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

Cited by (160)

Items 101–160 of 160

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  3. Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population
    Kalpana Bellary, Dwarkanath K. Murthy, Nagalla Balakrishna, Mohini Aiyengar Tupurani · 2019 · Indian Heart Journal
  4. Heterogeneous expression of alternatively spliced lncRNA mediates vascular smooth cell plasticity
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  5. Intracranial aneurysm risk factor genes: relationship with intracranial aneurysm risk in a Chinese Han population
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  6. The impact of coronary artery disease risk loci on ischemic heart failure severity and prognosis: association analysis in the COntrolled ROsuvastatin multiNAtional trial in heart failure (CORONA)
    Vincent G. Haver, Niek Verweij, JOHN K. KJEKSHUS, Jayne C. Fox, Hans Wedel, John Wikstrand, Wiek H. van Gilst, Rudolf A. de Boer, Dirk Jan van Veldhuisen, Pim van der Harst · 2014 · BMC Medical Genetics
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  8. The cardiovascular implication of single nucleotide polymorphisms of chromosome 9p21 locus among Arab population
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  10. The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs
    Salma Majid Wakil, Cao Nguyen, Nzioka P. Muiya, Editha Andres, Agnieszka Lykowska-Tarnowska, Batoul Baz, Asma I. Tahir, Brian F. Meyer, Grant Morahan, Nduna Dzimiri · 2015 · Disease Markers
  11. The Chromosome 9p21 Variant Not Predicting Long-Term Cardiovascular Mortality in Chinese with Established Coronary Artery Disease: An Eleven-Year Follow-Up Study
    I‐Te Lee, Mark O. Goodarzi, Wen‐Jane Lee, Jerome I. Rotter, Yii-Der Ida Chen, Kae‐Woei Liang, Wen-Lieng Lee, Wayne Huey‐Herng Sheu · 2014 · BioMed Research International
  12. CDKN2A and CDKN2B methylation in coronary heart disease cases and controls
    Jinyan Zhong, Xiaoying Chen, Huadan Ye, Nan Wu, Xiaomin Chen, Shiwei Duan · 2017 · Experimental and Therapeutic Medicine
  13. miR-3646 promotes vascular inflammation and augments vascular smooth muscle cell proliferation and migration in progression of coronary artery disease by directly targeting RHOH.
    Xiaoli Kang, Simin Cao, Zheng Ji, Yu Zhang, Shuxian Sun, Xiaoming Shang · 2018 · Europe PMC (PubMed Central)
  14. Association of Myocardial Infarction with CDKN2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 Polymorphism in Slovenian Subjects with Type 2 Diabetes Mellitus
    Miha Tibaut, Franjo Husam Naji, Daniel Petrovič · 2022 · Genes
  15. Non-Coding RNA Polymorphisms (rs2910164 and rs1333049) Associated With Prognosis of Lung Cancer Under Platinum-Based Chemotherapy
    Yixin Chen, Juan Chen, Ji‐Ye Yin, Hong‐Hao Zhou, Baimei He, Zhaoqian Liu · 2021 · Frontiers in Pharmacology
  16. CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MI
    Ivan Životić, Tamara Djurić, Aleksandra Stanković, Dejan Milašinović, Goran R. Stankovic, Milica Dekleva, Nataša Marković, Dragan Alavantić, Maja Živković · 2019 · Clinical Biochemistry
  17. The mechanisms of Chr.9p21.3 risk locus in coronary artery disease: where are we today?
    Anna‐Kaisa Ruotsalainen, Sanna Kettunen, Tuisku Suoranta, Minna Unelma Kaikkonen, Seppo Ylä‐Herttuala, Rédouane Aherrahrou · 2024 · American Journal of Physiology-Heart and Circulatory Physiology
  18. Elevated methylation of cyclin dependent kinase inhibitor 2B contributes to the risk of coronary heart disease in women
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  19. The role of CDKN2B in cardiovascular risk in ethnic Saudi Arabs: A validation study
    Maha M. Al-Rasheed, MennatAllah M. Hefnawy, Nourhan N. Elsherif, Tariq M. Alhawassi, Norah Othman Abanmy, Nora M. AlRasheed, Fulwah Yahya Alqahtani, Fadilah Sfouq Aleanizy, Paul Muiya, Olayan M Al-Boudari et al. · 2018 · Gene
  20. Dysregulation of the Urothelial Cancer Associated 1 Long Noncoding RNA Promotes Proliferation of Vascular Smooth Muscle Cells by Modulating Expression of P27KIP1/CDK2
    Haikuo Zheng, Ming-Hui Dong, Guohui Liu, Zhe An, Liang Zhang, Rui‐Ting Shan, Wenqi Zhang · 2020 · Genetic Testing and Molecular Biomarkers
  21. Quest for Genes and Mechanisms Linking the Human Chromosome 9p21.3 Locus to Cardiovascular Disease
    Anders Hamsten, Per Olof Eriksson · 2012 · Circulation
  22. Genetic association of ANRIL with susceptibility to Ischemic stroke: A comprehensive meta-analysis
    Na Bai, Wei Liu, Tao Xiang, Qiang Zhou, Jun Pu, Jing Zhao, Danyang Luo, Xindong Liu, Hua Liu · 2022 · PLoS ONE
  23. Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions
    I‐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
  24. Association of ANRIL Gene Polymorphisms with Acute Myeloid Leukemia in an Iranian Population
    Arezou Sayad, Abbas Hajifathali, Mohammad Naser Taheri · 2017 · International Journal of Cancer Management
  25. Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3
    Valeriy V. Benberin, Raushan Karabayeva, Nazgul Kulmyrzaeva, Rauza Bigarinova, Tamara A. Vochshenkova · 2023 · Medicine
  26. Genetic association between the lncRNA ANRIL rs10757272 polymorphism and intracranial aneurysm susceptibility in Asians
    Wei Zhao, Aijie He, Peng Zou · 2022 · Neurosurgical Review
  27. Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese population
    Jianjun Yan, Jinmei Zeng, Zhiyong Xie, Dongchen Liu, Liansheng Wang, Zhong Chen · 2016 · Lipids in Health and Disease
  28. The 9p21 Rs 1333040 polymorphism is associated with coronary microvascular obstruction in ST-segment elevation myocardial infarction treated by primary angioplasty
    Francesco 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
  29. Evaluation of the role of CDKN2B gene in type 2 diabetes mellitus and hypertension in ethnic Saudi Arabs
    Maha M. Al-Rasheed · 2018 · Saudi Pharmaceutical Journal
  30. Single‐nucleotide polymorphisms at the 9p21.3 genomic region not associated with the risk of cardiovascular disease in patients with rheumatoid arthritis
    Mercedes 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
  31. Analysis on the Polymorphism of Chromosome Region 9p21 and the Susceptibility of Carotid Plaque
    Jialan Sun, Fenghua Sun, Kang Yang, Ningzhen Fu, Longxuan Li · 2016 · European Neurology
  32. A Missing LNC in Vascular Diseases
    John P. Cooke, Nicholas James Leeper · 2017 · Circulation Research
  33. Methylation of Tumor Suppressor Genes on Chromosome 9: Diagnostic Insights from a Nasopharyngeal Carcinoma in Vietnam
    Thiều Hồng Huệ, Thuy Ai Huyen Le, Thuan Duc Lao · 2025 · Asian Pacific Journal of Cancer Prevention
  34. Deoxyribonucleic acid methylation in the enhancer region of the CDKN2A/2B and CDKN2B-AS1 genes in blood vessels and cells in patients with carotid atherosclerosis
    Iuliia 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
  35. Inference of causal relationships based on the genetics of cardiometabolic traits and conditions unique to females in >50,000 participants
    Brenda 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
  36. Influence of Chromosome 9p21.3 rs1333049 Variant on Telomere Length and Their Interactive Impact on the Prognosis of Coronary Artery Disease
    Andrea Borghini, Antonella Mercuri, Jonica Campolo, Marina Parolini, Rudina Ndreu, Stefano Turchi, Maria Grazia Andreassi · 2023 · Journal of Cardiovascular Development and Disease
  37. Progress and trends in myocardial infarction-related long non-coding RNAs: a bibliometric analysis
    Qingkun Meng, Hao Tan, Chengfu Wang, Zhijun Sun · 2024 · Frontiers in Molecular Biosciences
  38. Association of ANRIL Gene Polymorphisms with Gastric Cancer Risk: A Case–Control Study
    Samaneh Hasani, Farhad Pourfarzi, Mohammad Mazani, Abbas Yazdanbod, Aliakbar Fazaeli · 2024 · Genetic Testing and Molecular Biomarkers
  39. Association Study of Polymorphic Variants in 9P21 Locus and the Manifestation of Coronary Artery Disease in Bulgarians
    Reni Tzveova, Galya Naydenova Atanasova, Teodora Yaneva-Sirakova, Silvia Vandeva, P. Atanasov, Vanio Mitev, Р. Kaneva, D. Pendicheva-Duhlenska · 2025 · Acta Medica Bulgarica
  40. The Genetic and Proteomic Detereminants of the Risk of Coronary Artery Disease
    Naif A. M. Almontashiri · 2015 · uO Research (University of Ottawa)
  41. Identification and Characterization of novel long non-coding RNAs in vascular smooth cells
    Charles 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)
  42. The Non-Coding RNA Journal Club: Highlights on Recent Papers—13
    Patrick 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
  43. A framework for studying multi-omic risk factors and their interplay: application to coronary artery disease
    Jiaqi Hu, Chen Lin, Hongyu Zhao, Andrew Thomas DeWan · 2025 · medRxiv
  44. Genetics of Coronary Artery Disease
    Valentı́n Fuster, Jason C. Kovacic · 2014
  45. Investigating Genetic Risk Factors of Coronary Artery Disease Using Genome Editing
    David G. McVey · 2016 · Leicester Research Archive (University of Leicester)
  46. Genetic variation, telomeres and heart failure
    Vincent G. Haver · 2015 · University of Groningen research database (University of Groningen / Centre for Information Technology)
  47. Population-based studies of risk factors for subarachnoid hemorrhage
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  48. TCF7L2 Regulation of GATA6-dependent and -Independent Vascular Smooth Muscle Cell Plasticity and Intimal Hyperplasia
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  49. Deoxyribonucleic acid damage gene expression, ligase activity and correlation with coronary atherosclerotic plaque morphology.
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  50. Kardiyovasküler Hastalıklarda Uzun Kodlamayan RNA’lar ve Sirküler RNA’ların Önemi
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  51. Knockout of the Murine Ortholog to the Human 9p21 Coronary Artery Disease Locus Leads to SMC Proliferation, Vascular Calcification, and Advanced Atherosclerosis
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  52. Periodontal Disease
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  54. DNA Methylation Pattern and mRNA Expression Level of E-Cadherin and P16 Genes in Thrombotic Disorders
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  55. Allelic Variation at 9p21.3 Orchestrates Widespread RNA Splicing Shifts Governing Vascular Smooth Muscle Cell Plasticity
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  56. Shared Genetic Liability Between Heart Failure and Myocardial Infarction Revealed by Genome-Wide Cross-Trait Analysis
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