Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: NR1H3[original query] |
---|
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Nature genetics 2009 Jan 41 (1): 35-46. Sabatti Chiara, Service Susan K, Hartikainen Anna-Liisa, Pouta Anneli, Ripatti Samuli, Brodsky Jae, Jones Chris G, Zaitlen Noah A, Varilo Teppo, Kaakinen Marika, Sovio Ulla, Ruokonen Aimo, Laitinen Jaana, Jakkula Eveliina, Coin Lachlan, Hoggart Clive, Collins Andrew, Turunen Hannu, Gabriel Stacey, Elliot Paul, McCarthy Mark I, Daly Mark J, Järvelin Marjo-Riitta, Freimer Nelson B, Peltonen Lee |
Association between liver X receptor alpha gene polymorphisms and risk of metabolic syndrome in French populations. International journal of obesity (2005) 2008 Mar 32 (3): 421-8. Legry V, Cottel D, Ferrières J, Chinetti G, Deroide T, Staels B, Amouyel P, Meirhaeghe |
Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes. BMC cancer 2010 10 (1): 484. Andersen Vibeke, Christensen Jane, Overvad Kim, Tjønneland Anne, Vogel Ul |
Genetic variation within the NR1H2 gene encoding liver X receptor ß associates with insulin secretion in subjects at increased risk for type 2 diabetes. Journal of molecular medicine (Berlin, Germany) 2011 Jan 89 (1): 75-81. Ketterer Caroline, Müssig Karsten, Machicao Fausto, Stefan Norbert, Fritsche Andreas, Häring Hans-Ulrich, Staiger Hara |
Liver X receptor a gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study. Pharmacogenetics and genomics 2011 Jun 21 (6): 333-40. Price Elvin Tyrone, Pacanowski Michael A, Martin Michael A, Cooper-DeHoff Rhonda M, Pepine Carl J, Zineh Issam, Johnson Julie |
Associations between common genetic polymorphisms in the liver X receptor alpha and its target genes with the serum HDL-cholesterol concentration in adolescents of the HELENA Study. Atherosclerosis 2011 May 216 (1): 166-9. Legry Vanessa, Bokor Szilvia, Beghin Laurent, Galfo Myriam, Gonzalez-Gross Marcela, Molnar Denes, Moreno Luis A, Amouyel Philippe, Dallongeville Jean, Meirhaeghe Aline, |
A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia. BMC medical genetics 2011 12 (1): 145. Mouzat Kevin, Mercier Eric, Polge Anne, Evrard Alexandre, Baron Silvère, Balducchi Jean-Pierre, Brouillet Jean-Paul, Lumbroso Serge, Gris Jean-Christop |
Genetic analysis of genes involved in amyloid-ß degradation and clearance in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2012 28 (3): 553-9. Natunen Teemu, Helisalmi Seppo, Vepsäläinen Saila, Sarajärvi Timo, Antikainen Leila, Mäkinen Petra, Herukka Sanna-Kaisa, Koivisto Anne Maria, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
Genome-wide and candidate gene association studies of placental abruption. International journal of molecular epidemiology and genetics 2013 4 (3): 128-39. Workalemahu Tsegaselassie, Enquobahrie Daniel A, Moore Amy, Sanchez Sixto E, Ananth Cande V, Pacora Percy N, Liang Liming, Salazar Manuel, Williams Michelle |
The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. PloS one 2013 8 (6): e66976. Alobeidy Barrak F, Li Cong, Alzobair Alya A, Liu Tao, Zhao Junzhang, Fang Yuan, Zheng Fa |
Association of LXRa polymorphisms with obesity and obesity-related phenotypes in an Iranian population. Annals of human biology 0 41 (3): 214-9. Rooki Hassan, Ghayour-Mobarhan Majid, Pourhosseingholi Mohamad-Amin, Azarpazhooh Mahmoud-Reza, Ebrahimi Mahmoud, Ferns Gordon, Zali Mohammad-Re |
Effects of NR1H3 genetic variation on the expression of liver X receptor a and the progression of Alzheimer's disease. PloS one 2013 8 (11): e80700. Natunen Teemu, Martiskainen Henna, Sarajärvi Timo, Helisalmi Seppo, Pursiheimo Juha-Pekka, Viswanathan Jayashree, Laitinen Marjo, Mäkinen Petra, Kauppinen Tarja, Rauramaa Tuomas, Leinonen Ville, Alafuzoff Irina, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
Lack of association between LXRa and LXRß gene polymorphisms and prevalence of metabolic syndrome: a case-control study of an Iranian population. Gene 2013 Dec 532 (2): 288-93. Rooki Hassan, Ghayour-Mobarhan Manjid, Haerian Monir-Sadat, Ebrahimi Mahmoud, Azimzadeh Pedram, Heidari-Bakavoli Alireza, Mirfakhraei Reza, Tavallaie Shima, Mirhafez Reza, Ferns Gordon, Zali Mohammad-Re |
Liver X receptors alpha gene (NR1H3) promoter polymorphisms are associated with systemic lupus erythematosus in Koreans. Arthritis research & therapy 2014 16 (3): R112. Jeon Ja-Young, Nam Jin-Young, Kim Hyoun-Ah, Park Yong-Beom, Bae Sang-Cheol, Suh Chang-H |
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular genetics 2014 Jun 7 (3): 374-82. Cornes Belinda K, Brody Jennifer A, Nikpoor Naghmeh, Morrison Alanna C, Dang Huan Chu Pham, Ahn Byung Soo, Wang Shuai, Dauriz Marco, Barzilay Joshua I, Dupuis Josée, Florez Jose C, Coresh Josef, Gibbs Richard A, Kao W H Linda, Liu Ching-Ti, McKnight Barbara, Muzny Donna, Pankow James S, Reid Jeffrey G, White Charles C, Johnson Andrew D, Wong Tien Y, Psaty Bruce M, Boerwinkle Eric, Rotter Jerome I, Siscovick David S, Sladek Robert, Meigs James |
Many obesity-associated SNPs strongly associate with DNA methylation changes at proximal promoters and enhancers. Genome medicine 2015 7 (1): 103. Voisin Sarah, Almén Markus Sällman, Zheleznyakova Galina Y, Lundberg Lina, Zarei Sanaz, Castillo Sandra, Eriksson Fia Ence, Nilsson Emil K, Blüher Matthias, Böttcher Yvonne, Kovacs Peter, Klovins Janis, Rask-Andersen Mathias, Schiöth Helgi |
Nuclear Receptor NR1H3 in Familial Multiple Sclerosis. Neuron 2016 Jun 90 (5): 948-54. Wang Zhe, Sadovnick A Dessa, Traboulsee Anthony L, Ross Jay P, Bernales Cecily Q, Encarnacion Mary, Yee Irene M, de Lemos Madonna, Greenwood Talitha, Lee Joshua D, Wright Galen, Ross Colin J, Zhang Si, Song Weihong, Vilariño-Güell Carl |
Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease. Nature genetics 2016 May . Helgadottir Anna, Gretarsdottir Solveig, Thorleifsson Gudmar, Hjartarson Eirikur, Sigurdsson Asgeir, Magnusdottir Audur, Jonasdottir Aslaug, Kristjansson Helgi, Sulem Patrick, Oddsson Asmundur, Sveinbjornsson Gardar, Steinthorsdottir Valgerdur, Rafnar Thorunn, Masson Gisli, Jonsdottir Ingileif, Olafsson Isleifur, Eyjolfsson Gudmundur I, Sigurdardottir Olof, Daneshpour Maryam S, Khalili Davood, Azizi Fereidoun, Swinkels Dorine W, Kiemeney Lambertus, Quyyumi Arshed A, Levey Allan I, Patel Riyaz S, Hayek Salim S, Gudmundsdottir Ingibjorg J, Thorgeirsson Gudmundur, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
Publicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple Sclerosis. Neuron 2016 Oct 92 (2): 336-338. Minikel Eric Vallabh, MacArthur Daniel |
NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk. Neuron 2016 Oct 92 (2): 333-335. , |
Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study. American journal of obstetrics and gynecology 2018 Sep . Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Thornton Timothy A, Tekola-Ayele Fasil, Sanchez Sixto E, Garcia Pedro J, Palomino Henry G, Hajat Anjum, Romero Roberto, Ananth Cande V, Williams Michelle |
Genome-wide association analyses identify new loci influencing intraocular pressure.
Human molecular genetics 2018 Mar . Gao X Raymond, Huang Hua, Nannini Drew R, Fan Fangda, Kim Heej |
Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis.
Neurology(R) neuroimmunology & neuroinflammation 2021 Nov 8 (6): . Tietz Anja K, Angstwurm Klemens, Baumgartner Tobias, Doppler Kathrin, Eisenhut Katharina, Elisak Martin, Franke Andre, Golombeck Kristin S, Handreka Robert, Kaufmann Max, Kraemer Markus, Kraft Andrea, Lewerenz Jan, Lieb Wolfgang, Madlener Marie, Melzer Nico, Mojzisova Hana, Möller Peter, Pfefferkorn Thomas, Prüss Harald, Rostásy Kevin, Schnegelsberg Margret, Schröder Ina, Siebenbrodt Kai, Sühs Kurt-Wolfram, Wickel Jonathan, Wandinger Klaus-Peter, Leypoldt Frank, Kuhlenbäumer Gregor, |
GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. Frontiers in molecular biosciences 2021 8 632314. Kretzschmar Gabriela Canalli, Alencar Nina Moura, da Silva Saritha Suellen Lopes, Sulzbach Carla Daniela, Meissner Caroline Grisbach, Petzl-Erler Maria Luiza, Souza Ricardo Lehtonen R, Boldt Angelica Beate Wint |
New associations of serum ?-carotene, lycopene, and zeaxanthin concentrations with NR1H3, APOB, RDH12, AND CYP genes. Food science & nutrition 2022 3 10 (3): 763-771. Domarkien? Ingrida, Mažeikien? Asta, Petrauskait? Guost?, Ku?inskien? Zita Aušrel?, Ku?inskas Vaidut |
Association of insulin signaling pathway-related gene polymorphisms and gene-gene interactions with MAFLD in obese children. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2023 6 48 (4): 516-525. Xiang Xiao, Junxia Yan, Ning'an Xu, Rutong Kang, Jiayou Luo, Yan Zho |
Pharmacogenetic association of the NR1H3 promoter variant with antihypertensive response among patients with hypertension: A longitudinal study. Frontiers in pharmacology 2023 3 14 1083134. Chen Yu, Han Yuqing, Wu Yiyi, Hui Rutai, Yang Yunyun, Zhong Yixuan, Zhang Shuyuan, Zhang Wei |
Contributions of NR1H3 genetic polymorphisms to susceptibility and effects of narrowband UVB phototherapy to nonsegmental vitiligo. Scientific reports 2023 2 13 (1): 3384. Xu Meifeng, Xu Qiuyu, Liu Yan, Li Xiaoli, Wang Mei, Dong Wei, Song Yuning, Xiao Shengxia |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: