HuGE Literature Finder
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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 |
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 |
[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 |
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, |
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 |
[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 |
[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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
NOS3 gene polymorphisms and exercise hemodynamics in postmenopausal women. International journal of sports medicine 2006 Dec 27 (12): 951-8. Hand B D, McCole S D, Brown M D, Park J J, Ferrell R E, Huberty A, Douglass L W, Hagberg J |
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 |
Promoter polymorphisms in the nitric oxide synthase 3 gene are associated with ischemic stroke susceptibility in young black women. Stroke; a journal of cerebral circulation 2005 Sep 36 (9): 1848-51. Howard Timothy D, Giles Wayne H, Xu Jianfeng, Wozniak Marcella A, Malarcher Ann M, Lange Leslie A, Macko Richard F, Basehore Monica J, Meyers Deborah A, Cole John W, Kittner Steven |
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- Page last updated:Aug 03, 2022
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