Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: PTPRN2[original query] |
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Genetic variants associated with syncope implicate neural and autonomic processes.
European heart journal 2023 2 44 (12): 1070-1080. Aegisdottir Hildur M, Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Stefansson Olafur A, Gunnarsson Bjarni, Tragante Vinicius, Thorleifsson Gudmar, Stefansdottir Lilja, Thorgeirsson Thorgeir E, Ferkingstad Egil, Sulem Patrick, Norddahl Gudmundur, Rutsdottir Gudrun, Banasik Karina, Christensen Alex Hoerby, Mikkelsen Christina, Pedersen Ole Birger, Brunak Søren, Bruun Mie Topholm, Erikstrup Christian, Jacobsen Rikke Louise, Nielsen Kaspar Rene, Sørensen Erik, Frigge Michael L, Hjorleifsson Kristjan E, Ivarsdottir Erna V, Helgadottir Anna, Gretarsdottir Solveig, Steinthorsdottir Valgerdur, Oddsson Asmundur, Eggertsson Hannes P, Halldorsson Gisli H, Jones David A, Anderson Jeffrey L, Knowlton Kirk U, Nadauld Lincoln D, , Haraldsson Magnus, Thorgeirsson Gudmundur, Bundgaard Henning, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Ostrowski Sisse R, Holm Hilma, Stefansson Ka |
Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients. Genes, chromosomes & cancer 2008 Aug 47 (8): 680-96. Nordgard Silje H, Johansen Fredrik E, Alnaes Grethe I G, Bucher Elmar, Syvänen Ann-Christine, Naume Bjørn, Børresen-Dale Anne-Lise, Kristensen Vessela |
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
Association of genetic variants with chronic kidney disease in Japanese individuals with or without hypertension or diabetes mellitus. Experimental and therapeutic medicine 2012 11 1 (1): 137-145. Yoshida Tetsuro, Kato Kimihiko, Yokoi Kiyoshi, Oguri Mitsutoshi, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nozawa Yoshinori, Yamada Yoshi |
Host genetic predictors of the kynurenine pathway of tryptophan catabolism among treated HIV-infected Ugandans. AIDS (London, England) 2016 Apr . Lee Sulggi A, Mefford Joel A, Huang Yong, Witte John S, Martin Jeffrey N, Haas David W, Mclaren Paul J, Mushiroda Taisei, Kubo Michiaki, Byakwaga Helen, Hunt Peter W, Kroetz Deanna |
An investigation of obesity susceptibility genes in Northern Han Chinese by targeted resequencing. Medicine 2017 Feb 96 (7): e6117. Wu Yili, Wang Weijing, Jiang Wenjie, Yao Jie, Zhang Dongfe |
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity. European journal of human genetics : EJHG 2018 Jul . Selvanayagam Thanuja, Walker Susan, Gazzellone Matthew J, Kellam Barbara, Cytrynbaum Cheryl, Stavropoulos Dimitri J, Li Ping, Birken Catherine S, Hamilton Jill, Weksberg Rosanna, Scherer Stephen |
Novel CSF biomarkers in genetic frontotemporal dementia identified by proteomics. Annals of clinical and translational neurology 2019 4 6 (4): 698-707. van der Ende Emma L, Meeter Lieke H, Stingl Christoph, van Rooij Jeroen G J, Stoop Marcel P, Nijholt Diana A T, Sanchez-Valle Raquel, Graff Caroline, Öijerstedt Linn, Grossman Murray, McMillan Corey, Pijnenburg Yolande A L, Laforce Robert, Binetti Giuliano, Benussi Luisa, Ghidoni Roberta, Luider Theo M, Seelaar Harro, van Swieten John |
The association of genetically controlled CpG methylation (cg158269415) of protein tyrosine phosphatase, receptor type N2 (PTPRN2) with childhood obesity. Scientific reports 2019 Mar 9 (1): 4855. Lee Sum |
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke. Stroke 2020 3 51 (4): 1056-1063. Ilinca Andreea, Martinez-Majander Nicolas, Samuelsson Sofie, Piccinelli Paul, Truvé Katarina, Cole John, Kittner Steven, Soller Maria, Kristoffersson Ulf, Tatlisumak Turgut, Puschmann Andreas, Putaala Jukka, Lindgren Ar |
Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population.
Journal of cellular and molecular medicine 2020 Nov . Niu Yuguang, Xie Chengyong, Du Zhenhua, Zeng Jifeng, Chen Hongxia, Jin Liang, Zhang Qing, Yu Huiying, Wang Yahui, Ping Jie, Yang Chenning, Liu Xinyi, Li Yuanfeng, Zhou Gangqi |
Developing a novel DNA methylation risk score for survival and identification of prognostic gene mutations in endometrial cancer: a study based on TCGA data. Japanese journal of clinical oncology 2022 5 52 (9): 992-1000. Shen Po-Chien, Wang Ying-Fu, Chang Hao-Chih, Huang Wen-Yen, Lo Cheng-Hsiang, Su Yu-Fu, Yang Jen-Fu, Lin Chun-Shu, Dai Yang-Ho |
Sweet Taste Preference: Relationships with Other Tastes, Liking for Sugary Foods and Exploratory Genome-Wide Association Analysis in Subjects with Metabolic Syndrome. Biomedicines 2022 1 10 (1): . Fernández-Carrión Rebeca, Sorlí Jose V, Coltell Oscar, Pascual Eva C, Ortega-Azorín Carolina, Barragán Rocío, Giménez-Alba Ignacio M, Alvarez-Sala Andrea, Fitó Montserrat, Ordovas Jose M, Corella Dolor |
Establishment of a novel signature to predict prognosis and immune characteristics of pancreatic cancer based on necroptosis-related long non-coding RNA. Molecular biology reports 2023 7 . Yuanpeng Xiong, Xiaoyu Kong, Kang Fang, Gen Sun, Shuju Tu, Yongyang Wei, Yonghao Ouyang, Renhua Wan, Weidong Xi |
Genome-wide association study identifies WWC2 as a possible locus associated with persistent pulmonary hypertension of the newborn in the Thai population. Translational pediatrics 2023 2 12 (1): 1-12. Nakwan Narongsak, Kunhapan Punna, Chaiyasung Tassamonwan, Satproedprai Nusara, Singkhamanan Kamonnut, Mahasirimongkol Surakameth, Charalsawadi Chariyaw |
Screening of genes interacting with high myopia and neuropsychiatric disorders. Scientific reports 2023 10 13 (1): 18347. Yang Liu, Yang Liu, Wen Zhang, Zhong-Qi Xue, Fang-Xia Zhang, Wei-Gang Xu, Wen-Juan Zhua |
Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China. BMC medical genomics 2024 1 17 (1): 18. Shan Wu, Zhidan Wu, Manlian Chen, Xiangbin Zhong, Haoyan Gu, Wenjing Du, Weidong Liu, Li Lang, Junyi Wa |
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- Page last updated:Apr 22, 2024
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