Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: Stroke and NOS3[original query] |
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NOS3 polymorphisms, cigarette smoking, and cardiovascular disease risk: the Atherosclerosis Risk in Communities study. Pharmacogenetics and genomics 2006 Dec 16 (12): 891-9. Lee Craig R, North Kari E, Bray Molly S, Avery Christy L, Mosher Mary Jane, Couper David J, Coresh Josef, Folsom Aaron R, Boerwinkle Eric, Heiss Gerardo, Zeldin Darryl |
Endothelial nitric oxide synthase gene polymorphisms and cardiovascular disease: a HuGE review. American journal of epidemiology 2006 Nov 164 (10): 921-35. Casas Juan P, Cavalleri Gianpiero L, Bautista Leonelo E, Smeeth Liam, Humphries Steve E, Hingorani Aroon |
Renin-angiotensin system and nitric oxide synthase gene polymorphisms in relation to stroke. American journal of hypertension 2007 Jul 20 (7): 764-70. Henskens Léon H, Kroon Abraham A, van der Schouw Yvonne T, Schiffers Paul M, Grobbee Diederick E, de Leeuw Peter W, Bots Michiel |
The intron 4c allele of the NOS3 gene is associated with ischemic stroke in African Americans. BMC medical genetics 2007 8 (1): 76. Grewal R P, Dutra A V C, Liao Yi C, Juo Ss H, Papamitsakis N I |
Common genetic variation in six lipid-related and statin-related genes, statin use and risk of incident nonfatal myocardial infarction and stroke. Pharmacogenetics and genomics 2008 Aug 18 (8): 677-82. Hindorff Lucia A, Lemaitre Rozenn N, Smith Nicholas L, Bis Joshua C, Marciante Kristin D, Rice Kenneth M, Lumley Thomas, Enquobahrie Daniel A, Li Guo, Heckbert Susan R, Psaty Bruce |
Association of acute ischemic stroke with the MTHFR C677T polymorphism but not with NOS3 gene polymorphisms in a Singapore population. European journal of neurology : the official journal of the European Federation of Neurological Societies 2008 Dec 15 (12): 1309-14. Moe K T, Woon F P, De Silva D A, Wong P, Koh T H, Kingwell B, Chin-Dusting J, Wong M |
Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study. Stroke; a journal of cerebral circulation 2009 Oct 40 (10): e550-7. MacClellan Leah R, Howard Timothy D, Cole John W, Stine O Colin, Giles Wayne H, O'Connell Jeffery R, Wozniak Marcella A, Stern Barney J, Mitchell Braxton D, Kittner Steven |
Genetic and pharmacogenetic associations between NOS3 polymorphisms, blood pressure, and cardiovascular events in hypertension. American journal of hypertension 2009 Jul 22 (7): 748-53. Pacanowski Michael A, Zineh Issam, Cooper-Dehoff Rhonda M, Pepine Carl J, Johnson Julie |
NOS3 gene rs1799983 polymorphism and incident dementia in elderly stroke survivors. Neurobiology of aging 2011 Mar 32 (3): 554.e1-6. Morris Christopher M, Ballard Clive G, Allan Louise, Rowan Elise, Stephens Sally, Firbank Michael, Ford Gary A, Kenny Rose Anne, O'Brien John T, Kalaria Raj |
MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection. International journal of stroke : official journal of the International Stroke Society 2010 Apr 5 (2): 80-5. Jara-Prado A, Alonso M E, Martínez Ruano L, Guerrero Camacho J, Leyva A, López M, Gutierrez-Castrellon P, Arauz |
Screening the single nucleotide polymorphisms in patients with internal carotid artery stenosis by oligonucleotide-based custom DNA array. Bioinformatics and biology insights 2009 1 63-9. Nakai Kenji, Oyanagi Mayu, Hitomi Jiro, Ogasawara Kuniaki, Inoue Takashi, Kobayashi Masakazu, Nakai Keiko, Suwabe Akira, Habano Wataru, Baba Toshiaki, Yoshida Hiroshi, Ogawa Aki |
Variants within the nitric oxide synthase 1 gene are associated with stroke susceptibility. Atherosclerosis 2012 Feb 220 (2): 443-8. Manso Helena, Krug Tiago, Sobral João, Albergaria Isabel, Gaspar Gisela, Ferro José M, Oliveira Sofia A, Vicente Astrid |
Predictive role of polymorphisms in interleukin-5 receptor alpha-subunit, lipoprotein lipase, integrin A2 and nitric oxide synthase genes on ischemic stroke in type 2 diabetes--an 8-year prospective cohort analysis of 1327 Chinese patients. Atherosclerosis 2011 1 215 (1): 130-5. Luk Andrea O Y, Wang Ying, Ma Ronald C W, Tam Claudia H T, Ng Maggie C Y, Lam Vincent, Yang Xilin, Baum Larry, Tong Peter C Y, Chan Juliana C N, So Wing-Y |
Pharmacogenetic association of NOS3 variants with cardiovascular disease in patients with hypertension: the GenHAT study. PloS one 2012 7 (3): e34217. Zhang Xue, Lynch Amy I, Davis Barry R, Ford Charles E, Boerwinkle Eric, Eckfeldt John H, Leiendecker-Foster Catherine, Arnett Donna |
Gene polymorphisms in association with self-reported stroke in US adults. The application of clinical genetics 2013 6 3 23-8. Fan Amy Z, Fang Jing, Yesupriya Ajay, Chang Man-Huei, Kilmer Greta, House Meaghan, Hayes Donald, Ned Renée M, Dowling Nicole F, Mokdad Ali |
Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians. Journal of the neurological sciences 2014 Sep 344 (1-2): 69-75. Akhter Mohd Suhail, Biswas Arijit, Rashid Hina, Devi Luxmi, Behari Madhuri, Saxena Re |
Importance of NOS3 genetic polymorphisms in the risk of development of ischemic stroke in the Turkish population. Genetic testing and molecular biomarkers 2014 Dec 18 (12): 797-803. Türkano?lu Özçelik Aysun, Can Demirdö?en Birsen, Demirkaya ?eref, Adal? Orh |
An Inflammatory Polymorphisms Risk Scoring System for the Differentiation of Ischemic Stroke Subtypes. Mediators of inflammation 2015 2015 569714. Muiño Elena, Krupinski Jurek, Carrera Caty, Gallego-Fabrega Cristina, Montaner Joan, Fernández-Cadenas Isra |
[GENDER-SPECIFIC DIFFERENCES OF ENDOTHELIAL NITRIC OXIDE SYNTHASE E298D POLYMORPHISM AND THE RISK OF STROKE]. Klinicheskaia meditsina 2015 93 (2): 34-40. Bushueva O Yu, Stetskaya T A, Korogodina G V, Ivanov V P, Polonikov A |
[The combined effect of E298D polymorphism of the endothelial nitric oxide synthase gene and smoking on the risk of cerebral stroke]. Genetika 2015 Feb 51 (2): 256-62. Bushueva O Yu, Stetskaya T A, Korogodina T V, Ivanov V P, Polonikov A |
Clinical implications of nonsarcomeric gene polymorphisms in hypertrophic cardiomyopathy. European journal of clinical investigation 2015 Nov . García-Honrubia Antonio, Hernández-Romero Diana, Orenes-Piñero Esteban, Romero-Aniorte Ana Isabel, Climent Vicente, García Miriam, Garrigos-Gómez Noemí, Moro Concepción, Valdés Mariano, Marín Francis |
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Circulation 2017 10 137 (3): 222-232. Emdin Connor A, Khera Amit V, Klarin Derek, Natarajan Pradeep, Zekavat Seyedeh M, Nomura Akihiro, Haas Mary, Aragam Krishna, Ardissino Diego, Wilson James G, Schunkert Heribert, McPherson Ruth, Watkins Hugh, Elosua Roberto, Bown Matthew J, Samani Nilesh J, Baber Usman, Erdmann Jeanette, Gormley Padhraig, Palotie Aarno, Stitziel Nathan O, Gupta Namrata, Danesh John, Saleheen Danish, Gabriel Stacey, Kathiresan Sek |
Genome-wide meta-analysis identifies 3 novel loci associated with stroke.
Annals of neurology 2018 Dec 84 (6): 934-939. Malik Rainer, Rannikmäe Kristiina, Traylor Matthew, Georgakis Marios K, Sargurupremraj Muralidharan, Markus Hugh S, Hopewell Jemma C, Debette Stephanie, Sudlow Cathie L M, Dichgans Martin, |
[A clinical and genetic analysis of risk factors for the development of acute and chronic cerebral ischemia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (3. Vyp. 2): 62-67. Anisimova A V, Gunchenko A S, Ikonnikova A Yu, Galkin S S, Avdonina M A, Nasedkina T |
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Stroke 2020 07 51 (7): 2111-2121. Armstrong Nicola J, Mather Karen A, Sargurupremraj Muralidharan, Knol Maria J, Malik Rainer, Satizabal Claudia L, Yanek Lisa R, Wen Wei, Gudnason Vilmundur G, Dueker Nicole D, Elliott Lloyd T, Hofer Edith, Bis Joshua, Jahanshad Neda, Li Shuo, Logue Mark A, Luciano Michelle, Scholz Markus, Smith Albert V, Trompet Stella, Vojinovic Dina, Xia Rui, Alfaro-Almagro Fidel, Ames David, Amin Najaf, Amouyel Philippe, Beiser Alexa S, Brodaty Henry, Deary Ian J, Fennema-Notestine Christine, Gampawar Piyush G, Gottesman Rebecca, Griffanti Ludovica, Jack Clifford R, Jenkinson Mark, Jiang Jiyang, Kral Brian G, Kwok John B, Lampe Leonie, C M Liewald David, Maillard Pauline, Marchini Jonathan, Bastin Mark E, Mazoyer Bernard, Pirpamer Lukas, Rafael Romero José, Roshchupkin Gennady V, Schofield Peter R, Schroeter Matthias L, Stott David J, Thalamuthu Anbupalam, Trollor Julian, Tzourio Christophe, van der Grond Jeroen, Vernooij Meike W, Witte Veronica A, Wright Margaret J, Yang Qiong, Morris Zoe, Siggurdsson Siggi, Psaty Bruce, Villringer Arno, Schmidt Helena, Haberg Asta K, van Duijn Cornelia M, Jukema J Wouter, Dichgans Martin, Sacco Ralph L, Wright Clinton B, Kremen William S, Becker Lewis C, Thompson Paul M, Mosley Thomas H, Wardlaw Joanna M, Ikram M Arfan, Adams Hieab H H, Seshadri Sudha, Sachdev Perminder S, Smith Stephen M, Launer Lenore, Longstreth William, DeCarli Charles, Schmidt Reinhold, Fornage Myriam, Debette Stephanie, Nyquist Paul |
Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia. Blood cells, molecules & diseases 2020 Jul 83 102436. Silva Marisa, Vargas Sofia, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Maia Raquel, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Silva Rita, Kjöllerström Paula, Faustino Pau |
Endothelial NO synthase 786T/T polymorphism increases hemorrhagic transformation after endovascular thrombectomy. Nitric oxide : biology and chemistry 2022 Sep 129 8-15. de la Riva Patricia, Rodríguez-Antigüedad Jon, Gómez Virginia, Arenaza Gorka, Gorostidi Ana, Díez Noemí, de Arce Ana, Martínez-Zabaleta Maite, González Félix, Luttich Alex, Garmendia Eñaut, Sola Ana, Larrea Jose Angel, Bergareche Alberto, Sobrino Tom |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
Model based on single-nucleotide polymorphism to discriminate aspirin resistance patients. Stroke and vascular neurology 2023 8 . Qingyuan Liu, Shuaiwei Guo, Nuochuan Wang, Kaiwen Wang, Shaohua Mo, Xiong Li, Yanan Zhang, Hongwei He, Shuo Wang, Jun |
Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathy. Human genomics 2023 3 17 (1): 24. Guey Stéphanie, Hervé Dominique, Kossorotoff Manoëlle, Ha Guillaume, Aloui Chaker, Bergametti Françoise, Arnould Minh, Guenou Hind, Hadjadj Jessica, Dubois Teklali Fanny, Riant Florence, Balligand Jean-Luc, Uzan Georges, Villoutreix Bruno O, Tournier-Lasserve Elisabe |
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