Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
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| Development of a human acute myeloid leukaemia screening panel and consequent identification of novel gene mutation in FLT3 and CCND3. British journal of haematology 2005 1 128 (3): 318-23. Smith Matthew L, Arch Rachael, Smith Lan-Lan, Bainton Nigel, Neat Michael, Taylor Claire, Bonnet Dominique, Cavenagh Jamie D, Andrew Lister T, Fitzgibbon Ju |
| Influence of a single nucleotide polymorphism in the P1 promoter of the furin gene on transcription activity and hepatitis B virus infection. Hepatology (Baltimore, Md.) 2009 Sep 50 (3): 763-71. Lei Rui Xiang, Shi Hong, Peng Xiao Mou, Zhu Yin Hong, Cheng Jie, Chen Gui H |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
| SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. The Journal of clinical endocrinology and metabolism 2013 May 98 (5): E973-80. He Huiling, Bronisz Agnieszka, Liyanarachchi Sandya, Nagy Rebecca, Li Wei, Huang Yungui, Akagi Keiko, Saji Motoyasu, Kula Dorota, Wojcicka Anna, Sebastian Nikhil, Wen Bernard, Puch Zbigniew, Kalemba Michal, Stachlewska Elzbieta, Czetwertynska Malgorzata, Dlugosinska Joanna, Dymecka Kinga, Ploski Rafal, Krawczyk Marek, Morrison Patrick J, Ringel Matthew D, Kloos Richard T, Jazdzewski Krystian, Symer David E, Vieland Veronica J, Ostrowski Michael, Jarz?b Barbara, de la Chapelle Albe |
| Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
Human molecular genetics 2013 Jul 22 (13): 2754-64. Stambolian Dwight, Wojciechowski Robert, Oexle Konrad, Pirastu Mario, Li Xiaohui, Raffel Leslie J, Cotch Mary Frances, Chew Emily Y, Klein Barbara, Klein Ronald, Wong Tien Y, Simpson Claire L, Klaver Caroline C W, van Duijn Cornelia M, Verhoeven Virginie J M, Baird Paul N, Vitart Veronique, Paterson Andrew D, Mitchell Paul, Saw Seang Mei, Fossarello Maurizio, Kazmierkiewicz Krista, Murgia Federico, Portas Laura, Schache Maria, Richardson Andrea, Xie Jing, Wang Jie Jin, Rochtchina Elena, , Viswanathan Ananth C, Hayward Caroline, Wright Alan F, Polasek Ozren, Campbell Harry, Rudan Igor, Oostra Ben A, Uitterlinden André G, Hofman Albert, Rivadeneira Fernando, Amin Najaf, Karssen Lennart C, Vingerling Johannes R, Hosseini S M, Döring Angela, Bettecken Thomas, Vatavuk Zoran, Gieger Christian, Wichmann H-Erich, Wilson James F, Fleck Brian, Foster Paul J, Topouzis Fotis, McGuffin Peter, Sim Xueling, Inouye Michael, Holliday Elizabeth G, Attia John, Scott Rodney J, Rotter Jerome I, Meitinger Thomas, Bailey-Wilson Joan |
| Protein Kinase Activity Decreases with Higher Braak Stages of Alzheimer's Disease Pathology. Journal of Alzheimer's disease : JAD 2015 Oct . Rosenberger Andrea F N, Hilhorst Riet, Coart Elisabeth, García Barrado Leandro, Naji Faris, Rozemuller Annemieke J M, van der Flier Wiesje M, Scheltens Philip, Hoozemans Jeroen J M, van der Vies Saskia |
| Association between function and structure of the triple network and catechol-O-methyltransferase valmet polymorphism in the first episode schizophrenia. Neuroscience letters 2018 9 687 65-70. Kang Yafei, Huang Kexin, Cai Suping, Wang Haidong, Liu Jixin, Wang Yubo, Lv Yahui, Zhang Wei, Wang Qiang, Huang Liyu, Wang Jijun, Tian J |
| Genetic contribution of catechol-O-methyltransferase in dorsolateral prefrontal cortex functional changes in the first episode schizophrenia. Behavioural brain research 2019 Feb . Kang Yafei, Huang Kexin, Lv Yahui, Zhang Wei, Cai Suping, Wang Yubo, Wang Qiang, Huang Liyu, Wang Jijun, Tian J |
| Genetic polymorphism in catechol-O-methyltransferase associated with the functional connectivity of frontostriatal circuits in first episode schizophrenia patients. The European journal of neuroscience 2019 Dec . Kang Yafei, Zhang Wei, Lv Yahui, Xu Hanxiao, Lin Yanyan, Cai Suping, Wang Jijun, Huang Li |
| Gender differences of neurocognitive functioning in patients with first-episode schizophrenia in China. Comprehensive psychiatry 2019 11 95 152132. Pu Chengcheng, Qiu Yujia, Zhou Tianhang, Yang Fude, Lu Zheng, Wang Chuanyue, Deng Hong, Zhao Jingping, Shi Chuan, Yu X |
| Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
eLife 2019 01 8 . Timmers Paul Rhj, Mounier Ninon, Lall Kristi, Fischer Krista, Ning Zheng, Feng Xiao, Bretherick Andrew D, Clark David W, , Shen Xia, Esko Tõnu, Kutalik Zoltán, Wilson James F, Joshi Peter |
| FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration. Journal of the American Heart Association 2020 Feb 9 (4): e014333. Yang Xu, Yang Wei, McVey David G, Zhao Guojun, Hu Jinfu, Poston Robin N, Ren Meixia, Willeit Karin, Coassin Stefan, Willeit Johann, Webb Thomas R, Samani Nilesh J, Mayr Manuel, Kiechl Stefan, Ye S |
| SAP97 rs3915512 Polymorphism Affects the Neurocognition of Schizophrenic Patients: A Genetic Neuroimaging Study. Frontiers in genetics 2020 11 11 572414. Xu Xusan, He Bin, Lin Zhixiong, Wang Xiaoxia, Yin Jingwen, Luo Xudong, Luo Shucun, Liang Chunmei, Wen Xia, Xiong Susu, Zhu Dongjian, Fu Jiawu, Lv Dong, Dai Zhun, Lin Juda, Li You, Chen Wubiao, Luo Zebin, Wang Yajun, Ma Guo |
| Uncovering potential single nucleotide polymorphisms, copy number variations and related signaling pathways in primary Sjogren's syndrome. Bioengineered 2021 11 12 (2): 9313-9331. Qi Xuan, Wang Xi-Qin, Jin Lu, Gao Li-Xia, Guo Hui-Fa |
| Salivary microbiome profiling reveals a dysbiotic schizophrenia-associated microbiota. NPJ schizophrenia 2021 10 7 (1): 51. Qing Ying, Xu Lihua, Cui Gaoping, Sun Liya, Hu Xiaowen, Yang Xuhan, Jiang Jie, Zhang Juan, Zhang Tianhong, Wang Tao, He Lin, Wang Jijun, Wan Chunli |
| The genetic influence of the DRD3 rs6280 polymorphism (Ser9Gly) on functional connectivity and gray matter volume of the hippocampus in patients with first-episode, drug-naïve schizophrenia. Behavioural brain research 2022 9 437 114124. Kang Yafei, Zhang Youming, Huang Kexin, Wang Zhenho |
| The oral selective estrogen receptor degrader GDC-0810 (ARN-810) in postmenopausal women with hormone receptor-positive HER2-negative (HR?+?/HER2?-) advanced/metastatic breast cancer. Breast cancer research and treatment 2022 11 197 (2): 319-331. Bardia Aditya, Mayer Ingrid, Winer Eric, Linden Hannah M, Ma Cynthia X, Parker Barbara A, Bellet Meritxell, Arteaga Carlos L, Cheeti Sravanthi, Gates Mary, Chang Ching-Wei, Fredrickson Jill, Spoerke Jill M, Moore Heather M, Giltnane Jennifer, Friedman Lori S, Chow Maneval Edna, Chan Iris, Jhaveri Kom |
| Genetic contribution of synapse-associated protein 97 to cerebellar functional connectivity changes in first-episode schizophrenia. BMC psychiatry 2023 8 23 (1): 630. Xusan Xu, Shucun Luo, Xiaoxia Wang, Xia Wen, Jingwen Yin, Xudong Luo, Bin He, Chunmei Liang, Susu Xiong, Dongjian Zhu, Dong Lv, Zhun Dai, Juda Lin, You Li, Zhixiong Lin, Wubiao Chen, Zebin Luo, Yajun Wang, Guoda |
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