Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 32 Records) |
| Query Trace: Disease and FOXO1[original query] |
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| Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182. Journal of molecular medicine (Berlin, Germany) 2014 Sep 92 (9): 961-7. Yu Hongsong, Liu Yunjia, Bai Lin, Kijlstra Aize, Yang Peize |
| Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese. PloS one 2014 9 (1): e86252. Zhao Ying, Yu Yanbo, Tian Xiaoli, Yang Xi, Li Xueqi, Jiang Feng, Chen Yundai, Shi Maow |
| FOXO1 locus and acetylcholinesterase inhibitors in elderly patients with Alzheimer's disease. Clinical interventions in aging 2014 9 1783-91. Paroni Giulia, Seripa Davide, Fontana Andrea, D'Onofrio Grazia, Gravina Carolina, Urbano Maria, Cascavilla Leandro, Pellegrini Fabio, Greco Antonio, Pilotto Alber |
| Integration of gene mutations in risk prognostication for patients receiving first-line immunochemotherapy for follicular lymphoma: a retrospective analysis of a prospective clinical trial and validation in a population-based registry. The Lancet. Oncology 2015 Sep 16 (9): 1111-22. Pastore Alessandro, Jurinovic Vindi, Kridel Robert, Hoster Eva, Staiger Annette M, Szczepanowski Monika, Pott Christiane, Kopp Nadja, Murakami Mark, Horn Heike, Leich Ellen, Moccia Alden A, Mottok Anja, Sunkavalli Ashwini, Van Hummelen Paul, Ducar Matthew, Ennishi Daisuke, Shulha Hennady P, Hother Christoffer, Connors Joseph M, Sehn Laurie H, Dreyling Martin, Neuberg Donna, Möller Peter, Feller Alfred C, Hansmann Martin L, Stein Harald, Rosenwald Andreas, Ott German, Klapper Wolfram, Unterhalt Michael, Hiddemann Wolfgang, Gascoyne Randy D, Weinstock David M, Weigert Oliv |
| Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. Journal of negative results in biomedicine 2015 14 10. Abu-Amero Khaled K, Helwa Inas, Al-Muammar Abdulrahman, Strickland Shelby, Hauser Michael A, Allingham R Rand, Liu Yut |
| The BANK1 SLE-risk variants are associated with alterations in peripheral B cell signaling and development in humans. Clinical immunology (Orlando, Fla.) 2016 Dec 173 171-180. Dam Elizabeth M, Habib Tania, Chen Janice, Funk Andrew, Glukhova Veronika, Davis-Pickett Mel, Wei Shan, James Richard, Buckner Jane H, Cerosaletti Kar |
| A clinicopathologic study of head and neck rhabdomyosarcomas showing FOXO1 fusion-positive alveolar and MYOD1-mutant sclerosing are associated with unfavorable outcome. Oral oncology 2016 Oct 61 89-97. Owosho Adepitan A, Huang Shih-Chiang, Chen Sonja, Kashikar Shruti, Estilo Cherry L, Wolden Suzanne L, Wexler Leonard H, Huryn Joseph M, Antonescu Cristina |
| Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
| Identification of the functional variant driving ORMDL3 and GSDMB expression in human chromosome 17q12-21 in primary biliary cholangitis. Scientific reports 2017 Jun 7 (1): 2904. Hitomi Yuki, Kojima Kaname, Kawashima Minae, Kawai Yosuke, Nishida Nao, Aiba Yoshihiro, Yasunami Michio, Nagasaki Masao, Nakamura Minoru, Tokunaga Katsus |
| Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
| Prostaglandin receptor EP4 expression by Th17 cells is associated with high disease activity in ankylosing spondylitis. Arthritis research & therapy 2019 6 21 (1): 159. Klasen Charlotte, Meyer Anja, Wittekind Paula S, Waqué Iris, Nabhani Schafiq, Kofler David |
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants.
Scientific reports 2019 Jun 9 (1): 9143. Fung Kenneth, Ramírez Julia, Warren Helen R, Aung Nay, Lee Aaron M, Tzanis Evan, Petersen Steffen E, Munroe Patricia |
| Promoter methylation and functional variants in arachidonate 5-lipoxygenase and forkhead box protein O1 genes associated with coronary artery disease. Journal of cellular biochemistry 2019 Mar . Heidari Laleh, Ghaderian Sayyed Mohammad Hossein, Vakili Hossein, Salmani Tayyeb A |
| Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer's disease created by integrative analysis of multi-omics data. Alzheimer's research & therapy 2020 Nov 12 (1): 145. Shigemizu Daichi, Akiyama Shintaro, Higaki Sayuri, Sugimoto Taiki, Sakurai Takashi, Boroevich Keith A, Sharma Alok, Tsunoda Tatsuhiko, Ochiya Takahiro, Niida Shumpei, Ozaki Kouic |
| Predisposition to Graves' disease and Graves' ophthalmopathy by genetic variants of IL2RA. Journal of molecular medicine (Berlin, Germany) 2021 Jul . Du Juan, Wang Xin, Tan Guiqin, Wei Wenwen, Zhou Fangyu, Liang Zhongzhi, Li Hua, Yu Hongso |
| Genomic Classification and Clinical Outcome in Rhabdomyosarcoma: A Report From an International Consortium. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2021 6 39 (26): 2859-2871. Shern Jack F, Selfe Joanna, Izquierdo Elisa, Patidar Rajesh, Chou Hsien-Chao, Song Young K, Yohe Marielle E, Sindiri Sivasish, Wei Jun, Wen Xinyu, Rudzinski Erin R, Barkauskas Donald A, Lo Tammy, Hall David, Linardic Corinne M, Hughes Debbie, Jamal Sabri, Jenney Meriel, Chisholm Julia, Brown Rebecca, Jones Kristine, Hicks Belynda, Angelini Paola, George Sally, Chesler Louis, Hubank Michael, Kelsey Anna, Gatz Susanne A, Skapek Stephen X, Hawkins Douglas S, Shipley Janet M, Khan Jav |
| Exercise Training-Increased FBXO32 and FOXO1 in a Gender-Dependent Manner in Mild Cognitively Impaired African Americans: GEMS-1 Study. Frontiers in aging neuroscience 2021 5 13 641758. Bedada Fikru B, Ntekim Oyonumo E, Nwulia Evaristus O, Fungwe Thomas V, Nadarajah Sheeba Raaj, Obisesan Thomas |
| Analysis of the Serum Peptidomics Profile for Cats With Sarcomeric Gene Mutation and Hypertrophic Cardiomyopathy. Frontiers in veterinary science 2021 11 8 771408. Sukumolanan Pratch, Phanakrop Narumon, Thaisakun Siriwan, Roytrakul Sittiruk, Petchdee Soontar |
| Epstein-Barr virus status of sporadic Burkitt lymphoma is associated with patient age and mutational features. British journal of haematology 2021 10 196 (3): 681-689. Richter Julia, John Katharina, Staiger Annette M, Rosenwald Andreas, Kurz Katrin, Michgehl Ulf, Ott German, Franzenburg Sören, Kohler Christian, Finger Jasmin, Oschlies Ilske, Paul Ulrike, Siebert Reiner, Spang Rainer, Burkhardt Birgit, Klapper Wolfr |
| Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
| Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids. Hepatology communications 2022 Sep . Handelman Samuel K, Puentes Yindra M, Kuppa Annapurna, Chen Yanhua, Du Xiaomeng, Feitosa Mary F, Palmer Nicholette D, Speliotes Elizabeth |
| A minority of somatically mutated genes in pre-existing fatty liver disease have prognostic importance in the development of NAFLD. Liver international : official journal of the International Association for the Study of the Liver 2022 4 42 (8): 1823-1835. Mann Jake P, Hoare Matth |
| Diffuse large B-cell lymphoma and red cell autoimmunity: clinical role and pathogenesis. Pathology 2022 11 55 (1): 104-112. Coombes Caitlin, Horikawa Keisuke, Jain Sanjiv, Jiang Simon, Lim Jun Hee, Saxena Kartik, Shadbolt Bruce, Smyth Lillian, Tobin Joshua, Talaulikar Dip |
| Molecular Characterization of Circulating Tumor DNA in Pediatric Rhabdomyosarcoma: A Feasibility Study. JCO precision oncology 2022 10 6 e2100534. Ruhen Olivia, Lak Nathalie S M, Stutterheim Janine, Danielli Sara G, Chicard Mathieu, Iddir Yasmine, Saint-Charles Alexandra, Di Paolo Virginia, Tombolan Lucia, Gatz Susanne A, Aladowicz Ewa, Proszek Paula, Jamal Sabri, Stankunaite Reda, Hughes Deborah, Carter Paul, Izquierdo Elisa, Wasti Ajla, Chisholm Julia C, George Sally L, Pace Erika, Chesler Louis, Aerts Isabelle, Pierron Gaelle, Zaidi Sakina, Delattre Olivier, Surdez Didier, Kelsey Anna, Hubank Michael, Bonvini Paolo, Bisogno Gianni, Di Giannatale Angela, Schleiermacher Gudrun, Schäfer Beat W, Tytgat Godelieve A M, Shipley Jan |
| Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. NPJ precision oncology 2023 2 7 (1): 21. Christodoulou Eirini, Yellapantula Venkata, O'Halloran Katrina, Xu Liya, Berry Jesse L, Cotter Jennifer A, Zdanowicz Anya, Mascarenhas Leo, Amatruda James F, Ostrow Dejerianne, Bootwalla Moiz, Gai Xiaowu, Navid Fariba, Biegel Jaclyn |
| Specific Mutation Predict Relapse/Refractory Diffuse Large B-Cell Lymphoma. Journal of blood medicine 2024 9 15 407-419. Jing Wang, Lei Tian, Weilong Zhang, Shuhan Tang, Wei Zhao, Yu Guo, Chaoling Wu, Yuansheng Lin, Xiaoyan Ke, Hongmei Ji |
| FOXO1 Single-Nucleotide Polymorphisms Are Associated with Bleeding Severity and Sensitivity of Glucocorticoid Treatment of Pediatric Immune Thrombocytopenia. DNA and cell biology 2024 4 . Xingjuan Xie, Hao Gu, Jingyao Ma, Lingling Fu, Jie Ma, Jialu Zhang, Runhui Wu, Zhenping Ch |
| Prognostic Model for High-Grade Neuroendocrine Carcinoma of the Lung Incorporating Genomic Profiling and Poly (ADP-ribose) Polymerase-1 Expression. JCO precision oncology 2024 4 8 e2300495. Hye Sook Kim, Jong Kwang Kim, Jeong Hyeon Lee, Young Joo Lee, Geon-Kuk Lee, Ji-Youn H |
| Molecular Features of HHV8 Monoclonal Microlymphoma Associated with Kaposi Sarcoma and Multicentric Castleman Disease in an HIV-Negative Patient. International journal of molecular sciences 2024 4 25 (7): . Evelina Rogges, Sabrina Pelliccia, Camilla Savio, Gianluca Lopez, Irene Della Starza, Giacinto La Verde, Arianna Di Napo |
| Prognostic factors in patients with localized and metastatic alveolar rhabdomyosarcoma. A report from two studies and two registries of the Cooperative Weichteilsarkom Studiengruppe CWS. Cancer medicine 2025 1 14 (1): e70215. Ewa Koscielniak, Sabine Stegmaier, Gustaf Ljungman, Bernarda Kazanowska, Felix Niggli, Ruth Ladenstein, Bernd Blank, Erika Hallmen, Christian Vokuhl, Claudia Blattmann, Monika Sparber-Sauer, Thomas Klingebi |
- Page last reviewed:Feb 1, 2024
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