Ugrás a tartalomhoz

Genetika és genomika

Falus András, László Valéria, Tóth Sára, Oberfrank Ferenc, Pap Erna, Dr. Szalai Csaba (2014)

Typotex Kiadó



[12.1] Laland KN, Odling–Smee J, Myles S. How culture shaped the human genome: bringing genetics and the human sciences together. Nat Rev Genet. 2010 Feb;11(2):137–48.

[12.2] International Human Genome Sequencing Consortium: Initial sequencing and analysis of the human genome. Nature 2001; 409:860–921.

[12.3] Venter JC et al. The sequence of the Human Genome. Science 2001; 291:1304–51.

[12.4] Barreiro LB, Quintana-Murci L. From evolutionary genetics to human immunology: how selection shapes host defence genes. Nat Rev Genet. 2010 Jan; 11(1):17–30.

[12.5] Fumagalli M, et al. Genome-wide identification of susceptibility alleles for viral infections through a population genetics approach. PLoS Genet. 2010 Feb 19; 6(2):e1000849.

[12.6] Szalai Cs, Czinner A, Császár A, Szabó T, Falus A: Frequency of the HIV-1 resistance CCR5 deletion allele in Hungarian newborns. Eur J Pediat 1998: 157:/9:782.

[12.7] Hütter G, Ganepola S. The CCR5-delta32 polymorphism as a model to study host adaptation against infectious diseases and to develop new treatment strategies. Exp Biol Med (Maywood). 2011 Aug 1; 236(8):938–43.

[12.8] Tishkoff SA, et al. Convergent adaptation of human lactase persistence in Africa and Europe. Nat Genet. 2007 Jan; 39(1):31–40.

[12.9] Tully G. Genotype versus phenotype: human pigmentation. Forensic Sci Int Genet. 2007 Jun;1(2):105–10.

[12.10] Reich D, et al. Denisova admixture and the first modern human dispersals into Southeast Asia and Oceania. Am J Hum Genet. 2011 Oct 7; 89(4):516–28.

[12.11] Chambers V, et al. Haemochromatosis-associated HFE genotypes in English blood donors: age-related frequency and biochemical expression. J Hepatol. 2003 Dec;39(6): 925–31.

[12.12] Erblich J, et al. Stress-induced cigarette craving: effects of the DRD2 TaqI RFLP and SLC6A3 VNTR polymorphisms. Pharmacogenomics J. 2004; 4(2):102–9.

[12.13] Minematsu N, et al. Association of CYP2A6 deletion polymorphism with smoking habit and development of pulmonary emphysema. Thorax. 2003 Jul; 58(7):623–8.

[12.14] Stevens VL, et al. Nicotinic receptor gene variants influence susceptibility to heavy smoking. Cancer Epidemiol Biomarkers Prev. 2008 Dec; 17(12):3517–25.

[12.15] Füst G, Arason GJ, Kramer J, Szalai C, et al. Genetic basis of tobacco smoking: strong association of a specific major histocompatibility complex haplotype on chromosome 6 with smoking behavior. Int Immunol. 2004 Oct; 16(10):1507–14.

[12.16] Lundström E, et al.Gene-environment interaction between the DRB1 shared epitope and smoking in the risk of anti-citrullinated protein antibody-positive rheumatoid arthritis: all alleles are important. Arthritis Rheum. 2009 Jun; 60(6):1597–603.

[12.17] Criswell LA, et al. Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women. Ann Rheum Dis. 2006 Sep; 65(9):1163–7.

[12.18] Blaskó B, et al. Low complement C4B gene copy number predicts short-term mortality after acute myocardial infarction. Int Immunol. 2008 Jan; 20(1):31–7.

[12.19] Füst György, Kramer Judit, Kiszel Petra, Blaskó Bernadette, Szalai Csaba, Gudmundur Johann Arason, Chack Yung Yu . C4BQ0, egy génvariáns, amely jelentősen csökkenti az esélyt az egészséges öregkor megélésére. Magyar Tudomány, 2006/3 266. o.

[12.20] Lee KM, et al. Paternal smoking, genetic polymorphisms in CYP1A1 and childhood leukemia risk. Leuk Res. 2009 Feb; 33(2):250–8.

[12.21] Susan Colilla, et al. Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. J Allergy Clin Immunol 2003; 111:840–6.

[12.22] Wang Z, et al. Association of asthma with beta(2)-adrenergic receptor gene polymorphism and cigarette smoking. Am J Respir Crit Care Med. 2001 May; 163(6):1404–9.

[12.23] Wang XL, et al. Effect of CYP1A1 MspI polymorphism on cigarette smoking related coronary artery disease and diabetes.Atherosclerosis. 2002 Jun; 162(2):391–7.

[12.24] Talmud PJ, Hawe E, Miller GJ. Analysis of gene-environment interaction in coronary artery disease: lipoprotein lipase and smoking as examples. Ital Heart J. 2002 Jan; 3(1):6–9.

[12.25] Kivipelto M, et al. Apolipoprotein E epsilon4 magnifies lifestyle risks for dementia: a population-based study. J Cell Mol Med. 2008 Dec; 12(6B):2762–71.

[12.26] Rusanen M, et al. Midlife smoking, apolipoprotein E and risk of dementia and Alzheimer's disease: a population-based cardiovascular risk factors, aging and dementia study. Dement Geriatr Cogn Disord. 2010; 30(3):277–84.

[12.27] Drenos F, Kirkwood TB. Selection on alleles affecting human longevity and late-life disease: the example of apolipoprotein E. PLoS One. 2010 Apr 2; 5(4):e10022.

[12.28] Dwyer JH, et al. Arachidonate 5-lipoxygenase promoter genotype, dietary arachidonic acid, and atherosclerosis. N Engl J Med. 2004 Jan 1; 350(1):29–37.

[12.29] Zhang G, et al. Opposite gene by environment interactions in Karelia for CD14 and CC16 single nucleotide polymorphisms and allergy. Allergy. 2009 Sep; 64(9):1333–41.

[12.30] Alam MA, et al. Association of polymorphism in the thermolabile 5, 10-methylene tetrahydrofolate reductase gene and hyperhomocysteinemia with coronary artery disease. Mol Cell Biochem. 2008 Mar; 310(1-2):111–7.

[12.31] Bufalino A,. Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population. Birth Defects Res A Clin Mol Teratol. 2010 Nov; 88(11):980–6.

[12.32] Chen L, et al. Alcohol intake and blood pressure: a systematic review implementing a Mendelian randomization approach. PLoS Med. 2008 Mar 4; 5(3):e52.

[12.33] Hines LM, et al. Genetic variation in alcohol dehydrogenase and the beneficial effect of moderate alcohol consumption on myocardial infarction. N Engl J Med. 2001 Feb 22; 344(8):549–55.

[12.34] Capri M, et al. Human longevity within an evolutionary perspective: the peculiar paradigm of a post-reproductive genetics. Exp Gerontol. 2008 Feb; 43(2):53–60.

[12.35] Candore G, et al. Inflammation, longevity, and cardiovascular diseases: role of polymorphisms of TLR4. Ann N Y Acad Sci. 2006 May; 1067:282–7.

[12.36] Do R et al. The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study. PLoS Medicine 2011; 9 (10)

[12.37] Li S, et al. Physical activity attenuates the genetic predisposition to obesity in 20,000 men and women from EPIC-Norfolk prospective population study. PLoS Med. 2010 Aug 31; 7(8). pii: e1000332. PubMed PMID: 20824172; PubMed Central PMCID: PMC2930873.

[12.38] Lu Y, Feskens EJ, Dolle ME, et al. Dietary n-3 and n-6 polyunsaturated fatty acid intake interacts with FADS1 genetic variation to affect total and HDLcholesterol concentrations in the Doetinchem Cohort Study. Am J Clin Nutr 2010; 92:258–265.

[12.39] Ordovás JM, Robertson R, Cléirigh EN. Gene-gene and gene-environment interactions defining lipid-related traits. Curr Opin Lipidol. 2011 Apr; 22(2):129–36.

[12.40] Hamza TH, et al. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. PLoS Genet. 2011 Aug; 7(8):e1002237.