Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells
Motterle, A., Pu, X., Wood, H., Xiao, Q., Gor, S., Liang Ng, F., Chan, K., Cross, F. +5 more·2012·Human Molecular Genetics
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- Non-Coding RNA Polymorphisms (rs2910164 and rs1333049) Associated With Prognosis of Lung Cancer Under Platinum-Based ChemotherapyYixin Chen, Juan Chen, Ji‐Ye Yin, Hong‐Hao Zhou, Baimei He, Zhaoqian Liu · 2021 · Frontiers in Pharmacology
- CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MIIvan Životić, Tamara Djurić, Aleksandra Stanković, Dejan Milašinović, Goran R. Stankovic, Milica Dekleva, Nataša Marković, Dragan Alavantić, Maja Živković · 2019 · Clinical Biochemistry
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- Elevated methylation of cyclin dependent kinase inhibitor 2B contributes to the risk of coronary heart disease in womenXiaomin Chen, Danjie Jiang, Limin Xu, Liyuan Han, Haochang Hu, Yi Huang, Deyi Lu, Huihui Ji, Bin Li, Yong Yang et al. · 2018 · Experimental and Therapeutic Medicine
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- Quest for Genes and Mechanisms Linking the Human Chromosome 9p21.3 Locus to Cardiovascular DiseaseAnders Hamsten, Per Olof Eriksson · 2012 · Circulation
- Genetic association of ANRIL with susceptibility to Ischemic stroke: A comprehensive meta-analysisNa Bai, Wei Liu, Tao Xiang, Qiang Zhou, Jun Pu, Jing Zhao, Danyang Luo, Xindong Liu, Hua Liu · 2022 · PLoS ONE
- Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary LesionsI‐Te Lee, Kae‐Woei Liang, Jun‐Sing Wang, Wen‐Jane Lee, Yii-Der Ida Chen, Shih-Yi Lin, Wen-Lieng Lee, Wayne Huey‐Herng Sheu · 2015 · Medicine
- Association of ANRIL Gene Polymorphisms with Acute Myeloid Leukemia in an Iranian PopulationArezou Sayad, Abbas Hajifathali, Mohammad Naser Taheri · 2017 · International Journal of Cancer Management
- Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3Valeriy V. Benberin, Raushan Karabayeva, Nazgul Kulmyrzaeva, Rauza Bigarinova, Tamara A. Vochshenkova · 2023 · Medicine
- Genetic association between the lncRNA ANRIL rs10757272 polymorphism and intracranial aneurysm susceptibility in AsiansWei Zhao, Aijie He, Peng Zou · 2022 · Neurosurgical Review
- Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese populationJianjun Yan, Jinmei Zeng, Zhiyong Xie, Dongchen Liu, Liansheng Wang, Zhong Chen · 2016 · Lipids in Health and Disease
- The 9p21 Rs 1333040 polymorphism is associated with coronary microvascular obstruction in ST-segment elevation myocardial infarction treated by primary angioplastyFrancesco Fracassi, Giampaolo Niccoli, Vincenzo Vetrugno, Michele Cauteruccio, Antonino Buffon, Ilaria Gatto, Igor Giarretta, Paolo Tondi, Roberto Pola, Filippo Crea · 2017 · European Heart Journal Acute Cardiovascular Care
- Evaluation of the role of CDKN2B gene in type 2 diabetes mellitus and hypertension in ethnic Saudi ArabsMaha M. Al-Rasheed · 2018 · Saudi Pharmaceutical Journal
- Single‐nucleotide polymorphisms at the 9p21.3 genomic region not associated with the risk of cardiovascular disease in patients with rheumatoid arthritisMercedes García-Bermúdez, Raquel López‐Mejías, Fernanda Genre, Santos Castañeda, Carlos González‐Juanatey, Javier Llorca, Alfonso Corrales, José Alberto Miranda-Filloy, Trinitario Pina, Carmen Gómez‐Vaquero et al. · 2013 · Tissue Antigens
- Analysis on the Polymorphism of Chromosome Region 9p21 and the Susceptibility of Carotid PlaqueJialan Sun, Fenghua Sun, Kang Yang, Ningzhen Fu, Longxuan Li · 2016 · European Neurology
- A Missing LNC in Vascular DiseasesJohn P. Cooke, Nicholas James Leeper · 2017 · Circulation Research
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- Deoxyribonucleic acid methylation in the enhancer region of the CDKN2A/2B and CDKN2B-AS1 genes in blood vessels and cells in patients with carotid atherosclerosisIuliia A. Koroleva, Anton Markov, Irina A. Goncharova, А. А. Слепцов, Н. П. Бабушкина, Nail Raushanovich Valiakhmetov, Diana Sharysh, А. А. Зарубин, М. С. Кузнецов, Boris N. Kozlov et al. · 2020 · Russian Journal of Cardiology
- Inference of causal relationships based on the genetics of cardiometabolic traits and conditions unique to females in >50,000 participantsBrenda Xiao, Digna R. Velez Edwards, Anastasia Lucas, Theodore G. Drivas, Kathryn J. Gray, Brendan J. Keating, Chunhua Weng, Gail Pairitz Jarvik, Hakon H. Hakonarson, Leah Claire Kottyan et al. · 2022 · medRxiv
- Influence of Chromosome 9p21.3 rs1333049 Variant on Telomere Length and Their Interactive Impact on the Prognosis of Coronary Artery DiseaseAndrea Borghini, Antonella Mercuri, Jonica Campolo, Marina Parolini, Rudina Ndreu, Stefano Turchi, Maria Grazia Andreassi · 2023 · Journal of Cardiovascular Development and Disease
- Progress and trends in myocardial infarction-related long non-coding RNAs: a bibliometric analysisQingkun Meng, Hao Tan, Chengfu Wang, Zhijun Sun · 2024 · Frontiers in Molecular Biosciences
- Association of ANRIL Gene Polymorphisms with Gastric Cancer Risk: A Case–Control StudySamaneh Hasani, Farhad Pourfarzi, Mohammad Mazani, Abbas Yazdanbod, Aliakbar Fazaeli · 2024 · Genetic Testing and Molecular Biomarkers
- Association Study of Polymorphic Variants in 9P21 Locus and the Manifestation of Coronary Artery Disease in BulgariansReni Tzveova, Galya Naydenova Atanasova, Teodora Yaneva-Sirakova, Silvia Vandeva, P. Atanasov, Vanio Mitev, Р. Kaneva, D. Pendicheva-Duhlenska · 2025 · Acta Medica Bulgarica
- The Genetic and Proteomic Detereminants of the Risk of Coronary Artery DiseaseNaif A. M. Almontashiri · 2015 · uO Research (University of Ottawa)
- Identification and Characterization of novel long non-coding RNAs in vascular smooth cellsCharles Ugochukwu Solomon, David G. McVey, Catherine Andreadi, Peng Gong, Lanka Turner, Sonja Khemiri, Julie C. Chamberlain, Tom R. Webb, Nilesh J. Samani, Shu Ye · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
- The Non-Coding RNA Journal Club: Highlights on Recent Papers—13Patrick Shiu, Johanna Kay DiStefano, Suresh K. Alahari, Francisco J. Enguita, Mark W. Feinberg, Nikolaos Sideris, Salih Bayraktar, Leandro Castellano, Diana Luna Buitrago, Andrea Caporali et al. · 2023 · Non-Coding RNA
- A framework for studying multi-omic risk factors and their interplay: application to coronary artery diseaseJiaqi Hu, Chen Lin, Hongyu Zhao, Andrew Thomas DeWan · 2025 · medRxiv
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- Genetic variation, telomeres and heart failureVincent G. Haver · 2015 · University of Groningen research database (University of Groningen / Centre for Information Technology)
- Population-based studies of risk factors for subarachnoid hemorrhageMartin Söderholm · 2016 · Lund University Publications (Lund University)
- TCF7L2 Regulation of GATA6-dependent and -Independent Vascular Smooth Muscle Cell Plasticity and Intimal HyperplasiaRoshni Srivastava, Harshvardhan Rolyan, Yi Xie, Na Li, Neha Bhat, Lingjuan Hong, Fatemehsadat Esteghamat, Adebowale Adeniran, Arnar Geirsson, Jiasheng Zhang et al. · 2018 · bioRxiv (Cold Spring Harbor Laboratory)
- Deoxyribonucleic acid damage gene expression, ligase activity and correlation with coronary atherosclerotic plaque morphology.Nikunj R. Shah · 2019 · Surrey Research Insight Open Access (The University of Surrey)
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- Allelic Variation at 9p21.3 Orchestrates Widespread RNA Splicing Shifts Governing Vascular Smooth Muscle Cell PlasticityS. Suryavanshi, Huan Yang, Elsa Salido, Valentina Lo Sardo · 2026 · bioRxiv (Cold Spring Harbor Laboratory)
- Shared Genetic Liability Between Heart Failure and Myocardial Infarction Revealed by Genome-Wide Cross-Trait AnalysisRuikang Liu, Chiyun Sun, Nan Jiang, Yang Liu, Jun Li, Fuyuan Zhang, Cong Chen, Yiying Liu, Xiaodi Qi, B Y Guo et al. · 2026 · Journal of Cardiovascular Pharmacology and Therapeutics
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