Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: ETS2[original query] |
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Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2011 Jan 6 (1): 132-8. Sato Yasunori, Yamamoto Noboru, Kunitoh Hideo, Ohe Yuichiro, Minami Hironobu, Laird Nan M, Katori Noriko, Saito Yoshiro, Ohnami Sumiko, Sakamoto Hiromi, Sawada Jun-Ichi, Saijo Nagahiro, Yoshida Teruhiko, Tamura Tomohi |
Exploratory investigation on functional significance of ETS2 and SIM2 genes in Down syndrome. Disease markers 2011 31 (5): 247-57. Chatterjee Arpita, Dutta Samikshan, Sinha Swagata, Mukhopadhyay Kanch |
Genomic alterations in breast cancer patients in betel quid and non betel quid chewers. PloS one 2012 7 (8): e43789. Kaushal Mishi, Mishra Ashwani K, Sharma Jagannath, Zomawia Eric, Kataki Amal, Kapur Sujala, Saxena Suni |
TERT promoter mutations in bladder cancer affect patient survival and disease recurrence through modification by a common polymorphism. Proceedings of the National Academy of Sciences of the United States of America 2013 Oct 110 (43): 17426-31. Rachakonda P Sivaramakrishna, Hosen Ismail, de Verdier Petra J, Fallah Mahdi, Heidenreich Barbara, Ryk Charlotta, Wiklund N Peter, Steineck Gunnar, Schadendorf Dirk, Hemminki Kari, Kumar Raj |
Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies. BMC medical genetics 2013 Jan 14 (1): 1. Chatterjee A, Dutta S, Mukherjee S, Mukherjee N, Dutta A, Mukherjee A, Sinha S, Panda CK, Chaudhuri K, Roy AL, Mukhopadhyay K |
TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma. Oncotarget 2015 Jun 6 (18): 16663-73. Mosrati Mohamed Ali, Malmström Annika, Lysiak Malgorzata, Krysztofiak Adam, Hallbeck Martin, Milos Peter, Hallbeck Anna-Lotta, Bratthäll Charlotte, Strandéus Michael, Stenmark-Askmalm Marie, Söderkvist Pet |
Prognostic quality of activating TERT promoter mutations in glioblastoma: interaction with the rs2853669 polymorphism and patient age at diagnosis. Neuro-oncology 2015 Sep 17 (9): 1231-40. Spiegl-Kreinecker Sabine, Lötsch Daniela, Ghanim Bahil, Pirker Christine, Mohr Thomas, Laaber Magdalena, Weis Serge, Olschowski Alfred, Webersinke Gerald, Pichler Josef, Berger Walt |
A genetic variation in microRNA target site of ETS2 is associated with clinical outcomes of paclitaxel-cisplatin chemotherapy in non-small cell lung cancer. Oncotarget 2016 Feb . Hong Mi Jeong, Lee Shin Yup, Choi Jin Eun, Jin Cheng Cheng, Kang Hyo Jung, Baek Sun Ah, Lee So Yeon, Shin Kyung Min, Jeong Ji Yun, Lee Won Kee, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Son Ji Woong, Park Jae Yo |
Functional dissection of breast cancer risk-associated TERT promoter variants. Oncotarget 2017 10 8 (40): 67203-67217. Helbig Sonja, Wockner Leesa, Bouendeu Annick, Hille-Betz Ursula, McCue Karen, French Juliet D, Edwards Stacey L, Pickett Hilda A, Reddel Roger R, Chenevix-Trench Georgia, Dörk Thilo, Beesley Jonath |
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.
BMJ (Clinical research ed.) 2018 Aug 362 k3225. Trajanoska Katerina, Morris John A, Oei Ling, Zheng Hou-Feng, Evans David M, Kiel Douglas P, Ohlsson Claes, Richards J Brent, Rivadeneira Fernando, |
Genomewide association study of C-peptide surfaces key regulatory genes in Indians.
Journal of genetics 2019 Mar 98 (1): . Bandesh Khushdeep, Prasad Gauri, Giri Anil Kumar, Saroja Voruganti V, Butte Nancy F, Cole Shelley A, Comuzzie Anthony G, , Tandon Nikhil, Bharadwaj Dwaipay |
Obesity Genes and Weight Loss During Lifestyle Intervention in Children With Obesity. JAMA pediatrics 2020 Dec e205142. Heitkamp Melanie, Siegrist Monika, Molnos Sophie, Brandmaier Stefan, Wahl Simone, Langhof Helmut, Grallert Harald, Halle Mart |
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.
American journal of human genetics 2020 12 108 (1): 84-99. Ortiz-Fernández Lourdes, Saruhan-Direskeneli Güher, Alibaz-Oner Fatma, Kaymaz-Tahra Sema, Coit Patrick, Kong Xiufang, Kiprianos Allan P, Maughan Robert T, Aydin Sibel Z, Aksu Kenan, Keser Gokhan, Kamali Sevil, Inanc Murat, Springer Jason, Akar Servet, Onen Fatos, Akkoc Nurullah, Khalidi Nader A, Koening Curry, Karadag Omer, Kiraz Sedat, Forbess Lindsy, Langford Carol A, McAlear Carol A, Ozbalkan Zeynep, Yavuz Sule, Çetin Gozde Yildirim, Alpay-Kanitez Nilufer, Chung Sharon, Ates Askin, Karaaslan Yasar, McKinnon-Maksimowicz Kathleen, Monach Paul A, Ozer Hüseyin T E, Seyahi Emire, Fresko Izzet, Cefle Ayse, Seo Philip, Warrington Kenneth J, Ozturk Mehmet A, Ytterberg Steven R, Cobankara Veli, Onat Ahmet Mesut, Duzgun Nur?en, B?cakc?gil Muge, Yentür Sibel P, Lally Lindsay, Manfredi Angelo A, Baldissera Elena, Erken Eren, Yazici Ayten, K?sac?k Bünyamin, Ka?ifo?lu Timuçin, Dalkilic Ediz, Cuthbertson David, Pagnoux Christian, Sreih Antoine, Reales Guillermo, Wallace Chris, Wren Jonathan D, Cunninghame-Graham Deborah S, Vyse Timothy J, Sun Ying, Chen Huiyong, Grayson Peter C, Tombetti Enrico, Jiang Lindi, Mason Justin C, Merkel Peter A, Direskeneli Haner, Sawalha Amr |
Noonan syndrome-like phenotype in a patient with heterozygous ERF truncating variant. Congenital anomalies 2021 6 61 (6): 226-230. Yamada Mamiko, Funato Michinori, Kondo Goro, Suzuki Hisato, Uehara Tomoko, Takenouchi Toshiki, Sakamoto Yoshiaki, Kosaki Kenji |
Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia. Nature communications 2021 5 12 (1): 2833. Ochi Yotaro, Yoshida Kenichi, Huang Ying-Jung, Kuo Ming-Chung, Nannya Yasuhito, Sasaki Ko, Mitani Kinuko, Hosoya Noriko, Hiramoto Nobuhiro, Ishikawa Takayuki, Branford Susan, Shanmuganathan Naranie, Ohyashiki Kazuma, Takahashi Naoto, Takaku Tomoiku, Tsuchiya Shun, Kanemura Nobuhiro, Nakamura Nobuhiko, Ueda Yasunori, Yoshihara Satoshi, Bera Rabindranath, Shiozawa Yusuke, Zhao Lanying, Takeda June, Watatani Yosaku, Okuda Rurika, Makishima Hideki, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Sanada Masashi, Takaori-Kondo Akifumi, Miyano Satoru, Ogawa Seishi, Shih Lee-Yu |
Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations. Clinical epigenetics 2021 3 13 (1): 61. Pei J, Schuldt M, Nagyova E, Gu Z, El Bouhaddani S, Yiangou L, Jansen M, Calis J J A, Dorsch L M, Blok C Snijders, van den Dungen N A M, Lansu N, Boukens B J, Efimov I R, Michels M, Verhaar M C, de Weger R, Vink A, van Steenbeek F G, Baas A F, Davis R P, Uh H W, Kuster D W D, Cheng C, Mokry M, van der Velden J, Asselbergs F W, Harakalova |
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia. Blood cancer discovery 2022 7 3 (5): 410-427. Takeda June, Yoshida Kenichi, Nakagawa Masahiro M, Nannya Yasuhito, Yoda Akinori, Saiki Ryunosuke, Ochi Yotaro, Zhao Lanying, Okuda Rurika, Qi Xingxing, Mori Takuto, Kon Ayana, Chiba Kenichi, Tanaka Hiroko, Shiraishi Yuichi, Kuo Ming-Chung, Kerr Cassandra M, Nagata Yasunobu, Morishita Daisuke, Hiramoto Nobuhiro, Hangaishi Akira, Nakazawa Hideyuki, Ishiyama Ken, Miyano Satoru, Chiba Shigeru, Miyazaki Yasushi, Kitano Toshiyuki, Usuki Kensuke, Sezaki Nobuo, Tsurumi Hisashi, Miyawaki Shuichi, Maciejewski Jaroslaw P, Ishikawa Takayuki, Ohyashiki Kazuma, Ganser Arnold, Heuser Michael, Thol Felicitas, Shih Lee-Yung, Takaori-Kondo Akifumi, Makishima Hideki, Ogawa Seis |
Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing.
Annals of the rheumatic diseases 2023 2 . Ortiz-Fernández Lourdes, Carmona Elio G, Kerick Martin, Lyons Paul, Carmona Francisco David, López Mejías Raquel, Khor Chiea Chuen, Grayson Peter C, Tombetti Enrico, Jiang Lindi, Direskeneli Haner, Saruhan-Direskeneli Guher, Callejas-Rubio José-Luis, Vaglio Augusto, Salvarani Carlo, Hernández-Rodríguez Jose, Cid Maria Cinta, Morgan Ann W, Merkel Peter A, Burgner David, Smith Kenneth Gc, Gonzalez-Gay Miguel Angel, Sawalha Amr H, Martin Javier, Marquez A |
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