Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: ZFPM2[original query] |
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ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia. American journal of medical genetics. Part A 2005 Feb 133A (1): 68-70. Sarkozy Anna, Conti Emanuela, D'Agostino Rita, Digilio Maria Cristina, Formigari Roberto, Picchio Fernando, Marino Bruno, Pizzuti Antonio, Dallapiccola Bru |
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. Clinical genetics 2011 Aug 80 (2): 184-90. De Luca Alessandro, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici M L, Vergara P, De Zorzi A, Versacci P, Digilio M C, Marino B, Dallapiccola |
Association of the ZFPM2 gene with antipsychotic-induced parkinsonism in schizophrenia patients. Psychopharmacology 2012 Apr 220 (3): 519-28. Greenbaum Lior, Smith Robert C, Lorberboym Mordechai, Alkelai Anna, Zozulinsky Polina, Lifschytz Tzuri, Lifshytz Tzuri, Kohn Yoav, Djaldetti Ruth, Lerer Berna |
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.
Circulation research 2011 Aug 109 (5): 554-63. Debette Stephanie, Visvikis-Siest Sophie, Chen Ming-Huen, Ndiaye Ndeye-Coumba, Song Ci, Destefano Anita, Safa Radwan, Azimi Nezhad Mohsen, Sawyer Douglas, Marteau Jean-Brice, Xanthakis Vanessa, Siest Gerard, Sullivan Lisa, Pfister Michele, Smith Holly, Choi Seung-Hoan, Lamont John, Lind Lars, Yang Qiong, Fitzgerald Peter, Ingelsson Erik, Vasan Ramachandran S, Seshadri Sud |
Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4. PloS one 2014 9 (7): e102379. Zhang Wenwen, Shen Li, Deng Zhantao, Ding Yibing, Mo Xuming, Xu Zhengfeng, Gao Qian, Yi Lo |
DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Investigative ophthalmology & visual science 2014 Dec 55 (12): 8251-8. Liu Yutao, Garrett Melanie E, Yaspan Brian L, Bailey Jessica Cooke, Loomis Stephanie J, Brilliant Murray, Budenz Donald L, Christen William G, Fingert John H, Gaasterland Douglas, Gaasterland Terry, Kang Jae H, Lee Richard K, Lichter Paul, Moroi Sayoko E, Realini Anthony, Richards Julia E, Schuman Joel S, Scott William K, Singh Kuldev, Sit Arthur J, Vollrath Douglas, Weinreb Robert, Wollstein Gadi, Zack Donald J, Zhang Kang, Pericak-Vance Margaret A, Haines Jonathan L, Pasquale Louis R, Wiggs Janey L, Allingham R Rand, Ashley-Koch Allison E, Hauser Michael |
Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population. Molecular biology reports 2014 41 (4): 2671-7. Huang Xiaomin, Niu Wenquan, Zhang Zhen, Zhou Chunxia, Xu Zhiwei, Liu Jinfen, Su Zhaokang, Ding Wenxiang, Zhang Hai |
Glioma Association and Balancing Selection of ZFPM2. PloS one 2015 10 (7): e0133003. Tsang Shui-Ying, Mei Lingling, Wan Weiqing, Li Jun, Li Yi, Zhao Cunyou, Ding Xiaofan, Pun Frank W, Hu Xiaoxia, Wang Jianmin, Zhang Junyi, Luo Rongcheng, Cheung Siu-Tim, Leung Gilberto K K, Poon Wai-Sang, Ng Ho-Keung, Zhang Liwei, Xue Ho |
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect. Genetics in medicine : official journal of the American College of Medical Genetics 2015 May . D'Alessandro Lisa C A, Al Turki Saeed, Manickaraj Ashok Kumar, Manase Dorin, Mulder Barbara J M, Bergin Lynn, Rosenberg Herschel C, Mondal Tapas, Gordon Elaine, Lougheed Jane, Smythe John, Devriendt Koen, Bhattacharya Shoumo, Watkins Hugh, Bentham Jamie, Bowdin Sarah, Hurles Matthew E, Mital See |
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS genetics 2016 Apr 12 (4): e1005963. Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan |
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity. Schizophrenia research 2016 Feb . Gadelha Ary, Coleman Jonathan, Breen Gerome, Mazzoti Diego Robles, Yonamine Camila M, Pellegrino Renata, Ota Vanessa Kiyomi, Belangero Sintia Iole, Glessner Joseph, Sleiman Patrick, Hakonarson Hakon, Hayashi Mirian A F, Bressan Rodrigo |
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies.
PLoS genetics 2016 Feb 12 (2): e1005874. Choi Seung Hoan, Ruggiero Daniela, Sorice Rossella, Song Ci, Nutile Teresa, Vernon Smith Albert, Concas Maria Pina, Traglia Michela, Barbieri Caterina, Ndiaye Ndeye Coumba, Stathopoulou Maria G, Lagou Vasiliki, Maestrale Giovanni Battista, Sala Cinzia, Debette Stephanie, Kovacs Peter, Lind Lars, Lamont John, Fitzgerald Peter, Tönjes Anke, Gudnason Vilmundur, Toniolo Daniela, Pirastu Mario, Bellenguez Celine, Vasan Ramachandran S, Ingelsson Erik, Leutenegger Anne-Louise, Johnson Andrew D, DeStefano Anita L, Visvikis-Siest Sophie, Seshadri Sudha, Ciullo Mari |
Vascular Endothelial Growth Factor and Ischemic Heart Disease Risk: A Mendelian Randomization Study. Journal of the American Heart Association 2017 8 6 (8): . Au Yeung Shiu Lun, Lam Hugh Simon Hung San, Schooling C Ma |
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Klarin Derek, Emdin Connor A, Natarajan Pradeep, Conrad Mark F, , Kathiresan Sek |
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing. Prenatal diagnosis 2018 Jul . Kammoun Molka, Souche Erika, Brady Paul, Ding Jia, Cosemans Nele, Gratacos Eduard, Devriendt Koen, Eixarch Elisenda, Deprest Jan, Vermeesch Joris Robe |
Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease. Pediatric cardiology 2018 Jan . Pulignani Silvia, Vecoli Cecilia, Borghini Andrea, Foffa Ilenia, Ait-Alì Lamia, Andreassi Maria Graz |
Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect. Genesis (New York, N.Y. : 2000) 2019 Sep e23333. Zhao Zhengshan, Zhan Yongkun, Chen Weicheng, Ma Xiaojing, Sheng Wei, Huang Guoyi |
Association between SNPs of Circulating Vascular Endothelial Growth Factor Levels, Hypercholesterolemia and Metabolic Syndrome. Medicina (Kaunas, Lithuania) 2019 Aug 55 (8): . Salami Ali, El Shamieh Sa |
Genome-wide identification of circulating-miRNA expression quantitative trait loci reveals the role of several miRNAs in the regulation of cardiometabolic phenotypes. Cardiovascular research 2019 Jan . Nikpay Majid, Beehler Kaitlyn, Valsesia Armand, Hager Jorg, Harper Mary-Ellen, Dent Robert, McPherson Ru |
Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy.
American journal of human genetics 2019 Dec 105 (6): 1076-1090. Nath Artika P, Ritchie Scott C, Grinberg Nastasiya F, Tang Howard Ho-Fung, Huang Qin Qin, Teo Shu Mei, Ahola-Olli Ari V, Würtz Peter, Havulinna Aki S, Santalahti Kristiina, Pitkänen Niina, Lehtimäki Terho, Kähönen Mika, Lyytikäinen Leo-Pekka, Raitoharju Emma, Seppälä Ilkka, Sarin Antti-Pekka, Ripatti Samuli, Palotie Aarno, Perola Markus, Viikari Jorma S, Jalkanen Sirpa, Maksimow Mikael, Salmi Marko, Wallace Chris, Raitakari Olli T, Salomaa Veikko, Abraham Gad, Kettunen Johannes, Inouye Micha |
Implications of venous thromboembolism GWAS reported genetic makeup in the clinical outcome of ovarian cancer patients. The pharmacogenomics journal 2020 Nov . Tavares Valéria, Pinto Ricardo, Assis Joana, Coelho Sara, Brandão Mariana, Alves Sara, Pereira Deolinda, Medeiros R |
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- Page last updated:Apr 22, 2024
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