chen E., amp; Brody, G. H. Self-control forecasts better psychosocial outcomes but faster epigenetic aging in low-SES youth // Proceedings of the National Academy of Sciences of the United States of America. 2015; 112 (33), 10325-10330.