Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 16 (of 16 Records) |
Query Trace: Spontaneous Coronary Artery Dissection[original query] |
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Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.
Nature genetics 2023 5 55 (6): 964-972. Adlam David, Berrandou Takiy-Eddine, Georges Adrien, Nelson Christopher P, Giannoulatou Eleni, Henry Joséphine, Ma Lijiang, Blencowe Montgomery, Turley Tamiel N, Yang Min-Lee, Chopade Sandesh, Finan Chris, Braund Peter S, Sadeg-Sayoud Ines, Iismaa Siiri E, Kosel Matthew L, Zhou Xiang, Hamby Stephen E, Cheng Jenny, Liu Lu, Tarr Ingrid, Muller David W M, d'Escamard Valentina, King Annette, Brunham Liam R, Baranowska-Clarke Ania A, Debette Stéphanie, Amouyel Philippe, Olin Jeffrey W, Patil Snehal, Hesselson Stephanie E, Junday Keerat, Kanoni Stavroula, Aragam Krishna G, Butterworth Adam S, , , , Tweet Marysia S, Gulati Rajiv, Combaret Nicolas, , Kadian-Dodov Daniella, Kalman Jonathan M, Fatkin Diane, Hingorani Aroon D, Saw Jacqueline, Webb Tom R, Hayes Sharonne N, Yang Xia, Ganesh Santhi K, Olson Timothy M, Kovacic Jason C, Graham Robert M, Samani Nilesh J, Bouatia-Naji Nabi |
Spontaneous coronary artery dissection and associated myocardial bridging: Current evidence from cohort study and case reports. Medical hypotheses 2019 6 128 50-53. Tajrishi Farbod Zahedi, Ahmad Asrar, Jamil Adeel, Sharfaei Sadaf, Goudarzi Sogand, Homayounieh Fatemeh, Pitliya Anmol, Kahe Farima, Chi Gera |
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection. Circulation. Genomic and precision medicine 2019 3 12 (4): e002437. Turley Tamiel N, Theis Jeanne L, Sundsbak Rhianna S, Evans Jared M, O'Byrne Megan M, Gulati Rajiv, Tweet Marysia S, Hayes Sharonne N, Olson Timothy |
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. Journal of the American College of Cardiology 2019 1 73 (1): 58-66. Adlam David, Olson Timothy M, Combaret Nicolas, Kovacic Jason C, Iismaa Siiri E, Al-Hussaini Abtehale, O'Byrne Megan M, Bouajila Sara, Georges Adrien, Mishra Ketan, Braund Peter S, d'Escamard Valentina, Huang Siying, Margaritis Marios, Nelson Christopher P, de Andrade Mariza, Kadian-Dodov Daniella, Welch Catherine A, Mazurkiewicz Stephani, Jeunemaitre Xavier, , Wong Claire Mei Yi, Giannoulatou Eleni, Sweeting Michael, Muller David, Wood Alice, McGrath-Cadell Lucy, Fatkin Diane, Dunwoodie Sally L, Harvey Richard, Holloway Cameron, Empana Jean-Philippe, Jouven Xavier, , Olin Jeffrey W, Gulati Rajiv, Tweet Marysia S, Hayes Sharonne N, Samani Nilesh J, Graham Robert M, Motreff Pascal, Bouatia-Naji Nabi |
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Nature communications 2020 09 11 (1): 4432. Saw Jacqueline, Yang Min-Lee, Trinder Mark, Tcheandjieu Catherine, Xu Chang, Starovoytov Andrew, Birt Isabelle, Mathis Michael R, Hunker Kristina L, Schmidt Ellen M, Jackson Linda, Fendrikova-Mahlay Natalia, Zawistowski Matthew, Brummett Chad M, Zoellner Sebastian, Katz Alexander, Coleman Dawn M, Swan Kirby, O'Donnell Christopher J, , Zhou Xiang, Li Jun Z, Gornik Heather L, Assimes Themistocles L, Stanley James C, Brunham Liam R, Ganesh Santhi |
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular research 2020 6 117 (4): 1154-1165. Georges Adrien, Albuisson Juliette, Berrandou Takiy, Dupré Délia, Lorthioir Aurélien, D'Escamard Valentina, Di Narzo Antonio F, Kadian-Dodov Daniella, Olin Jeffrey W, Warchol-Celinska Ewa, Prejbisz Aleksander, Januszewicz Andrzej, Bruneval Patrick, Baranowska Anna A, Webb Tom R, Hamby Stephen E, Samani Nilesh J, Adlam David, Fendrikova-Mahlay Natalia, Hazen Stanley, Wang Yu, Yang Min-Lee, Hunker Kristina, Combaret Nicolas, Motreff Pascal, Chédid Antoine, Fiquet Béatrice, Plouin Pierre-François, Mousseaux Elie, Azarine Arshid, Amar Laurence, Azizi Michel, Gornik Heather L, Ganesh Santhi K, Kovacic Jason C, Jeunemaitre Xavier, Bouatia-Naji Nabi |
Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
JAMA cardiology 2020 May . Turley Tamiel N, O'Byrne Megan M, Kosel Matthew L, de Andrade Mariza, Gulati Rajiv, Hayes Sharonne N, Tweet Marysia S, Olson Timothy |
Spontaneous coronary artery dissection: Role of prognostic markers and relationship with genetic analysis. International journal of cardiology 2020 11 326 19-29. Antonutti Marco, Baldan Federica, Lanera Corrado, Spedicato Leonardo, Zanuttini Davide, Bisceglia Teodoro, Favaretto Enrico, Poli Stefano, Tioni Chiara, Sut Dario, Gregori Dario, Damante Giuseppe, Proclemer Alessand |
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circulation. Genomic and precision medicine 2020 10 13 (6): e003030. Carss Keren J, Baranowska Anna A, Armisen Javier, Webb Tom R, Hamby Stephen E, Premawardhana Diluka, Al-Hussaini Abtehale, Wood Alice, Wang Quanli, Deevi Sri V V, Vitsios Dimitrios, Lewis Samuel H, Kotecha Deevia, Bouatia-Naji Nabila, Hesselson Stephanie, Iismaa Siiri E, Tarr Ingrid, McGrath-Cadell Lucy, Muller David W, Dunwoodie Sally L, Fatkin Diane, Graham Robert M, Giannoulatou Eleni, Samani Nilesh J, Petrovski Slavé, Haefliger Carolina, Adlam Dav |
Genome-Wide Identification of RNA Modifications for Spontaneous Coronary Aortic Dissection. Frontiers in genetics 2021 12 696562. Chai Tianci, Tian Mengyue, Yang Xiaojie, Qiu Zhihuang, Lin Xinjian, Chen Liangw |
Burden of Rare Genetic Variants in Spontaneous Coronary Artery Dissection With High-risk Features. JAMA cardiology 2022 9 7 (10): 1045-1055. Wang Yu, Starovoytov Andrew, Murad Andrea M, Hunker Kristina L, Brunham Liam R, Li Jun Z, Saw Jacqueline, Ganesh Santhi |
PHACTR1 modulates vascular compliance but not endothelial function: a translational study. Cardiovascular research 2022 Jun . Wood Alice, Antonopoulos Alexios, Chuaiphichai Surawee, Kyriakou Theodosios, Diaz Rebeca, Al Hussaini Abtehale, Marsh Anna-Marie, Sian Manjit, Meisuria Mitul, McCann Gerry, Rashbrook Victoria S, Drydale Edward, Draycott Sally, Polkinghorne Murray David, Akoumianakis Ioannis, Antoniades Charalambos, Watkins Hugh, Channon Keith M, Adlam David, Douglas Gilli |
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing. Circulation. Genomic and precision medicine 2022 May 101161CIRCGEN121003527. Tarr Ingrid, Hesselson Stephanie, Iismaa Siiri E, Rath Emma, Monger Steven, Troup Michael, Mishra Ketan, Wong Claire M Y, Hsu Pei-Chen, Junday Keerat, Humphreys David T, Adlam David, Webb Tom R, Baranowska-Clarke Anna A, Hamby Stephen E, Carss Keren J, Samani Nilesh J, Bax Monique, McGrath-Cadell Lucy, Kovacic Jason C, Dunwoodie Sally L, Fatkin Diane, Muller David W M, Graham Robert M, Giannoulatou Ele |
Association of Circulating Cathepsin B Levels With Blood Pressure and Aortic Dilation. Frontiers in cardiovascular medicine 2022 4 9 762468. Chai Tianci, Tian Mengyue, Yang Xiaojie, Qiu Zhihuang, Lin Xinjian, Chen Liangw |
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility. American journal of medical genetics. Part A 2022 Jan . Murad Andrea M, Hill Hannah L, Wang Yu, Ghannam Michael, Yang Min-Lee, Pugh Norma L, Asch Federico M, Hornsby Whitney, Driscoll Anisa, McNamara Jennifer, Willer Cristen J, Regalado Ellen S, , , Milewicz Dianna M, Eagle Kim A, Ganesh Santhi |
Polygenic Risk in Families With Spontaneous Coronary Artery Dissection. JAMA cardiology 2024 1 . Ingrid Tarr, Stephanie Hesselson, Michael Troup, Paul Young, Jamie-Lee Thompson, Lucy McGrath-Cadell, Diane Fatkin, Sally L Dunwoodie, David W M Muller, Siiri E Iismaa, Jason C Kovacic, Robert M Graham, Eleni Giannoulat |
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