Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: LRP8[original query] |
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Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's disease. Neuroscience letters 2002 Nov 332 (3): 216-8. Ma Suk Ling, Ng Ho Keung, Baum Larry, Pang Jesse Chung Sean, Chiu Helen Fung Kum, Woo Jean, Tang Nelson Leung Sang, Lam Linda Chiu |
Polymorphism in maternal LRP8 gene is associated with fetal growth. American journal of human genetics 2006 May 78 (5): 770-7. Wang Lin, Wang Xiaobin, Laird Nan, Zuckerman Barry, Stubblefield Philip, Xu X |
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction. American journal of human genetics 2007 Oct 81 (4): 780-91. Shen Gong-Qing, Li Lin, Girelli Domenico, Seidelmann Sara B, Rao Shaoqi, Fan Chun, Park Jeong Euy, Xi Quansheng, Li Jing, Hu Ying, Olivieri Oliviero, Marchant Kandice, Barnard John, Corrocher Roberto, Elston Robert, Cassano June, Henderson Susan, Hazen Stanley L, Plow Edward F, Topol Eric J, Wang Qing |
Low-density lipoprotein receptor-related protein 8 gene polymorphisms and dementia. Neurobiology of aging 2009 Feb 30 (2): 266-71. Helbecque Nicole, Cottel Dominique, Amouyel Philip |
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction. Journal of molecular medicine (Berlin, Germany) 2008 Oct 86 (10): 1163-70. Lieb Wolfgang, Zeller Tanja, Mangino Massimo, Götz Anika, Braund Peter, Wenzel Juergen J, Horn Christian, Proust Carole, Linsel-Nitschke Patrick, Amouyel Philippe, Bruse Petra, Arveiler Dominique, König Inke R, Ferrières Jean, Ziegler Andreas, Balmforth Anthony J, Evans Alun, Ducimetière Pierre, Cambien Francois, Hengstenberg Christian, Stark Klaus, Hall Alistair S, Schunkert Heribert, Blankenberg Stefan, Samani Nilesh J, Erdmann Jeanette, Tiret Lauren |
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study. BMC medical genetics 2009 10 41. Martinelli Nicola, Olivieri Oliviero, Shen Gong-Qing, Trabetti Elisabetta, Pizzolo Francesca, Busti Fabiana, Friso Simonetta, Bassi Antonella, Li Lin, Hu Ying, Pignatti Pier Franco, Corrocher Roberto, Wang Qing Kenneth, Girelli Domeni |
Investigation of LRP8 gene in 1p31 QTL linked to LDL peak particle diameter in the Quebec family study. Molecular genetics and metabolism 2011 Apr 102 (4): 448-52. Dolley G, Lamarche B, Després J P, Bouchard C, Pérusse L, Vohl M |
Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population. Neurological research 2012 Sep 34 (7): 725-9. Chen Ke, Chen Yong Ping, Song Wei, Huang Rui, Zhao Bi, Cao Bei, Yang Yuan, Satake Wataru, Toda Tatsushi, Shang Hui-Fa |
Genetic variant R952Q in LRP8 is associated with increased plasma triglyceride levels in patients with early-onset CAD and MI. Annals of human genetics 2012 May 76 (3): 193-9. Shen Gong-Qing, Li Lin, Wang Qing |
Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI. Gene 2013 May 521 (1): 78-81. Shen Gong-Qing, Girelli Domenico, Li Lin, Olivieri Oliviero, Martinelli Nicola, Chen Qiuyun, Topol Eric J, Wang Qing |
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. Circulation. Cardiovascular genetics 2014 Aug 7 (4): 514-20. Shen Gong-Qing, Girelli Domenico, Li Lin, Rao Shaoqi, Archacki Stephen, Olivieri Oliviero, Martinelli Nicola, Park Jeong Euy, Chen Qiuyun, Topol Eric J, Wang Qing |
Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population. Autism research : official journal of the International Society for Autism Research 2015 Aug . Shen Yidong, Xun Guanglei, Guo Hui, He Yiqun, Ou Jianjun, Dong Huixi, Xia Kun, Zhao Jingpi |
Integrative mutation, haplotype and G?×?G interaction evidence connects ABGL4, LRP8 and PCSK9 genes to cardiometabolic risk. Scientific reports 2016 Nov 6 37375. Guo Tao, Yin Rui-Xing, Yao Li-Mei, Huang Feng, Pan Ling, Lin Wei-Xiong, Yang De-Zhai, Pan Shang-Li |
Further evidence for the association between LRP8 and schizophrenia. Schizophrenia research 2017 May . Xiao Xiao, Yu Hao, Li Jun, Wang Lu, Li Lingyi, Chang Hong, Zhang Dai, Yue Weihua, Li Mi |
TG haplotype in the LRP8 is associated with myocardial infarction in south Indian population. Gene 2017 10 642 225-229. Asif Muhammed, Bhat Shivarama, Nizamuddin Sheikh, Mustak Mohammed |
Reversal of ApoE4-induced recycling block as a novel prevention approach for Alzheimer's disease. eLife 2018 10 7 . Xian Xunde, Pohlkamp Theresa, Durakoglugil Murat S, Wong Connie H, Beck Jürgen K, Lane-Donovan Courtney, Plattner Florian, Herz Joach |
Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia. The heart surgery forum 2020 Jul 23 (4): E517-E523. Ai-Ghalayini Kamal W, Salama Mohammed A, Al Mahdi Hadia Bassam, Al-Harthi Sameer, Alhejily Wesam A, Alasnag Mirvat A, Tasbhji Noura O, Al-Quwaie Diana A H, Deloukas Panos, Edris Sher |
LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population. Psychiatric genetics 2020 Oct . Poursaei Elham, Daneshmandpour Yousef, Aghaei Moghadam Ehsan, Abolghasemi Mahsa, Jamshidi Javad, Baradaran Behzad, Asadi Milad, Kazeminasab Somayeh, Emamalizadeh Bab |
Relationship between RELN signaling pathway genes and language development of autism based on a cluster model. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2022 8 47 (7): 858-864. Shen Yidong, Dong Huixi, Zhao Jingping, Xia Kun, Ou Jianj |
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. NPJ Parkinson's disease 2023 8 9 (1): 128. Alejandro Martinez-Carrasco, Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela M X Tan, Lesley Wu, Nigel M Williams, Camille Carroll, Michele T M Hu, Donald G Grosset, John Hardy, Mina Ryten, Tom Foltynie, Yoav Ben-Shlomo, Maryam Shoai, Huw R Morr |
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. medRxiv : the preprint server for health sciences 2023 7 . Alejandro Martinez-Carrasco, Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela M X Tan, Lesley Wu, Nigel M Williams, Camille Carroll, Michele T M Hu, Donald G Grosset, John Hardy, Mina Ryten, Tom Foltynie, Yoav Ben-Shlomo, Maryam Shoai, Huw R Morr |
Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis.
JAMA psychiatry 2023 2 . Gong Weiming, Guo Ping, Li Yuanming, Liu Lu, Yan Ran, Liu Shuai, Wang Shukang, Xue Fuzhong, Zhou Xiang, Yuan Zhongsha |
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- Page last updated:Apr 22, 2024
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