Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: Coronary Artery Disease and SORT1[original query] |
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Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Nature genetics 2008 Feb 40 (2): 161-9. Willer Cristen J, Sanna Serena, Jackson Anne U, Scuteri Angelo, Bonnycastle Lori L, Clarke Robert, Heath Simon C, Timpson Nicholas J, Najjar Samer S, Stringham Heather M, Strait James, Duren William L, Maschio Andrea, Busonero Fabio, Mulas Antonella, Albai Giuseppe, Swift Amy J, Morken Mario A, Narisu Narisu, Bennett Derrick, Parish Sarah, Shen Haiqing, Galan Pilar, Meneton Pierre, Hercberg Serge, Zelenika Diana, Chen Wei-Min, Li Yun, Scott Laura J, Scheet Paul A, Sundvall Jouko, Watanabe Richard M, Nagaraja Ramaiah, Ebrahim Shah, Lawlor Debbie A, Ben-Shlomo Yoav, Davey-Smith George, Shuldiner Alan R, Collins Rory, Bergman Richard N, Uda Manuela, Tuomilehto Jaakko, Cao Antonio, Collins Francis S, Lakatta Edward, Lathrop G Mark, Boehnke Michael, Schlessinger David, Mohlke Karen L, Abecasis Gonçalo |
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Nature genetics 2008 Feb 40 (2): 189-97. Kathiresan Sekar, Melander Olle, Guiducci Candace, Surti Aarti, Burtt Noël P, Rieder Mark J, Cooper Gregory M, Roos Charlotta, Voight Benjamin F, Havulinna Aki S, Wahlstrand Björn, Hedner Thomas, Corella Dolores, Tai E Shyong, Ordovas Jose M, Berglund Göran, Vartiainen Erkki, Jousilahti Pekka, Hedblad Bo, Taskinen Marja-Riitta, Newton-Cheh Christopher, Salomaa Veikko, Peltonen Leena, Groop Leif, Altshuler David M, Orho-Melander Mar |
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 2010 Jan 208 (1): 183-9. Linsel-Nitschke Patrick, Heeren Jörg, Aherrahrou Zouhair, Bruse Petra, Gieger Christian, Illig Thomas, Prokisch Holger, Heim Katharina, Doering Angela, Peters Annette, Meitinger Thomas, Wichmann H-Erich, Hinney Anke, Reinehr Thomas, Roth Christian, Ortlepp Jan R, Soufi Mouhidien, Sattler Alexander M, Schaefer Jürgen, Stark Klaus, Hengstenberg Christian, Schaefer Arne, Schreiber Stefan, Kronenberg Florian, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanet |
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population. Annals of human genetics 2011 Jul 75 (4): 475-82. Wang Annabel Z, Li Lin, Zhang Bin, Shen Gong-Qing, Wang Qing Kenne |
The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations. Pediatric research 2011 Jun 69 (6): 538-43. Devaney Joseph M, Thompson Paul D, Visich Paul S, Saltarelli William A, Gordon Paul M, Orkunoglu-Suer E Funda, Gordish-Dressman Heather, Harmon Brennan T, Bradbury Margaret K, Panchapakesan Karuna, Khianey Rahul, Hubal Monica J, Clarkson Priscilla M, Pescatello Linda S, Zoeller Robert F, Moyna Niall M, Angelopoulos Theodore J, Kraus William E, Hoffman Eric |
A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics 2012 2012 . Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqi |
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PloS one 2012 7 (5): e37056. Braun Timothy R, Been Latonya F, Singhal Akhil, Worsham Jacob, Ralhan Sarju, Wander Gurpreet S, Chambers John C, Kooner Jaspal S, Aston Christopher E, Sanghera Dharambir |
Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals. PloS one 2012 7 (9): e46385. Takeuchi Fumihiko, Isono Masato, Katsuya Tomohiro, Yokota Mitsuhiro, Yamamoto Ken, Nabika Toru, Shimokawa Kazuro, Nakashima Eitaro, Sugiyama Takao, Rakugi Hiromi, Yamaguchi Shuhei, Ogihara Toshio, Yamori Yukio, Kato Norihi |
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PloS one 2011 6 (12): e29427. Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A, |
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. Human molecular genetics 2013 Jul 22 (14): 2941-7. Jones Gregory T, Bown Matthew J, Gretarsdottir Solveig, Romaine Simon P R, Helgadottir Anna, Yu Grace, Tromp Gerard, Norman Paul E, Jin Cao, Baas Annette F, Blankensteijn Jan D, Kullo Iftikhar J, Phillips L Victoria, Williams Michael J A, Topless Ruth, Merriman Tony R, Vasudevan Thodor M, Lewis David R, Blair Ross D, Hill Andrew A, Sayers Robert D, Powell Janet T, Deloukas Panagiotis, Thorleifsson Gudmar, Matthiasson Stefan E, Thorsteinsdottir Unnur, Golledge Jonathan, Ariëns Robert A, Johnson Anne, Sohrabi Soroush, Scott D Julian, Carey David J, Erdman Robert, Elmore James R, Kuivaniemi Helena, Samani Nilesh J, Stefansson Kari, van Rij Andre |
A genome-wide association study of a coronary artery disease risk variant.
Journal of human genetics 2013 Jan . Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, Joong Kim K, Heo L, Young Lee J, Kyoung Kim Y, Jin Kim Y, Bum Hong C, Lee SH, Yoon D, Jung Ku H, Oh IY, Kim BJ, Lee J, Park SJ, Kim J, Kawk HK, Lee JE, Park HK, Lee JE, Nam HY, Park HY, Shin C, Yokota M, Asano H, Nakatochi M, Matsubara T, Kitajima H, Yamamoto K, Kim HL, Han BG, Cho MC, Jang Y, Kim HS, Euy Park J, Lee JY |
LDL-c-linked SNPs are associated with LDL-c and myocardial infarction despite lipid-lowering therapy in patients with established vascular disease. European journal of clinical investigation 2013 Nov . van de Woestijne AP, van der Graaf Y, de Bakker PI, Asselbergs FW, de Borst GJ, Algra A, Spiering W, Visseren FL |
CELSR2-PSRC1-SORT1 gene expression and association with coronary artery disease and plasma lipid levels in an Asian Indian cohort. Journal of cardiology 2014 Nov 64 (5): 339-46. Arvind Prathima, Nair Jiny, Jambunathan Srikarthika, Kakkar Vijay V, Shanker Jayashr |
Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study. Circulation. Cardiovascular genetics 2014 Apr 7 (2): 178-88. Kocarnik Jonathan M, Pendergrass Sarah A, Carty Cara L, Pankow James S, Schumacher Fredrick R, Cheng Iona, Durda Peter, Ambite José Luis, Deelman Ewa, Cook Nancy R, Liu Simin, Wactawski-Wende Jean, Hutter Carolyn, Brown-Gentry Kristin, Wilson Sarah, Best Lyle G, Pankratz Nathan, Hong Ching-Ping, Cole Shelley A, Voruganti V Saroja, B?žkova Petra, Jorgensen Neal W, Jenny Nancy S, Wilkens Lynne R, Haiman Christopher A, Kolonel Laurence N, Lacroix Andrea, North Kari, Jackson Rebecca, Le Marchand Loic, Hindorff Lucia A, Crawford Dana C, Gross Myron, Peters Ulri |
Macrophage sortilin promotes LDL uptake, foam cell formation, and atherosclerosis. Circulation research 2015 Feb 116 (5): 789-96. Patel Kevin M, Strong Alanna, Tohyama Junichiro, Jin Xueting, Morales Carlos R, Billheimer Jeffery, Millar John, Kruth Howard, Rader Daniel |
Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease. Cytokine 2017 Jul . Ansari Wafa M, Humphries Steve E, Naveed Abdul K, Khan Omer J, Khan Dilshad A, Khattak Ejaz Hass |
Replication and fine-mapping of genetic predictors of lipid traits in African-Americans. Journal of human genetics 2017 May . Feng QiPing, Wei Wei-Qi, Levinson Rebecca T, Mosley Jonathan D, Stein C Micha |
Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants. Atherosclerosis 2017 Jan 258 1-7. Shahid Saleem Ullah, Shabana , Cooper Jackie A, Beaney Katherine E, Li Kawah, Rehman Abdul, Humphries Steve |
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population. Disease markers 2020 2020 9738567. Cheema Asma Naseer, Pirim Dilek, Wang Xingbin, Ali Jabar, Bhatti Attya, John Peter, Feingold Eleanor, Demirci F Yesim, Kamboh M Ily |
Sortilin as a Biomarker for Cardiovascular Disease Revisited.
Frontiers in cardiovascular medicine 2021 5 8 652584. Møller Peter Loof, Rohde Palle D, Winther Simon, Breining Peter, Nissen Louise, Nykjaer Anders, Bøttcher Morten, Nyegaard Mette, Kjolby Ma |
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography. Nutrition, metabolism, and cardiovascular diseases : NMCD 2021 Feb . Noto Davide, Cefalù Angelo B, Martinelli Nicola, Giammanco Antonina, Spina Rossella, Barbagallo Carlo M, Caruso Marco, Novo Salvatore, Sarullo Filippo, Pernice Vincenzo, Brucato Federica, Ingrassia Valeria, Fayer Francesca, Altieri Grazia I, Scrimali Chiara, Misiano Gabriella, Olivieri Oliviero, Girelli Domenico, Averna Maurizio |
In silico genome-wide gene-based association analysis reveals new genes predisposing to coronary artery disease. Clinical genetics 2021 10 101 (1): 78-86. Zorkoltseva Irina, Shadrina Alexandra, Belonogova Nadezhda, Kirichenko Anatoly, Tsepilov Yakov, Axenovich Tatia |
PSRC1 May Affect Coronary Artery Disease Risk by Altering CELSR2, PSRC1, and SORT1 Gene Expression and Circulating Granulin and Apolipoprotein B Protein Levels. Frontiers in cardiovascular medicine 2022 3 9 763015. Chai Tianci, Wang Zhisheng, Yang Xiaojie, Qiu Zhihuang, Chen Liangw |
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. European heart journal 2023 4 . Chen Hao Yu, Dina Christian, Small Aeron M, Shaffer Christian M, Levinson Rebecca T, Helgadóttir Anna, Capoulade Romain, Munter Hans Markus, Martinsson Andreas, Cairns Benjamin J, Trudsø Linea C, Hoekstra Mary, Burr Hannah A, Marsh Thomas W, Damrauer Scott M, Dufresne Line, Le Scouarnec Solena, Messika-Zeitoun David, Ranatunga Dilrini K, Whitmer Rachel A, Bonnefond Amélie, Sveinbjornsson Garðar, Daníelsen Ragnar, Arnar David O, Thorgeirsson Gudmundur, Thorsteinsdottir Unnur, Gudbjartsson Daníel F, Hólm Hilma, Ghouse Jonas, Olesen Morten Salling, Christensen Alex H, Mikkelsen Susan, Jacobsen Rikke Louise, Dowsett Joseph, Pedersen Ole Birger Vesterager, Erikstrup Christian, Ostrowski Sisse R, , O'Donnell Christopher J, Budoff Matthew J, Gudnason Vilmundur, Post Wendy S, Rotter Jerome I, Lathrop Mark, Bundgaard Henning, Johansson Bengt, Ljungberg Johan, Näslund Ulf, Le Tourneau Thierry, Smith J Gustav, Wells Quinn S, Söderberg Stefan, Stefánsson Kári, Schott Jean-Jacques, Rader Daniel J, Clarke Robert, Engert James C, Thanassoulis Geor |
Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis. Journal of cardiovascular development and disease 2023 3 10 (3): . Castillo-Avila Rosa Giannina, González-Castro Thelma Beatriz, Tovilla-Zárate Carlos Alfonso, Martínez-Magaña José Jaime, López-Narváez María Lilia, Juárez-Rojop Isela Esther, Arias-Vázquez Pedro Iván, Borgonio-Cuadra Verónica Marusa, Pérez-Hernández Nonanzit, Rodríguez-Pérez José Manu |
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- Page last updated:Apr 29, 2024
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