Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and NT5C2[original query] |
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A comprehensive family-based replication study of schizophrenia genes.
JAMA psychiatry 2013 Jun 70 (6): 573-81. Aberg Karolina A, Liu Youfang, Bukszár Jozsef, McClay Joseph L, Khachane Amit N, Andreassen Ole A, Blackwood Douglas, Corvin Aiden, Djurovic Srdjan, Gurling Hugh, Ophoff Roel, Pato Carlos N, Pato Michele T, Riley Brien, Webb Todd, Kendler Kenneth, O'Donovan Mick, Craddock Nick, Kirov George, Owen Mike, Rujescu Dan, St Clair David, Werge Thomas, Hultman Christina M, Delisi Lynn E, Sullivan Patrick, van den Oord Edwin |
| SLC28A3 genotype and gemcitabine rate of infusion affect dFdCTP metabolite disposition in patients with solid tumours. British journal of cancer 2014 Jan 110 (2): 304-12. Khatri A, Williams B W, Fisher J, Brundage R C, Gurvich V J, Lis L G, Skubitz K M, Dudek A Z, Greeno E W, Kratzke R A, Lamba J K, Kirstein M |
| Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Stroke; a journal of cerebral circulation 2014 Jan 45 (1): 24-36. Dichgans Martin, Malik Rainer, König Inke R, Rosand Jonathan, Clarke Robert, Gretarsdottir Solveig, Thorleifsson Gudmar, Mitchell Braxton D, Assimes Themistocles L, Levi Christopher, O'Donnell Christopher J, Fornage Myriam, Thorsteinsdottir Unnur, Psaty Bruce M, Hengstenberg Christian, Seshadri Sudha, Erdmann Jeanette, Bis Joshua C, Peters Annette, Boncoraglio Giorgio B, März Winfried, Meschia James F, Kathiresan Sekar, Ikram M Arfan, McPherson Ruth, Stefansson Kari, Sudlow Cathie, Reilly Muredach P, Thompson John R, Sharma Pankaj, Hopewell Jemma C, Chambers John C, Watkins Hugh, Rothwell Peter M, Roberts Robert, Markus Hugh S, Samani Nilesh J, Farrall Martin, Schunkert Heribert, , , , |
| Two-stage replication of previous genome-wide association studies of AS3MT-CNNM2-NT5C2 gene cluster region in a large schizophrenia case-control sample from Han Chinese population. Schizophrenia research 2016 Jul . Guan Fanglin, Zhang Tianxiao, Li Lu, Fu Dongke, Lin Huali, Chen Gang, Chen Te |
| Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis. Scientific reports 2017 Jan 7 40303. López-Mejías Raquel, Corrales Alfonso, Vicente Esther, Robustillo-Villarino Montserrat, González-Juanatey Carlos, Llorca Javier, Genre Fernanda, Remuzgo-Martínez Sara, Dierssen-Sotos Trinidad, Miranda-Filloy José A, Huaranga Marco A Ramírez, Pina Trinitario, Blanco Ricardo, Alegre-Sancho Juan J, Raya Enrique, Mijares Verónica, Ubilla Begoña, Ferraz-Amaro Iván, Gómez-Vaquero Carmen, Balsa Alejandro, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Ocejo-Vinyals J Gonzalo, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Castañeda Santos, Martín Javier, González-Gay Miguel |
| NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia.
Leukemia 2018 Sep . Tulstrup Morten, Grosjean Marie, Nielsen Stine Nygaard, Grell Kathrine, Wolthers Benjamin Ole, Wegener Peder Skov, Jonsson Olafur Gisli, Lund Bendik, Harila-Saari Arja, Abrahamsson Jonas, Vaitkeviciene Goda, Pruunsild Kaie, Toft Nina, Holm Mette, Hulegårdh Erik, Liestøl Sigurd, Griskevicius Laimonas, Punab Mari, Wang Jinhua, Carroll William L, Zhang Zeyu, Dalgaard Marlene D, Gupta Ramneek, Nersting Jacob, Schmiegelow Kje |
| NT5C2 Gene Polymorphisms and the Risk of Coronary Heart Disease. Public health genomics 2020 Jun 1-10. Chen Xianghong, Zhang Zaozhang, Wang Xingfan, Chen Yuewu, Wang Ch |
| First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
| 5'-nucleotidase, cytosolic II genotype, and clinical outcome in patients with acute myeloid leukemia with intermediate-risk cytogenetics. European journal of haematology 2022 Sep . Díaz-Santa Johana, Rodríguez-Romanos Rocío, Coll Rosa, Osca Gemma, Pratcorona Marta, González-Bártulos Marta, Garrido Ana, Angona Anna, Talarn Carme, Tormo Mar, Arnan Montserrat, Vives Susanna, Salamero Olga, Tuset Esperanza, Lloveras Natàlia, Díez Isabel, Zamora Lurdes, Bargay Joan, Sampol Antonia, Cruz David, Vila Jordi, Sitges Marta, Garcia Antoni, Vall-Llovera Ferran, Esteve Jordi, Sierra Jorge, Gallardo David, |
| Whole-exome sequencing reveals a comprehensive germline mutation landscape and identifies twelve novel predisposition genes in Chinese prostate cancer patients. PLoS genetics 2022 Sep 18 (9): e1010373. Liang Yonghao, Chiu Peter Ka-Fung, Zhu Yao, Wong Christine Yim-Ping, Xiong Qing, Wang Lin, Teoh Jeremy Yuen-Chun, Cao Qin, Wei Yu, Ye Ding-Wei, Tsui Stephen Kwok-Wing, Ng Chi-F |
| Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype. Vavilovskii zhurnal genetiki i selektsii 2021 Dec 25 (8): 855-863. Goncharova I A, Bragina E Yu, Zhalsanova I Zh, Freidin M B, Nazarenko M |
| Chromosome 10q24.32 Variants Associate With Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study. Journal of the American Heart Association 2023 12 12 (23): e030935. Minghua Liu, Farid Khasiyev, Sanjeev Sariya, Antonio Spagnolo-Allende, Danurys L Sanchez, Howard Andrews, Qiong Yang, Alexa Beiser, Ye Qiao, Emy A Thomas, Jose Rafael Romero, Tatjana Rundek, Adam M Brickman, Jennifer J Manly, Mitchell Sv Elkind, Sudha Seshadri, Christopher Chen, Saima Hilal, Bruce A Wasserman, Giuseppe Tosto, Myriam Fornage, Jose Gutierr |
| Clinical Utility of a Novel Triplex Digital PCR Assay for Clone Monitoring in Sequential and Relapsed Pediatric B-Cell Acute Lymphoblastic Leukemia Patients. Pediatric blood & cancer 2024 11 e31443. Prateek Bhatia, Rozy Thakur, Sreejesh Sreedharanunni, Minu Singh, Meenakshi Malhotra, Swati Arora, Ashish George, Amita Treh |
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