Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Hypertension and NPR3[original query] |
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Polygenic prediction of preeclampsia and gestational hypertension.
Nature medicine 2023 5 29 (6): 1540-1549. Honigberg Michael C, Truong Buu, Khan Raiyan R, Xiao Brenda, Bhatta Laxmi, Vy Ha My T, Guerrero Rafael F, Schuermans Art, Selvaraj Margaret Sunitha, Patel Aniruddh P, Koyama Satoshi, Cho So Mi Jemma, Vellarikkal Shamsudheen Karuthedath, Trinder Mark, Urbut Sarah M, Gray Kathryn J, Brumpton Ben M, Patil Snehal, Zöllner Sebastian, Antopia Mariah C, Saxena Richa, Nadkarni Girish N, Do Ron, Yan Qi, Pe'er Itsik, Verma Shefali Setia, Gupta Rajat M, Haas David M, Martin Hilary C, van Heel David A, Laisk Triin, Natarajan Prade |
| Allelic variants of natriuretic peptide receptor genes are associated with family history of hypertension and cardiovascular phenotype. Journal of hypertension 2003 Aug 21 (8): 1491-6. Pitzalis Maria Vittoria, Sarzani Riccardo, Dessì-Fulgheri Paolo, Iacoviello Massimo, Forleo Cinzia, Lucarelli Katya, Pietrucci Francesca, Salvi Fabio, Sorrentino Sandro, Romito Roberta, Guida Pietro, Rappelli Alessandro, Rizzon Pao |
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
| Impact of natriuretic peptide clearance receptor (NPR3) gene variants on blood pressure in type 2 diabetes. Diabetes care 2011 May 34 (5): 1199-204. Saulnier Pierre-Jean, Roussel Ronan, Halimi Jean Michel, Lebrec Jeremie, Dardari Dured, Maimaitiming Sulyia, Guilloteau Gérard, Prugnard Xavier, Marechaud Richard, Ragot Stephanie, Marre Michel, Hadjadj Samy, |
| Association of a single nucleotide polymorphism of the NPR3 gene promoter with early onset ischemic stroke in an Italian cohort. European journal of internal medicine 2013 Jan 24 (1): 80-2. Rubattu Speranza, Giusti Betti, Lotta Luca Andrea, Peyvandi Flora, Cotugno Maria, Stanzione Rosita, Marchitti Simona, Palombella Anna Maria, Di Castro Sara, Rasura Maurizia, Mannucci Pier Mannuccio, Volpe Massi |
| Association of natriuretic peptide receptor-C gene with ischemic stroke and hypertension in Chinese Han population. Clinical and experimental hypertension (New York, N.Y. : 1993) 2012 34 (7): 504-9. Liu Ying, Li Shuyuan, Chen Xingdong, Zheng Lijuan, Yang Yajun, Jin Li, Wang Xiaofe |
| Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium. European heart journal 2012 Sep 33 (18): 2331-41. Fedorowski Artur, Franceschini Nora, Brody Jennifer, Liu Chunyu, Verwoert Germaine C, Boerwinkle Eric, Couper David, Rice Kenneth M, Rotter Jerome I, Mattace-Raso Francesco, Uitterlinden Andre, Hofman Albert, Almgren Peter, Sjögren Marketa, Hedblad Bo, Larson Martin G, Newton-Cheh Christopher, Wang Thomas J, Rose Kathryn M, Psaty Bruce M, Levy Daniel, Witteman Jacqueline, Melander Ol |
| A functional genetic variant (N521D) in natriuretic peptide receptor 3 is associated with diastolic dysfunction: the prevalence of asymptomatic ventricular dysfunction study. PloS one 2014 9 (1): e85708. Pereira Naveen L, Redfield Margaret M, Scott Christopher, Tosakulwong Nirubol, Olson Timothy M, Bailey Kent R, Rodeheffer Richard J, Burnett John |
| Correlation between natriuretic peptide receptor C (NPR3) gene polymorphisms and hypertension in the Dai people of China. Genetics and molecular research : GMR 2015 14 (3): 8786-95. Sun H, Yang Z Q, Liu S Y, Yu L, Huang K, Lin K Q, Chu J Y, Huang X |
| Association of NPR3 polymorphism with risk of essential hypertension in a Chinese population. Journal of clinical pharmacy and therapeutics 2017 May . Kuang D-B, Zhou J-P, Li M-P, Tang J, Chen X |
| The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle. Human molecular genetics 2017 10 27 (1): 199-210. Ren Meixia, Ng Fu Liang, Warren Helen R, Witkowska Kate, Baron Michael, Jia Zhilong, Cabrera Claudia, Zhang Ruoxin, Mifsud Borbala, Munroe Patricia B, Xiao Qingzhong, Townsend-Nicholson Andrea, Hobbs Adrian J, Ye Shu, Caulfield Mark |
| Association of genetic variation with blood pressure traits among East Africans. Clinical genetics 2017 Jan . Kayima James, Liang Jingjing, Natanzon Yanina, Nankabirwa Joaniter, Ssinabulya Isaac, Nakibuuka Jane, Katamba Achilles, Mayanja-Kizza Harriet, Miron Alexander, Li Chun, Zhu Xiaofe |
| Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta. Physiological genomics 2019 4 51 (6): 177-185. LaDisa John F, Tomita-Mitchell Aoy, Stamm Karl, Bazan Kathleen, Mahnke Donna K, Goetsch Mary A, Wegter Brandon J, Gerringer Jesse W, Repp Kathryn, Palygin Oleg, Zietara Adrian P, Krolikowski Mary M, Eddinger Thomas J, Alli Abdel A, Mitchell Michael |
| Association of JAG1 gene polymorphism with systemic blood pressure in patients with obstructive sleep apnea: a prospective cohort study. Croatian medical journal 2019 Oct 60 (5): 421-430. Parani?ová Ivana, Habalová Viera, Klim?áková Lucia, Trojová Ivana, Židzik Jozef, Tká? Ivan, Tká?ová Ružena, Joppa Pav |
| The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. PloS one 2020 6 15 (6): e0234547. Soltész Beáta, Pikó Péter, Sándor János, Kósa Zsigmond, Ádány Róza, Fiatal Szilv |
| Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.
JAMA cardiology 2023 6 . Jaakko S Tyrmi, Tea Kaartokallio, A Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori, |
| Physiological role and mechanisms of action for a long noncoding haplotype region. bioRxiv : the preprint server for biology 2024 9 . Hong Xue, Manoj K Mishra, Yong Liu, Pengyuan Liu, Michael Grzybowski, Rajan Pandey, Kristie Usa, Mark A Vanden Avond, Niharika Bala, Abdel A Alli, Allen W Cowley, Qiongzi Qiu, Andrew S Greene, Sridhar Rao, Caitlin C O'Meara, Aron M Geurts, Mingyu Lia |
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