Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 47 Records) |
Query Trace: PSRC1[original query] |
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Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study. European heart journal 2013 Apr 34 (13): 982-92. Hopewell Jemma C, Parish Sarah, Offer Alison, Link Emma, Clarke Robert, Lathrop Mark, Armitage Jane, Collins Rory, |
Identification of candidate oncogenes in human colorectal cancers with microsatellite instability. Gastroenterology 2013 Sep 145 (3): 540-3.e22. Gylfe Alexandra E, Kondelin Johanna, Turunen Mikko, Ristolainen Heikki, Katainen Riku, Pitkänen Esa, Kaasinen Eevi, Rantanen Ville, Tanskanen Tomas, Varjosalo Markku, Lehtonen Heli, Palin Kimmo, Taipale Minna, Taipale Jussi, Renkonen-Sinisalo Laura, Järvinen Heikki, Böhm Jan, Mecklin Jukka-Pekka, Ristimäki Ari, Kilpivaara Outi, Tuupanen Sari, Karhu Auli, Vahteristo Pia, Aaltonen Lauri |
Association of common genetic variants with lipid traits in the Indian population. PloS one 2014 9 (7): e101688. Walia Gagandeep Kaur, Gupta Vipin, Aggarwal Aastha, Asghar Mohammad, Dudbridge Frank, Timpson Nicholas, Singh Nongmaithem Suraj, Kumar M Ravi, Kinra Sanjay, Prabhakaran Dorairaj, Reddy K Srinath, Chandak Giriraj Ratan, Smith George Davey, Ebrahim Sh |
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 |
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
Nature communications 2014 5 5068. Postmus Iris, Trompet Stella, Deshmukh Harshal A, Barnes Michael R, Li Xiaohui, Warren Helen R, Chasman Daniel I, Zhou Kaixin, Arsenault Benoit J, Donnelly Louise A, Wiggins Kerri L, Avery Christy L, Griffin Paula, Feng QiPing, Taylor Kent D, Li Guo, Evans Daniel S, Smith Albert V, de Keyser Catherine E, Johnson Andrew D, de Craen Anton J M, Stott David J, Buckley Brendan M, Ford Ian, Westendorp Rudi G J, Slagboom P Eline, Sattar Naveed, Munroe Patricia B, Sever Peter, Poulter Neil, Stanton Alice, Shields Denis C, O'Brien Eoin, Shaw-Hawkins Sue, Chen Y-D Ida, Nickerson Deborah A, Smith Joshua D, Dubé Marie Pierre, Boekholdt S Matthijs, Hovingh G Kees, Kastelein John J P, McKeigue Paul M, Betteridge John, Neil Andrew, Durrington Paul N, Doney Alex, Carr Fiona, Morris Andrew, McCarthy Mark I, Groop Leif, Ahlqvist Emma, , Bis Joshua C, Rice Kenneth, Smith Nicholas L, Lumley Thomas, Whitsel Eric A, Stürmer Til, Boerwinkle Eric, Ngwa Julius S, O'Donnell Christopher J, Vasan Ramachandran S, Wei Wei-Qi, Wilke Russell A, Liu Ching-Ti, Sun Fangui, Guo Xiuqing, Heckbert Susan R, Post Wendy, Sotoodehnia Nona, Arnold Alice M, Stafford Jeanette M, Ding Jingzhong, Herrington David M, Kritchevsky Stephen B, Eiriksdottir Gudny, Launer Leonore J, Harris Tamara B, Chu Audrey Y, Giulianini Franco, MacFadyen Jean G, Barratt Bryan J, Nyberg Fredrik, Stricker Bruno H, Uitterlinden André G, Hofman Albert, Rivadeneira Fernando, Emilsson Valur, Franco Oscar H, Ridker Paul M, Gudnason Vilmundur, Liu Yongmei, Denny Joshua C, Ballantyne Christie M, Rotter Jerome I, Adrienne Cupples L, Psaty Bruce M, Palmer Colin N A, Tardif Jean-Claude, Colhoun Helen M, Hitman Graham, Krauss Ronald M, Wouter Jukema J, Caulfield Mark |
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 |
A genetic risk score is significantly associated with statin therapy response in the elderly population. Clinical genetics 2016 Oct . Ciuculete D M, Bandstein M, Benedict C, Waeber G, Vollenweider P, Lind L, Schiöth H B, Mwinyi |
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin.
Human molecular genetics 2018 Feb 27 (3): 546-558. Tönjes Anke, Scholz Markus, Krüger Jacqueline, Krause Kerstin, Schleinitz Dorit, Kirsten Holger, Gebhardt Claudia, Marzi Carola, Grallert Harald, Ladenvall Claes, Heyne Henrike, Laurila Esa, Kriebel Jennifer, Meisinger Christa, Rathmann Wolfgang, Gieger Christian, Groop Leif, Prokopenko Inga, Isomaa Bo, Beutner Frank, Kratzsch Jürgen, Fischer-Rosinsky Antje, Pfeiffer Andreas, Krohn Knut, Spranger Joachim, Thiery Joachim, Blüher Matthias, Stumvoll Michael, Kovacs Pet |
Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities).
Arteriosclerosis, thrombosis, and vascular biology 2017 Jan . Pankow James S, Tang Weihong, Pankratz Nathan, Guan Weihua, Weng Lu-Chen, Cushman Mary, Boerwinkle Eric, Folsom Aaron |
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.
PloS one 2019 14 (8): e0220827. Andaleon Angela, Mogil Lauren S, Wheeler Heather |
The Association of Polymorphisms in Circadian Clock and Lipid Metabolism Genes With 2 Trimester Lipid Levels and Preterm Birth. Frontiers in genetics 2019 10 540. Kovac Ursa, Jasper Elizabeth A, Smith Caitlin J, Baer Rebecca J, Bedell Bruce, Donovan Brittney M, Weathers Nancy, Prosenc Zmrzljak Ursula, Jelliffe-Pawlowski Laura L, Rozman Damjana, Ryckman Kelli |
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 |
Genetically programmed changes in transcription of the novel progranulin regulator. Journal of molecular medicine (Berlin, Germany) 2020 Jul . Keller Maria, Gebhardt Claudia, Huth Sandra, Schleinitz Dorit, Heyne Henrike, Scholz Markus, Stumvoll Michael, Böttcher Yvonne, Tönjes Anke, Kovacs Pet |
Quantile-specific heritability of total cholesterol and its pharmacogenetic and nutrigenetic implications. International journal of cardiology 2020 12 327 185-192. Williams Paul |
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 |
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
NPJ genomic medicine 2020 5 1. Oni-Orisan Akinyemi, Haldar Tanushree, Ranatunga Dilrini K, Medina Marisa W, Schaefer Catherine, Krauss Ronald M, Iribarren Carlos, Risch Neil, Hoffmann Thomas |
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 |
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC Study. Arteriosclerosis, thrombosis, and vascular biology 2022 12 43 (2): 367-378. Steffen Brian T, Pankow James S, Norby Faye L, Lutsey Pamela L, Demmer Ryan T, Guan Weihua, Pankratz Nathan, Li Aixin, Liu Guning, Matsushita Kunihiro, Tin Adrienne, Tang Weiho |
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 |
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- Page last updated:Apr 22, 2024
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