Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: LOXL4[original query] |
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Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms. Human genetics 2007 May 121 (3-4): 377-87. Akagawa Hiroyuki, Narita Akira, Yamada Haruhiko, Tajima Atsushi, Krischek Boris, Kasuya Hidetoshi, Hori Tomokatsu, Kubota Motoo, Saeki Naokatsu, Hata Akira, Mizutani Tohru, Inoue Itu |
Single-nucleotide polymorphisms in the lysyl oxidase-like protein 4 and complement component 3 genes are associated with increased risk for endometriosis and endometriosis-associated infertility. Fertility and sterility 2011 Aug 96 (2): 512-5. Ruiz Lynnette A, Dutil Julie, Ruiz Abigail, Fourquet Jessica, Abac Sonia, Laboy Joaquín, Flores Idhal |
Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype. BMC medical genetics 2011 12 (1): 92. McGregor Tracy L, Gurnett Christina A, Dobbs Matthew B, Wise Carol A, Morcuende Jose A, Morgan Thomas M, Menon Ramkumar, Muglia Louis |
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
Nature communications 2018 12 9 (1): 5141. Franceschini Nora, Giambartolomei Claudia, de Vries Paul S, Finan Chris, Bis Joshua C, Huntley Rachael P, Lovering Ruth C, Tajuddin Salman M, Winkler Thomas W, Graff Misa, Kavousi Maryam, Dale Caroline, Smith Albert V, Hofer Edith, van Leeuwen Elisabeth M, Nolte Ilja M, Lu Lingyi, Scholz Markus, Sargurupremraj Muralidharan, Pitkänen Niina, Franzén Oscar, Joshi Peter K, Noordam Raymond, Marioni Riccardo E, Hwang Shih-Jen, Musani Solomon K, Schminke Ulf, Palmas Walter, Isaacs Aaron, Correa Adolfo, Zonderman Alan B, Hofman Albert, Teumer Alexander, Cox Amanda J, Uitterlinden André G, Wong Andrew, Smit Andries J, Newman Anne B, Britton Annie, Ruusalepp Arno, Sennblad Bengt, Hedblad Bo, Pasaniuc Bogdan, Penninx Brenda W, Langefeld Carl D, Wassel Christina L, Tzourio Christophe, Fava Cristiano, Baldassarre Damiano, O'Leary Daniel H, Teupser Daniel, Kuh Diana, Tremoli Elena, Mannarino Elmo, Grossi Enzo, Boerwinkle Eric, Schadt Eric E, Ingelsson Erik, Veglia Fabrizio, Rivadeneira Fernando, Beutner Frank, Chauhan Ganesh, Heiss Gerardo, Snieder Harold, Campbell Harry, Völzke Henry, Markus Hugh S, Deary Ian J, Jukema J Wouter, de Graaf Jacqueline, Price Jacqueline, Pott Janne, Hopewell Jemma C, Liang Jingjing, Thiery Joachim, Engmann Jorgen, Gertow Karl, Rice Kenneth, Taylor Kent D, Dhana Klodian, Kiemeney Lambertus A L M, Lind Lars, Raffield Laura M, Launer Lenore J, Holdt Lesca M, Dörr Marcus, Dichgans Martin, Traylor Matthew, Sitzer Matthias, Kumari Meena, Kivimaki Mika, Nalls Mike A, Melander Olle, Raitakari Olli, Franco Oscar H, Rueda-Ochoa Oscar L, Roussos Panos, Whincup Peter H, Amouyel Philippe, Giral Philippe, Anugu Pramod, Wong Quenna, Malik Rainer, Rauramaa Rainer, Burkhardt Ralph, Hardy Rebecca, Schmidt Reinhold, de Mutsert Renée, Morris Richard W, Strawbridge Rona J, Wannamethee S Goya, Hägg Sara, Shah Sonia, McLachlan Stela, Trompet Stella, Seshadri Sudha, Kurl Sudhir, Heckbert Susan R, Ring Susan, Harris Tamara B, Lehtimäki Terho, Galesloot Tessel E, Shah Tina, de Faire Ulf, Plagnol Vincent, Rosamond Wayne D, Post Wendy, Zhu Xiaofeng, Zhang Xiaoling, Guo Xiuqing, Saba Yasaman, , Dehghan Abbas, Seldenrijk Adrie, Morrison Alanna C, Hamsten Anders, Psaty Bruce M, van Duijn Cornelia M, Lawlor Deborah A, Mook-Kanamori Dennis O, Bowden Donald W, Schmidt Helena, Wilson James F, Wilson James G, Rotter Jerome I, Wardlaw Joanna M, Deanfield John, Halcox Julian, Lyytikäinen Leo-Pekka, Loeffler Markus, Evans Michele K, Debette Stéphanie, Humphries Steve E, Völker Uwe, Gudnason Vilmundur, Hingorani Aroon D, Björkegren Johan L M, Casas Juan P, O'Donnell Christopher |
Familial Alzheimer's Disease and Recessive Modifiers. Molecular neurobiology 2019 10 57 (2): 1035-1043. Vélez Jorge I, Lopera Francisco, Silva Claudia T, Villegas Andrés, Espinosa Lady G, Vidal Oscar M, Mastronardi Claudio A, Arcos-Burgos Mauric |
Polymorphisms in Lysyl Oxidase Family Genes Are Associated With Intracranial Aneurysm Susceptibility in a Chinese Population. Frontiers in endocrinology 2021 12 642698. Luo Chun, Hu Chongyu, Li Bingyang, Liu Junyu, Hu Liming, Dong Rui, Liao Xin, Zhou Jilin, Xu Lu, Liu Songlin, Li Yifeng, Yuan Dun, Jiang Weixi, Yan Junx |
Collagen type 1A1, type 3A1, and LOXL1/4 polymorphisms as risk factors of pelvic organ prolapse. BMC research notes 2021 Jan 14 (1): 15. Ashikari Asuka, Suda Tetsuji, Miyazato Mino |
Lysyl oxidase family gene polymorphisms and risk of aneurysmal subarachnoid hemorrhage: a case-control study. Annals of translational medicine 2022 Sep 10 (17): 925. Luo Chun, Li Bingyang, Liu Chao, Dong Rui, Hu Chongyu, Liu Junyu, Hu Liming, Liao Xin, Zhou Jilin, Xu Lu, Liu Songlin, Yuan Dun, Jiang Weixi, Yan Junxia, Li Yife |
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