Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Disease and CTCF[original query] |
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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Nature genetics 2009 Jan 41 (1): 47-55. Aulchenko Yurii S, Ripatti Samuli, Lindqvist Ida, Boomsma Dorret, Heid Iris M, Pramstaller Peter P, Penninx Brenda W J H, Janssens A Cecile J W, Wilson James F, Spector Tim, Martin Nicholas G, Pedersen Nancy L, Kyvik Kirsten Ohm, Kaprio Jaakko, Hofman Albert, Freimer Nelson B, Jarvelin Marjo-Riitta, Gyllensten Ulf, Campbell Harry, Rudan Igor, Johansson Asa, Marroni Fabio, Hayward Caroline, Vitart Veronique, Jonasson Inger, Pattaro Cristian, Wright Alan, Hastie Nick, Pichler Irene, Hicks Andrew A, Falchi Mario, Willemsen Gonneke, Hottenga Jouke-Jan, de Geus Eco J C, Montgomery Grant W, Whitfield John, Magnusson Patrik, Saharinen Juha, Perola Markus, Silander Kaisa, Isaacs Aaron, Sijbrands Eric J G, Uitterlinden Andre G, Witteman Jacqueline C M, Oostra Ben A, Elliott Paul, Ruokonen Aimo, Sabatti Chiara, Gieger Christian, Meitinger Thomas, Kronenberg Florian, Döring Angela, Wichmann H-Erich, Smit Johannes H, McCarthy Mark I, van Duijn Cornelia M, Peltonen Leena, |
Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. American journal of human genetics 2009 Sep 85 (3): 377-93. Verlaan Dominique J, Berlivet Soizik, Hunninghake Gary M, Madore Anne-Marie, Larivière Mathieu, Moussette Sanny, Grundberg Elin, Kwan Tony, Ouimet Manon, Ge Bing, Hoberman Rose, Swiatek Marcin, Dias Joana, Lam Kevin C L, Koka Vonda, Harmsen Eef, Soto-Quiros Manuel, Avila Lydiana, Celedón Juan C, Weiss Scott T, Dewar Ken, Sinnett Daniel, Laprise Catherine, Raby Benjamin A, Pastinen Tomi, Naumova Anna |
Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved? The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2009 Aug 12 (7): 885-94. Baruch Kuti, Silberberg Gilad, Aviv Alex, Shamir Eyal, Bening-Abu-Shach Ulli, Baruch Yehuda, Darvasi Ariel, Navon Ru |
Human-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseases. Genome medicine 2014 3 6 (3): 19. Wilson Gareth A, Butcher Lee M, Foster Holly R, Feber Andrew, Roos Christian, Walter Lutz, Woszczek Grzegorz, Beck Stephan, Bell Christopher |
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia. Haematologica 2015 Jul . Vicente Carmen, Schwab Claire, Broux Michaël, Geerdens Ellen, Degryse Sandrine, Demeyer Sofie, Lahortiga Idoya, Elliott Alannah, Chilton Lucy, La Starza Roberta, Mecucci Cristina, Vandenberghe Peter, Goulden Nicholas, Vora Ajay, Moorman Anthony V, Soulier Jean, Harrison Christine J, Clappier Emmanuelle, Cools J |
A novel somatic MAPK1 mutation in primary ovarian mixed germ cell tumors. Oncology reports 2015 Nov . Zou Yang, Deng Wei, Wang Feng, Yu Xiao-Hong, Liu Fa-Ying, Yang Bi-Cheng, Huang Mei-Zhen, Guo Jiu-Bai, Xie Qiu-Hua, He Ming, Huang Ou-Pi |
Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity. eLife 2016 Feb 5 . Raj Prithvi, Rai Ekta, Song Ran, Khan Shaheen, Wakeland Benjamin E, Viswanathan Kasthuribai, Arana Carlos, Liang Chaoying, Zhang Bo, Dozmorov Igor, Carr-Johnson Ferdicia, Mitrovic Mitja, Wiley Graham B, Kelly Jennifer A, Lauwerys Bernard R, Olsen Nancy J, Cotsapas Chris, Garcia Christine K, Wise Carol A, Harley John B, Nath Swapan K, James Judith A, Jacob Chaim O, Tsao Betty P, Pasare Chandrashekhar, Karp David R, Li Quan Zhen, Gaffney Patrick M, Wakeland Edward |
IL-10 and integrin signaling pathways are associated with head and neck cancer progression. BMC genomics 2016 17 (1): 38. Bornstein Sophia, Schmidt Mark, Choonoo Gabrielle, Levin Trevor, Gray Joe, Thomas Charles R, Wong Melissa, McWeeney Shann |
Novel CTCF mutations in Chinese patients with ovarian endometriosis. Molecular medicine reports 2018 May . Guo Jiubai, Cao Bianna, Xu Xiaoyun, Wu Fei, Zhu B |
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2018 12 29 (1): 156-170. Budde Monika, Friedrichs Stefanie, Alliey-Rodriguez Ney, Ament Seth, Badner Judith A, Berrettini Wade H, Bloss Cinnamon S, Byerley William, Cichon Sven, Comes Ashley L, Coryell William, Craig David W, Degenhardt Franziska, Edenberg Howard J, Foroud Tatiana, Forstner Andreas J, Frank Josef, Gershon Elliot S, Goes Fernando S, Greenwood Tiffany A, Guo Yiran, Hipolito Maria, Hood Leroy, Keating Brendan J, Koller Daniel L, Lawson William B, Liu Chunyu, Mahon Pamela B, McInnis Melvin G, McMahon Francis J, Meier Sandra M, Mühleisen Thomas W, Murray Sarah S, Nievergelt Caroline M, Nurnberger John I, Nwulia Evaristus A, Potash James B, Quarless Danjuma, Rice John, Roach Jared C, Scheftner William A, Schork Nicholas J, Shekhtman Tatyana, Shilling Paul D, Smith Erin N, Streit Fabian, Strohmaier Jana, Szelinger Szabolcs, Treutlein Jens, Witt Stephanie H, Zandi Peter P, Zhang Peng, Zöllner Sebastian, Bickeböller Heike, Falkai Peter G, Kelsoe John R, Nöthen Markus M, Rietschel Marcella, Schulze Thomas G, Malzahn Dört |
Defining functional variants associated with Alzheimer's disease in the induced immune response. Brain communications 2021 5 3 (2): fcab083. Harwood Janet C, Leonenko Ganna, Sims Rebecca, Escott-Price Valentina, Williams Julie, Holmans Pet |
Enhancer release and retargeting activates disease-susceptibility genes. Nature 2021 5 595 (7869): 735-740. Oh Soohwan, Shao Jiaofang, Mitra Joydeep, Xiong Feng, D'Antonio Matteo, Wang Ruoyu, Garcia-Bassets Ivan, Ma Qi, Zhu Xiaoyu, Lee Joo-Hyung, Nair Sreejith J, Yang Feng, Ohgi Kenneth, Frazer Kelly A, Zhang Zhengdong D, Li Wenbo, Rosenfeld Michael |
A Low-Producing Haplotype of Interleukin-6 Disrupting CTCF Binding Is Protective against Severe COVID-19. mBio 2021 10 12 (5): e0137221. Chen Tao, Lin Yu-Xin, Zha Yan, Sun Ying, Tian Jinxiu, Yang Zhiying, Lin Shan-Wen, Yu Fuxun, Chen Zi-Sheng, Kuang Bo-Hua, Lei Jin-Ju, Nie Ying-Jie, Xu Yonghao, Tian Dong-Bo, Li Ying-Zi, Yang Bin, Xu Qiang, Yang Li, Zhong Nanshan, Zheng Meizhen, Li Yimin, Zhao Jincun, Zhang Xiang-Yan, Feng L |
Genomic imbalances in the placenta are associated with poor fetal growth. Molecular medicine (Cambridge, Mass.) 2021 1 27 (1): 3. Del Gobbo Giulia F, Yin Yue, Choufani Sanaa, Butcher Emma A, Wei John, Rajcan-Separovic Evica, Bos Hayley, von Dadelszen Peter, Weksberg Rosanna, Robinson Wendy P, Yuen Ryan K |
Severe COVID-19 associated variants linked to chemokine receptor gene control in monocytes and macrophages. bioRxiv : the preprint server for biology 2021 Jan . Stikker Bernard, Stik Grégoire, Hendriks Rudi W, Stadhouders Ral |
The Clinical Outcomes and Genomic Landscapes of Acute Lymphoblastic Leukemia Patients with E2A-PBX1: A 10-year Retrospective Study. American journal of hematology 2021 Aug . Zhou Biqi, Chu Xinran, Tian Hong, Liu Tianhui, Liu Hong, Gao Wei, Chen Suning, Hu Shaoyan, Wu Depei, Xu Ya |
Prognostic value of baseline genetic features and newly identified TP53 mutations in advanced breast cancer. Molecular oncology 2022 Jul . Zhang Lanxin, Sun Siwen, Zhao Xiaotian, Liu Jingwen, Xu Yang, Xu Lingzhi, Song Chen, Li Na, Yu Jing, Zhao Shanshan, Yu Peiyao, Fang Fengqi, Xie Jiping, Ji Xuening, Yu Ruoying, Ou Qiuxiang, Zhao Zuowei, Li M |
Discovery and Functional Characterization of Two Regulatory Variants Underlying Lupus Susceptibility at 2p13.1. Genes 2022 Jun 13 (6): . Fazel-Najafabadi Mehdi, Rallabandi Harikrishna-Reddy, Singh Manish K, Maiti Guru P, Morris Jacqueline, Looger Loren L, Nath Swapan |
Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants. BMC medicine 2022 2 20 (1): 68. Chen Rui, Liu Jiewei, Li Shiwu, Li Xiaoyan, Huo Yongxia, Yao Yong-Gang, Xiao Xiao, Li Ming, Luo Xiong-Ji |
The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung's disease. Frontiers in cell and developmental biology 2023 7 11 1184799. Shuiqing Chi, Shuai Li, Guoqing Cao, Jialing Guo, Yunqiao Han, Yun Zhou, Xi Zhang, Yibo Li, Zhibin Luo, Xiangyang Li, Liying Rong, Mengxin Zhang, Linglu Li, Shaotao Ta |
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