Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: Hypertension and MAF[original query] |
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Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn. Pediatric nephrology (Berlin, Germany) 2009 Jun 24 (6): 1151-7. Zhang Zhao, Quinlan Jackie, Grote David, Lemire Mathieu, Hudson Thomas, Benjamin Alice, Roy Anne, Pascuet Elena, Goodyer Meigan, Raju Chandhana, Houghton Fiona, Bouchard Maxime, Goodyer Pa |
CRP polymorphisms and progression of chronic kidney disease in African Americans. Clinical journal of the American Society of Nephrology : CJASN 2010 Jan 5 (1): 24-33. Hung Adriana M, Crawford Dana C, Griffin Marie R, Brown-Gentry Kristin, Lipkowitz Michael S, Siew Edward D, Cavanaugh Kerri, Lewis Julia B, Ikizler T Alp, |
Gene-environment interaction for hypertension among African American women across generations. Biological research for nursing 2010 Oct 12 (2): 149-55. Taylor Jacquelyn Y, Sun Yan V, Hunt Steven C, Kardia Sharon L |
Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area. Journal of human genetics 2011 Oct 56 (10): 716-9. Hotta Kikuko, Kitamoto Takuya, Kitamoto Aya, Mizusawa Seiho, Matsuo Tomoaki, Nakata Yoshio, Hyogo Hideyuki, Ochi Hidenori, Kamohara Seika, Miyatake Nobuyuki, Kotani Kazuaki, Komatsu Ryoya, Itoh Naoto, Mineo Ikuo, Wada Jun, Yoneda Masato, Nakajima Atsushi, Funahashi Tohru, Miyazaki Shigeru, Tokunaga Katsuto, Masuzaki Hiroaki, Ueno Takato, Chayama Kazuaki, Hamaguchi Kazuyuki, Yamada Kentaro, Hanafusa Toshiaki, Oikawa Shinichi, Yoshimatsu Hironobu, Sakata Toshiie, Tanaka Kiyoji, Matsuzawa Yuji, Nakao Kazuwa, Sekine Akihi |
Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population. Journal of human genetics 2011 Sep 56 (9): 647-51. Hotta Kikuko, Kitamoto Takuya, Kitamoto Aya, Mizusawa Seiho, Matsuo Tomoaki, Nakata Yoshio, Kamohara Seika, Miyatake Nobuyuki, Kotani Kazuaki, Komatsu Ryoya, Itoh Naoto, Mineo Ikuo, Wada Jun, Yoneda Masato, Nakajima Atsushi, Funahashi Tohru, Miyazaki Shigeru, Tokunaga Katsuto, Masuzaki Hiroaki, Ueno Takato, Hamaguchi Kazuyuki, Tanaka Kiyoji, Yamada Kentaro, Hanafusa Toshiaki, Oikawa Shinichi, Yoshimatsu Hironobu, Sakata Toshiie, Matsuzawa Yuji, Nakao Kazuwa, Sekine Akihi |
Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort. Clinical endocrinology 2012 Mar 76 (3): 365-72. Chang Yi-Cheng, Chiu Yen-Feng, Liu Pi-Hua, Shih Kuang-Chung, Lin Ming-Wei, Sheu Wayne H-H, Quertermous Thomas, Curb Jess David, Hsiung Chano A, Lee Wei-Jei, Lee Po-Chu, Chen Yuan-Tsong, Chuang Lee-Mi |
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. Diabetologia 2013 Feb 56 (2): 298-310. Albrechtsen A, Grarup N, Li Y, Sparsø T, Tian G, Cao H, Jiang T, Kim S Y, Korneliussen T, Li Q, Nie C, Wu R, Skotte L, Morris A P, Ladenvall C, Cauchi S, Stan?áková A, Andersen G, Astrup A, Banasik K, Bennett A J, Bolund L, Charpentier G, Chen Y, Dekker J M, Doney A S F, Dorkhan M, Forsen T, Frayling T M, Groves C J, Gui Y, Hallmans G, Hattersley A T, He K, Hitman G A, Holmkvist J, Huang S, Jiang H, Jin X, Justesen J M, Kristiansen K, Kuusisto J, Lajer M, Lantieri O, Li W, Liang H, Liao Q, Liu X, Ma T, Ma X, Manijak M P, Marre M, Mokrosi?ski J, Morris A D, Mu B, Nielsen A A, Nijpels G, Nilsson P, Palmer C N A, Rayner N W, Renström F, Ribel-Madsen R, Robertson N, Rolandsson O, Rossing P, Schwartz T W, , Slagboom P E, Sterner M, , Tang M, Tarnow L, Tuomi T, van't Riet E, van Leeuwen N, Varga T V, Vestmar M A, Walker M, Wang B, Wang Y, Wu H, Xi F, Yengo L, Yu C, Zhang X, Zhang J, Zhang Q, Zhang W, Zheng H, Zhou Y, Altshuler D, 't Hart L M, Franks P W, Balkau B, Froguel P, McCarthy M I, Laakso M, Groop L, Christensen C, Brandslund I, Lauritzen T, Witte D R, Linneberg A, Jørgensen T, Hansen T, Wang J, Nielsen R, Pedersen |
Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifs. Journal of hypertension 2012 Nov . Wei Z, Zhang K, Wen G, Balasubramanian K, Shih PA, Rao F, Friese RS, Miramontes-Gonzalez JP, Schmid-Schoenbein GW, Kim HS, Mahata SK, O'Connor DT |
Association of oxysterol binding protein-related protein 9 polymorphism with cerebral infarction in Hunan Han population. Irish journal of medical science 2014 Sep 183 (3): 439-48. Li Lingjuan, Qu Geyue, Wang Mingyue, Huang Qing, Liu Yunh |
Are ALOX5AP gene SNPs a risk or protective factor for stroke? Gene 2014 Sep 548 (1): 56-60. Papapostolou Apostolis, Spengos Kostas, Fylaktou Irene, Poulou Myrto, Gountas Ilias, Kitsiou-Tzeli Sophia, Kanavakis Emmanuel, Tzetis Mar |
Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia. Acta paediatrica (Oslo, Norway : 1992) 2014 Oct 103 (10): e439-43. Trittmann J K, Nelin L D, Zmuda E J, Gastier-Foster J M, Chen B, Backes C H, Frick J, Vaynshtok P, Vieland V J, Klebanoff M |
Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. PloS one 2014 9 (10): e109155. Morrison Alanna C, Bis Joshua C, Hwang Shih-Jen, Ehret Georg B, Lumley Thomas, Rice Kenneth, Muzny Donna, Gibbs Richard A, Boerwinkle Eric, Psaty Bruce M, Chakravarti Aravinda, Levy Dani |
Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study. Lipids in health and disease 2015 14 (1): 79. Yang Qian, Yin Rui-Xing, Zhou Yi-Jiang, Cao Xiao-Li, Guo Tao, Chen Wu-Xi |
The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans. Human heredity 2015 79 (1): 20-7. Sung Yun Ju, Basson Jacob, Cheng Nuo, Nguyen Khanh-Dung H, Nandakumar Priyanka, Hunt Steven C, Arnett Donna K, Dávila-Román Victor G, Rao Dabeeru C, Chakravarti Aravin |
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance. PLoS genetics 2016 Oct 12 (10): e1006367. Kiando Soto Romuald, Tucker Nathan R, Castro-Vega Luis-Jaime, Katz Alexander, D'Escamard Valentina, Tréard Cyrielle, Fraher Daniel, Albuisson Juliette, Kadian-Dodov Daniella, Ye Zi, Austin Erin, Yang Min-Lee, Hunker Kristina, Barlassina Cristina, Cusi Daniele, Galan Pilar, Empana Jean-Philippe, Jouven Xavier, Gimenez-Roqueplo Anne-Paule, Bruneval Patrick, Hyun Kim Esther Soo, Olin Jeffrey W, Gornik Heather L, Azizi Michel, Plouin Pierre-François, Ellinor Patrick T, Kullo Iftikhar J, Milan David J, Ganesh Santhi K, Boutouyrie Pierre, Kovacic Jason C, Jeunemaitre Xavier, Bouatia-Naji Nabi |
Lack of association of mirSNP rs11174811 in AVPR1A gene with arterial blood pressure and hypertension in South Indian population. Clinical and experimental hypertension (New York, N.Y. : 1993) 2017 Nov 1-5. Koshy Linda, Vijayalekshmi S V, Harikrishnan S, Raman Kutty V, Jissa V T, Jayakumaran Nair A, Gangaprasad A, Nair G M, Sudhakaran P |
Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies. Journal of hypertension and management 2018 3 3 (1): . Do Anh N, Zhao Wei, Srinivasasainagendra Vinodh, Aslibekyan Stella, Tiwari Hemant K, Limdi Nita, Shah Sanjiv J, Zhi Degui, Broeckel Uli, Gu C Charles, Rao D C, Schwander Karen, Smith Jennifer A, Kardia Sharon L R, Arnett Donna K, Irvin Marguerite |
Association of FMO3 Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study. International journal of hypertension 2019 3 2019 2137629. Bryant Tyler S, Duggal Priya, Yu Bing, Morrison Alanna C, Shafi Tariq, Ehret Georg, Franceschini Nora, Boerwinkle Eric, Coresh Josef, Tin Adrien |
The effect of genetic and nongenetic factors on warfarin dose variability in Qatari population. The pharmacogenomics journal 2019 Oct . Bader Loulia, Mahfouz Ahmad, Kasem Mohammed, Mohammed Shaban, Alsaadi Sumayya, Abdelsamad Osama, Elenani Rasha, Soaly Ezeldin, Elzouki Abdelnasser, Rizk Nasser, Khalifa Sherief, Shahin Mohamed H, Cavallari Larisa H, Mraiche Fatima, Elewa Haz |
Potential mechanisms underlying the association between single nucleotide polymorphism (BRAP and ALDH2) and hypertension among elderly Japanese population. Scientific reports 2020 Aug 10 (1): 14148. Shimizu Yuji, Arima Kazuhiko, Noguchi Yuko, Kawashiri Shin-Ya, Yamanashi Hirotomo, Tamai Mami, Nagata Yasuhiro, Maeda Takahi |
A variant in TMPRSS2 is associated with decreased disease severity in COVID-19. Meta gene 2021 May 100930. Ravikanth Vishnubhotla, Sasikala Mitnala, Naveen Vankadari, Latha Sabbu Sai, Parsa Kishore Venkata Laxmi, Vijayasarathy Ketavarapu, Amanchy Ramars, Avanthi Steffie, Govardhan Bale, Rakesh Kalapala, Kumari Daram Sarala, Srikaran Bojja, Rao Guduru Venkat, Reddy D Nageshw |
Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension. Pulse (Basel, Switzerland) 2021 Sep 9 (1-2): 17-29. Curtis Dav |
The MUC5B Promoter Polymorphism is Not Associated With Non-ILD Chronic Respiratory Diseases or Post-transplant Outcome. Transplant international : official journal of the European Society for Organ Transplantation 2022 35 10159. Goos Tinne, Verleden Stijn E, De Sadeleer Laurens J, Van Herck Anke, Sacreas Annelore, Vanstapel Arno, Kaes Janne, Geudens Vincent, Aelbrecht Celine, Ruttens David, Lambrechts Diether, Vermeer Sascha, Ceulemans Laurens J, Van Raemdonck Dirk E, Godinas Laurent, Yserbyt Jonas, Vanaudenaerde Bart M, Verleden Geert M, Vos Robin, Wuyts Wim |
Rare and Common Variants in COL4A1 in Chinese Patients With Intracerebral Hemorrhage. Frontiers in neurology 2022 6 13 827165. Liu Xiaolu, Yang Qiong, Tang Lu, He Ji, Tian Danyang, Wang Baojun, Xie Lihong, Li Changbao, Fan Dongshe |
Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort.
![]() Frontiers in genetics 2022 13 866042. Gyftopoulos Alex, Chen Yi-Ju, Wang Libin, Williams Charles H, Chun Young Wook, O'Connell Jeffery R, Perry James A, Hong Charles |
The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population. Frontiers in genetics 2022 4 13 875269. Yang Lincheng, Pu Tian, Zhang Yan, Yan Hua, Yu Haiyi, Gao W |
Association analyses of predicted loss-of-function variants prioritized 15 genes as blood pressure regulators. The Canadian journal of cardiology 2023 7 . Estelle Lecluze, Guillaume Lett |
Clinical exome sequencing unravels the diverse spectrum of genetic heterogeneity and genotype-phenotype correlations in hypertrophic cardiomyopathy. International journal of cardiology 2024 6 132273. Sivadasanpillai Harikrishnan, Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, N K Ramya Das, Madhusoodanan Urulangodi, M Madhuma, Y Vysakh, Anjana Subran, L R Lakshmikan |
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