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Polymorphisms of MRP2 (ABCC2) are associated with susceptibility to nonalcoholic fatty liver diseaseSOOKOIAN, Silvia; CASTANO, Gustavo; FEMANDEZ GIANOTTI, Tomas et al.Journal of nutritional biochemistry. 2009, Vol 20, Num 10, pp 765-770, issn 0955-2863, 6 p.Article

Gene-environment interaction and oxidative stress in cardiovascular diseaseSTEPHENS, Jeffrey W; BAIN, Stephen C; HUMPHRIES, Steve E et al.Atherosclerosis. 2008, Vol 200, Num 2, pp 229-238, issn 0021-9150, 10 p.Article

Tryptophan hydroxylase-1 gene variants associated with schizophreniaZABOLI, Ghazal; JÖNSSON, Erik G; GIZATULLIN, Rinat et al.Biological psychiatry (1969). 2006, Vol 60, Num 6, pp 563-569, issn 0006-3223, 7 p.Article

Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancySOOKOIAN, Silvia; CASTANO, Gustavo; BURGUENO, Adriana et al.Journal of hepatology. 2008, Vol 48, Num 1, pp 125-132, issn 0168-8278, 8 p.Article

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)BASSI, Maria T; BALOTTIN, Umberto; BORGATTI, Renato et al.Neurogenetics (Oxford. Print). 2005, Vol 6, Num 4, pp 185-193, issn 1364-6745, 9 p.Article

Tryptophan hydroxylase-I gene variants associate with a group of suicidal borderline womenZABOLI, Ghazal; GIZATULLIN, Rinat; NILSONNE, Asa et al.Neuropsychopharmacology (New York, NY). 2006, Vol 31, Num 9, pp 1982-1990, issn 0893-133X, 9 p.Article

Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarctionDE CATERINA, Raffaele; TALMUD, Philippa J; BERNARDINELLI, Luisa et al.Atherosclerosis. 2011, Vol 214, Num 2, pp 397-403, issn 0021-9150, 7 p.Article

The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver diseaseSOOKOIAN, Silvia; CASTANO, Gustavo O; BURGUENO, Adriana L et al.Pharmacogenetics and genomics (Print). 2010, Vol 20, Num 1, pp 1-8, issn 1744-6872, 8 p.Article

Variants of the peroxisome proliferator -activated receptor γ-and β-adrenergic receptor genes are associated with measures of compensatory eating behaviors in young childrenCECIL, Joanne E; PALMER, Colin N. A; FISCHER, Bettina et al.The American journal of clinical nutrition. 2007, Vol 86, Num 1, pp 167-173, issn 0002-9165, 7 p.Article

Gene variants associated with antisocial behaviour: a latent variable approachBENTLEY, Mary Jane; HAIQUN LIN; FERNANDEZ, Thomas V et al.Journal of child psychology and psychiatry and allied disciplines (Print). 2013, Vol 54, Num 10, pp 1074-1085, issn 0021-9630, 12 p.Article

Possible association between NOD2 variants and joint surgery in psoriatic arthritisGRAELL, E; AROSTEGUI, J. I; SANMARTI, R et al.Clinical and experimental rheumatology (Testo stampato). 2010, Vol 28, Num 1, pp 30-34, issn 0392-856X, 5 p.Article

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Influences of the phosphatidylcholine transfer protein gene variants on the LDL peak particle sizeDOLLEY, G; BERTHIER, M. T; LAMARCHE, B et al.Atherosclerosis. 2007, Vol 195, Num 2, pp 297-302, issn 0021-9150, 6 p.Article

Three novel missense Mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives implication of clinical phenotypesKAMIDE, Kei; TAKIUCHI, Shin; MIYATA, Toshiyuki et al.American journal of hypertension. 2004, Vol 17, Num 5, pp 446-449, issn 0895-7061, 4 p., 1Article

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Synonymous nucleotide polymorphisms influence Dombrock blood group protein expression in K562 cellsDUROUSSEAU DE COULGEANS, Cécile; SILVY, Monique; HALVERSON, Gregory et al.British journal of haematology. 2014, Vol 164, Num 1, pp 131-141, issn 0007-1048, 11 p.Article

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Mutations of the hexose-6-phosphate dehydrogenase gene rarely cause hyperandrogenemic polycystic ovary syndromeKENAN QIN; ROSENFIELD, Robert L.Steroids. 2011, Vol 76, Num 1-2, pp 135-139, issn 0039-128X, 5 p.Article

Melanocortin-3-receptor gene variants in morbid obesitySCHALIN-JÄNTTI, C; VALLI-JAAKOLA, K; OKSANEN, L et al.International journal of obesity. 2003, Vol 27, Num 1, pp 70-74, issn 0307-0565, 5 p.Article

A common variant of the eNOS gene (E298D) is an independent risk factor for left ventricular hypertrophy in human essential hypertensionXIN, Ying; SONG, Xiaodong; XUE, Hao et al.Clinical science (1979). 2009, Vol 117, Num 1-2, pp 67-73, issn 0143-5221, 7 p.Article

Association of putative functional variants in the PLAU gene and the PLAUR gene with myocardial infarctionXU, Jing; LI, Wenlong; YU, Hui et al.Clinical science (1979). 2010, Vol 119, Num 7-8, pp 353-359, issn 0143-5221, 7 p.Article