Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 6 (of 6 Records)

Query Trace: Disease and PLD1[original query]
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
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
Exome sequencing and analysis of 454,787 UK Biobank participants. GWAS Catalog
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
TOP