HuGE Literature Finder
Records 1-10
|
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
Oncotarget 2016 Mar . Hemminki Kari, Chen Bowang, Kumar Abhishek, Melander Olle, Manjer Jonas, Hallmans Göran, Pettersson-Kymmer Ulrika, Ohlsson Claes, Folprecht Gunnar, Löffler Harald, Krämer Alwin, Försti As |
|
[Association of TIAM1 gene polymorphisms with Kawasaki disease and its clinical characteristics].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2015 Nov 17 (11): 1217-20. Wang Xian, Zhu Tian-Jiao, Zhou Xiong-Fei, Wan Zhi-Ti |
|
Genome-wide association pathway analysis to identify candidate single nucleotide polymorphisms and molecular pathways for gastric adenocarcinoma.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Jul 36 (7): 5635-9. Zhu Hongcheng, Yang Meilin, Zhang Hao, Chen Xiaochen, Yang Xi, Zhang Chi, Qin Qin, Cheng Hongyan, Sun Xinch |
|
Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2014 Jul 35 (7): 1089-95. Chen Xueping, Huang Rui, Chen Yongping, Zheng Zhenzhen, Chen Ke, Song Wei, Zhao Bi, Yang Yuan, Yuan Lixing, Shang Huifa |
|
Landscape of the relationship between type 2 diabetes and coronary heart disease through an integrated gene network analysis.
Gene 2014 Apr 539 (1): 30-6. Dong Changzheng, Tang Linlin, Liu Zhifang, Bu Shizhong, Liu Qiong, Wang Qinwen, Mai Yifeng, Wang Dao Wen, Duan Shiw |
|
Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2014 Jan 23 (1): 98-106. Tang Hongwei, Wei Peng, Duell Eric J, Risch Harvey A, Olson Sara H, Bueno-de-Mesquita H Bas, Gallinger Steven, Holly Elizabeth A, Petersen Gloria M, Bracci Paige M, McWilliams Robert R, Jenab Mazda, Riboli Elio, Tjønneland Anne, Boutron-Ruault Marie Christine, Kaaks Rudolf, Trichopoulos Dimitrios, Panico Salvatore, Sund Malin, Peeters Petra H M, Khaw Kay-Tee, Amos Christopher I, Li Dongh |
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
Human molecular genetics 2013 Aug 22 (15): 3174-85. Kirin Mirna, Chandra Aman, Charteris David G, Hayward Caroline, Campbell Susan, Celap Ivana, Bencic Goran, Vatavuk Zoran, Kirac Iva, Richards Allan J, Tenesa Albert, Snead Martin P, Fleck Brian W, Singh Jaswinder, Harsum Steven, Maclaren Robert E, den Hollander Anneke I, Dunlop Malcolm G, Hoyng Carel B, Wright Alan F, Campbell Harry, Vitart Veronique, Mitry Dan |
|
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.
Genome medicine 2011 3 (1): 3. Wang Joanne H, Pappas Derek, De Jager Philip L, Pelletier Daniel, de Bakker Paul Iw, Kappos Ludwig, Polman Chris H, , Chibnik Lori B, Hafler David A, Matthews Paul M, Hauser Stephen L, Baranzini Sergio E, Oksenberg Jorge |
|
Mutation of ARHGAP9 in patients with coronary spastic angina.
Journal of human genetics 2010 Jan 55 (1): 42-9. Takefuji Mikito, Asano Hiroyuki, Mori Kazutaka, Amano Mutsuki, Kato Katsuhiro, Watanabe Takashi, Morita Yasuhiro, Katsumi Akira, Itoh Toshiki, Takenawa Tadaomi, Hirashiki Akihiro, Izawa Hideo, Nagata Kozo, Hirayama Haruo, Takatsu Fumimaro, Naoe Tomoki, Yokota Mitsuhiro, Kaibuchi Ko |
|
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Molecular medicine (Cambridge, Mass.) 0 16 (7-8): 247-53. Rose Jed E, Behm Frédérique M, Drgon Tomas, Johnson Catherine, Uhl George |
- Page last reviewed:Jul 30, 2019
- Page last updated:Feb 20, 2020
- Content source: