HuGE Literature Finder
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A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Nature genetics 2022 Jun 54 (6): 761-771. Vujkovic Marijana, Ramdas Shweta, Lorenz Kim M, Guo Xiuqing, Darlay Rebecca, Cordell Heather J, He Jing, Gindin Yevgeniy, Chung Chuhan, Myers Robert P, Schneider Carolin V, Park Joseph, Lee Kyung Min, Serper Marina, Carr Rotonya M, Kaplan David E, Haas Mary E, MacLean Matthew T, Witschey Walter R, Zhu Xiang, Tcheandjieu Catherine, Kember Rachel L, Kranzler Henry R, Verma Anurag, Giri Ayush, Klarin Derek M, Sun Yan V, Huang Jie, Huffman Jennifer E, Creasy Kate Townsend, Hand Nicholas J, Liu Ching-Ti, Long Michelle T, Yao Jie, Budoff Matthew, Tan Jingyi, Li Xiaohui, Lin Henry J, Chen Yii-Der Ida, Taylor Kent D, Chang Ruey-Kang, Krauss Ronald M, Vilarinho Silvia, Brancale Joseph, Nielsen Jonas B, Locke Adam E, Jones Marcus B, Verweij Niek, Baras Aris, Reddy K Rajender, Neuschwander-Tetri Brent A, Schwimmer Jeffrey B, Sanyal Arun J, Chalasani Naga, Ryan Kathleen A, Mitchell Braxton D, Gill Dipender, Wells Andrew D, Manduchi Elisabetta, Saiman Yedidya, Mahmud Nadim, Miller Donald R, Reaven Peter D, Phillips Lawrence S, Muralidhar Sumitra, DuVall Scott L, Lee Jennifer S, Assimes Themistocles L, Pyarajan Saiju, Cho Kelly, Edwards Todd L, Damrauer Scott M, Wilson Peter W, Gaziano J Michael, O'Donnell Christopher J, Khera Amit V, Grant Struan F A, Brown Christopher D, Tsao Philip S, Saleheen Danish, Lotta Luca A, Bastarache Lisa, Anstee Quentin M, Daly Ann K, Meigs James B, Rotter Jerome I, Lynch Julie A, , , , , Rader Daniel J, Voight Benjamin F, Chang Kyong- |
| Frequency of alleles and genotypes associated with alpha-1 antitrypsin deficiency in clinical and general populations: Revelations about underdiagnosis. Pulmonology 2022 3 . Hernández-Pérez J M, Ramos-Díaz R, Vaquerizo-Pollino C, Pérez J |
| Heterozygosity of the Alpha 1-Antitrypsin Pi*Z Allele and Risk of Liver Disease. Hepatology communications 2021 8 5 (8): 1348-1361. Hakim Aaron, Moll Matthew, Qiao Dandi, Liu Jiangyuan, Lasky-Su Jessica A, Silverman Edwin K, Vilarinho Silvia, Jiang Gordon Z, Hobbs Brian D, Cho Michael |
| Genome-wide Association Study and Meta-analysis on Alcohol-Associated Liver Cirrhosis Identifies Genetic Risk Factors.
Hepatology (Baltimore, Md.) 2020 Aug . Schwantes-An Tae-Hwi, Darlay Rebecca, Mathurin Philippe, Masson Steven, Liangpunsakul Suthat, Mueller Sebastian, Aithal Guruprasad P, Eyer Florian, Gleeson Dermot, Thompson Andrew, Muellhaupt Beat, Stickel Felix, Soyka Michael, Goldman David, Liang Tiebing, Lumeng Lawrence, Pirmohamed Munir, Nalpas Bertrand, Jacquet Jean-Marc, Moirand Romain, Nahon Pierre, Naveau Sylvie, Perney Pascal, Botwin Greg, Haber Paul S, Seitz Helmut K, Day Christopher P, Foroud Tatiana M, Daly Ann K, Cordell Heather J, Whitfield John B, Morgan Timothy R, Seth Devanshi, |
| Molecular diagnosis of alpha1-antitrypsin deficiency: A new method based on Luminex technology. Journal of clinical laboratory analysis 2020 3 34 (7): e23279. Ottaviani Stefania, Barzon Valentina, Buxens Amaya, Gorrini Marina, Larruskain Amaia, El Hamss Rachid, Balderacchi Alice M, Corsico Angelo G, Ferrarotti Ilar |
| Increased Frequency of Heterozygous Alpha-1-Antitrypsin Deficiency in Liver Explants From Nonalcoholic Steatohepatitis Patients. Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 2019 10 26 (1): 17-24. Cheeney Gregory, Pac Lincoln J, Gopal Purva, Landis Charles S, Konnick Eric Q, Swanson Paul E, Greene Dina N, Lockwood Christina M, Westerhoff Mar |
| Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ Mutation. Gastroenterology 2019 5 157 (3): 705-719.e18. Hamesch Karim, Mandorfer Mattias, Pereira Vítor M, Moeller Linda S, Pons Monica, Dolman Grace E, Reichert Matthias C, Schneider Carolin V, Woditsch Vivien, Voss Jessica, Lindhauer Cecilia, Fromme Malin, Spivak Igor, Guldiken Nurdan, Zhou Biaohuan, Arslanow Anita, Schaefer Benedikt, Zoller Heinz, Aigner Elmar, Reiberger Thomas, Wetzel Martin, Siegmund Britta, Simões Carolina, Gaspar Rui, Maia Luís, Costa Dalila, Bento-Miranda Mário, van Helden Josef, Yagmur Eray, Bzdok Danilo, Stolk Jan, Gleiber Wolfgang, Knipel Verena, Windisch Wolfram, Mahadeva Ravi, Bals Robert, Koczulla Rembert, Barrecheguren Miriam, Miravitlles Marc, Janciauskiene Sabina, Stickel Felix, Lammert Frank, Liberal Rodrigo, Genesca Joan, Griffiths William J, Trauner Michael, Krag Aleksander, Trautwein Christian, Strnad Pavel, |
| Identification and Replication of Six Loci Associated With Gallstone Disease.
Hepatology (Baltimore, Md.) 2018 Oct . Gellert-Kristensen Helene, Dalila Nawar, Fallgaard Nielsen Sune, Grønne Nordestgaard Børge, Tybjaerg-Hansen Anne, Stender Stef |
| Association between inherited monogenic liver disorders and chronic hepatitis C. World journal of hepatology 2014 Feb 6 (2): 92-7. Piekuse Linda, Kreile Madara, Zarina Agnese, Steinberga Zane, Sondore Valentina, Keiss Jazeps, Lace Baiba, Krumina Astri |
| Prevalence of genetic polymorphisms in the promoter region of the alpha-1 antitrypsin (SERPINA1) gene in chronic liver disease: a case control study. BMC gastroenterology 2010 10 (1): 22. Kok Karin F, te Morsche René H, van Oijen Martijn G H, Drenth Joost P |
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- Page last updated:Mar 22, 2023
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