Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and SLC39A8[original query] |
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| Pleiotropic genes for metabolic syndrome and inflammation. Molecular genetics and metabolism 2014 Aug 112 (4): 317-38. Kraja Aldi T, Chasman Daniel I, North Kari E, Reiner Alexander P, Yanek Lisa R, Kilpeläinen Tuomas O, Smith Jennifer A, Dehghan Abbas, Dupuis Josée, Johnson Andrew D, Feitosa Mary F, Tekola-Ayele Fasil, Chu Audrey Y, Nolte Ilja M, Dastani Zari, Morris Andrew, Pendergrass Sarah A, Sun Yan V, Ritchie Marylyn D, Vaez Ahmad, Lin Honghuang, Ligthart Symen, Marullo Letizia, Rohde Rebecca, Shao Yaming, Ziegler Mark A, Im Hae Kyung, , , , , , , , , , , , Schnabel Renate B, Jørgensen Torben, Jørgensen Marit E, Hansen Torben, Pedersen Oluf, Stolk Ronald P, Snieder Harold, Hofman Albert, Uitterlinden Andre G, Franco Oscar H, Ikram M Arfan, Richards J Brent, Rotimi Charles, Wilson James G, Lange Leslie, Ganesh Santhi K, Nalls Mike, Rasmussen-Torvik Laura J, Pankow James S, Coresh Josef, Tang Weihong, Linda Kao W H, Boerwinkle Eric, Morrison Alanna C, Ridker Paul M, Becker Diane M, Rotter Jerome I, Kardia Sharon L R, Loos Ruth J F, Larson Martin G, Hsu Yi-Hsiang, Province Michael A, Tracy Russell, Voight Benjamin F, Vaidya Dhananjay, O'Donnell Christopher J, Benjamin Emelia J, Alizadeh Behrooz Z, Prokopenko Inga, Meigs James B, Borecki Ingrid |
| Expression of RNAs Coding for Metal Transporters in Blood of Patients with Huntington's Disease. Neurochemical research 2015 Oct . Szeliga Monika, Ró?ycka Aleksandra, J?drak Paulina, Bara?ska Sylwia, Janik Piotr, Jamrozik Zygmunt, Albrecht J |
| A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition. Gastroenterology 2016 Aug . Li Dalin, Achkar Jean-Paul, Haritunians Talin, Jacobs Jonathan P, Hui Ken Y, D'Amato Mauro, Brand Stephan, Radford-Smith Graham, Halfvarson Jonas, Niess Jan-Hendrik, Kugathasan Subra, Büning Carsten, Schumm L Philip, Klei Lambertus, Ananthakrishnan Ashwin, Aumais Guy, Baidoo Leonard, Dubinsky Marla, Fiocchi Claudio, Glas Jürgen, Milgrom Raquel, Proctor Deborah D, Regueiro Miguel, Simms Lisa A, Stempak Joanne M, Targan Stephan R, Törkvist Leif, Sharma Yashoda, Devlin Bernie, Borneman James, Hakonarson Hakon, Xavier Ramnik J, Daly Mark, Brant Steven R, Rioux John D, Silverberg Mark S, Cho Judy H, Braun Jonathan, McGovern Dermot Pb, Duerr Richard |
Detection and interpretation of shared genetic influences on 42 human traits.
Nature genetics 2016 May . Pickrell Joseph K, Berisa Tomaz, Liu Jimmy Z, Ségurel Laure, Tung Joyce Y, Hinds David |
| Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.
Human molecular genetics 2016 Apr 25 (7): 1447-56. Johansson Åsa, Eriksson Niclas, Lindholm Daniel, Varenhorst Christoph, James Stefan, Syvänen Ann-Christine, Axelsson Tomas, Siegbahn Agneta, Barratt Bryan J, Becker Richard C, Himmelmann Anders, Katus Hugo A, Steg Philippe Gabriel, Storey Robert F, Wallentin Lars, |
| Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Circulation 2019 Jan 139 (5): 620-635. Sabater-Lleal Maria, Huffman Jennifer E, de Vries Paul S, Marten Jonathan, Mastrangelo Michael A, Song Ci, Pankratz Nathan, Ward-Caviness Cavin K, Yanek Lisa R, Trompet Stella, Delgado Graciela E, Guo Xiuqing, Bartz Traci M, Martinez-Perez Angel, Germain Marine, de Haan Hugoline G, Ozel Ayse B, Polasek Ozren, Smith Albert V, Eicher John D, Reiner Alex P, Tang Weihong, Davies Neil M, Stott David J, Rotter Jerome I, Tofler Geoffrey H, Boerwinkle Eric, de Maat Moniek P M, Kleber Marcus E, Welsh Paul, Brody Jennifer A, Chen Ming-Huei, Vaidya Dhananjay, Soria José Manuel, Suchon Pierre, van Hylckama Vlieg Astrid, Desch Karl C, Kolcic Ivana, Joshi Peter K, Launer Lenore J, Harris Tamara B, Campbell Harry, Rudan Igor, Becker Diane M, Li Jun Z, Rivadeneira Fernando, Uitterlinden André G, Hofman Albert, Franco Oscar H, Cushman Mary, Psaty Bruce M, Morange Pierre-Emmanuel, McKnight Barbara, Chong Michael R, Fernandez-Cadenas Israel, Rosand Jonathan, Lindgren Arne, , Gudnason Vilmundur, Wilson James F, Hayward Caroline, Ginsburg David, Fornage Myriam, Rosendaal Frits R, Souto Juan Carlos, Becker Lewis C, Jenny Nancy S, März Winfried, Jukema J Wouter, Dehghan Abbas, Trégouët David-Alexandre, Morrison Alanna C, Johnson Andrew D, O'Donnell Christopher J, Strachan David P, Lowenstein Charles J, Smith Nicholas |
| SLC39A8 is a risk factor for schizophrenia in Uygur Chinese: a case-control study. BMC psychiatry 2019 Sep 19 (1): 293. Jian Xuemin, Chen Jianhua, Li Zhiqiang, Song Zhijian, Zhou Juan, Xu Wei, Liu Yahui, Shen Jiawei, Wang Yonggang, Yi Qizhong, Shi Yongyo |
| SLC39A8 missense variant is associated with Crohn's disease but does not have a major impact on gut microbiome composition in healthy subjects. PloS one 2019 14 (1): e0211328. Collij Valerie, Imhann Floris, Vich Vila Arnau, Fu Jingyuan, Dijkstra Gerard, Festen Eleonora A M, Voskuil Michiel D, Daly Mark J, Xavier Ramnik J, Wijmenga Cisca, Zhernakova Alexandra, Weersma Rinse |
| Glycobiology and schizophrenia: a biological hypothesis emerging from genomic research. Molecular psychiatry 2020 5 25 (12): 3129-3139. Mealer Robert G, Williams Sarah E, Daly Mark J, Scolnick Edward M, Cummings Richard D, Smoller Jordan |
| Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis.
Journal of hepatology 2020 Aug 73 (2): 241-251. Parisinos Constantinos A, Wilman Henry R, Thomas E Louise, Kelly Matt, Nicholls Rowan C, McGonigle John, Neubauer Stefan, Hingorani Aroon D, Patel Riyaz S, Hemingway Harry, Bell Jimmy D, Banerjee Rajarshi, Yaghootkar Hani |
| Functional validity, role, and implications of heavy alcohol consumption genetic loci.
Science advances 2020 01 6 (3): eaay5034. Thompson Andrew, Cook James, Choquet Hélène, Jorgenson Eric, Yin Jie, Kinnunen Tarja, Barclay Jeff, Morris Andrew P, Pirmohamed Mun |
| Alcohol Consumption Is Associated with Poor Prognosis in Obese Patients with COVID-19: A Mendelian Randomization Study Using UK Biobank. Nutrients 2021 6 13 (5): . Fan Xiude, Liu Zhengwen, Poulsen Kyle L, Wu Xiaoqin, Miyata Tatsunori, Dasarathy Srinivasan, Rotroff Daniel M, Nagy Laura |
| Schizophrenia-associated SLC39A8 polymorphism is a loss-of-function allele altering glutamate receptor and innate immune signaling. Translational psychiatry 2021 Feb 11 (1): 136. Tseng Wei Chou, Reinhart Veronica, Lanz Thomas A, Weber Mark L, Pang Jincheng, Le Kevin Xuong Vinh, Bell Robert D, O'Donnell Patricio, Buhl Derek |
| C Deletion at the re74650330 Locus of the SLC39A8 Gene (rs74650330) Increases the Risk of Coronary Artery Disease in Individuals with Low-Density Lipoprotein Cholesterol Levels. Genetic testing and molecular biomarkers 2021 10 25 (10): 660-667. Zhang Jun, Yu Yang, Pan Lili, Yu Tianhong, Luo Guangh |
| A genome-wide association study for shoulder impingement and rotator cuff disease.
Journal of shoulder and elbow surgery 2021 Jan . Kim Stuart K, Nguyen Condor, Jones Kevin B, Tashjian Robert |
| Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.
Annals of the rheumatic diseases 2022 11 82 (3): 384-392. Henkel Cecilie, Styrkársdóttir Unnur, Thorleifsson Gudmar, Stefánsdóttir Lilja, Björnsdóttir Gyda, Banasik Karina, Brunak Søren, Erikstrup Christian, Dinh Khoa Manh, Hansen Thomas Folkmann, Nielsen Kaspar René, Bruun Mie Topholm, Dowsett Joseph, Brodersen Thorsten, , Thorgeirsson Thorgeir E, Gromov Kirill, Boesen Mikael Ploug, Ullum Henrik, Ostrowski Sisse Rye, Pedersen Ole Birger, Stefánsson Kári, Troelsen Ande |
| Influence of Metabolic, Transporter, and Pathogenic Genes on Pharmacogenetics and DNA Methylation in Neurological Disorders. Biology 2023 9 12 (9): . Olaia Martínez-Iglesias, Vinogran Naidoo, Iván Carrera, Juan Carlos Carril, Natalia Cacabelos, Ramón Cacabel |
| Does SLC39A8 Ala391Thr confer risk of chronic liver disease? Antioxidants & redox signaling 2024 4 . Anne-Sofie Seidelin, Boerge Nordestgaard, Anne Tybjærg-Hansen, Stefan Stend |
- Page last reviewed:Feb 1, 2024
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