Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: NR2F2[original query] |
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Web-based, participant-driven studies yield novel genetic associations for common traits.
PLoS genetics 2010 Jun 6 (6): e1000993. Eriksson Nicholas, Macpherson J Michael, Tung Joyce Y, Hon Lawrence S, Naughton Brian, Saxonov Serge, Avey Linda, Wojcicki Anne, Pe'er Itsik, Mountain Joan |
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.
PLoS genetics 2012 Jul 8 (7): 7. Coviello AD, Haring R, Wellons M, Vaidya D, Lehtimäki T, Keildson S, Lunetta KL, He C, Fornage M, Lagou V, Mangino M, Onland-Moret NC, Chen B, Eriksson J, Garcia M, Liu YM, Koster A, Lohman K, Lyytikäinen LP, Petersen AK, Prescott J, Stolk L, Vandenput L, Wood AR, Zhuang WV, Ruokonen A, Hartikainen AL, Pouta A, Bandinelli S, Biffar R, Brabant G, Cox DG, Chen Y, Cummings S, Ferrucci L, Gunter MJ, Hankinson SE, Martikainen H, Hofman A, Homuth G, Illig T, Jansson JO, Johnson AD, Karasik D, Karlsson M, Kettunen J, Kiel DP, Kraft P, Liu J, Ljunggren O, Lorentzon M, Maggio M, Markus MR, Mellström D, Miljkovic I, Mirel D, Nelson S, Morin Papunen L, Peeters PH, Prokopenko I, Raffel L, Reincke M, Reiner AP, Rexrode K, Rivadeneira F, Schwartz SM, Siscovick D, Soranzo N, Stöckl D, Tworoger S, Uitterlinden AG, van Gils CH, Vasan RS, Wichmann HE, Zhai G, Bhasin S, Bidlingmaier M, Chanock SJ, De Vivo I, Harris TB, Hunter DJ, Kähönen M, Liu S, Ouyang P, Spector TD, van der Schouw YT, Viikari J, Wallaschofski H, McCarthy MI, Frayling TM, Murray A, Franks S, Järvelin MR, de Jong FH, Raitakari O, Teumer A, Ohlsson C, Murabito JM, Perry JR |
Glucose-dependent regulation of NR2F2 promoter and influence of SNP-rs3743462 on whole body insulin sensitivity. PloS one 2012 7 (5): e35810. Boutant Marie, Ramos Oscar Henrique Pereira, Lecoeur Cécile, Vaillant Emmanuel, Philippe Julien, Zhang Pili, Perilhou Anaïs, Valcarcel Beatriz, Sebert Sylvain, Jarvelin Mario-Ritta, Balkau Beverley, Scott Donald, Froguel Philippe, Vaxillaire Martine, Vasseur-Cognet Mireil |
Rare variants in NR2F2 cause congenital heart defects in humans. American journal of human genetics 2014 Apr 94 (4): 574-85. Al Turki Saeed, Manickaraj Ashok K, Mercer Catherine L, Gerety Sebastian S, Hitz Marc-Phillip, Lindsay Sarah, D'Alessandro Lisa C A, Swaminathan G Jawahar, Bentham Jamie, Arndt Anne-Karin, Low Jacoba, Breckpot Jeroen, Gewillig Marc, Thienpont Bernard, Abdul-Khaliq Hashim, Harnack Christine, Hoff Kirstin, Kramer Hans-Heiner, Schubert Stephan, Siebert Reiner, Toka Okan, Cosgrove Catherine, Watkins Hugh, Lucassen Anneke M, O'Kelly Ita M, Salmon Anthony P, Bu'lock Frances A, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Brook J David, Mulder Barbara, Klaassen Sabine, Bhattacharya Shoumo, Devriendt Koen, Fitzpatrick David F, , Wilson David I, Mital Seema, Hurles Matthew |
Mutation within the hinge region of the transcription factor Nr2f2 attenuates salt-sensitive hypertension. Nature communications 2015 6 6252. Kumarasamy Sivarajan, Waghulde Harshal, Gopalakrishnan Kathirvel, Mell Blair, Morgan Eric, Joe Bi |
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Genetic epidemiology 2015 Mar 39 (3): 207-16. Springelkamp Henriët, Mishra Aniket, Hysi Pirro G, Gharahkhani Puya, Höhn René, Khor Chiea-Chuen, Cooke Bailey Jessica N, Luo Xiaoyan, Ramdas Wishal D, Vithana Eranga, Koh Victor, Yazar Seyhan, Xu Liang, Forward Hannah, Kearns Lisa S, Amin Najaf, Iglesias Adriana I, Sim Kar-Seng, van Leeuwen Elisabeth M, Demirkan Ayse, van der Lee Sven, Loon Seng-Chee, Rivadeneira Fernando, Nag Abhishek, Sanfilippo Paul G, Schillert Arne, de Jong Paulus T V M, Oostra Ben A, Uitterlinden André G, Hofman Albert, , Zhou Tiger, Burdon Kathryn P, Spector Timothy D, Lackner Karl J, Saw Seang-Mei, Vingerling Johannes R, Teo Yik-Ying, Pasquale Louis R, Wolfs Roger C W, Lemij Hans G, Tai E-Shyong, Jonas Jost B, Cheng Ching-Yu, Aung Tin, Jansonius Nomdo M, Klaver Caroline C W, Craig Jamie E, Young Terri L, Haines Jonathan L, MacGregor Stuart, Mackey David A, Pfeiffer Norbert, Wong Tien-Yin, Wiggs Janey L, Hewitt Alex W, van Duijn Cornelia M, Hammond Christopher |
Expression of genes involved in progesterone receptor paracrine signaling and their effect on litter size in pigs. Journal of animal science and biotechnology 2016 7 31. Chen Xiao, Fu Jinluan, Wang Aig |
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect. European journal of medical genetics 2017 12 61 (4): 197-203. Qiao Xiao-Hui, Wang Qian, Wang Juan, Liu Xing-Yuan, Xu Ying-Jia, Huang Ri-Tai, Xue Song, Li Yan-Jie, Zhang Min, Qu Xin-Kai, Li Ruo-Gu, Qiu Xing-Biao, Yang Yi-Qi |
Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing. Prenatal diagnosis 2018 Jul . Kammoun Molka, Souche Erika, Brady Paul, Ding Jia, Cosemans Nele, Gratacos Eduard, Devriendt Koen, Eixarch Elisenda, Deprest Jan, Vermeesch Joris Robe |
Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. Birth defects research 2018 3 110 (7): 610-617. Matsunami Nori, Shanmugam Hari, Baird Lisa, Stevens Jeff, Byrne Janice L, Barnhart Douglas C, Rau Carrie, Feldkamp Marcia L, Yoder Bradley A, Leppert Mark F, Yost H Joseph, Brunelli Lu |
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. American journal of human genetics 2018 2 102 (3): 487-493. Bashamboo Anu, Eozenou Caroline, Jorgensen Anne, Bignon-Topalovic Joelle, Siffroi Jean-Pierre, Hyon Capucine, Tar Attila, Nagy Péter, Sólyom Janos, Halász Zita, Paye-Jaouen Annnabel, Lambert Sophie, Rodriguez-Buritica David, Bertalan Rita, Martinerie Laetitia, Rajpert-De Meyts Ewa, Achermann John C, McElreavey K |
SNPs Associated With Testosterone Levels Influence Human Facial Morphology. Frontiers in genetics 2018 9 497. Roosenboom Jasmien, Indencleef Karlijne, Lee Myoung Keun, Hoskens Hanne, White Julie D, Liu Dongjing, Hecht Jacqueline T, Wehby George L, Moreno Lina M, Hodges-Simeon Carolyn, Feingold Eleanor, Marazita Mary L, Richmond Stephen, Shriver Mark D, Claes Peter, Shaffer John R, Weinberg Seth |
A genome-wide association study implicates NR2F2 in lymphangioleiomyomatosis pathogenesis.
The European respiratory journal 2019 Apr . Kim Wonji, Giannikou Krinio, Dreier John R, Lee Sanghun, Tyburczy Magdalena E, Silverman Edwin K, Radzikowska El?bieta, Wu Shulin, Wu Chin-Lee, Henske Elizabeth P, Hunninghake Gary, Carel Havi, Roman Antonio, Pujana Miquel Angel, Moss Joel, Won Sungho, Kwiatkowski David |
Prognostic Role of Chicken Ovalbumin Upstream Promoter Transcription Factor II in Isocitrate Dehydrogenase-Mutant Glioma with 1p19q Co-Deletion. Journal of molecular neuroscience : MN 2019 Mar . Chai Yi, Liu Wei, Wang Caixia, Rao Minchao, Zhang Yu |
NR2F2 loss?of?function mutation is responsible for congenital bicuspid aortic valve. International journal of molecular medicine 2019 2 43 (4): 1839-1846. Wang Juan, Abhinav Pradhan, Xu Ying-Jia, Li Ruo-Gu, Zhang Min, Qiu Xing-Biao, Di Ruo-Min, Qiao Qi, Li Xiu-Mei, Huang Ri-Tai, Xue Song, Yang Yi-Qi |
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants. American journal of surgery 2021 7 223 (1): 182-186. Schwab Marisa E, Dong Shan, Lianoglou Billie R, Aguilar Lucero Alessandra F, Schwartz Grace B, Norton Mary E, MacKenzie Tippi C, Sanders Stephan |
Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort. Frontiers in genetics 2022 9 13 900574. Zidoune Housna, Ladjouze Asmahane, Chellat-Rezgoune Djalila, Boukri Asma, Dib Scheher Aman, Nouri Nassim, Tebibel Meryem, Sifi Karima, Abadi Noureddine, Satta Dalila, Benelmadani Yasmina, Bignon-Topalovic Joelle, El-Zaiat-Munsch Maeva, Bashamboo Anu, McElreavey K |
A novel cuproptosis-related lncRNA signature predicts the prognosis and immune landscape in bladder cancer. Frontiers in immunology 2022 12 13 1027449. Bai Yuchen, Zhang Qi, Liu Feng, Quan Ji |
A genome-wide by PM exposure interaction study for blood pressure in Korean adults. Scientific reports 2023 8 13 (1): 13060. Hyun-Jin Kim, Ho-Young Son, Philiip Park, Jae Moon Yun, Hyuktae Kwon, Belong Cho, Jong-Il Kim, Jin-Ho Pa |
Genomic insights and advanced machine learning: characterizing autism spectrum disorder biomarkers and genetic interactions. Metabolic brain disease 2023 12 . Laila Dabab Nahas, Ankur Datta, Alsamman M Alsamman, Monica H Adly, Nader Al-Dewik, Karthik Sekaran, K Sasikumar, Kanika Verma, George Priya C Doss, Hatem Zay |
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