Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: AMT[original query] |
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Homozygosity for the C677-->T mutation of 5,10-methylenetetrahydrofolate reductase and total plasma homocyst(e) ine are not associated with greater than normal risk of a first myocardial infarction in northern Sweden. Coronary artery disease 2001 Mar 12 (2): 85-90. Thögersen AM, Nilsson TK, Dahlen G, Jansson JH, Boman K, Huhtasaari F, Hallmans G |
Association of mutations in the hemochromatosis gene with shorter life expectancy. Archives of internal medicine 2001 Nov 161 (20): 2441-4. Bathum L, Christiansen L, Nybo H, Ranberg K A, Gaist D, Jeune B, Petersen N E, Vaupel J, Christensen |
Association between CYP1A2 polymorphism and susceptibility to porphyria cutanea tarda. Human genetics 2000 Dec 107 (6): 612-4. Christiansen L, Bygum A, Jensen A, Thomsen K, Brandrup F, Hørder M, Petersen N |
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder. Molecular psychiatry 2002 7 (7): 745-54. Nyegaard M, Børglum A D, Bruun T G, Collier D A, Russ C, Mors O, Ewald H, Kruse T |
Apolipoprotein E genotype frequency patterns in aged Danes as revealed by logistic regression models. European journal of epidemiology 2004 19 (7): 651-6. Tan Qihua, Christiansen Lene, Christensen Kaare, Kruse Torben A, Bathum Li |
Evidence for an association of methylene tetrahydrofolate reductase polymorphism C677T and an increased risk of fractures: results from a population-based Danish twin study. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2004 Aug 15 (8): 659-64. Bathum Lise, von Bornemann Hjelmborg Jacob, Christiansen Lene, Madsen Jonna Skov, Skytthe Axel, Christensen Kaa |
Apolipoprotein e genotypes: relationship to cognitive functioning, cognitive decline, and survival in nonagenarians. Journal of the American Geriatrics Society 2006 Apr 54 (4): 654-8. Bathum Lise, Christiansen Lene, Jeune Bernard, Vaupel James, McGue Matt, Christensen Kaa |
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia. Human mutation 2006 Apr 27 (4): 343-52. Kure Shigeo, Kato Kumi, Dinopoulos Agirios, Gail Chuck, DeGrauw Ton J, Christodoulou John, Bzduch Vladimir, Kalmanchey Rozalia, Fekete Gyorgy, Trojovsky Alex, Plecko Barbara, Breningstall Galen, Tohyama Jun, Aoki Yoko, Matsubara Yoic |
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen study. Calcified tissue international 2007 Dec 81 (6): 421-9. Brixen K, Beckers S, Peeters A, Piters E, Balemans W, Nielsen T L, Wraae K, Bathum L, Brasen C, Hagen C, Andersen M, Van Hul W, Abrahamsen |
Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes. International journal of immunogenetics 2007 Dec 34 (6): 469-73. Nielsen C, Hansen D, Husby S, Lillevang S |
A phase II trial of triapine (NSC# 663249) and gemcitabine as second line treatment of advanced non-small cell lung cancer: Eastern Cooperative Oncology Group Study 1503. Investigational new drugs 2010 Feb 28 (1): 91-7. Traynor Anne M, Lee Ju-Whei, Bayer Gerald K, Tate John M, Thomas Sachdev P, Mazurczak Miroslaw, Graham David L, Kolesar Jill M, Schiller Joan |
Abnormal motor cortex plasticity in premanifest and very early manifest Huntington disease. Journal of neurology, neurosurgery, and psychiatry 2010 Mar 81 (3): 267-70. Orth Michael, Schippling Sven, Schneider Susanne A, Bhatia Kailash P, Talelli Penelope, Tabrizi Sarah J, Rothwell John |
Peroxisome proliferator-activated receptor-delta genotype influences metabolic phenotype and may influence lipid response to statin therapy in humans: a genetics of diabetes audit and research Tayside study. The Journal of clinical endocrinology and metabolism 2010 Apr 95 (4): 1830-7. Burch Lindsay R, Donnelly Louise A, Doney Alex S F, Brady Jeffrey, Tommasi Anna M, Whitley Adrian L, Goddard Catharine, Morris Andrew D, Hansen Michael K, Palmer Colin N |
Tryptophan hydroxylase(2) gene polymorphisms predict brain serotonin synthesis in the orbitofrontal cortex in humans. Molecular psychiatry 2012 Jul 17 (8): 809-17. Booij L, Turecki G, Leyton M, Gravel P, Lopez De Lara C, Diksic M, Benkelfat |
The folate hydrolase 1561C>T polymorphism is associated with depressive symptoms in Puerto Rican adults. Psychosomatic medicine 2011 Jun 73 (5): 385-92. Ye Xingwang, Lai Chao-Qiang, Crott Jimmy W, Troen Aron M, Ordovas Jose M, Tucker Katherine |
Renin-angiotensin-aldosterone system genotypes and haplotypes affect the susceptibility to nephropathy in type 2 diabetes patients. Journal of the renin-angiotensin-aldosterone system : JRAAS 2011 Dec 12 (4): 572-80. Mtiraoui Nabil, Ezzidi Intissar, Turki Amira, Chaieb Molka, Mahjoub Touhami, Almawi Wassim |
Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013 Jan 77 (2): 2. Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, Leclair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA |
Myopia and cognitive dysfunction among elderly Chinese adults: a propensity score matching analysis. Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 2015 Sep . Sun Hong-Peng, Liu Hu, Xu Yong, Pan Chen-W |
Genetic association of the glycine cleavage system genes and myelomeningocele. Birth defects research. Part A, Clinical and molecular teratology 2016 Sep . Shah Rita H, Northrup Hope, Hixson James E, Morrison Alanna C, Au Kit Si |
Prognostic Molecular and Imaging Biomarkers in Primary Glioblastoma. Clinical nuclear medicine 2017 Feb . Bosnyák Edit, Michelhaugh Sharon K, Klinger Neil V, Kamson David O, Barger Geoffrey R, Mittal Sandeep, Juhász Csa |
A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia. BMC medical genetics 2018 1 19 (1): 5. Lin Yiming, Zheng Zhenzhu, Sun Wenjia, Fu Qingl |
Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient. Journal of atherosclerosis and thrombosis 2019 5 27 (1): 100-103. Ueda Kazuki, Morishita Eriko, Shiraki Hironaga, Matsuoka Shunzo, Imashuku Shinsa |
Role of serum amitriptyline concentration and CYP2C19 polymorphism in predicting the response to low-dose amitriptyline in irritable bowel syndrome. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2021 Mar . Zhou Wen-Cong, Jia Lin, Deng Qi, Wen Yu-Guan, Shang De-Wei, Ni Xiao-Jia, Huang Yao-Xing, Liu Yao, Zhao Han-Bing, Yang Meng, Dou Guo-Yu |
BDNF polymorphism and interhemispheric balance of motor cortex excitability: a preliminary study. Journal of neurophysiology 2021 12 127 (1): 204-212. Dubbioso Raffaele, Pellegrino Giovanni, Ranieri Federico, Di Pino Giovanni, Capone Fioravante, Dileone Michele, Iodice Rosa, Ruggiero Lucia, Tozza Stefano, Uncini Antonino, Manganelli Fiore, Di Lazzaro Vincen |
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- Page last updated:Jun 03, 2024
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