Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 39 Records) |
| Query Trace: Disease and ABCG5[original query] |
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| Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus. Hepatology (Baltimore, Md.) 2013 Jun 57 (6): 2407-17. von Kampen Oliver, Buch Stephan, Nothnagel Michael, Azocar Lorena, Molina Hector, Brosch Mario, Erhart Wiebke, von Schönfels Witigo, Egberts Jan, Seeger Marcus, Arlt Alexander, Balschun Tobias, Franke Andre, Lerch Markus M, Mayerle Julia, Kratzer Wolfgang, Boehm Bernhard O, Huse Klaus, Schniewind Bodo, Tiemann Katharina, Jiang Zhao-Yan, Han Tian-Quan, Mittal Balraj, Srivastava Anshika, Fenger Mogens, Jørgensen Torben, Schirin-Sokhan Ramin, Tönjes Anke, Wittenburg Henning, Stumvoll Michael, Kalthoff Holger, Lammert Frank, Tepel Jürgen, Puschel Klaus, Becker Thomas, Schreiber Stefan, Platzer Matthias, Völzke Henry, Krawczak Michael, Miquel Juan Francisco, Schafmayer Clemens, Hampe Joch |
| Phytosterol and cholesterol precursor levels indicate increased cholesterol excretion and biosynthesis in gallstone disease. Hepatology (Baltimore, Md.) 2012 May 55 (5): 1507-17. Krawczyk Marcin, Lütjohann Dieter, Schirin-Sokhan Ramin, Villarroel Luis, Nervi Flavio, Pimentel Fernando, Lammert Frank, Miquel Juan Francis |
| Role of the ABCG8 19H risk allele in cholesterol absorption and gallstone disease. BMC gastroenterology 2013 13 (1): 30. Renner Olga, Lütjohann Dieter, Richter Dominique, Strohmeyer André, Schimmel Silke, Müller Oliver, Stange Eduard F, Harsch Simo |
| Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study. Investigative ophthalmology & visual science 2013 Mar 54 (3): 2333-45. Meyers Kristin J, Johnson Elizabeth J, Bernstein Paul S, Iyengar Sudha K, Engelman Corinne D, Karki Chitra K, Liu Zhe, Igo Robert P, Truitt Barbara, Klein Michael L, Snodderly D Max, Blodi Barbara A, Gehrs Karen M, Sarto Gloria E, Wallace Robert B, Robinson Jennifer, LeBlanc Erin S, Hageman Gregory, Tinker Lesley, Mares Julie |
| Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III). BMC medical genetics 2013 Nov 14 (1): 1. Goodloe R, Brown-Gentry K, Gillani NB, Jin H, Mayo P, Allen M, McClellan B, Boston J, Sutcliffe C, Schnetz-Boutaud N, Dilks HH, Crawford DC |
| ABCG5/8 variants are associated with susceptibility to coronary heart disease. Molecular medicine reports 2014 Jun 9 (6): 2512-20. Wu Ge, Li Gui-Bin, Yao Ming, Zhang Dong-Qing, Dai Bin, Ju Chuan-Jing, Han Mi |
| The ABCG5/8 cholesterol transporter and myocardial infarction versus gallstone disease. Journal of the American College of Cardiology 2014 May 63 (20): 2121-8. Stender Stefan, Frikke-Schmidt Ruth, Nordestgaard Børge G, Tybjaerg-Hansen An |
| Association of three common single nucleotide polymorphisms of ATP binding cassette G8 gene with gallstone disease: a meta-analysis. PloS one 2014 9 (1): e87200. Jiang Zhao-Yan, Cai Qu, Chen Er-Zh |
| Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array. European journal of human genetics : EJHG 2015 Apr . Rodriguez Santiago, Gaunt Tom R, Guo Yiran, Zheng Jie, Barnes Michael R, Tang Weihang, Danish Fazal, Johnson Andrew, Castillo Berta A, Li Yun R, Hakonarson Hakon, Buxbaum Sarah G, Palmer Tom, Tsai Michael Y, Lange Leslie A, Ebrahim Shah, Davey Smith George, Lawlor Debbie A, Folsom Aaron R, Hoogeveen Ron, Reiner Alex, Keating Brendan, Day Ian |
| ABCG8 polymorphisms and renal disease in type 2 diabetic patients. Metabolism: clinical and experimental 2015 Jun 64 (6): 713-9. Nicolas Anthony, Fatima Sehrish, Lamri Amel, Bellili-Muñoz Naima, Halimi Jean-Michel, Saulnier Pierre-Jean, Hadjadj Samy, Velho Gilberto, Marre Michel, Roussel Ronan, Fumeron Frédér |
| Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding. JIMD reports 2015 21 115-22. Tada Hayato, Kawashiri Masa-Aki, Takata Mutsuko, Matsunami Kunihiro, Imamura Atsushi, Matsuyama Misayo, Sawada Hirotake, Nunoi Hiroyuki, Konno Tetsuo, Hayashi Kenshi, Nohara Atsushi, Inazu Akihiro, Kobayashi Junji, Mabuchi Hiroshi, Yamagishi Masaka |
| Genetic determinants of lipid-lowering response to atorvastatin therapy in an Indian population. Journal of clinical pharmacy and therapeutics 2016 Jun 41 (3): 329-33. Kadam P, Ashavaid T F, Ponde C K, Rajani R |
| Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis. JAMA 2016 Oct 316 (13): 1383-1391. Lotta Luca A, Sharp Stephen J, Burgess Stephen, Perry John R B, Stewart Isobel D, Willems Sara M, Luan Jian'an, Ardanaz Eva, Arriola Larraitz, Balkau Beverley, Boeing Heiner, Deloukas Panos, Forouhi Nita G, Franks Paul W, Grioni Sara, Kaaks Rudolf, Key Timothy J, Navarro Carmen, Nilsson Peter M, Overvad Kim, Palli Domenico, Panico Salvatore, Quirós Jose-Ramón, Riboli Elio, Rolandsson Olov, Sacerdote Carlotta, Salamanca-Fernandez Elena, Slimani Nadia, Spijkerman Annemieke M W, Tjonneland Anne, Tumino Rosario, van der A Daphne L, van der Schouw Yvonne T, McCarthy Mark I, Barroso Inês, O'Rahilly Stephen, Savage David B, Sattar Naveed, Langenberg Claudia, Scott Robert A, Wareham Nicholas |
| Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease. Journal of clinical lipidology 2018 Aug . Tada Hayato, Kawashiri Masa-Aki, Nomura Akihiro, Teramoto Ryota, Hosomichi Kazuyoshi, Nohara Atsushi, Inazu Akihiro, Mabuchi Hiroshi, Tajima Atsushi, Yamagishi Masaka |
| Unusual genetic variants associated with hypercholesterolemia in Argentina. Atherosclerosis 2018 10 277 256-261. Corral Pablo, Geller Andrew S, Polisecki Eliana Y, Lopez Graciela I, Bañares Virginia G, Cacciagiu Leonardo, Berg Gabriela, Hegele Robert A, Schaefer Ernst J, Schreier Laura |
| Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial Hypercholesterolemia. The Canadian journal of cardiology 2018 10 34 (10): 1316-1324. Iacocca Michael A, Wang Jian, Sarkar Samantha, Dron Jacqueline S, Lagace Thomas, McIntyre Adam D, Lau Paulina, Robinson John F, Yang Ping, Knoll Joan H, Cao Henian, McPherson Ruth, Hegele Robert |
| Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease. Circulation. Genomic and precision medicine 2020 9 13 (5): 417-423. Nomura Akihiro, Emdin Connor A, Won Hong Hee, Peloso Gina M, Natarajan Pradeep, Ardissino Diego, Danesh John, Schunkert Heribert, Correa Adolfo, Bown Matthew J, Samani Nilesh J, Erdmann Jeanette, McPherson Ruth, Watkins Hugh, Saleheen Danish, Elosua Roberto, Kawashiri Masa-Aki, Tada Hayato, Gupta Namrata, Shah Svati H, Rader Daniel J, Gabriel Stacey, Khera Amit V, Kathiresan Sek |
| Targeted Genetic Analysis in a Chinese Cohort of 208 Patients Related to Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2020 Aug . Wang Hao, Yang Hang, Liu Zhaohui, Cui Kai, Zhang Yinhui, Zhang Yujing, Zhao Kun, Yin Kunlun, Li Wenke, Zhou Zh |
| Recent Advances in the Critical Role of the Sterol Efflux Transporters ABCG5/G8 in Health and Disease. Advances in experimental medicine and biology 2020 7 1276 105-136. Wang Helen H, Liu Min, Portincasa Piero, Wang David Q |
| Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease. European heart journal 2020 Jul 41 (28): 2618-2628. Helgadottir Anna, Thorleifsson Gudmar, Alexandersson Kristjan F, Tragante Vinicius, Thorsteinsdottir Margret, Eiriksson Finnur F, Gretarsdottir Solveig, Björnsson Eythór, Magnusson Olafur, Sveinbjornsson Gardar, Jonsdottir Ingileif, Steinthorsdottir Valgerdur, Ferkingstad Egil, Jensson Brynjar Ö, Stefansson Hreinn, Olafsson Isleifur, Christensen Alex H, Torp-Pedersen Christian, Køber Lars, Pedersen Ole B, Erikstrup Christian, Sørensen Erik, Brunak Søren, Banasik Karina, Hansen Thomas F, Nyegaard Mette, Eyjolfssson Gudmundur I, Sigurdardottir Olof, Thorarinsson Bjorn L, Matthiasson Stefan E, Steingrimsdottir Thora, Bjornsson Einar S, Danielsen Ragnar, Asselbergs Folkert W, Arnar David O, Ullum Henrik, Bundgaard Henning, Sulem Patrick, Thorsteinsdottir Unnur, Thorgeirsson Gudmundur, Holm Hilma, Gudbjartsson Daniel F, Stefansson Ka |
| Features of Sitosterolemia in Children. The American journal of cardiology 2020 3 125 (9): 1312-1316. Xu Liyuan, Wen Wenhui, Yang Ya, Xie Jinjie, Li Rongjuan, Wu Yue, Hu Yifei, Wang Luya, Chong M |
| ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia. Journal of clinical lipidology 2020 Jan . Reeskamp Laurens F, Volta Andrea, Zuurbier Linda, Defesche Joep C, Hovingh G Kees, Grefhorst Al |
| Cascade screening and genetic diagnosis of familial hypercholesterolemia in clusters of the Southeastern region from Brazil. Molecular biology reports 2020 11 47 (12): 9279-9288. de Paiva Silvino Júnea Paolucci, Jannes Cinthia Elim, Tada Mauricio Teruo, Lima Isabella Ramos, Silva Iêda de Fátima Oliveira, Pereira Alexandre Costa, Gomes Karina Bra |
| Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids. Hepatology communications 2022 Sep . Handelman Samuel K, Puentes Yindra M, Kuppa Annapurna, Chen Yanhua, Du Xiaomeng, Feitosa Mary F, Palmer Nicholette D, Speliotes Elizabeth |
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nature communications 2022 1 13 (1): 143. Scholz Markus, Horn Katrin, Pott Janne, Gross Arnd, Kleber Marcus E, Delgado Graciela E, Mishra Pashupati Prasad, Kirsten Holger, Gieger Christian, Müller-Nurasyid Martina, Tönjes Anke, Kovacs Peter, Lehtimäki Terho, Raitakari Olli, Kähönen Mika, Gylling Helena, Baber Ronny, Isermann Berend, Stumvoll Michael, Loeffler Markus, März Winfried, Meitinger Thomas, Peters Annette, Thiery Joachim, Teupser Daniel, Ceglarek U |
| Causal effect of gallstone disease on the risk of coronary heart disease or acute myocardial infarction: a Mendelian randomization study. Scientific reports 2023 11 13 (1): 18807. Qingan Fu, Tianzhou Shen, Qingyun Yu, Long Jiang, Renqiang Ya |
| Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning. Vavilovskii zhurnal genetiki i selektsii 2023 10 27 (5): 522-529. D E Ivanoshchuk, A B Kolker, O V Timoshchenko, S E Semaev, E V Shakhtshneid |
| Targeted sequencing of a gene panel in patients with Familial Hypercholesterolemia from Southern Poland. Polish archives of internal medicine 2023 1 . Toto?-?ura?ska Justyna, Wo?kow Pawe?, Kapusta Maria, Wójcik Ma?gorzata, Starzyk Jerzy, Kawalec Ewa, Idzior-Walu? Barbara, Walu?-Miarka Ma?gorza |
| Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis.
Gastroenterology 2023 2 . Bourgault Jérôme, Abner Erik, Manikpurage Hasanga D, Pujol-Gualdo Natàlia, Laisk Triin, , Gobeil Émilie, Gagnon Eloi, Girard Arnaud, Mitchell Patricia L, Thériault Sébastien, Esko Tõnu, Mathieu Patrick, Arsenault Benoit |
| Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol. Human genomics 2024 8 18 (1): 85. Jamil Alenbawi, Yasser A Al-Sarraj, Umm-Kulthum I Umlai, Ayat Kadhi, Nagham N Hendi, Georges Nemer, Omar M E Albag |
- Page last reviewed:Feb 1, 2024
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