Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CITED2[original query] |
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Identification and functional analysis of CITED2 mutations in patients with congenital heart defects. Human mutation 2005 Dec 26 (6): 575-82. Sperling Silke, Grimm Christina H, Dunkel Ilona, Mebus Siegrun, Sperling Hans-Peter, Ebner Arno, Galli Raffaello, Lehrach Hans, Fusch Christoph, Berger Felix, Hammer Stefan |
[Mutation analysis of Cited2 in patients with congenital heart disease]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2010 Apr 48 (4): 293-6. Yang Xiao-fei, Wu Xiao-yun, Li Mi, Li Yong-gang, Dai Jiang-tao, Bai Yong-hong, Tian J |
Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study. BMC medical genetics 2010 11 141. Lu Wei, Guzman Adrian R, Yang Wei, Chapa Claudia J, Shaw Gary M, Greene Robert M, Pisano M Michele, Lammer Edward J, Finnell Richard H, Zhu Huipi |
CITED2 mutations potentially cause idiopathic premature ovarian failure. Translational research : the journal of laboratory and clinical medicine 2012 Nov 160 (5): 384-8. Fonseca Dora Janeth, Ojeda Diego, Lakhal Besma, Braham Rim, Eggers Stefanie, Turbitt Erin, White Stefan, Grover Sonia, Warne Garry, Zacharin Margaret, Nevin Lam Alexandra, Landolsi Hanène, Elghezal Hatem, Saâd Ali, Restrepo Carlos Martín, Fellous Marc, Sinclair Andrew, Koopman Peter, Laissue Pa |
Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population. PloS one 2014 9 (5): e98157. Liu Yan, Wang Fengyu, Wu Yuan, Tan Sainan, Wen Qiaolian, Wang Jing, Zhu Xiaomei, Wang Xi, Li Congmin, Ma Xu, Pan Ho |
CITED2 mutation and methylation in children with congenital heart disease. Journal of biomedical science 2014 21 (1): 7. Xu Min, Wu Xiaoyun, Li Yonggang, Yang Xiaofei, Hu Jihua, Zheng Min, Tian J |
Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied biochemistry and biotechnology 2019 Sep . Dianatpour Sima, Khatami Mehri, Heidari Mohammad Mehdi, Hadadzadeh Meh |
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC genomics 2020 Mar 21 (1): 228. Hodonsky Chani J, Baldassari Antoine R, Bien Stephanie A, Raffield Laura M, Highland Heather M, Sitlani Colleen M, Wojcik Genevieve L, Tao Ran, Graff Marielisa, Tang Weihong, Thyagarajan Bharat, Buyske Steve, Fornage Myriam, Hindorff Lucia A, Li Yun, Lin Danyu, Reiner Alex P, North Kari E, Loos Ruth J F, Kooperberg Charles, Avery Christy |
Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.
Cell reports. Medicine 2022 12 3 (12): 100855. Park Joseph, MacLean Matthew T, Lucas Anastasia M, Torigian Drew A, Schneider Carolin V, Cherlin Tess, Xiao Brenda, Miller Jason E, Bradford Yuki, Judy Renae L, , Verma Anurag, Damrauer Scott M, Ritchie Marylyn D, Witschey Walter R, Rader Daniel |
Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal defects: Correlation with cardiac troponin T and caspase-3. Gene 2023 7 882 147660. Mohamed Taha, Nourhan Awny, Somaia Ismail, Engy A Ashaat, Mahmoud A Senou |
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- Page last updated:Apr 22, 2024
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