HuGE Literature Finder
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Coronary artery disease patient-derived iPSC-hepatocytes have distinct miRNA profile that may alter lipid metabolism. Scientific reports 2023 1 13 (1): 1706. Alexanova Anna, Raitoharju Emma, Valtonen Joona, Aalto-Setälä Katriina, Viiri Leena |
Src homology 2-B adapter protein 3 C784 T and Methylenetetrahydrofolate reductase C677 T Polymorphisms and Inflammation Markers in ST-segment Elevation Myocardial Infarction Patients. Angiology 2023 1 33197231152693. Golestani Amin, Rahimi Atefeh, Moezi Bady Seyed Ali, Azdaki Nahid, Sajjadi Seyed Meh |
Genetic Liability to Rheumatoid Arthritis in Relation to Coronary Artery Disease and Stroke Risk. Arthritis & rheumatology (Hoboken, N.J.) 2022 May . Yuan Shuai, Carter Paul, Mason Amy M, Yang Fangkun, Burgess Stephen, Larsson Susanna |
A novel anti-inflammatory role links the CARS2 locus to protection from coronary artery disease. Atherosclerosis 2022 4 348 8-15. Dang Anh-Thu, Turner Adam W, Lau Paulina, Mohottalage Dhanuddara, Stephanie Fong Yuet Kay, Eriksson Per, Folkersen Lasse, Matic Ljubica, Hedin Ulf, Soubeyrand Sébastien, McPherson Ru |
Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population. BMC cardiovascular disorders 2022 6 22 (1): 298. Rayat Sima, Ramezanidoraki Nasim, Kazemi Nima, Modarressi Mohammad H, Falah Masoumeh, Zardadi Safoura, Morovvati Sae |
Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation.
![]() PLoS biology 2022 2 20 (2): e3001547. Richardson Tom G, Leyden Genevieve M, Wang Qin, Bell Joshua A, Elsworth Benjamin, Davey Smith George, Holmes Michael |
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. Nature communications 2022 3 13 (1): 1222. Stacey David, Chen Lingyan, Stanczyk Paulina J, Howson Joanna M M, Mason Amy M, Burgess Stephen, MacDonald Stephen, Langdown Jonathan, McKinney Harriett, Downes Kate, Farahi Neda, Peters James E, Basu Saonli, Pankow James S, Tang Weihong, Pankratz Nathan, Sabater-Lleal Maria, de Vries Paul S, Smith Nicholas L, , Gelinas Amy D, Schneider Daniel J, Janjic Nebojsa, Samani Nilesh J, Ye Shu, Summers Charlotte, Chilvers Edwin R, Danesh John, Paul Dirk |
Evidence for Shared Genetic Aetiology Between Schizophrenia, Cardiometabolic, and Inflammation-Related Traits: Genetic Correlation and Colocalization Analyses. Schizophrenia bulletin open 2022 2 3 (1): sgac001. Perry Benjamin I, Bowker Nicholas, Burgess Stephen, Wareham Nicholas J, Upthegrove Rachel, Jones Peter B, Langenberg Claudia, Khandaker Golam |
Loss-of-function N178T variant of the human P2Y receptor is associated with decreased severity of coronary artery disease and improved glucose homeostasis. Frontiers in pharmacology 2022 12 13 1049696. Horckmans Michael, Diaz Villamil Esteban, Verdier Céline, Laurell Henrik, Ruidavets Jean-Bernard, De Roeck Lucas, Combes Guillaume, Martinez Laurent O, Communi Didi |
Vitamin D receptor gene polymorphism TaqI (rs731236) and its association with the susceptibility to coronary artery disease among Pakistani population. The journal of gene medicine 2021 Aug e3386. Kulsoom Ume, Khan Amber, Saghir Tahir, Nawab Syeda Nuzhat, Tabassum Atiya, Fatima Sehrish, Saleem Saima, Zehra Sitw |
Protective role of TIRAP functional variant against development of coronary artery disease. Saudi journal of biological sciences 2021 Jun 28 (6): 3548-3552. Noreen Mamoona, Imran Muhammad, Safi Sher Zaman, Bashir Muhammad Amjad, Gul Sana, Alkhuriji Afrah Fahad, Aloma Suliman Yousef, Alharbi Hanan Mualla, Arshad Muhamm |
LncRNA H19 rs4929984 Variant is Associated with Coronary Artery Disease Susceptibility in Han Chinese Female Population. Biochemical genetics 2021 Apr . Huang Jiao, Li Minhua, Li Jinhong, Liang Baoyun, Chen Zhaoxia, Yang Jialei, Guo Xiaojing, Huang Siyun, Gu Lian, Su |
The Association of IL-6, TNF? and CRP Gene Polymorphisms with Coronary Artery Disease in a Tunisian Population: A Case-Control study. Biochemical genetics 2021 Feb . Grira Nedra, Lahidheb Dhaker, Lamine Oussama, Ayoub Manel, Wassaifi Souhir, Aouni Zied, Fehri Wafa, Mazigh Chak |
Dissecting the IL-6 pathway in cardiometabolic disease: A Mendelian randomization study on both IL6 and IL6R. British journal of clinical pharmacology 2021 12 88 (6): 2875-2884. Cupido Arjen J, Asselbergs Folkert W, Natarajan Pradeep, , Ridker Paul M, Hovingh G Kees, Schmidt A Floria |
Two RECK Splice Variants (Long and Short) Are Differentially Expressed in Patients with Stable and Unstable Coronary Artery Disease: A Pilot Study. Genes 2021 7 12 (6): . Vancheri Chiara, Morini Elena, Prandi Francesca Romana, Alkhoury Elie, Celotto Roberto, Romeo Francesco, Novelli Giuseppe, Amati Frances |
Interaction between a haptoglobin genetic variant and coronary artery disease (CAD) risk factors on CAD severity in Singaporean Chinese population. Molecular genetics & genomic medicine 2020 Aug e1450. Chang Xuling, Dorajoo Rajkumar, Han Yi, Wang Ling, Liu Jianjun, Khor Chiea-Chuen, Low Adrian F, Chan Mark Yan-Yee, Yuan Jian-Min, Koh Woon-Puay, Friedlander Yechiel, Heng Chew-Ki |
Reverse expression pattern of sirtuin-1 and histone deacetylase-9 in coronary artery disease. Archives of physiology and biochemistry 2020 Aug 1-8. Heidari Laleh, Ghaderian Sayyed Mohammad Hossein, Bastami Milad, Hosseini Shadi, Alipour Parsa Saeed, Heidari Sahel, Jafari Hossein, Sohrabifar Nasim, Pirhoushiaran Mary |
A Meta-Analysis on the Association Between TNFSF4 Polymorphisms (rs3861950 T > C and rs1234313 A > G) and Susceptibility to Coronary Artery Disease. Frontiers in physiology 2020 12 11 539288. Liu Shuyan, Wang Xiju, Yu Shoujun, Yan Miao, Peng Yue, Zhang Guilong, Xu Zhaow |
Association of E-Selectin gene polymorphisms and serum E-Selectin level with risk of coronary artery disease in lur population of Iran. Archives of physiology and biochemistry 2020 10 1-6. Khoshbin Mobin, Ahmadi Seyyed Amir Yasin, Cheraghi Mostafa, Nouryazdan Negar, Birjandi Mehdi, Shahsavari Gholamre |
Functional Genetic Variant in ATG5 Gene Promoter in Acute Myocardial Infarction. Cardiology research and practice 2020 5 2020 9898301. Zhang Yexin, He Xiaohui, Li Jiarui, Yang Wentao, Cui Yinghua, Pang Shuchao, Wang Haihua, Yan |
Genetic determinants of circulating galectin-3 levels in patients with coronary artery disease. Molecular genetics & genomic medicine 2020 6 8 (9): e1370. Liao Yu-Huang, Teng Ming-Sheng, Juang Jyh-Ming J, Chiang Fu-Tien, Er Leay-Kiaw, Wu Semon, Ko Yu-L |
High-sensitivity C-reactive protein is associated with clonal hematopoiesis of indeterminate potential. Blood advances 2020 6 4 (11): 2430-2438. Busque Lambert, Sun Maxine, Buscarlet Manuel, Ayachi Sami, Feroz Zada Yassamin, Provost Sylvie, Bourgoin Vincent, Mollica Luigina, Meisel Marlies, Hinterleitner Reinhard, Jabri Bana, Dubé Marie-Pierre, Tardif Jean-Clau |
Hypermethylation of miR-181b in monocytes is associated with coronary artery disease and promotes M1 polarized phenotype via PIAS1-KLF4 axis. Cardiovascular diagnosis and therapy 2020 9 10 (4): 738-751. Wang Zhonghua, Li Chunlei, Sun Xinyong, Li Zhuqin, Li Jia, Wang Lanfeng, Sun Yanmi |
Plasma kynurenines and prognosis in patients with heart failure. PloS one 2020 1 15 (1): e0227365. Lund Anders, Nordrehaug Jan Erik, Slettom Grete, Solvang Stein-Erik Hafstad, Pedersen Eva Kristine Ringdal, Midttun Øivind, Ulvik Arve, Ueland Per Magne, Nygård Ottar, Giil Lasse Melva |
The Association Between Leukocyte Telomere Length and Cognitive Performance Among the American Elderly. Frontiers in aging neuroscience 2020 11 12 527658. Linghui Deng, Shi Qiu, Chi Chen, Xiaolei Liu, Lixing Zhou, Zhiliang Zuo, Birong Do |
Down-regulated RGS5 by genetic variants impairs endothelial cell function and contributes to coronary artery disease. Cardiovascular research 2019 (1): 240-255. Li Yang, Yan Han, Guo Jian, Han Yingchun, Zhang Cuifang, Liu Xiuying, Du Jie, Tian Xiao- |
Long- and short-term association of low-grade systemic inflammation with cardiovascular mortality in the LURIC study. Clinical research in cardiology : official journal of the German Cardiac Society 2019 Jul . Kälsch Anna-Isabelle, Scharnagl Hubert, Kleber Marcus E, Windpassinger Christian, Sattler Wolfgang, Leipe Jan, Krämer Bernhard K, März Winfried, Malle Ern |
Glutathione Transferase P1 Polymorphism Might Be a Risk Determinant in Heart Failure. Disease markers 2019 7 2019 6984845. Simeunovic Dejan, Odanovic Natalija, Pljesa-Ercegovac Marija, Radic Tanja, Radovanovic Slavica, Coric Vesna, Milinkovic Ivan, Matic Marija, Djukic Tatjana, Ristic Arsen, Risimic Dijana, Seferovic Petar, Simic Tatjana, Simic Dragan, Savic-Radojevic A |
Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing. Gene 2019 9 721 144107. Ghose Subhoshree, Ghosh Sourav, Tanwar Vinay Singh, Tolani Priya, Kutum Rintu, Sharma Anju, Bhardwaj Nitin, Shamsudheen K V, Verma Ankit, Jayarajan Rijith, Dash Debasis, Sivasubbu Sridhar, Scaria Vinod, Seth Sandeep, Sengupta Shanta |
Non-alcoholic fatty liver disease and cardiovascular disease: assessing the evidence for causality. Diabetologia 2019 11 63 (2): 253-260. Brouwers Martijn C G J, Simons Nynke, Stehouwer Coen D A, Isaacs Aar |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 29, 2023
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