Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: PLD1[original query] |
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A Single Nucleotide Polymorphism in the Phospholipase D1 Gene is Associated with Risk of Non-Small Cell Lung Cancer. International journal of biomedical science : IJBS 2012 Jun 8 (2): 121-8. Ahn Myung-Ju, Park Shin-Young, Kim Won Kyu, Cho Ju Hwan, Chang Brian Junho, Kim Dong Jo, Ahn Jin Seok, Park Keunchil, Han Joong-S |
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 |
Genome-Wide Association Studies of the Human Gut Microbiota.
![]() PloS one 2015 10 (10): e0140301. Davenport Emily R, Cusanovich Darren A, Michelini Katelyn, Barreiro Luis B, Ober Carole, Gilad Yo |
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities. Journal of neural transmission (Vienna, Austria : 1996) 2017 Nov . Chiocchetti Andreas G, Yousaf Afsheen, Bour Hannah S, Haslinger Denise, Waltes Regina, Duketis Eftichia, Jarczok Tomas, Sachse Michael, Biscaldi Monica, Degenhardt Franziska, Herms Stefan, Cichon Sven, Ackermann Jörg, Koch Ina, Klauck Sabine M, Freitag Christine |
Identification of Genes Associated With Hirschsprung Disease, Based on Whole-Genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development. Gastroenterology 2018 12 155 (6): 1908-1922.e5. Tang Clara Sze-Man, Li Peng, Lai Frank Pui-Ling, Fu Alexander Xi, Lau Sin-Ting, So Man Ting, Lui Kathy Nga-Chu, Li Zhixin, Zhuang Xuehan, Yu Michelle, Liu Xuelai, Ngo Ngoc D, Miao Xiaoping, Zhang Xi, Yi Bin, Tang Shaotao, Sun Xiaobing, Zhang Furen, Liu Hong, Liu Qiji, Zhang Ruizhong, Wang Hualong, Huang Liuming, Dong Xiao, Tou Jinfa, Cheah Kathryn Song-Eng, Yang Wanling, Yuan Zhenwei, Yip Kevin Yuk-Lap, Sham Pak-Chung, Tam Paul Kwang-Hang, Garcia-Barcelo Maria-Mercè, Ngan Elly Sau-W |
Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung's Disease in Han Chinese Population. Frontiers in genetics 2020 8 11 738. Niu Wei-Bo, Bai Mei-Rong, Song Huan-Lei, Lu Yan-Jiao, Wu Wen-Jie, Gong Yi-Ming, Yu Xian-Xian, Wei Zhi-Liang, Yu Wen-Wen, Gu Bei-Lin, Cai Wei, Chu X |
Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2020 11 58 (3): 377-387. Qiao F, Wang Y, Zhang C, Zhou R, Wu Y, Wang C, Meng L, Mao P, Cheng Q, Luo C, Hu P, Xu |
Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort.
![]() Bone & joint research 2021 Nov 10 (11): 734-741. Cheng Bolun, Wen Yan, Yang Xuena, Cheng Shiqiang, Liu Li, Chu Xiaomeng, Ye Jing, Liang Chujun, Yao Yao, Jia Yumeng, Zhang Fe |
Exome sequencing and analysis of 454,787 UK Biobank participants.
![]() Nature 2021 10 599 (7886): 628-634. Backman Joshua D, Li Alexander H, Marcketta Anthony, Sun Dylan, Mbatchou Joelle, Kessler Michael D, Benner Christian, Liu Daren, Locke Adam E, Balasubramanian Suganthi, Yadav Ashish, Banerjee Nilanjana, Gillies Christopher E, Damask Amy, Liu Simon, Bai Xiaodong, Hawes Alicia, Maxwell Evan, Gurski Lauren, Watanabe Kyoko, Kosmicki Jack A, Rajagopal Veera, Mighty Jason, , , Jones Marcus, Mitnaul Lyndon, Stahl Eli, Coppola Giovanni, Jorgenson Eric, Habegger Lukas, Salerno William J, Shuldiner Alan R, Lotta Luca A, Overton John D, Cantor Michael N, Reid Jeffrey G, Yancopoulos George, Kang Hyun M, Marchini Jonathan, Baras Aris, Abecasis Gonçalo R, Ferreira Manuel A |
Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects. Pharmacogenomics and personalized medicine 2023 3 16 173-181. Cai Rongqin, Tan Ya, Wang Mingming, Yu Huijun, Wang Jing, Ren Zhuo, Dong Zhe, He Yiwen, Li Zhi, Lin Li, Gu Yi |
Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning. Vavilovskii zhurnal genetiki i selektsii 2023 10 27 (5): 522-529. D E Ivanoshchuk, A B Kolker, O V Timoshchenko, S E Semaev, E V Shakhtshneid |
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- Page last updated:Jun 24, 2024
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