Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: ACTN1[original query] |
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Glutamate and synaptic plasticity systems and smoking behavior: results from a genetic association study. PloS one 2012 7 (6): e38666. dos Santos Vanessa Argondizo, Chatkin Jose Miguel, Bau Claiton Henrique Dotto, Paixão-Côrtes Vanessa Rodrigues, Sun Ye, Zamel Noe, Siminovitch Katheri |
[Association study between candidate genes involved in cell-cell adhesion and non-syndromic cleft lip with or without cleft palate in Chinese population]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2016 Jun 48 (3): 403-8. Yuan Y, Wang P, Wu-Chou Y H, Ye X Q, Huang S Z, Shi B, Wang K, Wang Z Q, Liu D J, Wang Z F, Wu T, Wang |
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
American journal of human genetics 2016 Feb 98 (2): 229-42. Schick Ursula M, Jain Deepti, Hodonsky Chani J, Morrison Jean V, Davis James P, Brown Lisa, Sofer Tamar, Conomos Matthew P, Schurmann Claudia, McHugh Caitlin P, Nelson Sarah C, Vadlamudi Swarooparani, Stilp Adrienne, Plantinga Anna, Baier Leslie, Bien Stephanie A, Gogarten Stephanie M, Laurie Cecelia A, Taylor Kent D, Liu Yongmei, Auer Paul L, Franceschini Nora, Szpiro Adam, Rice Ken, Kerr Kathleen F, Rotter Jerome I, Hanson Robert L, Papanicolaou George, Rich Stephen S, Loos Ruth J F, Browning Brian L, Browning Sharon R, Weir Bruce S, Laurie Cathy C, Mohlke Karen L, North Kari E, Thornton Timothy A, Reiner Alex |
Network based subcellular proteomics in monocyte membrane revealed novel candidate genes involved in osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2017 7 28 (10): 3033-3042. Zeng Y, Zhang L, Zhu W, He H, Sheng H, Tian Q, Deng F-Y, Zhang L-S, Hu H-G, Deng H |
Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura. Pediatric blood & cancer 2018 8 65 (12): e27418. Kanhai Danny, Mulder René, Ploos van Amstel Hans Kristian, Schutgens Roger, Lukens Michael, Tamminga Rienk Y |
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. British journal of haematology 2018 10 183 (2): 276-288. Faleschini Michela, Melazzini Federica, Marconi Caterina, Giangregorio Tania, Pippucci Tommaso, Cigalini Elena, Pecci Alessandro, Bottega Roberta, Ramenghi Ugo, Siitonen Timo, Seri Marco, Pastore Annalisa, Savoia Anna, Noris Patriz |
Gene-gene interaction among cell adhesion genes and risk of nonsyndromic cleft lip with or without cleft palate in Chinese case-parent trios. Molecular genetics & genomic medicine 2019 Aug e872. Liu Dongjing, Wang Mengying, Yuan Yuan, Schwender Holger, Wang Hong, Wang Ping, Zhou Zhibo, Li Jing, Wu Tao, Zhu Hongping, Beaty Terri |
Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.
Current Alzheimer research 2019 16 (13): 1163-1174. Li Jin, Chen Feng, Zhang Qiushi, Meng Xianglian, Yao Xiaohui, Risacher Shannon L, Yan Jingwen, Saykin Andrew J, Liang Hong, Shen Li, |
COVID-19 in pediatrics: Genetic susceptibility.
Frontiers in genetics 2022 9 13 928466. Glessner Joseph T, Chang Xiao, Mentch Frank, Qu Huiqi, Abrams Debra J, Thomas Alexandria, Sleiman Patrick M A, Hakonarson Hak |
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