Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and APOH[original query] |
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| Genetics of apolipoprotein H (beta2-glycoprotein I) polymorphism in India. Annals of human biology 0 29 (3): 247-55. Singh P, Singh M, Mastana S |
| Genetic polymorphism at the apolipoprotein E locus affects the outcome of chronic hepatitis B. Journal of medical virology 2010 Feb 82 (2): 224-331. Toniutto Pierluigi, Fattovich Giovanna, Fabris Carlo, Minisini Rosalba, Burlone Michela, Pravadelli Cecilia, Peraro Laura, Falleti Edmondo, Caldera Francesca, Bitetto Davide, Pirisi Mar |
| Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes. The Journal of rheumatology 2009 Feb 36 (2): 315-22. Suresh Sangita, Demirci F Yesim K, Jacobs Erin, Kao Amy H, Rhew Elisa Y, Sanghera Dharambir K, Selzer Faith, Sutton-Tyrrell Kim, McPherson David, Bontempo Franklin A, Kammerer Candace M, Ramsey-Goldman Rosalind, Manzi Susan, Kamboh M Ily |
| Association of anti-oxidized LDL and candidate genes with severity of coronary stenosis in the Women's Ischemia Syndrome Evaluation study. Journal of lipid research 2011 Apr 52 (4): 801-7. Chen Qi, Reis Steven E, Kammerer Candace, Craig Wendy, McNamara Dennis M, Holubkov Richard, Sharaf Barry L, Sopko George, Pauly Daniel F, Merz C Noel Bairey, Kamboh M Ilyas, |
Genetic determinants of plasma ß2-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.
Journal of thrombosis and haemostasis : JTH 2013 Jan . Athanasiadis G, Sabater-Lleal M, Buil A, Souto JC, Borrell M, Lathrop M, Watkins H, Almasy L, Hamsten A, Soria JM |
| Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†. Human molecular genetics 2016 Dec . Yu Yi, Wagner Erin K, Souied Eric H, Seitsonen Sanna, Immonen Ilkka J, Häppölä Paavo, Raychaudhuri Soumya, Daly Mark J, Seddon Johanna |
| Plasma apolipoproteins and physical and cognitive health in very old individuals. Neurobiology of aging 2017 07 55 49-60. Muenchhoff Julia, Song Fei, Poljak Anne, Crawford John D, Mather Karen A, Kochan Nicole A, Yang Zixuan, Trollor Julian N, Reppermund Simone, Maston Kate, Theobald Adam, Kirchner-Adelhardt Susanne, Kwok John B, Richmond Robyn L, McEvoy Mark, Attia John, Schofield Peter W, Brodaty Henry, Sachdev Perminder |
| Genome-wide association study of cardiac troponin I in the general population.
Human molecular genetics 2021 . Moksnes Marta R, Røsjø Helge, Richmond Anne, Lyngbakken Magnus N, Graham Sarah E, Hansen Ailin Falkmo, Wolford Brooke N, Gagliano Taliun Sarah A, LeFaive Jonathon, Rasheed Humaira, Thomas Laurent F, Zhou Wei, Aung Nay, Surakka Ida, Douville Nicholas J, Campbell Archie, Porteous David J, Petersen Steffen E, Munroe Patricia B, Welsh Paul, Sattar Naveed, Smith George Davey, Fritsche Lars G, Nielsen Jonas B, Åsvold Bjørn Olav, Hveem Kristian, Hayward Caroline, Willer Cristen J, Brumpton Ben M, Omland Torbjø |
| A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Nature genetics 2022 Jun 54 (6): 761-771. Vujkovic Marijana, Ramdas Shweta, Lorenz Kim M, Guo Xiuqing, Darlay Rebecca, Cordell Heather J, He Jing, Gindin Yevgeniy, Chung Chuhan, Myers Robert P, Schneider Carolin V, Park Joseph, Lee Kyung Min, Serper Marina, Carr Rotonya M, Kaplan David E, Haas Mary E, MacLean Matthew T, Witschey Walter R, Zhu Xiang, Tcheandjieu Catherine, Kember Rachel L, Kranzler Henry R, Verma Anurag, Giri Ayush, Klarin Derek M, Sun Yan V, Huang Jie, Huffman Jennifer E, Creasy Kate Townsend, Hand Nicholas J, Liu Ching-Ti, Long Michelle T, Yao Jie, Budoff Matthew, Tan Jingyi, Li Xiaohui, Lin Henry J, Chen Yii-Der Ida, Taylor Kent D, Chang Ruey-Kang, Krauss Ronald M, Vilarinho Silvia, Brancale Joseph, Nielsen Jonas B, Locke Adam E, Jones Marcus B, Verweij Niek, Baras Aris, Reddy K Rajender, Neuschwander-Tetri Brent A, Schwimmer Jeffrey B, Sanyal Arun J, Chalasani Naga, Ryan Kathleen A, Mitchell Braxton D, Gill Dipender, Wells Andrew D, Manduchi Elisabetta, Saiman Yedidya, Mahmud Nadim, Miller Donald R, Reaven Peter D, Phillips Lawrence S, Muralidhar Sumitra, DuVall Scott L, Lee Jennifer S, Assimes Themistocles L, Pyarajan Saiju, Cho Kelly, Edwards Todd L, Damrauer Scott M, Wilson Peter W, Gaziano J Michael, O'Donnell Christopher J, Khera Amit V, Grant Struan F A, Brown Christopher D, Tsao Philip S, Saleheen Danish, Lotta Luca A, Bastarache Lisa, Anstee Quentin M, Daly Ann K, Meigs James B, Rotter Jerome I, Lynch Julie A, , , , , Rader Daniel J, Voight Benjamin F, Chang Kyong- |
| Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease. Frontiers in genetics 2022 11 13 995488. Sabotta Caroline M, Kwan Suet-Ying, Petty Lauren E, Below Jennifer E, Joon Aron, Wei Peng, Fisher-Hoch Susan P, McCormick Joseph B, Beretta Lau |
| Levels of Angiotensin-Converting Enzyme and Apolipoproteins Are Associated with Alzheimer's Disease and Cardiovascular Diseases. Cells 2022 1 11 (1): . Xu Chun, Garcia Debra, Lu Yongke, Ozuna Kaysie, Adjeroh Donald A, Wang Kesheng, On Behalf Of The Alzheimer's Disease Neuroimaging Initiativ |
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