References
1. Van Zyl H., Levitt N.S. Pregnancy outcome in patients with pregestational and gestational diabetes attending Groote Schuur Hospital, Cape Town, South Africa. S Afr Med J. 2018; 108 (9): 772-6. doi: 10.7196/SAMJ.2018.v108i9.12992.
2. Akhmetova E.S., Lareva N.V., Mudrov V.A., Gergesova E.E. Features of pregnancy with gestational diabetes mellitus and prediction of diabetic fetopathy. Zhurnal akusherstva i zhenskikh bolezney [Journal of Obstetrics and Women's Diseases]. 2017; 66 (4): 14-24. (in Russian)
3. Lysenko S.N., Chechneva M.A., Petrukhin V.A., Burumkulova F.F., Ermakova L.B. Ultrasound diagnosis of diabetic fetopathy. Rossiyskiy vestnik akushera-ginecologa [Russian Bulletin of Obstetrician-Gynecologist]. 2016; 16 (3): 23-30. (in Russian)
4. Pakin V.S. Molecular genetic aspects of gestational diabetes. Prob-lemy endokrinologii [Problems of Endocrinology]. 2017; 63 (3): 204-7. (in Russian)
5. Davydov D.M., Nurbekov M.K. Central and peripheral pathogenetic forms of type 2 diabetes: a proof-of-concept study. Endocr Connect. 2016; 5 (2): 55-64. doi: 10.1530/EC-16-0009.
6. Balampanis K., Chasapi A., Kourea E., Tanoglidi A., et al. Intertissue expression patterns of the key metabolic biomarker PGC-1 a in severely obese individuals: implication in obesity-induced disease. Hellenic J Cardiol. 2018; Aug 20. pii: S1109-9666(18)30252-5. doi: 10.1016/j.hjc.2018.08.002.
7. Fang P., He B., Yu M., Shi M., et al. Treatment with celastrol protects against obesity through suppression of galanin-induced fat intake and activation of PGC-1a/GLUT4 axis-mediated glucose consumption. Biochim Biophys Acta Mol Basis Dis. 2019; Feb 10. pii: S0925-4439(19)30045-6. doi: 10.1016/j.bbadis.2019.02.002.
8. Masuzawa R., Konno R., Ohsawa I., Watanabe A., et al. Muscle type-specific RNA polymerase II recruitment during PGC-1a gene transcription after acute exercise in adult rats. J Appl Physiol. (1985). 2018; Aug 16. doi: 10.1152/japplphysiol.00202.2018
9. Azhibekov S.A., Putilova N.V., Tretyakova T.B., Pestryaeva L.A. Influence of energy exchange genes on lipid metabolism during pregnancy complicated by the development of fetal growth restriction. Rossiyskiy vestnik akushera-ginecologa [Russian Bulletin of Obstetrician-Gynecologist]. 2017. (6): 9-13 (in Russian)
10. Okauchi Y., Iwahashi H., Okita K., Yuan M., et al. PGC-1alpha Gly482Ser polymorphism is associated with the plasma adiponectin level in type 2 diabetic men. Endocr J. 2008; 55 (6): 991-7.
11. Shaat N., Lernmark A., Karlsson E., Ivarsson S., et al. A variant in the transcription factor 7-like 2 (TCF7L2) gene is associated with an increased risk of gestational diabetes mellitus. Diabetologia. 2007; 50 (5): 972-9.
12. Gronek P., Gronek J., Lulinska-Kuklik E., Spieszny M., et al. Polygenic study of endurance-associated genetic markers NOS3 (Glu298Asp), BDKRB2 (-9/+9), UCP2 (Ala55Val), AMPD1 (Gln45Ter) and ACE (I/D) in Polish male half marathoners. J Hum Kinet. 2018; 64: 87-98. doi: 10.1515/hukin-2017-0204.
13. Mestnikova E.N., Makharova N.V., Zkharova F.A., Akhmetov 1.1., Pinigina I.A. Interconnection of ACE and eNOS genes polymorphism with the level of arterial pressure among athletes of the Sakha (Yakutia) Republic. Pedagogiko-psikhologicheskie i medico-biologicheskie problemy fizicheskoy kul'tuty i sporta [Pedagogico-Phycological and Medico-Biological Problems of Physical Culture and Sports]. 2018; 13 (2): 243-50. (in Russian)
14. Raza S.T., Abbas S., Siddiqi Z., Mahdi F. Association between ACE (rs4646994), FABP2 (rs1799883), MTHFR (rs1801133), FTO (rs9939609) genes polymorphism and type 2 diabetes with dyslipidemia. Int J Mol Cell Med. 2017; 6 (2): 121-30. doi: 10.22088/acadpub.BUMS.6.2.6.
15. Al-Saikhan F.I., Abd-Elaziz M.A., Ashour R.H. Association between risk of type 2 diabetes mellitus and angiotensin-converting enzyme inser-tion/deletion gene polymorphisms in a Saudi Arabian population. Biomed Rep. 2017; 7 (1): 56-60. doi: 10.3892/br.2017.920.
16. Aggarwal P., Agarwal N., Das N., Dalal K. Association of polymorphisms in angiotensin-converting enzyme gene with gestational diabetes mellitus in Indian women. Int J Appl Basic Med Res. 2016; 6 (1): 31-7. doi: 10.4103/2229-516X.174006.
17. Jhawat V., Gupta S., Agarwal B.K., Roy P., et al. angiotensin converting enzyme gene insertion/deletion polymorphism is not responsible for antihypertensive therapy induced new onset of type 2 diabetes in essential hypertension. Clin Med Insights Endocrinol Diabetes. 2019; 12: 1179551418825037. doi: 10.1177/1179551418825037.
18. Dostalova Z., Bienertova-Vasku A.J., Vasku A., Gerychova R., et al. [Insertion-deletion polymorphism in the gene for angiotensin-converning enzyme (I/D ACE) in pregnant women with gestational diabetes]. Ceska Gy-nekol. 2006; 71 (5): 369-73.
19. Carranza-Gonzalez L., Leon-Cachon R.B.R., Gonzalez-Zavala M.A., Rios-Ibarra C., et al. ACE, APOA5, and MTP gene polymorphisms analysis in relation to triglyceride and insulin levels in pediatric patients. Arch Med Res. 2018; 49 (2): 94-100. doi: 10.1016/j.arcmed.2018.04.013.
20. Kibitov A.O., Kurylev A.A., Brodyanskiy V.M., Chuprova N.A., et al. Combination of dopamine receptor D2 (DRD2-141C INS/DEL) and protein kinase PKK2 (DRD2/ANKK1 TAQ1A) gene polymorphisms reduces genetic risk of paranoid schizophrenia. Sotsial'naya i klinicheskaya psihiatriya [Social and Clinical Psychiatry]. 2017; 27 (3): 72-63. (in Russian)
21. Alfimova M.V., Golimbet V.E., Korovaitseva G.I., Aksenova E.V.,. et al. The association of COMT and DRD2 gene polymorphisms with a cognitive ability to understand others in schizophrenic patients. Zhurnal nev-rologii i psikhiatrii imeni S.S. Korsakova [S.S. Korsakov's Journal of Neurology and Psychiatry]. 2013; (8): 50-6. (in Russian)
22. Lawford B.R., Barnes M., Morris C.P., Noble E.P., et al. Dopamine 2 receptor genes are associated with raised blood glucose in schizophrenia. Can J Psychiatry. 2016; 61 (5): 291-7. doi: 10.1177/0706743716644765.
23. Barnard N.D., Noble E.P., Ritchie T., Cohen J., et al. D2 dopamine receptor Taq1A polymorphism, body weight, and dietary intake in type 2 diabetes. Nutrition. 2009; 25 (1): 58-65. doi: 10.1016/j.nut.2008.07.012.
24. Guigas B., de Leeuw van Weenen J.E., van Leeuwen N., Simonis-Bik A.M., et al. Sex-specific effects of naturally occurring variants in the dopamine receptor D2 locus on insulin secretion and type 2 diabetes susceptibility. Diabet Med. 2014; 31 (8): 1001-8. doi: 10.1111/dme.12464.
25. Heni M., Kullmann S., Ahlqvist E., Wagner R., et al. Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1/TaqIA on insulin sensitivity. Diabetologia. 2016; 59 (12): 2622-31.
26. Sevgi M., Rigoux L., Kuhn A.B., Mauer J., et al. An obesity-predisposing variant of the FTO gene regulates D2R-dependent reward learning. J Neurosci. 2015; 35 (36): 12 584-92. doi: 10.1523/JNEUROSCI.1589-15.2015.