Human Genome Epidemiology Literature Finder
|
Records 1 - 22 (of 22 Records) |
| Query Trace: Fibrosis and SERPINA1[original query] |
|---|
| Genetic modifiers of liver disease in cystic fibrosis. JAMA 2009 Sep 302 (10): 1076-83. Bartlett Jaclyn R, Friedman Kenneth J, Ling Simon C, Pace Rhonda G, Bell Scott C, Bourke Billy, Castaldo Giuseppe, Castellani Carlo, Cipolli Marco, Colombo Carla, Colombo John L, Debray Dominique, Fernandez Adriana, Lacaille Florence, Macek Milan, Rowland Marion, Salvatore Francesco, Taylor Christopher J, Wainwright Claire, Wilschanski Michael, Zemková Dana, Hannah William B, Phillips M James, Corey Mary, Zielenski Julian, Dorfman Ruslan, Wang Yunfei, Zou Fei, Silverman Lawrence M, Drumm Mitchell L, Wright Fred A, Lange Ethan M, Durie Peter R, Knowles Michael R, |
| The tumor necrosis factor a (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients. PloS one 2014 9 (3): e90945. Sanchez-Dominguez Celia N, Reyes-Lopez Miguel A, Bustamante Adriana, Cerda-Flores Ricardo M, Villalobos-Torres Maria Del C, Gallardo-Blanco Hugo L, Rojas-Martinez Augusto, Martinez-Rodriguez Herminia G, Barrera-Saldaña Hugo A, Ortiz-Lopez Roc |
| Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis. Hepatology research : the official journal of the Japan Society of Hepatology 2015 Jun . Goldschmidt Monique L, Mourya Reena, Connor Jessica, Dexheimer Phillip, Karns Rebekah, Miethke Alexander, Sheridan Rachel, Zhang Kejian, Bezerra Jorge |
| Increased Transcript Complexity in Genes Associated with Chronic Obstructive Pulmonary Disease. PloS one 2015 10 (10): e0140885. Lackey Lela, McArthur Evonne, Laederach Ala |
| A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height. Journal of medical genetics 2016 Feb . North Teri-Louise, Ben-Shlomo Yoav, Cooper Cyrus, Deary Ian J, Gallacher John, Kivimaki Mika, Kumari Meena, Martin Richard M, Pattie Alison, Sayer Avan Aihie, Starr John M, Wong Andrew, Kuh Diana, Rodriguez Santiago, Day Ian N |
| Liver disease in adults with ?1-antitrypsin deficiency. United European gastroenterology journal 2018 Jun 6 (5): 710-718. Mandorfer Mattias, Bucsics Theresa, Hutya Veronika, Schmid-Scherzer Karin, Schaefer Benedikt, Zoller Heinz, Ferlitsch Arnulf, Peck-Radosavljevic Markus, Trauner Michael, Ferenci Peter, Kneussl Meinhard, Reiberger Thom |
| SERPINA1 and HSD17B13 Gene Variants in Patients with Liver Fibrosis and Cirrhosis. Journal of gastrointestinal and liver diseases : JGLD 2019 Sep 28 (3): 297-302. Basyte-Bacevice Viktorija, Skieceviciene Jurgita, Valantiene Irena, Sumskiene Jolanta, Petrenkiene Vitalija, Kondrackiene Jurate, Petrauskas Dalius, Lammert Frank, Kupcinskas Juoz |
| 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, |
| SERPINA1 Z allele is associated with cystic fibrosis liver disease. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb . Boëlle Pierre-Yves, Debray Dominique, Guillot Loic, Corvol Harriet, |
Genetic variants that associate with cirrhosis have pleiotropic effects on human traits.
Liver international : official journal of the International Association for the Study of the Liver 2019 Dec . Chen Vincent L, Chen Yanhua, Du Xiaomeng, Handelman Samuel K, Speliotes Elizabeth |
| 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 |
| A Data-Driven Approach to Carrier Screening for Common Recessive Diseases. Journal of personalized medicine 2020 9 10 (3): . Kiseleva Anna V, Klimushina Marina V, Sotnikova Evgeniia A, Divashuk Mikhail G, Ershova Alexandra I, Skirko Olga P, Kurilova Olga V, Zharikova Anastasia A, Khlebus Eleonora Yu, Efimova Irina A, Pokrovskaya Maria S, Slominsky Petr A, Shalnova Svetlana A, Meshkov Alexey N, Drapkina Oxana |
| Insights into genetic variants associated with NASH-fibrosis from metabolite profiling. Human molecular genetics 2020 Jul . Mann Jake P, Pietzner Maik, Wittemans Laura B, Rolfe Emmanuela De Lucia, Kerrison Nicola D, Imamura Fumiaki, Forouhi Nita G, Fauman Eric, Allison Michael E, Griffin Jules L, Koulman Albert, Wareham Nicholas J, Langenberg Claud |
| Non-Invasive Assessment and Management of Liver Involvement in Adults With Alpha-1 Antitrypsin Deficiency. Chronic obstructive pulmonary diseases (Miami, Fla.) 2020 7 7 (3): 260-271. Hamesch Karim, Strnad Pav |
| Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond. Gastroenterology 2020 2 158 (7): 1865-1880.e1. Krawczyk Marcin, Liebe Roman, Lammert Fra |
| Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases. Journal of personalized medicine 2022 7 12 (7): . Sotnikova Evgeniia A, Kiseleva Anna V, Kutsenko Vladimir A, Zharikova Anastasia A, Ramensky Vasily E, Divashuk Mikhail G, Vyatkin Yuri V, Klimushina Marina V, Ershova Alexandra I, Revazyan Karina Z, Skirko Olga P, Zaicenoka Marija, Efimova Irina A, Pokrovskaya Maria S, Kopylova Oksana V, Glechan Anush M, Shalnova Svetlana A, Meshkov Alexey N, Drapkina Oxana |
| COVID-19 Survivor Patients Carrying the Rs35705950 Risk Allele in MUC5B Have Higher Plasma Levels of Mucin 5B. Current issues in molecular biology 2022 Jul 44 (8): 3283-3290. García-Carmona Salvador, Falfán-Valencia Ramcés, Verónica-Aguilar Abigail, Buendía-Roldán Ivette, Chávez-Galán Leslie, Hernández-Zenteno Rafael de Jesús, Martínez-Morales Alfonso, Fricke-Galindo Ingrid, Alanis-Ponce Jesús, Valencia-Pérez Rea Daniela, Gutiérrez-Pérez Ilse Adriana, Zaragoza-García Oscar, Nava-Quiroz Karol J, Camarena Angel, Mejía Mayra, Guzmán-Guzmán Iris Paola, Pérez-Rubio Glor |
| Liver disease progression in patients with alpha-1 antitrypsin deficiency and protease inhibitor ZZ genotype with or without lung disease. Alimentary pharmacology & therapeutics 2023 9 . Tiffany Wu, May Hagiwara, Esteban Gnass, Hannah Barman, David Sasson, William Treem, Kaili Ren, Ed G Marins, Chitra Karki, Harmeet Mal |
| Impact of Bronchiectasis on COPD Severity and Alpha-1 Antitrypsin Deficiency as a Risk Factor in Individuals with a Heavy Smoking History. Chronic obstructive pulmonary diseases (Miami, Fla.) 2023 5 . Manuel Izquierdo, Chad R Marion, Frank Genese, John D Newell, Wanda K O'Neal, Xingnan Li, Gregory A Hawkins, Igor Barjaktarevic, R Graham Barr, Stephanie Christenson, Christopher B Cooper, David Couper, Jeffrey Curtis, Meilan K Han, Nadia N Hansel, Richard E Kanner, Fernando J Martinez, Robert Paine, Vickram Tejwani, Prescott G Woodruff, Joe G Zein, Eric A Hoffman, Stephen P Peters, Deborah A Meyers, Eugene R Bleecker, Victor E Ortega, |
| Association of Alpha-1 Antitrypsin Pi*Z Allele Frequency and Progressive Liver Fibrosis in Two Chronic Hepatitis C Cohorts. Journal of clinical medicine 2023 1 12 (1): . Mücke Victoria Therese, Fischer Janett, Mücke Marcus Maximilian, Teumer Alexander, Koch Alexander, Vermehren Johannes, Fromme Malin, Zeuzem Stefan, Trautwein Christian, Sarrazin Christoph, Berg Thomas, Zhou Biaohuan, Hamesch Kar |
| The impact of genetic risk on the prevalence of advanced fibrosis and cirrhosis in prospectively assessed patients with type 2 diabetes. Alimentary pharmacology & therapeutics 2024 6 . Lana Bridi, Saaket Agrawal, Kaleb Tesfai, Egbert Madamba, Ricki Bettencourt, Lisa M Richards, Amit V Khera, Rohit Loomba, Veeral Ajme |
| Genetic and clinical factors influencing CF-associated liver disease: the impact of SERPINA1 variants and CFTR genotypes in Romanian pediatric cystic fibrosis patients. Medicine and pharmacy reports 2024 11 97 (4): 429-437. Elena-Simona Moiceanu, Iustina Violeta Stan, Simona Elena Mo?escu, Adina Chi?, Romana Vulturar, Daniel-Corneliu Leucu?a, Gabriela Viorela Ni?escu, Maria Iacobescu, Elena M?d?lina Petran, Dan Lucian Dumitra? |
- Page last reviewed:Feb 1, 2024
- Content source: