Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 57 Records) |
| Query Trace: AGTR2[original query] |
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Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.
Nature communications 2015 Sep 6 8382. Corvol Harriet, Blackman Scott M, Boëlle Pierre-Yves, Gallins Paul J, Pace Rhonda G, Stonebraker Jaclyn R, Accurso Frank J, Clement Annick, Collaco Joseph M, Dang Hong, Dang Anthony T, Franca Arianna, Gong Jiafen, Guillot Loic, Keenan Katherine, Li Weili, Lin Fan, Patrone Michael V, Raraigh Karen S, Sun Lei, Zhou Yi-Hui, O'Neal Wanda K, Sontag Marci K, Levy Hara, Durie Peter R, Rommens Johanna M, Drumm Mitchell L, Wright Fred A, Strug Lisa J, Cutting Garry R, Knowles Michael |
| Detection of human genome mutations associated with pregnancy complications using 3-D microarray based on macroporous polymer monoliths. Talanta 2016 Jan 147 537-46. Glotov A S, Sinitsyna E S, Danilova M M, Vashukova E S, Walter J G, Stahl F, Baranov V S, Vlakh E G, Tennikova T |
| Blood pressure, arterial stiffness and endogenous lithium clearance in relation to AGTR1 A1166C and AGTR2 G1675A gene polymorphisms. Journal of the renin-angiotensin-aldosterone system : JRAAS 0 17 (2): 1470320316655669. Cwynar Marcin, Gasowski Jerzy, Gluszewska Anna, Królczyk Jaroslaw, Barton Henryk, Slowik Agnieszka, Grodzicki Toma |
| Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
The New England journal of medicine 2017 Sep . Zhang Ge, Feenstra Bjarke, Bacelis Jonas, Liu Xueping, Muglia Lisa M, Juodakis Julius, Miller Daniel E, Litterman Nadia, Jiang Pan-Pan, Russell Laura, Hinds David A, Hu Youna, Weirauch Matthew T, Chen Xiaoting, Chavan Arun R, Wagner Günter P, Pavli?ev Mihaela, Nnamani Mauris C, Maziarz Jamie, Karjalainen Minna K, Rämet Mika, Sengpiel Verena, Geller Frank, Boyd Heather A, Palotie Aarno, Momany Allison, Bedell Bruce, Ryckman Kelli K, Huusko Johanna M, Forney Carmy R, Kottyan Leah C, Hallman Mikko, Teramo Kari, Nohr Ellen A, Davey Smith George, Melbye Mads, Jacobsson Bo, Muglia Louis |
| Association and Interaction Effect of AGTR1 and AGTR2 Gene Polymorphisms with Dietary Pattern on Metabolic Risk Factors of Cardiovascular Disease in Malaysian Adults. Nutrients 2017 Aug 9 (8): . Yap Roseline Wai Kuan, Shidoji Yoshihiro, Yap Wai Sum, Masaki Motofu |
| Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies. Journal of human hypertension 2017 Apr . Ji L-D, Li J-Y, Yao B-B, Cai X-B, Shen Q-J, Xu |
| Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population.
Gene 2018 Aug . Domínguez-Cruz Miriam Givisay, Muñoz María de Lourdes, Totomoch-Serra Armando, García-Escalante María Guadalupe, Burgueño Juan, Valadez-González Nina, Pinto-Escalantes Doris, Díaz-Badillo Álva |
| AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2018 Jun . Darrah Rebecca J, Jacono Frank J, Joshi Neha, Mitchell Anna L, Sattar Abdus, Campanaro Cara K, Litman Paul, Frey Jennifer, Nethery David E, Barbato Eric S, Hodges Craig A, Corvol Harriet, Cutting Garry R, Knowles Michael R, Strug Lisa J, Drumm Mitchell |
| The AGTR2 rs11091046 (A>C) polymorphism and power athletic status in top-level Brazilian athletes. Journal of sports sciences 2018 Mar 1-6. Guilherme João Paulo Limongi França, Silva Mariana Sussi, Bertuzzi Rômulo, Lancha Junior Antonio Herbe |
| AGTR2 and sprint/power performance: a case-control replication study for rs11091046 polymorphism in two ethnicities. Biology of sport 2018 Jun 35 (2): 105-109. Yvert Thomas P, Zempo Hirofumi, Gabdrakhmanova Leysan J, Kikuchi Naoki, Miyamoto-Mikami Eri, Murakami Haruka, Naito Hisashi, Cieszczyk Pawel, Leznicka Katarzyna, Kostryukova Elena S, Alexeev Dmitry G, Egorova Emiliya S, Maciejewska-Skrendo Agnieszka, Larin Andrey K, Generozov Edward V, Kulemin Nickolay A, Ospanova Elena A, Pavlenko Alexander V, Sawczuk Marek, Zmijewski Piotr, Lulinska-Kuklik Ewelina, Govorun Vadim M, Miyachi Motohiko, Ahmetov Ildus I, Fuku Noriyu |
| Copy number variations in a population with prune belly syndrome. American journal of medical genetics. Part A 2018 10 176 (11): 2276-2283. Iqbal Nida S, Jascur Thomas A, Harrison Steven, Chen Catherine, Arevalo Michelle K, Wong Daniel, Sanchez Emma, Grimsby Gwen, Wilson Kathleen, Baker Linda |
| Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Nature communications 2018 01 9 (1): 321. Bonàs-Guarch Sílvia, Guindo-Martínez Marta, Miguel-Escalada Irene, Grarup Niels, Sebastian David, Rodriguez-Fos Elias, Sánchez Friman, Planas-Fèlix Mercè, Cortes-Sánchez Paula, González Santi, Timshel Pascal, Pers Tune H, Morgan Claire C, Moran Ignasi, Atla Goutham, González Juan R, Puiggros Montserrat, Martí Jonathan, Andersson Ehm A, Díaz Carlos, Badia Rosa M, Udler Miriam, Leong Aaron, Kaur Varindepal, Flannick Jason, Jørgensen Torben, Linneberg Allan, Jørgensen Marit E, Witte Daniel R, Christensen Cramer, Brandslund Ivan, Appel Emil V, Scott Robert A, Luan Jian'an, Langenberg Claudia, Wareham Nicholas J, Pedersen Oluf, Zorzano Antonio, Florez Jose C, Hansen Torben, Ferrer Jorge, Mercader Josep Maria, Torrents Dav |
| Renin-angiotensin system gene variants and risk of early- and late-onset preeclampsia: A single center case-control study. Pregnancy hypertension 2019 Aug 18 1-8. Procopciuc Lucia Maria, Nemeti Georgiana, Buzdugan Elena, Iancu Mihaela, Stamatian Florin, Caracostea Gabrie |
| Genetic associations between genes in the renin-angiotensin-aldosterone system and renal disease: a systematic review and meta-analysis. BMJ open 2019 5 9 (4): e026777. Smyth Laura Jane, Cañadas-Garre Marisa, Cappa Ruaidhri C, Maxwell Alexander P, McKnight Amy Jay |
| AGT rs699 and AGTR1 rs5186 gene variants are associated with cardiovascular-related phenotypes in atherosclerotic peripheral arterial obstructive disease. Irish journal of medical science 2019 Dec . Junusbekov Yerik, Bayoglu Burcu, Cengiz Mujgan, Dirican Ahmet, Arslan Can |
| Association of Polymorphisms in the Genes of Angiotensinogen and Angiotensin Receptors With Risk for Basal Cell Carcinoma. Anticancer research 2019 Oct 39 (10): 5525-5530. Papaggelopoulos John, Angelopoulou Antonia, Avgoustidis Dimitris, Koronellos Nikolas, Derka Spyridoula, Vassiliou Stavros, Yapijakis Christ |
| Association of CYP11B2 gene polymorphism with preeclampsia in north east of Iran (Khorasan province). Gene 2020 Jan 144358. Azimi-Nezhad Mohsen, Teymoori Atieha, Ebrahimzadeh-Vesal Re |
| Pan-Cancer Analysis of Genomic and Prognostic Characteristics Associated With Coronavirus Disease 2019 Regulators. Frontiers in medicine 2021 8 8 662460. Zhang Jian, Jiang Huali, Du Kunpeng, Xie Tao, Wang Baiyao, Chen Chengcong, Cen Bohong, Yuan Yawei, Ye Jiac |
| Gene Polymorphisms of the Renin-Angiotensin System and Bleeding Complications of Warfarin: Genetic-Based Machine Learning Models. Pharmaceuticals (Basel, Switzerland) 2021 8 14 (8): . Kim Joo-Hee, Yee Jeong, Chang Byung-Chul, Gwak Hye-S |
| Genetic polymorphisms in the renin-angiotensin system and cognitive decline in Parkinson's disease. Molecular biology reports 2021 Jul . Pierzchli?ska Anna, S?awek Jaros?aw, Mak Monika, Gawro?ska-Szklarz Barbara, Bia?ecka Moni |
| Gene Polymorphisms of the Renin-Angiotensin-Aldosterone System as Risk Factors for the Development of In-Stent Restenosis in Patients with Stable Coronary Artery Disease. Biomolecules 2021 May 11 (5): . Azova Madina, Timizheva Kalima, Ait Aissa Amira, Blagonravov Mikhail, Gigani Olga, Aghajanyan Anna, Tskhovrebova Ley |
| Technologies for Prediction of Preeclampsia. Sovremennye tekhnologii v meditsine 2021 11 12 (5): 78-84. Rok?tyansk?ya E A, Panova I A, Malyshkina A I, Fetisova I N, Fetisov N S, Kharlamova N V, Kuligina M |
| Genetic Factors of Renin-Angiotensin System Associated with Major Bleeding for Patients Treated with Direct Oral Anticoagulants. Pharmaceutics 2022 Jan 14 (2): . Yee Jeong, Song Tae-Jin, Yoon Ha-Young, Park Junbeom, Gwak Hye-S |
| The Role of ACE, ACE2, and AGTR2 Polymorphisms in COVID-19 Severity and the Presence of COVID-19-Related Retinopathy. Genes 2022 Jun 13 (7): . Jevnikar Kristina, Lapajne Luka, Petrovi? Daniel, Megli? Andrej, Logar Mateja, Vidovi? Valentin?i? Nataša, Globo?nik Petrovi? Mojca, Cilenšek Ines, Mekjavi? Polona Ja |
| Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families. International journal of molecular sciences 2023 7 24 (14): . I-Hang Chung, Yu-Shu Huang, Ting-Hsuan Fang, Chia-Hsiang Ch |
| A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth. BMC medicine 2023 7 21 (1): 258. Li Wang, Robert M Rossi, Xiaoting Chen, Jing Chen, Jilian Runyon, Mehak Chawla, Daniel Miller, Carmy Forney, Arthur Lynch, Xuzhe Zhang, Fansheng Kong, Bo Jacobsson, Leah C Kottyan, Matthew T Weirauch, Ge Zhang, Louis J Mugl |
| The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia). Annals of human genetics 2023 11 . Oksana Yurievna Bordaeva, Ekaterina Grigorievna Derevyanchuk, Dema Alset, Maria Aleksandrovna Amelina, Tatiana Pavlovna Shkur |
| Early Evidence on Genetic Polymorphisms in Conferring A "Two-Hit" Propensity to Renal Injury in Asian Indian Children. Journal of Indian Association of Pediatric Surgeons 2023 1 27 (6): 741-746. Anand Suramya, Bajpai Minu, Kumar Alok, Kapahtia Siddhar |
| Association of the Single Nucleotide Polymorphisms in the Renin-Angiotensin-Aldosterone System with Hypertension in the Uzbek Population. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2024 4 52 (3): 182-188. Darya Zakirova, Guzal Abdullaeva, Zaringiz Mashkurova, Sevara Bekmetova, Elina Aguryanova, Fozilakhon Omonova, Alisher Abdulla |
| [Polymorphism of RAAS genes in patients with COVID-19: comparison with frequency in population and relationship with severity of course]. Terapevticheskii arkhiv 2024 10 96 (9): 872-878. A E Bragina, Y N Rodionova, E S Ogibenina, A S Fomin, V I Podzolk |
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