HuGE Literature Finder
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| Matched Paired Primary and Recurrent Meningiomas Points to Cell-Death Program Contributions to Genomic and Epigenomic Instability along Tumor Progression. Cancers 2022 8 14 (16): . San-Miguel Teresa, Megías Javier, Monleón Daniel, Navarro Lara, Muñoz-Hidalgo Lisandra, Montoliu Carmina, Meri Marina, Roldán Pedro, Cerdá-Nicolás Miguel, López-Ginés Conc |
| Systematic review of genome-wide association studies of abdominal aortic aneurysm. Atherosclerosis 2021 May 327 39-48. Singh Tejas P, Field Matt A, Bown Matthew J, Jones Gregory T, Golledge Jonath |
| Genome-wide scan of long noncoding RNA single nucleotide polymorphisms and pancreatic cancer susceptibility. International journal of cancer 2021 Feb . Corradi Chiara, Gentiluomo Manuel, Gajdán László, Cavestro Giulia Martina, Kreivenaite Edita, Di Franco Gregorio, Sperti Cosimo, Giaccherini Matteo, Petrone Maria Chiara, Tavano Francesca, Gioffreda Domenica, Morelli Luca, Soucek Pavel, Andriulli Angelo, Izbicki Jakob R, Napoli Niccolò, Ma?ecka-Panas Ewa, Hegyi Péter, Neoptolemos John P, Landi Stefano, Vashist Yogesh, Pasquali Claudio, Lu Ye, Cervena Klara, Theodoropoulos George E, Moz Stefania, Capurso Gabriele, Strobel Oliver, Carrara Silvia, Hackert Thilo, Hlavac Viktor, Archibugi Livia, Oliverius Martin, Vanella Giuseppe, Vodicka Pavel, Arcidiacono Paolo Giorgio, Pezzilli Raffaele, Milanetto Anna Caterina, Lawlor Rita T, Ivanauskas Audrius, Szentesi Andrea, Kupcinskas Juozas, Testoni Sabrina G G, Lovecek Martin, Nentwich Michael, Gazouli Maria, Luchini Claudio, Zuppardo Raffaella Alessia, Darvasi Erika, Brenner Hermann, Gheorghe Cristian, Jamroziak Krzysztof, Canzian Federico, Campa Danie |
| Comprehensive genomic profile of Chinese lung cancer patients and mutation characteristics of individuals resistant to icotinib/gefitinib. Scientific reports 2020 Nov 10 (1): 20243. Shang Yanhong, Li Xiaofang, Liu Weiwei, Shi Xiaoliang, Yuan Shaohua, Huo Ran, Fang Guotao, Han Xiao, Zhang Jingnan, Wang Kunjie, Dou Zhengyue, Zhang Yan, Zang Aimin, Zhang L |
| Susceptible gene polymorphism in patients with three-vessel coronary artery disease. BMC cardiovascular disorders 2020 Apr 20 (1): 172. Liu Ru, Song Lei, Jiang Lin, Tang Xiaofang, Xu Lianjun, Gao Zhan, Zhao Xueyan, Xu Jingjing, Gao Runlin, Yuan Jinqi |
| Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma. PloS one 2020 15 (6): e0233692. Moschos Marilita M, Dettoraki Maria, Karekla Aggela, Lamprinakis Ioannis, Damaskos Christos, Gouliopoulos Nikolaos, Tibilis Marios, Gazouli Mar |
| Genetic polymorphisms of diabetes-related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project. Molecular carcinogenesis 2019 03 58 (3): 436-446. Parada Humberto, Cleveland Rebecca J, North Kari E, Stevens June, Teitelbaum Susan L, Neugut Alfred I, Santella Regina M, Martinez Maria E, Gammon Marilie |
| A genetic variant in CDKN2A/2B locus was associated with poor prognosis in patients with esophageal squamous cell carcinoma. Journal of cellular physiology 2018 Sep . Ghobadi Niloofar, Mehramiz Mehrane, ShahidSales Soodabeh, Rezaei Brojerdi Arezou, Anvari Kazem, Khazaei Majid, Rezayi Majid, Sadegh Khorrami Mohammad, Joudi-Mashhad Mona, Ramshini Hassan, Ahmadi-Simab Saeideh, Moradi Ali, Hassanian Seyed Mahdi, Ghayour-Mobarhan Majid, Boroushaki Mohammad Taher, Ferns Gordon A, Avan Am |
| Clinical and Genetic Implications of Mutation Burden in Squamous Cell Carcinoma of the Lung. Annals of surgical oncology 2018 3 25 (6): 1564-1571. Okamoto Tatsuro, Takada Kazuki, Sato Seijiro, Toyokawa Gouji, Tagawa Tetsuzo, Shoji Fumihiro, Nakanishi Ryota, Oki Eiji, Koike Terumoto, Nagahashi Masayuki, Ichikawa Hiroshi, Shimada Yoshifumi, Watanabe Satoshi, Kikuchi Toshiaki, Akazawa Kouhei, Lyle Stephen, Takabe Kazuaki, Okuda Shujiro, Sugio Kenji, Wakai Toshifumi, Tsuchida Masanori, Maehara Yoshihi |
| Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion. Haematologica 2018 9 104 (1): 128-137. Ohki Kentaro, Kiyokawa Nobutaka, Saito Yuya, Hirabayashi Shinsuke, Nakabayashi Kazuhiko, Ichikawa Hitoshi, Momozawa Yukihide, Okamura Kohji, Yoshimi Ai, Ogata-Kawata Hiroko, Sakamoto Hiromi, Kato Motohiro, Fukushima Keitaro, Hasegawa Daisuke, Fukushima Hiroko, Imai Masako, Kajiwara Ryosuke, Koike Takashi, Komori Isao, Matsui Atsushi, Mori Makiko, Moriwaki Koichi, Noguchi Yasushi, Park Myoung-Ja, Ueda Takahiro, Yamamoto Shohei, Matsuda Koichi, Yoshida Teruhiko, Matsumoto Kenji, Hata Kenichiro, Kubo Michiaki, Matsubara Yoichi, Takahashi Hiroyuki, Fukushima Takashi, Hayashi Yasuhide, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira, |
| The 9p21 locus as a potential therapeutic target and prognostic marker in colorectal cancer. Pharmacogenomics 2018 04 19 (5): 463-474. Bahrami Afsane, Hassanian Seyed Mahdi, Khazaei Majid, Gharib Masoumeh, Rahmani Mahsa, Fiuji Hamid, Jazayeri Mir Hadi, Moetamani-Ahmadi Mehrdad, Ferns Gordon A, Avan Am |
| MGMT and CALCA promoter methylation are associated with poor prognosis in testicular germ cell tumor patients. Oncotarget 2017 9 8 (31): 50608-50617. Martinelli Camila Maria da Silva, Lengert André van Helvoort, Cárcano Flavio Mavignier, Silva Eduardo Caetano Albino, Brait Mariana, Lopes Luiz Fernando, Vidal Daniel Onof |
| The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues. PloS one 2012 7 (6): e39574. Pilbrow Anna P, Folkersen Lasse, Pearson John F, Brown Chris M, McNoe Les, Wang Nancy M, Sweet Wendy E, Tang W H Wilson, Black Michael A, Troughton Richard W, Richards A Mark, Franco-Cereceda Anders, Gabrielsen Anders, Eriksson Per, Moravec Christine S, Cameron Vicky |
Genome-wide association study of intracranial aneurysm identifies three new risk loci.
Nature genetics 2010 May 42 (5): 420-5. Yasuno Katsuhito, Bilguvar Kaya, Bijlenga Philippe, Low Siew-Kee, Krischek Boris, Auburger Georg, Simon Matthias, Krex Dietmar, Arlier Zulfikar, Nayak Nikhil, Ruigrok Ynte M, Niemelä Mika, Tajima Atsushi, von und zu Fraunberg Mikael, Dóczi Tamás, Wirjatijasa Florentina, Hata Akira, Blasco Jordi, Oszvald Agi, Kasuya Hidetoshi, Zilani Gulam, Schoch Beate, Singh Pankaj, Stüer Carsten, Risselada Roelof, Beck Jürgen, Sola Teresa, Ricciardi Filomena, Aromaa Arpo, Illig Thomas, Schreiber Stefan, van Duijn Cornelia M, van den Berg Leonard H, Perret Claire, Proust Carole, Roder Constantin, Ozturk Ali K, Gaál Emília, Berg Daniela, Geisen Christof, Friedrich Christoph M, Summers Paul, Frangi Alejandro F, State Matthew W, Wichmann H Erich, Breteler Monique M B, Wijmenga Cisca, Mane Shrikant, Peltonen Leena, Elio Vivas, Sturkenboom Miriam C J M, Lawford Patricia, Byrne James, Macho Juan, Sandalcioglu Erol I, Meyer Bernhard, Raabe Andreas, Steinmetz Helmuth, Rüfenacht Daniel, Jääskeläinen Juha E, Hernesniemi Juha, Rinkel Gabriel J E, Zembutsu Hitoshi, Inoue Ituro, Palotie Aarno, Cambien François, Nakamura Yusuke, Lifton Richard P, Günel Mur |
| DNA hypermethylation profiles in squamous cell carcinoma of the vulva. International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2008 12 28 (1): 63-75. Stephen Josena K, Chen Kang Mei, Raitanen Misa, Grénman Seija, Worsham Maria |
| Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort. Breast cancer research : BCR 2008 10 (3): R47. Azzato Elizabeth M, Driver Kristy E, Lesueur Fabienne, Shah Mitul, Greenberg David, Easton Douglas F, Teschendorff Andrew E, Caldas Carlos, Caporaso Neil E, Pharoah Paul D |
| A common allele on chromosome 9 associated with coronary heart disease. Science (New York, N.Y.) 2007 Jun 316 (5830): 1488-91. McPherson Ruth, Pertsemlidis Alexander, Kavaslar Nihan, Stewart Alexandre, Roberts Robert, Cox David R, Hinds David A, Pennacchio Len A, Tybjaerg-Hansen Anne, Folsom Aaron R, Boerwinkle Eric, Hobbs Helen H, Cohen Jonathan |
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- Page last updated:Mar 20, 2023
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