Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: SATB1[original query] |
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The haplotype of three polymorphisms in the SATB1 promoter region impacts survival in breast cancer patients. Oncology letters 2014 Jun 7 (6): 2007-2012. Heubner Martin, Kimmig Rainer, Aktas Bahriye, Siffert Winfried, Frey Ulrich |
Susceptibility to chronic mucus hypersecretion, a genome wide association study.
PloS one 2014 9 (4): e91621. Dijkstra Akkelies E, Smolonska Joanna, van den Berge Maarten, Wijmenga Ciska, Zanen Pieter, Luinge Marjan A, Platteel Mathieu, Lammers Jan-Willem, Dahlback Magnus, Tosh Kerrie, Hiemstra Pieter S, Sterk Peter J, Spira Avi, Vestbo Jorgen, Nordestgaard Borge G, Benn Marianne, Nielsen Sune F, Dahl Morten, Verschuren W Monique, Picavet H Susan J, Smit Henriette A, Owsijewitsch Michael, Kauczor Hans U, de Koning Harry J, Nizankowska-Mogilnicka Eva, Mejza Filip, Nastalek Pawel, van Diemen Cleo C, Cho Michael H, Silverman Edwin K, Crapo James D, Beaty Terri H, Lomas David A, Bakke Per, Gulsvik Amund, Bossé Yohan, Obeidat Ma'en, Obeidat M A, Loth Daan W, Lahousse Lies, Rivadeneira Fernando, Uitterlinden Andre G, Hofman Andre, Stricker Bruno H, Brusselle Guy G, van Duijn Cornelia M, Brouwer Uilke, Koppelman Gerard H, Vonk Judith M, Nawijn Martijn C, Groen Harry J M, Timens Wim, Boezen H Marike, Postma Dirkje S, |
Single nucleotide variants in metastasis-related genes are associated with breast cancer risk, by lymph node involvement and estrogen receptor status, in women with European and African ancestry. Molecular carcinogenesis 2016 Sep . Roberts Michelle R, Sucheston-Campbell Lara E, Zirpoli Gary R, Higgins Michael, Freudenheim Jo L, Bandera Elisa V, Ambrosone Christine B, Yao So |
Genetic variants in chromatin-remodeling pathway associated with lung cancer risk in a Chinese population. Gene 2016 May . Geng Liguo, Zhu Meng, Wang Yuzhuo, Cheng Yang, Liu Jia, Shen Wei, Li Zhihua, Zhang Jiahui, Wang Cheng, Jin Guangfu, Ma Hongxia, Shen Hongbing, Hu Zhibin, Dai Junche |
Expression profile analysis of two antisense lncRNAs to improve prognosis prediction of colorectal adenocarcinoma. Cancer cell international 2019 11 19 278. Shademan Milad, Naseri Salanghuch Azam, Zare Khadijeh, Zahedi Morteza, Foroughi Mohammad Ali, Akhavan Rezayat Kambiz, Mosannen Mozaffari Hooman, Ghaffarzadegan Kamran, Goshayeshi Ladan, Dehghani Hes |
Association of GALC, ZNF184, IL1R2 and ELOVL7 With Parkinson's Disease in Southern Chinese. Frontiers in aging neuroscience 2019 1 10 402. Li Gen, Cui Shishuang, Du Juanjuan, Liu Jin, Zhang Pingchen, Fu Yang, He Yixi, Zhou Haiyan, Ma Jianfang, Chen Sheng |
Differential SATB1 Expression Reveals Heterogeneity of Cutaneous T-Cell Lymphoma. The Journal of investigative dermatology 2020 8 141 (3): 607-618.e6. Gao Yumei, Liu Fengjie, Sun Jingru, Wen Yujie, Tu Ping, Kadin Marshall E, Wang Ya |
Special AT-rich Sequence Binding-Protein 1 (SATB1) Correlates with Immune Infiltration in Breast, Head and Neck, and Prostate Cancer. Medical science monitor : international medical journal of experimental and clinical research 2020 6 26 e923208. Ge Hua, Yan Yan, Yan Maozhao, Guo Lingfei, Mao K |
Association analysis of 15 GWAS-linked loci with Parkinson's disease in Chinese Han population. Neuroscience letters 2020 3 725 134867. Hu Xinchao, Mao Chengyuan, Hu Zhengwei, Zhang Zhongxian, Zhang Shuo, Yang Zhihua, Fan Yu, Fan Liyuan, Zheng Huimin, Yang Jing, Liu Yutao, Yuan Yanpeng, Wang Yaohe, Shi Changhe, Xu Yumi |
Reproducible Genetic Risk Loci for Anxiety: Results From ~200,000 Participants in the Million Veteran Program.
The American journal of psychiatry 2020 03 177 (3): 223-232. Levey Daniel F, Gelernter Joel, Polimanti Renato, Zhou Hang, Cheng Zhongshan, Aslan Mihaela, Quaden Rachel, Concato John, Radhakrishnan Krishnan, Bryois Julien, Sullivan Patrick F, , Stein Murray |
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nature communications 2021 11 12 (1): 6618. Grosche Sarah, Marenholz Ingo, Esparza-Gordillo Jorge, Arnau-Soler Aleix, Pairo-Castineira Erola, Rüschendorf Franz, Ahluwalia Tarunveer S, Almqvist Catarina, Arnold Andreas, , Baurecht Hansjörg, Bisgaard Hans, Bønnelykke Klaus, Brown Sara J, Bustamante Mariona, Curtin John A, Custovic Adnan, Dharmage Shyamali C, Esplugues Ana, Falchi Mario, Fernandez-Orth Dietmar, Ferreira Manuel A R, Franke Andre, Gerdes Sascha, Gieger Christian, Hakonarson Hakon, Holt Patrick G, Homuth Georg, Hubner Norbert, Hysi Pirro G, Jarvelin Marjo-Riitta, Karlsson Robert, Koppelman Gerard H, Lau Susanne, Lutz Manuel, Magnusson Patrik K E, Marks Guy B, Müller-Nurasyid Martina, Nöthen Markus M, Paternoster Lavinia, Pennell Craig E, Peters Annette, Rawlik Konrad, Robertson Colin F, Rodriguez Elke, Sebert Sylvain, Simpson Angela, Sleiman Patrick M A, Standl Marie, Stölzl Dora, Strauch Konstantin, Szwajda Agnieszka, Tenesa Albert, Thompson Philip J, Ullemar Vilhelmina, Visconti Alessia, Vonk Judith M, Wang Carol A, Weidinger Stephan, Wielscher Matthias, Worth Catherine L, Xu Chen-Jian, Lee Young- |
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. American journal of human genetics 2021 Jan . den Hoed Joery, de Boer Elke, Voisin Norine, Dingemans Alexander J M, Guex Nicolas, Wiel Laurens, Nellaker Christoffer, Amudhavalli Shivarajan M, Banka Siddharth, Bena Frederique S, Ben-Zeev Bruria, Bonagura Vincent R, Bruel Ange-Line, Brunet Theresa, Brunner Han G, Chew Hui B, Chrast Jacqueline, Cimbalistien? Loreta, Coon Hilary, , Délot Emmanuèlle C, Démurger Florence, Denommé-Pichon Anne-Sophie, Depienne Christel, Donnai Dian, Dyment David A, Elpeleg Orly, Faivre Laurence, Gilissen Christian, Granger Leslie, Haber Benjamin, Hachiya Yasuo, Abedi Yasmin Hamzavi, Hanebeck Jennifer, Hehir-Kwa Jayne Y, Horist Brooke, Itai Toshiyuki, Jackson Adam, Jewell Rosalyn, Jones Kelly L, Joss Shelagh, Kashii Hirofumi, Kato Mitsuhiro, Kattentidt-Mouravieva Anja A, Kok Fernando, Kotzaeridou Urania, Krishnamurthy Vidya, Ku?inskas Vaidutis, Kuechler Alma, Lavillaureix Alinoë, Liu Pengfei, Manwaring Linda, Matsumoto Naomichi, Mazel Benoît, McWalter Kirsty, Meiner Vardiella, Mikati Mohamad A, Miyatake Satoko, Mizuguchi Takeshi, Moey Lip H, Mohammed Shehla, Mor-Shaked Hagar, Mountford Hayley, Newbury-Ecob Ruth, Odent Sylvie, Orec Laura, Osmond Matthew, Palculict Timothy B, Parker Michael, Petersen Andrea K, Pfundt Rolph, Preikšaitien? Egl?, Radtke Kelly, Ranza Emmanuelle, Rosenfeld Jill A, Santiago-Sim Teresa, Schwager Caitlin, Sinnema Margje, Snijders Blok Lot, Spillmann Rebecca C, Stegmann Alexander P A, Thiffault Isabelle, Tran Linh, Vaknin-Dembinsky Adi, Vedovato-Dos-Santos Juliana H, Schrier Vergano Samantha A, Vilain Eric, Vitobello Antonio, Wagner Matias, Waheeb Androu, Willing Marcia, Zuccarelli Britton, Kini Usha, Newbury Dianne F, Kleefstra Tjitske, Reymond Alexandre, Fisher Simon E, Vissers Lisenka E L |
Neurodevelopmental disorders and anti-epileptic treatment in a patient with a SATB1 mutation: A case report. Frontiers in pediatrics 2022 9 10 931667. Yu Ying, Li Cuiyun, Li Wei, Chen Liting, Wang Dan, Wang Jie, Wang Jian, Yao Ru |
Evaluation of 41 single nucleotide polymorphisms in canine diffuse large B-cell lymphomas using MassARRAY. Scientific reports 2022 3 12 (1): 5120. Sirivisoot Sirintra, Kasantikul Tanit, Techangamsuwan Somporn, Radtanakatikanon Araya, Chen Ken, Lin Tzu-Yin, Rungsipipat Anud |
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