Human Genome Epidemiology Literature Finder
|
Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and SORCS1[original query] |
|---|
| Assessment of Alzheimer's disease case-control associations using family-based methods. Neurogenetics 2009 Feb 10 (1): 19-25. Schjeide Brit-Maren M, McQueen Matthew B, Mullin Kristina, DiVito Jason, Hogan Meghan F, Parkinson Michele, Hooli Basavaraj, Lange Christoph, Blacker Deborah, Tanzi Rudolph E, Bertram La |
| Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's disease : JAD 2010 20 (4): 1181-8. Laumet Geoffroy, Chouraki Vincent, Grenier-Boley Benjamin, Legry Vanessa, Heath Simon, Zelenika Diana, Fievet Nathalie, Hannequin Didier, Delepine Marc, Pasquier Florence, Hanon Olivier, Brice Alexis, Epelbaum Jacques, Berr Claudine, Dartigues Jean-Francois, Tzourio Christophe, Campion Dominique, Lathrop Mark, Bertram Lars, Amouyel Philippe, Lambert Jean-Charl |
| SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk. Annals of neurology 2011 Jan 69 (1): 47-64. Reitz Christiane, Tokuhiro Shinya, Clark Lorraine N, Conrad Christopher, Vonsattel Jean-Paul, Hazrati Lili-Naz, Palotás András, Lantigua Raphael, Medrano Martin, Z Jiménez-Velázquez Ivonne, Vardarajan Badri, Simkin Irene, Haines Jonathan L, Pericak-Vance Margaret A, Farrer Lindsay A, Lee Joseph H, Rogaeva Ekaterina, George-Hyslop Peter St, Mayeux Richa |
| Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways. International journal of Alzheimer's disease 2011 2011 . Olgiati P, Politis AM, Papadimitriou GN, De Ronchi D, Serretti A |
| A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics 2012 2012 . Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqi |
| SORCS1 and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in a Northern Han Chinese population. Brain research 2012 Apr 1448 111-6. Wang Hui-Fu, Yu Jin-Tai, Zhang Wei, Wang Wei, Liu Qiu-Yan, Ma Xiao-Ying, Ding Hua-Min, Tan L |
| SORCS1 contributes to the development of renal disease in rats and humans. Physiological genomics 2013 Aug 45 (16): 720-8. Lazar Jozef, O'Meara Caitlin C, Sarkis Allison B, Prisco Sasha Z, Xu Haiyan, Fox Caroline S, Chen Ming-Huei, Broeckel Ulrich, Arnett Donna K, Moreno Carol, Provoost Abraham P, Jacob Howard |
| The genetic variation of SORCS1 is associated with late-onset Alzheimer's disease in Chinese Han population. PloS one 2013 8 (5): e63621. Xu Wei, Xu Jun, Wang Ying, Tang Huidong, Deng Yulei, Ren Rujing, Wang Gang, Niu Wenquan, Ma Jianfang, Wu Yiwen, Zheng Jialin, Chen Shengdi, Ding Jianqi |
| Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational psychiatry 2013 3 e256. Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers R S, Conrad C, Haines J L, Pericak-Vance M A, Fallin M D, Foroud T, Farrer L A, Schellenberg G D, George-Hyslop P S, Mayeux R, |
| Sortilin-related VPS10 domain containing receptor 1 and Alzheimer's disease-associated allelic variations preferentially exist in female or type 2 diabetes mellitus patients in southern Han Chinese. Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society 2012 Dec 12 (4): 4. He Y, Fang Z, Yu G |
| The A-B-C for SORting APP. Journal of neurochemistry 2015 Oct 135 (1): 1-3. Coulson Elizabeth J, Andersen Olav |
| Effects of genetic variation on the dynamics of neurodegeneration in Alzheimer's disease. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2014 2014 2464-7. Printy Blake P, Verma Nishant, Cowperthwaite Matthew C, Markey Mia K, |
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
Scientific reports 2019 Apr 9 (1): 6077. Hellwege Jacklyn N, Stallings Sarah, Torstenson Eric S, Carroll Robert, Borthwick Kenneth M, Brilliant Murray H, Crosslin David, Gordon Adam, Hripcsak George, Jarvik Gail P, Linneman James G, Devi Parimala, Peissig Peggy L, Sleiman Patrick A M, Hakonarson Hakon, Ritchie Marylyn D, Verma Shefali Setia, Shang Ning, Denny Josh C, Roden Dan M, Velez Edwards Digna R, Edwards Todd |
| Novel Alzheimer's disease risk variants identified based on whole-genome sequencing of APOE ?4 carriers.
Translational psychiatry 2021 May 11 (1): 296. Park Jong-Ho, Park Inho, Youm Emilia Moonkyung, Lee Sejoon, Park June-Hee, Lee Jongan, Lee Dong Young, Byun Min Soo, Lee Jun Ho, Yi Dahyun, Chung Sun Ju, Park Kye Won, Choi Nari, Kim Seong Yoon, Yoon Woon, An Hoyoung, Kim Ki Woong, Choi Seong Hye, Jeong Jee Hyang, Kim Eun-Joo, Kang Hyojin, Lee Junehawk, Kim Younghoon, Lee Eunjung Alice, Seo Sang Won, Na Duk L, Kim Jong-W |
| Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity. Frontiers in genetics 2022 3 13 839349. Loid Petra, Pekkinen Minna, Mustila Taina, Tossavainen Päivi, Viljakainen Heli, Lindstrand Anna, Mäkitie Ou |
| Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
| The Association of Selected GWAS Reported AD Risk Loci with CSF Biomarker Levels and Cognitive Decline in Slovenian Patients. International journal of molecular sciences 2023 8 24 (16): . David Vogrinc, Milica Gregori? Kramberger, Andreja Emerši?, Saša ?u?nik, Katja Gori?ar, Vita Dolž |
| Unraveling the genetic architecture of blood unfolded p-53 among non-demented elderlies: novel candidate genes for early Alzheimer's disease. BMC genomics 2024 5 25 (1): 440. Arash Yaghoobi, Seyed Amir Malekpo |
| Consistent genes associated with structural changes in clinical Alzheimer's disease spectrum. Frontiers in neuroscience 2024 11 18 1376288. Yingqi Lu, Xiaodong Zhang, Liyu Hu, Qinxiu Cheng, Zhewei Zhang, Haoran Zhang, Zhuoran Xie, Yiheng Gao, Dezhi Cao, Shangjie Chen, Jinping |
- Page last reviewed:Feb 1, 2024
- Content source: