AHA/ASA Expert Consensus Document: An updated definition of stroke for the 21st century a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2013;44:2064-89.

Sommer CJ. Ischemic stroke: experimental models and reality. Acta Neuropathol. 2017;133(2):245-61. https://doi.org/10.1007/s00401-017-1667-0

Meschia JF, Bushnell C, Boden-Albala B, Braun LT, Bravata DM, Chaturvedi S, Creager MA, Eckel RH, Elkind MSV, Fornage M, Goldstein LB, Greenberg SM, Horvath SE, Iadecola C, Jauch EC, Moore WS, Wilson JA. Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2014;45(12):3754-832. https://doi.org/10.1161/STR.0000000000000046

Shahar E, Chambless LE, Rosamond WD, Boland LL, Ballantyne CM, McGovern PG, Sharrett AR. Plasma lipid profile and incident ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study. Stroke. 2003;34(3):623-31. https://doi.org/10.1161/01.STR.0000057812.51734.FF

Zhou YJ, Hong SC, Yin RX, Yang Q, Cao XL, Chen WX. Polymorphisms in the GCKR are associated with serum lipid traits, the risk of coronary artery disease and ischemic stroke. Int J Clin Exp Med. 2015;8(7):10678-86.

Perez-Martinez P, Corella D, Shen J Arnett DK, Yiannakouris N, Tai ES, Orho-Melander M, Tucker KL, Tsai M, Straka RJ, Province M, Kai CS, Perez-Jimenez F, Lai CQ, Lopez-Miranda J, Guillen M, Parnell LD, Borecki I, Kathiresan S, Ordovas JM. Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states. Am J Clin Nutr. 2008;89(1):391-9. https://doi.org/10.3945/ajcn.2008.26363

Pollin TI, Jablonski KA, McAteer JB Saxena R, Kathiresan S, Kahn SE, Goldberg RB, Altshuler D, Florez JC. Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism. J Clin Endocrinol Metab. 2011;96(7):E1142-7. https://doi.org/10.1210/jc.2010-2324

Mohás M, Kisfali P, Járomi L, Maász A, Fehér E, Csöngei V, Polgár N, Sáfrány E, Cseh J, Sümegi K, Hetyésy K, Wittmann I, Melegh B. GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness? Cardiovasc Diabetol. 2010;9:79. https://doi.org/10.1186/1475-2840-9-79

Transcript: GCKR-201. Ensembl genome browser 104 for Human GCKR gene [Internet]. EMBL-EBI. Ensembl release 104 - November 2021 [Cited 2021 Nov 18]. Available from: http://www.ensembl.org/Homo_sapiens/Transcript/Summary?db=core;g=ENSG00000084734;r=2:27496839-27523684;t=ENST00000264717

Shen H, Pollin TI, Damcott CM, McLenithan JC, Mitchell BD, Shuldiner AR. Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study. Hum Genet. 2009;126(4):567-74. https://doi.org/10.1007/s00439-009-0700-3

Bi M, Kao WH, Boerwinkle E, Hoogeveen RC, Rasmussen-Torvik LJ, Astor BC, North KE, Coresh J, Kottgen A. Association of rs780094 in GCKR with Metabolic Traits and Incident Diabetes and Cardiovascular Disease: The ARIC Study. PLoS One. 2010;5(7):e11690. https://doi.org/10.1371/journal.pone.0011690

Járomi L, Csöngei V, Polgár N, Szolnoki Z, Maász A, Horvatovich K, Faragó B, Sipeky C, Sáfrány E, Magyari L, Kisfali P, Mohás M, Janicsek I, Lakner L, Melegh B. Functional variants of glucokinase regulatory protein and apolipoprotein A5 genes in ischemic stroke. J Mol Neurosci. 2010;41:121-8. https://doi.org/10.1007/s12031-009-9301-9

Beer NL, Tribble ND, McCulloch LJ Roos C, Johnson PRV, Orho-Melander M, Gloyn AL. The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver. Hum Mol Genet. 2009;18(21):4081-8. https://doi.org/10.1093/hmg/ddp357

Rees MG, Wincovitch S, Schultz J, Waterstradt R, Beer NL, Baltrusch S, Collins FS, Gloyn AL. Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk. Diabetologia. 2012; 55(1): 114-22. https://doi.org/10.1007/s00125-011-2348-5

Raimondo A, Rees MG, Gloyn AL. Glucokinase regulatory protein: complexity at the crossroads of triglyceride and glucose metabolism. Curr Opin Lipidol. 2015;26(2):88-95. https://doi.org/10.1097/MOL.0000000000000155

López Rodríguez M, Kaminska D, Lappalainen K, Pihlajamäki J, Kaikkonen MU, Laakso M. Identification and characterization of a FOXA2-regulated transcriptional enhancer at a type 2 diabetes intronic locus that controls GCKR expression in liver cells. Genome Med. 2017;9(1):63. https://doi.org/10.1186/s13073-017-0453-x

Onuma H, Tabara Y, Kawamoto R Shimizu I, Kawamura R, Takata Y, Nishida W, Ohashi J, Miki T, Kohara K, Makino H, Osawa H. The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population. J Hum Genet. 2010;55(9):600-4. https://doi.org/10.1038/jhg.2010.75

Vaxillaire M, Cavalcanti-Proença C, Dechaume A, Tichet J, Marre M, Balkau B, Froguel P. The common P446L polymorphism in GCKR inversely modulates fasting glucose and triglyceride levels and reduces type 2 diabetes risk in the DESIR prospective general French population. Diabetes. 2008;57(8):2253-7. https://doi.org/10.2337/db07-1807

Sennblad B, Basu S, Mazur J, Suchon P, Martinez-Perez A, van Hylckama Vlieg A, Truong V, Li Y, Gådin JR, Tang W, Grossman V, de Haan HG, Handin N, Silveira A, Souto JC, Franco-Cereceda A, Morange PE, Gagnon F, Soria JM, Eriksson P, Hamsten A, Maegdefessel L, Rosendaal FR, Wild P, Folsom AR, Trégouët DA, Sabater-Lleal M. Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels. Hum Mol Genet. 2017;26(3):637-49. https://doi.org/10.1093/hmg/ddw401

Jevtovic Stoimenov T, Despotovic M, Stojanovic S, Basic J, Pavlovic D. Polymorphic variants of antioxidative defense enzymes and their gene-gene epistatic interactions in systemic lupus erythematodes patients. Clin Rheumatol. 2017;36(9):2019-26. https://doi.org/10.1007/s10067-017-3755-x

Despotovic M, Jevtovic Stoimenov T, Stankovic I, Basic J, Pavlovic D. Vitamin D Receptor Gene Polymorphisms in Serbian Patients with Bronchial Asthma: A Case-ControlStudy. J Cell Biochem. 2017;118(11):3986-92. https://doi.org/10.1002/jcb.26054

Despotović M, Jevtović Stoimenov T, Stojanović S, Bašić J, Kundalić J, Đorđević B, Ranđelović M., Pavlović D. Association of vitamin D receptor genetic variants with bone mineral density and inflammatory markers in rheumatoid arthritis. Clin Biochem. 2021;87:26-31. https://doi.org/10.1016/j.clinbiochem.2020.10.006

Despotović M, Jevtović Stoimenov T, Stanković I, Bašić J, Đorđević B. Genetic variants of vitamin D receptor and antioxidant enzyme genes in bronchial asthma: Epistatic interactions. Ann Allergy Asthma Immunol. 2020;125(6):701-3. https://doi.org/10.1016/j.anai.2020.07.020

Bašić J, Milošević V, Stanković M, Jevtović-Stoimenov T, Cvetković T, Despotović M, Pavlović D. The influence of rs53576 and rs2254298 oxytocin receptor gene polymorphisms on plasma oxytocin levels and measures of empathy. Arch Biol Sci. 2019;71(1):159-65. https://doi.org/10.2298/ABS181206057B

Man AWC, Li H, Xia N. Impact of Lifestyles (Diet and Exercise) on Vascular Health: Oxidative Stress and Endothelial Function. Oxid Med Cell Longev. 2020;2020:1496462. https://doi.org/10.1155/2020/1496462

Ljubisavljevic S, Stojanovic I, Pavlovic R, Pavlovic D. The importance of nitric oxide and arginase in the pathogenesis of acute neuroinflammation: are those contra players with the same direction? Neurotox Res. 2014;26(4):392-9. https://doi.org/10.1007/s12640-014-9470-3

Ljubisavljevic S, Stojanovic I, Pavlovic R, Sokolovic D, Pavlovic D, Cvetkovic T, Stevanovic I. Modulation of nitric oxide synthase by arginase and methylated arginines during the acute phase of experimental multiple sclerosis. J Neurol Sci. 2012;318(1-2):106-11. https://doi.org/10.1016/j.jns.2012.03.015