Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: QKI[original query] |
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No association found between the promoter variations of QKI and schizophrenia in the Chinese population. Progress in neuro-psychopharmacology & biological psychiatry 2009 Feb 33 (1): 33-6. Huang Ke, Tang Wei, Xu Zhao, Li Zhiqiang, He Zhangdong, Tang Ruqi, Che Ronglin, Xu Yifeng, Li Xingwang, Feng Guoyin, He Lin, Shi Yongyo |
Linkage and association of successful aging to the 6q25 region in large Amish kindreds.
Age (Dordrecht, Netherlands) 2013 Aug 35 (4): 1467-77. Edwards Digna R Velez, Gilbert John R, Hicks James E, Myers Jamie L, Jiang Lan, Cummings Anna C, Guo Shengru, Gallins Paul J, Konidari Ioanna, Caywood Laura, Reinhart-Mercer Lori, Fuzzell Denise, Knebusch Claire, Laux Renee, Jackson Charles E, Pericak-Vance Margaret A, Haines Jonathan L, Scott William |
Comprehensive replication of the relationship between myopia-related genes and refractive errors in a large Japanese cohort. Investigative ophthalmology & visual science 2014 Nov 55 (11): 7343-54. Yoshikawa Munemitsu, Yamashiro Kenji, Miyake Masahiro, Oishi Maho, Akagi-Kurashige Yumiko, Kumagai Kyoko, Nakata Isao, Nakanishi Hideo, Oishi Akio, Gotoh Norimoto, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa, |
Linkage and whole genome sequencing identify a locus on 6q25-26 for formal thought disorder and implicate MEF2A regulation. Schizophrenia research 2015 Sep . Thygesen Johan Hilge, Zambach Sine Katharina, Ingason Andrés, Lundin Pär, Hansen Thomas, Berlatan Marcelo, Rosengren Anders, Bjerre Ditte, Ferrero-Miliani Laura, Rasmussen Henrik Berg, Parnas Josef, Werge Thom |
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.
PloS one 2016 11 (3): e0144997. Dehghan Abbas, Bis Joshua C, White Charles C, Smith Albert Vernon, Morrison Alanna C, Cupples L Adrienne, Trompet Stella, Chasman Daniel I, Lumley Thomas, Völker Uwe, Buckley Brendan M, Ding Jingzhong, Jensen Majken K, Folsom Aaron R, Kritchevsky Stephen B, Girman Cynthia J, Ford Ian, Dörr Marcus, Salomaa Veikko, Uitterlinden André G, Eiriksdottir Gudny, Vasan Ramachandran S, Franceschini Nora, Carty Cara L, Virtamo Jarmo, Demissie Serkalem, Amouyel Philippe, Arveiler Dominique, Heckbert Susan R, Ferrières Jean, Ducimetière Pierre, Smith Nicholas L, Wang Ying A, Siscovick David S, Rice Kenneth M, Wiklund Per-Gunnar, Taylor Kent D, Evans Alun, Kee Frank, Rotter Jerome I, Karvanen Juha, Kuulasmaa Kari, Heiss Gerardo, Kraft Peter, Launer Lenore J, Hofman Albert, Markus Marcello R P, Rose Lynda M, Silander Kaisa, Wagner Peter, Benjamin Emelia J, Lohman Kurt, Stott David J, Rivadeneira Fernando, Harris Tamara B, Levy Daniel, Liu Yongmei, Rimm Eric B, Jukema J Wouter, Völzke Henry, Ridker Paul M, Blankenberg Stefan, Franco Oscar H, Gudnason Vilmundur, Psaty Bruce M, Boerwinkle Eric, O'Donnell Christopher |
Comprehensive Genomic Profiling of 282 Pediatric Low- and High-Grade Gliomas Reveals Genomic Drivers, Tumor Mutational Burden, and Hypermutation Signatures. The oncologist 2017 9 22 (12): 1478-1490. Johnson Adrienne, Severson Eric, Gay Laurie, Vergilio Jo-Anne, Elvin Julia, Suh James, Daniel Sugganth, Covert Mandy, Frampton Garrett M, Hsu Sigmund, Lesser Glenn J, Stogner-Underwood Kimberly, Mott Ryan T, Rush Sarah Z, Stanke Jennifer J, Dahiya Sonika, Sun James, Reddy Prasanth, Chalmers Zachary R, Erlich Rachel, Chudnovsky Yakov, Fabrizio David, Schrock Alexa B, Ali Siraj, Miller Vincent, Stephens Philip J, Ross Jeffrey, Crawford John R, Ramkissoon Shakti |
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors. Neuro-oncology 2017 Jan . Ramkissoon Shakti H, Bandopadhayay Pratiti, Hwang Jaeho, Ramkissoon Lori A, Greenwald Noah F, Schumacher Steven E, O'Rourke Ryan, Pinches Nathan, Ho Patricia, Malkin Hayley, Sinai Claire, Filbin Mariella, Plant Ashley, Bi Wenya Linda, Chang Michael S, Yang Edward, Wright Karen D, Manley Peter E, Ducar Matthew, Alexandrescu Sanda, Lidov Hart, Delalle Ivana, Goumnerova Liliana C, Church Alanna J, Janeway Katherine A, Harris Marian H, MacConaill Laura E, Folkerth Rebecca D, Lindeman Neal I, Stiles Charles D, Kieran Mark W, Ligon Azra H, Santagata Sandro, Dubuc Adrian M, Chi Susan N, Beroukhim Rameen, Ligon Keith |
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Journal of human genetics 2019 Jun 64 (6): 573-587. Bandesh Khushdeep, Prasad Gauri, Giri Anil K, Kauser Yasmeen, Upadhyay Medha, , Basu Analabha, Tandon Nikhil, Bharadwaj Dwaipay |
Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation. Journal of neuropathology and experimental neurology 2021 8 80 (9): 821-829. Ida Cristiane M, Johnson Derek R, Nair Asha A, Davila Jaime, Kollmeyer Thomas M, Minn Kay, Fadra Numrah M, Balcom Jessica R, Fung Kar-Ming A, Kim Dong Kun, Kaufmann Timothy J, Kipp Benjamin R, Halling Kevin C, Jenkins Robert B, Giannini Cateri |
Epidemiologic association and shared genetic architecture between cataract and hearing difficulties among middle-aged and older adults. Human genomics 2024 4 18 (1): 39. Xiayin Zhang, Shan Wang, Shunming Liu, Zijing Du, Guanrong Wu, Yingying Liang, Yu Huang, Xianwen Shang, Yijun Hu, Zhuoting Zhu, Wei Sun, Xueli Zhang, Honghua |
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- Page last updated:Apr 22, 2024
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