Human Genome Epidemiology Literature Finder
|
Records 1 - 29 (of 29 Records) |
| Query Trace: Disease and PSRC1[original query] |
|---|
| The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol. Journal of molecular medicine (Berlin, Germany) 2008 Nov 86 (11): 1233-41. Samani Nilesh J, Braund Peter S, Erdmann Jeanette, Götz Anika, Tomaszewski Maciej, Linsel-Nitschke Patrick, Hajat Cother, Mangino Massimo, Hengstenberg Christian, Stark Klaus, Ziegler Andreas, Caulfield Mark, Burton Paul R, Schunkert Heribert, Tobin Martin |
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
American journal of human genetics 2008 Jan 82 (1): 139-49. Wallace Chris, Newhouse Stephen J, Braund Peter, Zhang Feng, Tobin Martin, Falchi Mario, Ahmadi Kourosh, Dobson Richard J, Marçano Ana Carolina B, Hajat Cother, Burton Paul, Deloukas Panagiotis, Brown Morris, Connell John M, Dominiczak Anna, Lathrop G Mark, Webster John, Farrall Martin, Spector Tim, Samani Nilesh J, Caulfield Mark J, Munroe Patricia |
| 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 |
| Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2011 Feb 27 (2): 245-52. Roder Constantin, Peters Vera, Kasuya Hidetoshi, Nishizawa Tsutomu, Takehara Yayoi, Berg Daniela, Schulte Claudia, Khan Nadia, Tatagiba Marcos, Krischek Bor |
| Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.
PLoS genetics 2010 Apr 6 (4): e1000928. Suchindran Sunil, Rivedal David, Guyton John R, Milledge Tom, Gao Xiaoyi, Benjamin Ashlee, Rowell Jennifer, Ginsburg Geoffrey S, McCarthy Jeanette |
| Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk. Human molecular genetics 2010 May 19 (10): 2068-78. Reynolds Chandra A, Hong Mun-Gwan, Eriksson Ulrika K, Blennow Kaj, Wiklund Fredrik, Johansson Boo, Malmberg Bo, Berg Stig, Alexeyenko Andrey, Grönberg Henrik, Gatz Margaret, Pedersen Nancy L, Prince Jonathan |
| Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies. Journal of the American College of Cardiology 2011 Dec 58 (25): 2675-82. Qi Lu, Parast Layla, Cai Tianxi, Powers Christine, Gervino Ernest V, Hauser Thomas H, Hu Frank B, Doria Alessand |
| Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses. BMC medical genetics 2011 12 (1): 131. Trompet Stella, de Craen Anton J M, Postmus Iris, Ford Ian, Sattar Naveed, Caslake Muriel, Stott David J, Buckley Brendan M, Sacks Frank, Devlin James J, Slagboom P Eline, Westendorp Rudi G J, Jukema J Wouter, |
| Genetic risk score and risk of myocardial infarction in Hispanics. Circulation 2011 Feb 123 (4): 374-80. Qi Lu, Ma Jiantao, Qi Qibin, Hartiala Jaana, Allayee Hooman, Campos Hann |
| 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 |
| 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, |
| Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. Cardiovascular diabetology 2014 13 (1): 77. Adams Jeremy N, Raffield Laura M, Freedman Barry I, Langefeld Carl D, Ng Maggie C Y, Carr J Jeffrey, Cox Amanda J, Bowden Donald |
| 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 |
| Association of a transcription factor 21 gene polymorphism with hypertension. Biomedical reports 2015 Jan 3 (1): 118-122. Fujimaki Tetsuo, Oguri Mitsutoshi, Horibe Hideki, Kato Kimihiko, Matsuoka Reiko, Abe Shintaro, Tokoro Fumitaka, Arai Masazumi, Noda Toshiyuki, Watanabe Sachiro, Yamada Yoshi |
| Association of genetic variants with dyslipidemia. Molecular medicine reports 2015 Oct 12 (4): 5429-36. Abe Shintaro, Tokoro Fumitaka, Matsuoka Reiko, Arai Masazumi, Noda Toshiyuki, Watanabe Sachiro, Horibe Hideki, Fujimaki Tetsuo, Oguri Mitsutoshi, Kato Kimihiko, Minatoguchi Shinya, Yamada Yoshi |
| Connecting SNPs in Diabetes: A Spatial Analysis of Meta-GWAS Loci. Frontiers in endocrinology 2015 6 102. Schierding William, O'Sullivan Justin |
| Association of six genetic variants with myocardial infarction. International journal of molecular medicine 2015 May 35 (5): 1451-9. Matsuoka Reiko, Abe Shintaro, Tokoro Fumitaka, Arai Masazumi, Noda Toshiyuki, Watanabe Sachiro, Horibe Hideki, Fujimaki Tetsuo, Oguri Mitsutoshi, Kato Kimihiko, Minatoguchi Shinya, Yamada Yoshi |
| Association of genetic variants with atrial fibrillation. Biomedical reports 2016 Feb 4 (2): 178-182. Yamase Yuichiro, Kato Kimihiko, Horibe Hideki, Ueyama Chikara, Fujimaki Tetsuo, Oguri Mitsutoshi, Arai Masazumi, Watanabe Sachiro, Murohara Toyoaki, Yamada Yoshi |
| Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.
PloS one 2019 14 (8): e0220827. Andaleon Angela, Mogil Lauren S, Wheeler Heather |
| There is an association between a genetic polymorphism in the ZNF259 gene involved in lipid metabolism and coronary artery disease. Gene 2019 Mar . Mirhafez Seyed Reza, Avan Amir, Khatamianfar Sara, Ghasemi Faezeh, Moohebati Mohsen, Ebrahimi Mahmoud, Ghazizadeh Hamideh, Ghayour-Mobarhan Majid, Pasdar Alire |
| Coronary artery disease, genetic risk and the metabolome in young individuals. Wellcome open research 2019 2 3 114. Battram Thomas, Hoskins Luke, Hughes David A, Kettunen Johannes, Ring Susan M, Smith George Davey, Timpson Nicholas |
| Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. Medicina (Kaunas, Lithuania) 2020 8 56 (9): . Rodríguez-Arellano Martha Eunice, Solares-Tlapechco Jacqueline, Costa-Urrutia Paula, Cárdenas-Hernández Helios, Vallejo-Gómez Marajael, Granados Julio, Salas-Padilla Serg |
| Influence of PSRC1, CELSR2, and SORT1 Gene Polymorphisms on the Variability of Warfarin Dosage and Susceptibility to Cardiovascular Disease. Pharmacogenomics and personalized medicine 2020 11 13 619-632. Al-Eitan Laith N, Elsaqa Barakat Z, Almasri Ayah Y, Aman Hatem A, Khasawneh Rame H, Alghamdi Mansour |
| Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease. Computational and mathematical methods in medicine 2021 8 2021 7036592. Hu Yang, Qiu Shizheng, Cheng Lia |
| 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 |
| 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 |
| 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 |
| Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population. Journal of cardiovascular and thoracic research 2023 11 15 (3): 168-173. Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, Niloofar Naderi, Maryam Pourirahim, Katayoun Heshmatzad, Majid Maleki, Samira Kalayin |
- Page last reviewed:Feb 1, 2024
- Content source: