Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: PLD3[original query] |
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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease. Nature 2014 Jan 505 (7484): 550-4. Cruchaga Carlos, Karch Celeste M, Jin Sheng Chih, Benitez Bruno A, Cai Yefei, Guerreiro Rita, Harari Oscar, Norton Joanne, Budde John, Bertelsen Sarah, Jeng Amanda T, Cooper Breanna, Skorupa Tara, Carrell David, Levitch Denise, Hsu Simon, Choi Jiyoon, Ryten Mina, , Hardy John, Ryten Mina, Trabzuni Daniah, Weale Michael E, Ramasamy Adaikalavan, Smith Colin, Sassi Celeste, Bras Jose, Gibbs J Raphael, Hernandez Dena G, Lupton Michelle K, Powell John, Forabosco Paola, Ridge Perry G, Corcoran Christopher D, Tschanz Joann T, Norton Maria C, Munger Ronald G, Schmutz Cameron, Leary Maegan, Demirci F Yesim, Bamne Mikhil N, Wang Xingbin, Lopez Oscar L, Ganguli Mary, Medway Christopher, Turton James, Lord Jenny, Braae Anne, Barber Imelda, Brown Kristelle, , Passmore Peter, Craig David, Johnston Janet, McGuinness Bernadette, Todd Stephen, Heun Reinhard, Kölsch Heike, Kehoe Patrick G, Hooper Nigel M, Vardy Emma R L C, Mann David M, Pickering-Brown Stuart, Brown Kristelle, Kalsheker Noor, Lowe James, Morgan Kevin, David Smith A, Wilcock Gordon, Warden Donald, Holmes Clive, Pastor Pau, Lorenzo-Betancor Oswaldo, Brkanac Zoran, Scott Erick, Topol Eric, Morgan Kevin, Rogaeva Ekaterina, Singleton Andrew B, Hardy John, Kamboh M Ilyas, St George-Hyslop Peter, Cairns Nigel, Morris John C, Kauwe John S K, Goate Alison |
Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China. Neurobiology of aging 2014 Oct 35 (10): 2422.e9-2422.e11. Jiao Bin, Liu Xiaoyan, Tang Beisha, Hou Lihua, Zhou Lin, Zhang Fufeng, Zhou Yafang, Guo Jifeng, Yan Xinxiang, Shen |
PLD3 is accumulated on neuritic plaques in Alzheimer's disease brains. Alzheimer's research & therapy 2014 6 (9): 70. Satoh Jun-Ichi, Kino Yoshihiro, Yamamoto Yoji, Kawana Natsuki, Ishida Tsuyoshi, Saito Yuko, Arima Kunima |
Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort. Human mutation 2015 Sep . Cacace Rita, Van den Bossche Tobi, Engelborghs Sebastiaan, Geerts Nathalie, Laureys Annelies, Dillen Lubina, Graff Caroline, Thonberg Håkan, Chiang Huei-Hsin, Pastor Pau, Ortega-Cubero Sara, Pastor Maria A, Diehl-Schmid Janine, Alexopoulos Panagiotis, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Nacmias Benedetta, Sorbi Sandro, Sanchez-Valle Raquel, Lladó Albert, Gelpi Ellen, Almeida Maria Rosário, Santana Isabel, Tsolaki Magda, Koutroumani Maria, Clarimon Jordi, Lleó Alberto, Fortea Juan, de Mendonça Alexandre, Martins Madalena, Borroni Barbara, Padovani Alessandro, Matej Radoslav, Rohan Zdenek, Vandenbulcke Mathieu, Vandenberghe Rik, De Deyn Peter P, Cras Patrick, van der Zee Julie, Sleegers Kristel, Van Broeckhoven Christine, |
Common Variants in PLD3 and Correlation to Amyloid-Related Phenotypes in Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2015 May 46 (2): 491-5. Wang Chong, Tan Lan, Wang Hui-Fu, Yu Wan-Jiang, Liu Ying, Jiang Teng, Tan Meng-Shan, Hao Xiao-Ke, Zhang Dao-Qiang, Yu Jin-T |
Alzheimer's disease: rare variants with large effect sizes. Current opinion in genetics & development 2015 Aug 33 49-55. Del-Aguila Jorge L, Koboldt Daniel C, Black Kathleen, Chasse Rachel, Norton Joanne, Wilson Richard K, Cruchaga Carl |
Impact of Common Variations in PLD3 on Neuroimaging Phenotypes in Non-demented Elders. Molecular neurobiology 2015 Aug . Wang Chong, Wang Hui-Fu, Tan Meng-Shan, Liu Ying, Jiang Teng, Zhang Dao-Qiang, Tan Lan, Yu Jin-Tai, |
PLD3 in Alzheimer's Disease: a Modest Effect as Revealed by Updated Association and Expression Analyses. Molecular neurobiology 2015 Jul . Zhang Deng-Feng, Fan Yu, Wang Dong, Bi Rui, Zhang Chen, Fang Yiru, Yao Yong-Ga |
PLD3 gene variants and Alzheimer's disease. Nature 2015 Apr 520 (7545): E7-8. Hooli Basavaraj V, Lill Christina M, Mullin Kristina, Qiao Dandi, Lange Christoph, Bertram Lars, Tanzi Rudolph |
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.
Scientific reports 2016 6 33240. Einarsdottir Elisabet, Hafrén Lena, Leinonen Eira, Bhutta Mahmood F, Kentala Erna, Kere Juha, Mattila Petri |
Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's disease. Human genome variation 2016 4 2 14028. Schulte Eva C, Kurz Alexander, Alexopoulos Panagiotis, Hampel Harald, Peters Annette, Gieger Christian, Rujescu Dan, Diehl-Schmid Janine, Winkelmann Julia |
Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population. Oncotarget 2017 Feb . Lin Eugene, Tsai Shih-Jen, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Fe |
Common Variant in PLD3 Influencing Cerebrospinal Fluid Total Tau Levels and Hippocampal Volumes in Mild Cognitive Impairment Patients from the ADNI Cohort. Journal of Alzheimer's disease : JAD 2018 Jul . Tan Meng-Shan, Wang Ping, Ma Fang-Chen, Li Jie-Qiong, Tan Chen-Chen, Yu Jin-Tai, Tan Lan, |
Rare Variants in PLD3 Increase Risk for Alzheimer's Disease in Han Chinese. Journal of Alzheimer's disease : JAD 2018 64 (1): 55-59. Tan Meng-Shan, Zhu Jun-Xia, Cao Xi-Peng, Yu Jin-Tai, Tan L |
Whole-Exome Sequencing of an Exceptional Longevity Cohort. The journals of gerontology. Series A, Biological sciences and medical sciences 2018 5 74 (9): 1386-1390. Nygaard Haakon B, Erson-Omay E Zeynep, Wu Xiujuan, Kent Brianne A, Bernales Cecily Q, Evans Daniel M, Farrer Matthew J, Vilariño-Güell Carles, Strittmatter Stephen |
The effect of rare variants in TREM2 and PLD3 on longitudinal cognitive function in the Wisconsin Registry for Alzheimer's Prevention. Neurobiology of aging 2018 06 66 177.e1-177.e5. Engelman Corinne D, Darst Burcu F, Bilgel Murat, Vasiljevic Eva, Koscik Rebecca L, Jedynak Bruno M, Johnson Sterling |
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
Association of rare variants in neurodegenerative genes with familial Alzheimer's disease. Annals of clinical and translational neurology 2020 Sep . Zhang Weiwei, Jiao Bin, Xiao Tingting, Liu Xixi, Liao Xinxin, Xiao Xuewen, Guo Lina, Yuan Zhenhua, Yan Xinxiang, Tang Beisha, Shen |
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- Page last updated:Mar 25, 2024
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