NOS3 c.-52+1009A>T

Variant ID: 7-150689397-A-T

NM_000603.5(NOS3):c.-52+1009A>T

This variant was identified in 30 publications

View GRCh38 version.




Publications:


Genetic Predictors of the Development of Complications after Coronary Stenting.

Journal Of Personalized Medicine
Taizhanova, Dana D; Kalimbetova, Akerke A; Bodaubay, Roza R; Toleuova, Aliya A; Toiynbekova, Rakhima R; Beysenbekova, Zhazira Z; Visternichan, Olga O; Tauesheva, Zauresh Z; Kadyrova, Irina I; Babenko, Dmitriy D; Akhmaltdinova, Lyudmila L; Kolesnichenko, Svetlana S; Kolesnikova, Yevgeniya Y; Avdienko, Olga V OV; Akilzhanova, Ainur A; Gerotziafas, Grigorios T GT
Publication Date: 2022-12-22

Variant appearance in text: rs1800783
PubMed Link: 36675675
Variant Present in the following documents:
  • jpm-13-00014.pdf
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The NESHIE and CP Genetics Resource (NCGR): A database of genes and variants reported in neonatal encephalopathy with suspected hypoxic ischemic encephalopathy (NESHIE) and consequential cerebral palsy (CP).

Genomics
Holborn, Megan A MA; Ford, Graeme G; Turner, Sarah S; Mellet, Juanita J; van Rensburg, Jeanne J; Joubert, Fourie F; Pepper, Michael S MS
Publication Date: 2022-10-18

Variant appearance in text: rs1800783
PubMed Link: 36270382
Variant Present in the following documents:
  • Main text
  • main.pdf
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A systematic review to guide future efforts in the determination of genetic causes of pregnancy loss.

Frontiers In Reproductive Health
Carey, Andrew Z AZ; Blue, Nathan R NR; Varner, Michael W MW; Page, Jessica M JM; Chaiyakunapruk, Nathorn N; Quinlan, Aaron R AR; Branch, D Ware DW; Silver, Robert M RM; Workalemahu, Tsegaselassie T
Publication Date: 2021

Variant appearance in text: rs1800783
PubMed Link: 35462723
Variant Present in the following documents:
  • Main text
  • frph-03-770517.pdf
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Nutrigenetics, omega-3 and plasma lipids/lipoproteins/apolipoproteins with evidence evaluation using the GRADE approach: a systematic review.

Bmj Open
Keathley, Justine J; Garneau, Véronique V; Marcil, Valérie V; Mutch, David M DM; Robitaille, Julie J; Rudkowska, Iwona I; Sofian, Gabriela Magdalena GM; Desroches, Sophie S; Vohl, Marie-Claude MC
Publication Date: 2022-02-22

Variant appearance in text: rs1800783
PubMed Link: 35193914
Variant Present in the following documents:
  • bmjopen-2021-054417.draft_revisions.pdf
  • bmjopen-2021-054417supp001.pdf
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Diabetic kidney disease: Are the reported associations with single-nucleotide polymorphisms disease-specific?

World Journal Of Diabetes
Saracyn, Marek M; Kisiel, Bartłomiej B; Franaszczyk, Maria M; Brodowska-Kania, Dorota D; Żmudzki, Wawrzyniec W; Małecki, Robert R; Niemczyk, Longin L; Dyrla, Przemysław P; Kamiński, Grzegorz G; Płoski, Rafał R; Niemczyk, Stanisław S
Publication Date: 2021-10-15

Variant appearance in text: rs1800783
PubMed Link: 34754377
Variant Present in the following documents:
  • Main text
  • WJD-12-1765.pdf
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Study on Risk Factors of Diabetic Nephropathy in Obese Patients with Type 2 Diabetes Mellitus.

International Journal Of General Medicine
Hu, Fan F; Zhang, Taotao T
Publication Date: 2020

Variant appearance in text: rs1800783
PubMed Link: 32753935
Variant Present in the following documents:
  • Main text
  • ijgm-13-351.pdf
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Genetic Factors of Nitric Oxide's System in Psychoneurologic Disorders.

International Journal Of Molecular Sciences
Nasyrova, Regina F RF; Moskaleva, Polina V PV; Vaiman, Elena E EE; Shnayder, Natalya A NA; Blatt, Nataliya L NL; Rizvanov, Albert A AA
Publication Date: 2020-02-26

Variant appearance in text: rs1800783
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
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Genetic findings in sport-related concussions: potential for individualized medicine?

Concussion (London, England)
McDevitt, Jane J; Krynetskiy, Evgeny E
Publication Date: 2017-03

Variant appearance in text: rs1800783
PubMed Link: 30202567
Variant Present in the following documents:
  • Main text
  • cnc-02-26.pdf
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Genetic studies of human neuropathic pain conditions: a review.

Pain
Zorina-Lichtenwalter, Katerina K; Parisien, Marc M; Diatchenko, Luda L
Publication Date: 2018-03

Variant appearance in text: rs1800783
PubMed Link: 29240606
Variant Present in the following documents:
  • jop-159-583.pdf
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The Association between NOS3 Gene Polymorphisms and Hypoxic-Ischemic Encephalopathy Susceptibility and Symptoms in Chinese Han Population.

Biomed Research International
Wu, Yongqin Y; Zhu, Zhiling Z; Fang, Xiaoxia X; Yin, Ling L; Liu, Yuxia Y; Xu, Shouxia S; Li, Aixue A
Publication Date: 2016

Variant appearance in text: rs1800783
PubMed Link: 28070505
Variant Present in the following documents:
  • Main text
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Genetic Regulation of Endothelial Vasomotor Function.

Frontiers In Physiology
Kim, Seung Kyum SK; Massett, Michael P MP
Publication Date: 2016

Variant appearance in text: rs1800783
PubMed Link: 27932996
Variant Present in the following documents:
  • Main text
  • fphys-07-00571.pdf
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Biological Basis for the Clustering of Symptoms.

Seminars In Oncology Nursing
Lynch Kelly, Debra D; Dickinson, Kristin K; Hsiao, Chao-Pin CP; Lukkahatai, Nada N; Gonzalez-Marrero, Velda V; McCabe, Margaret M; Saligan, Leorey N LN
Publication Date: 2016-11

Variant appearance in text: rs1800783
PubMed Link: 27776832
Variant Present in the following documents:
  • Main text
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Gene variants as risk factors for gastroschisis.

American Journal Of Medical Genetics. Part A
Padula, Amy M AM; Yang, Wei W; Schultz, Kathleen K; Tom, Lauren L; Lin, Bin B; Carmichael, Suzan L SL; Lammer, Edward J EJ; Shaw, Gary M GM
Publication Date: 2016-11

Variant appearance in text: rs1800783
PubMed Link: 27616475
Variant Present in the following documents:
  • Main text
  • AJMG-170-2788.pdf
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Nutritional Modulation of Gene Expression: Might This be of Benefit to Individuals with Crohn's Disease?

Frontiers In Immunology
Ferguson, Lynnette R LR
Publication Date: 2015

Variant appearance in text: rs1800783
PubMed Link: 26441972
Variant Present in the following documents:
  • Main text
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Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.

Environmental Health Perspectives
Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y
Publication Date: 2015-05

Variant appearance in text: rs1800783
PubMed Link: 25575156
Variant Present in the following documents:
  • Main text
  • ehp.1307883.pdf
  • ehp.1307883.s001.508.pdf
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Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
Kuzmanić Šamija, R R; Primorac, D D; Rešić, B B; Pavlov, V V; Čapkun, V V; Punda, H H; Lozić, B B; Zemunik, T T
Publication Date: 2014-10

Variant appearance in text: rs1800783
PubMed Link: 25140814
Variant Present in the following documents:
  • Main text
  • 1414-431X-bjmbr-47-10-00869.pdf
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Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies.

American Journal Of Medical Genetics. Part A
Browne, Marilyn L ML; Carter, Tonia C TC; Kay, Denise M DM; Kuehn, Devon D; Brody, Lawrence C LC; Romitti, Paul A PA; Liu, Aiyi A; Caggana, Michele M; Druschel, Charlotte M CM; Mills, James L JL
Publication Date: 2012-10

Variant appearance in text: rs1800783
PubMed Link: 22965740
Variant Present in the following documents:
  • Main text
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Interactions between dietary n-3 fatty acids and genetic variants and risk of disease.

The British Journal Of Nutrition
Corella, Dolores D; Ordovás, José M JM
Publication Date: 2012-06

Variant appearance in text: rs1800783
PubMed Link: 22591901
Variant Present in the following documents:
  • Main text
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Ovarian cancer risk associated with inherited inflammation-related variants.

Cancer Research
White, Kristin L KL; Schildkraut, Joellen M JM; Palmieri, Rachel T RT; Iversen, Edwin S ES; Berchuck, Andrew A; Vierkant, Robert A RA; Rider, David N DN; Charbonneau, Bridget B; Cicek, Mine S MS; Sutphen, Rebecca R; Birrer, Michael J MJ; Pharoah, Paul P D PP; Song, Honglin H; Tyrer, Jonathan J; Gayther, Simon A SA; Ramus, Susan J SJ; Wentzensen, Nicolas N; Yang, Hannah P HP; Garcia-Closas, Montserrat M; Phelan, Catherine M CM; Cunningham, Julie M JM; Fridley, Brooke L BL; Sellers, Thomas A TA; Goode, Ellen L EL; ,
Publication Date: 2012-03-01

Variant appearance in text: rs1800783
PubMed Link: 22282663
Variant Present in the following documents:
  • Main text
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Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.

Hypertension (Dallas, Tex. : 1979)
Salvi, Erika E; Kutalik, Zoltán Z; Glorioso, Nicola N; Benaglio, Paola P; Frau, Francesca F; Kuznetsova, Tatiana T; Arima, Hisatomi H; Hoggart, Clive C; Tichet, Jean J; Nikitin, Yury P YP; Conti, Costanza C; Seidlerova, Jitka J; Tikhonoff, Valérie V; Stolarz-Skrzypek, Katarzyna K; Johnson, Toby T; Devos, Nabila N; Zagato, Laura L; Guarrera, Simonetta S; Zaninello, Roberta R; Calabria, Andrea A; Stancanelli, Benedetta B; Troffa, Chiara C; Thijs, Lutgarde L; Rizzi, Federica F; Simonova, Galina G; Lupoli, Sara S; Argiolas, Giuseppe G; Braga, Daniele D; D'Alessio, Maria C MC; Ortu, Maria F MF; Ricceri, Fulvio F; Mercurio, Maurizio M; Descombes, Patrick P; Marconi, Maurizio M; Chalmers, John J; Harrap, Stephen S; Filipovsky, Jan J; Bochud, Murielle M; Iacoviello, Licia L; Ellis, Justine J; Stanton, Alice V AV; Laan, Maris M; Padmanabhan, Sandosh S; Dominiczak, Anna F AF; Samani, Nilesh J NJ; Melander, Olle O; Jeunemaitre, Xavier X; Manunta, Paolo P; Shabo, Amnon A; Vineis, Paolo P; Cappuccio, Francesco P FP; Caulfield, Mark J MJ; Matullo, Giuseppe G; Rivolta, Carlo C; Munroe, Patricia B PB; Barlassina, Cristina C; Staessen, Jan A JA; Beckmann, Jacques S JS; Cusi, Daniele D
Publication Date: 2012-02

Variant appearance in text: rs1800783
PubMed Link: 22184326
Variant Present in the following documents:
  • Main text
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Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.

Croatian Medical Journal
Kuzmanić Samija, Radenka R; Primorac, Dragan D; Resić, Biserka B; Lozić, Bernarda B; Krzelj, Vjekoslav V; Tomasović, Maja M; Stoini, Eugenio E; Samanović, Ljubo L; Benzon, Benjamin B; Pehlić, Marina M; Boraska, Vesna V; Zemunik, Tatijana T
Publication Date: 2011-06

Variant appearance in text: rs1800783
PubMed Link: 21674837
Variant Present in the following documents:
  • Main text
  • CroatMedJ_52_0396.pdf
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.

American Journal Of Human Genetics
Lanktree, Matthew B MB; Guo, Yiran Y; Murtaza, Muhammed M; Glessner, Joseph T JT; Bailey, Swneke D SD; Onland-Moret, N Charlotte NC; Lettre, Guillaume G; Ongen, Halit H; Rajagopalan, Ramakrishnan R; Johnson, Toby T; Shen, Haiqing H; Nelson, Christopher P CP; Klopp, Norman N; Baumert, Jens J; Padmanabhan, Sandosh S; Pankratz, Nathan N; Pankow, James S JS; Shah, Sonia S; Taylor, Kira K; Barnard, John J; Peters, Bas J BJ; Maloney, Cliona M CM; Lobmeyer, Maximilian T MT; Stanton, Alice A; Zafarmand, M Hadi MH; Romaine, Simon P R SP; Mehta, Amar A; van Iperen, Erik P A EP; Gong, Yan Y; Price, Tom S TS; Smith, Erin N EN; Kim, Cecilia E CE; Li, Yun R YR; Asselbergs, Folkert W FW; Atwood, Larry D LD; Bailey, Kristian M KM; Bhatt, Deepak D; Bauer, Florianne F; Behr, Elijah R ER; Bhangale, Tushar T; Boer, Jolanda M A JM; Boehm, Bernhard O BO; Bradfield, Jonathan P JP; Brown, Morris M; Braund, Peter S PS; Burton, Paul R PR; Carty, Cara C; Chandrupatla, Hareesh R HR; Chen, Wei W; Connell, John J; Dalgeorgou, Chrysoula C; Boer, Anthonius de Ad; Drenos, Fotios F; Elbers, Clara C CC; Fang, James C JC; Fox, Caroline S CS; Frackelton, Edward C EC; Fuchs, Barry B; Furlong, Clement E CE; Gibson, Quince Q; Gieger, Christian C; Goel, Anuj A; Grobbee, Diederik E DE; Hastie, Claire C; Howard, Philip J PJ; Huang, Guan-Hua GH; Johnson, W Craig WC; Li, Qing Q; Kleber, Marcus E ME; Klein, Barbara E K BE; Klein, Ronald R; Kooperberg, Charles C; Ky, Bonnie B; Lacroix, Andrea A; Lanken, Paul P; Lathrop, Mark M; Li, Mingyao M; Marshall, Vanessa V; Melander, Olle O; Mentch, Frank D FD; Meyer, Nuala J NJ; Monda, Keri L KL; Montpetit, Alexandre A; Murugesan, Gurunathan G; Nakayama, Karen K; Nondahl, Dave D; Onipinla, Abiodun A; Rafelt, Suzanne S; Newhouse, Stephen J SJ; Otieno, F George FG; Patel, Sanjey R SR; Putt, Mary E ME; Rodriguez, Santiago S; Safa, Radwan N RN; Sawyer, Douglas B DB; Schreiner, Pamela J PJ; Simpson, Claire C; Sivapalaratnam, Suthesh S; Srinivasan, Sathanur R SR; Suver, Christine C; Swergold, Gary G; Sweitzer, Nancy K NK; Thomas, Kelly A KA; Thorand, Barbara B; Timpson, Nicholas J NJ; Tischfield, Sam S; Tobin, Martin M; Tomaszewski, Maciej M; Tomaszweski, Maciej M; Verschuren, W M Monique WM; Wallace, Chris C; Winkelmann, Bernhard B; Zhang, Haitao H; Zheng, Dongling D; Zhang, Li L; Zmuda, Joseph M JM; Clarke, Robert R; Balmforth, Anthony J AJ; Danesh, John J; Day, Ian N IN; Schork, Nicholas J NJ; de Bakker, Paul I W PI; Delles, Christian C; Duggan, David D; Hingorani, Aroon D AD; Hirschhorn, Joel N JN; Hofker, Marten H MH; Humphries, Steve E SE; Kivimaki, Mika M; Lawlor, Debbie A DA; Kottke-Marchant, Kandice K; Mega, Jessica L JL; Mitchell, Braxton D BD; Morrow, David A DA; Palmen, Jutta J; Redline, Susan S; Shields, Denis C DC; Shuldiner, Alan R AR; Sleiman, Patrick M PM; Smith, George Davey GD; Farrall, Martin M; Jamshidi, Yalda Y; Christiani, David C DC; Casas, Juan P JP; Hall, Alistair S AS; Doevendans, Pieter A PA; Christie, Jason D JD; Berenson, Gerald S GS; Murray, Sarah S SS; Illig, Thomas T; Dorn, Gerald W GW; Cappola, Thomas P TP; Boerwinkle, Eric E; Sever, Peter P; Rader, Daniel J DJ; Reilly, Muredach P MP; Caulfield, Mark M; Talmud, Philippa J PJ; Topol, Eric E; Engert, James C JC; Wang, Kai K; Dominiczak, Anna A; Hamsten, Anders A; Curtis, Sean P SP; Silverstein, Roy L RL; Lange, Leslie A LA; Sabatine, Marc S MS; Trip, Mieke M; Saleheen, Danish D; Peden, John F JF; Cruickshanks, Karen J KJ; März, Winfried W; O'Connell, Jeffrey R JR; Klungel, Olaf H OH; Wijmenga, Cisca C; Maitland-van der Zee, Anke Hilse AH; Schadt, Eric E EE; Johnson, Julie A JA; Jarvik, Gail P GP; Papanicolaou, George J GJ; , ; Grant, Struan F A SF; Munroe, Patricia B PB; North, Kari E KE; Samani, Nilesh J NJ; Koenig, Wolfgang W; Gaunt, Tom R TR; Anand, Sonia S SS; van der Schouw, Yvonne T YT; , ; Soranzo, Nicole N; Fitzgerald, Garret A GA; Reiner, Alex A; Hegele, Robert A RA; Hakonarson, Hakon H; Keating, Brendan J BJ
Publication Date: 2011-01-07

Variant appearance in text: rs1800783
PubMed Link: 21194676
Variant Present in the following documents:
  • Main text
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Genetic associations of brain structural networks in schizophrenia: a preliminary study.

Biological Psychiatry
Jagannathan, Kanchana K; Calhoun, Vince D VD; Gelernter, Joel J; Stevens, Michael C MC; Liu, Jingyu J; Bolognani, Federico F; Windemuth, Andreas A; Ruaño, Gualberto G; Assaf, Michal M; Pearlson, Godfrey D GD
Publication Date: 2010-10-01

Variant appearance in text: rs1800783
PubMed Link: 20691427
Variant Present in the following documents:
  • Main text
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Fenofibrate and metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets
Kraja, Aldi T AT; Province, Michael A MA; Straka, Robert J RJ; Ordovas, Jose M JM; Borecki, Ingrid B IB; Arnett, Donna K DK
Publication Date: 2010-06

Variant appearance in text: rs1800783
PubMed Link: 20406163
Variant Present in the following documents:
  • Main text
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Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study.

Stroke
MacClellan, Leah R LR; Howard, Timothy D TD; Cole, John W JW; Stine, O Colin OC; Giles, Wayne H WH; O'Connell, Jeffery R JR; Wozniak, Marcella A MA; Stern, Barney J BJ; Mitchell, Braxton D BD; Kittner, Steven J SJ
Publication Date: 2009-10

Variant appearance in text: rs1800783
PubMed Link: 19661472
Variant Present in the following documents:
  • Main text
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Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.

Neurogenetics
Hancock, Dana B DB; Martin, Eden R ER; Vance, Jeffery M JM; Scott, William K WK
Publication Date: 2008-10

Variant appearance in text: rs1800783
PubMed Link: 18663495
Variant Present in the following documents:
  • Main text
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Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.

American Journal Of Hypertension
Vimaleswaran, Karani S KS; Franks, Paul W PW; Barroso, Inês I; Brage, Soren S; Ekelund, Ulf U; Wareham, Nicholas J NJ; Loos, Ruth J F RJ
Publication Date: 2008-03

Variant appearance in text: rs1800783
PubMed Link: 18246059
Variant Present in the following documents:
  • Main text
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Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.

Bone
Cho, K K; Demissie, S S; Dupuis, J J; Cupples, L A LA; Kathiresan, S S; Beck, T J TJ; Karasik, D D; Kiel, D P DP
Publication Date: 2008-01

Variant appearance in text: rs1800783
PubMed Link: 17980690
Variant Present in the following documents:
  • Main text
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The diploid genome sequence of an individual human.

Plos Biology
Levy, Samuel S; Sutton, Granger G; Ng, Pauline C PC; Feuk, Lars L; Halpern, Aaron L AL; Walenz, Brian P BP; Axelrod, Nelson N; Huang, Jiaqi J; Kirkness, Ewen F EF; Denisov, Gennady G; Lin, Yuan Y; MacDonald, Jeffrey R JR; Pang, Andy Wing Chun AW; Shago, Mary M; Stockwell, Timothy B TB; Tsiamouri, Alexia A; Bafna, Vineet V; Bansal, Vikas V; Kravitz, Saul A SA; Busam, Dana A DA; Beeson, Karen Y KY; McIntosh, Tina C TC; Remington, Karin A KA; Abril, Josep F JF; Gill, John J; Borman, Jon J; Rogers, Yu-Hui YH; Frazier, Marvin E ME; Scherer, Stephen W SW; Strausberg, Robert L RL; Venter, J Craig JC
Publication Date: 2007-09-04

Variant appearance in text: rs1800783
PubMed Link: 17803354
Variant Present in the following documents:
  • pbio.0050254.pdf
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Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults.

Atherosclerosis
Kullo, Iftikhar J IJ; Greene, M Todd MT; Boerwinkle, Eric E; Chu, Jian J; Turner, Stephen T ST; Kardia, Sharon L R SL
Publication Date: 2008-02

Variant appearance in text: rs1800783
PubMed Link: 17367796
Variant Present in the following documents:
  • Main text
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