Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 36 Records) |
| Query Trace: Aneuploidy and TP53[original query] |
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Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.
Nature genetics 2017 May 49 (5): 674-679. Wright Daniel J, Day Felix R, Kerrison Nicola D, Zink Florian, Cardona Alexia, Sulem Patrick, Thompson Deborah J, Sigurjonsdottir Svanhvit, Gudbjartsson Daniel F, Helgason Agnar, Chapman J Ross, Jackson Steve P, Langenberg Claudia, Wareham Nicholas J, Scott Robert A, Thorsteindottir Unnur, Ong Ken K, Stefansson Kari, Perry John R |
| Aneuploidy, TP53 mutation, and amplification of MYC correlate with increased intratumor heterogeneity and poor prognosis of breast cancer patients. Genes, chromosomes & cancer 2017 Nov . Oltmann Johanna, Heselmeyer-Haddad Kerstin, Hernandez Leanora S, Meyer Rüdiger, Torres Irianna, Hu Yue, Doberstein Natalie, Killian J Keith, Petersen David, Zhu Yuelin Jack, Edelman Daniel C, Meltzer Paul S, Schwartz Russell, Gertz E Michael, Schäffer Alejandro A, Auer Gert, Habermann Jens K, Ried Thom |
| Aneuploidy of chromosome 8 and mutation of circulating tumor cells predict pathologic complete response in the treatment of locally advanced rectal cancer. Oncology letters 2018 7 16 (2): 1863-1868. Wan Jue-Feng, Li Xue-Qin, Zhang Jing, Yang Li-Feng, Zhu Ji, Li Gui-Chao, Liang Li-Ping, Shen Li-Jun, Zhang Hui, Li Jing, Zhang Yi-Tong, Chen Chang-Yue, Zhang Zh |
| DNA content analysis of colorectal serrated lesions detects an aneuploid subset of inflammatory bowel disease-associated serrated epithelial change and traditional serrated adenomas. Histopathology 2018 5 73 (3): 464-472. Choi Won-Tak, Wen Kwun Wah, Rabinovitch Peter S, Huang Danning, Mattis Aras N, Gill Ryan |
| Detection of Mutations in Barrett's Esophagus Before Progression to High-Grade Dysplasia or Adenocarcinoma. Gastroenterology 2018 4 155 (1): 156-167. Stachler Matthew D, Camarda Nicholas D, Deitrick Christopher, Kim Anthony, Agoston Agoston T, Odze Robert D, Hornick Jason L, Nag Anwesha, Thorner Aaron R, Ducar Matthew, Noffsinger Amy, Lash Richard H, Redston Mark, Carter Scott L, Davison Jon M, Bass Adam |
| NSAID use and somatic exomic mutations in Barrett's esophagus. Genome medicine 2018 3 10 (1): 17. Galipeau Patricia C, Oman Kenji M, Paulson Thomas G, Sanchez Carissa A, Zhang Qing, Marty Jerry A, Delrow Jeffrey J, Kuhner Mary K, Vaughan Thomas L, Reid Brian J, Li Xiaoho |
| Systematic identification of mutations and copy number alterations associated with cancer patient prognosis. eLife 2018 12 7 . Smith Joan C, Sheltzer Jason |
| Genomic characterization in triple-negative primary myelofibrosis and other myeloid neoplasms with bone marrow fibrosis. Annals of hematology 2019 8 98 (10): 2319-2328. Alvarez-Larrán Alberto, López-Guerra Mónica, Rozman María, Correa Juan-Gonzalo, Hernández-Boluda Juan Carlos, Tormo Mar, Martínez Daniel, Martín Iván, Colomer Dolors, Esteve Jordi, Cervantes Francis |
| Targeted next generation sequencing reveals a common genetic pathway for colorectal cancers with chromosomal instability and those with microsatellite and chromosome stability. Pathology, research and practice 2019 May 152445. Ham-Karim Hersh A, Ebili Henry O, Bradshaw Kirsty, Richman Susan D, Fadhil Wakkas, Domingo Enric, Tomlinson Ian, Ilyas Mohamm |
| Genotypic and Phenotypic Variables Affect Meiotic Cell Cycle Progression, Tumor Ploidy, and Cancer-Associated Mortality in a brca2-Mutant Zebrafish Model. Journal of oncology 2019 4 2019 9218251. Mensah L, Ferguson J L, Shive H |
| Aneuploidy in children with relapsed B-cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse. British journal of haematology 2019 2 185 (2): 266-283. Groeneveld-Krentz Stefanie, Schroeder Michael P, Reiter Michael, Pogodzinski Malwine J, Pimentel-Gutiérrez Helia J, Vagkopoulou Renia, Hof Jana, Chen-Santel Christiane, Nebral Karin, Bradtke Jutta, Türkmen Seval, Baldus Claudia D, Gattenlöhner Stefan, Haas Oskar A, von Stackelberg Arend, Karawajew Leonid, Eckert Cornelia, Kirschner-Schwabe Rena |
| A pan-cancer analysis of the frequency of DNA alterations across cell cycle activity levels. Oncogene 2020 6 39 (32): 5430-5440. Lundberg Arian, Lindström Linda S, Parker Joel S, Löverli Elinor, Perou Charles M, Bergh Jonas, Tobin Nicholas |
| Genomic profiles and clinical outcomes of de novo blastoid/pleomorphic MCL are distinct from those of transformed MCL. Blood advances 2020 Mar 4 (6): 1038-1050. Jain Preetesh, Zhang Shaojun, Kanagal-Shamanna Rashmi, Ok Chi Young, Nomie Krystle, Gonzalez Graciela Nogueras, Gonzalez-Pagan Omarya, Hill Holly A, Lee Hun Ju, Fayad Luis, Westin Jason, Nastoupil Loretta, Hagemeister Frederick, Chen Wendy, Oriabure Onyeka, Badillo Maria, Jiang Changying, Yixin Yao, Li Shaoying, Tang Guilin, Yin C Cameron, Patel Keyur P, Medeiros Leonard Jeffrey, Nair Ranjit, Ahmed Sairah, Iyer Swaminathan P, Thirumurthi Selvi, Champlin Richard, Xu Guofan, Tinsu Pan, Santos David, Wang Ruiping, Han Guangchun, Zhang Jianhua, Song Xingzhi, Neelapu Sattva, Romaguera Jorge, Futreal Andy, Flowers Christopher, Fowler Nathan, Wang Linghua, Wang Michael |
| Genetic alterations associated with F-fluorodeoxyglucose positron emission tomography/computed tomography in head and neck squamous cell carcinoma. Translational oncology 2020 12 14 (2): 100988. Han Sangwon, Oh Jungsu S, Lee Hyo Sang, Kim Jae Seu |
| CDKN2C-Null Leiomyosarcoma: A Novel, Genomically Distinct Class of TP53/RB1-Wild-Type Tumor With Frequent CIC Genomic Alterations and 1p/19q-Codeletion. JCO precision oncology 2020 10 4 . Williams Erik A, Sharaf Radwa, Decker Brennan, Werth Adrienne J, Toma Helen, Montesion Meagan, Sokol Ethan S, Pavlick Dean C, Shah Nikunj, Williams Kevin Jon, Venstrom Jeffrey M, Alexander Brian M, Ross Jeffrey S, Albacker Lee A, Lin Douglas I, Ramkissoon Shakti H, Elvin Julia |
| Molecular profile of FLT3-mutated relapsed/refractory patients with AML in the phase 3 ADMIRAL study of gilteritinib. Blood advances 2022 2 6 (7): 2144-2155. Smith Catherine C, Levis Mark J, Perl Alexander E, Hill Jason E, Rosales Matt, Bahceci Erk |
| High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13. Acta neuropathologica 2022 2 143 (3): 403-414. Pratt Drew, Abdullaev Zied, Papanicolau-Sengos Antonios, Ketchum Courtney, Panneer Selvam Pavalan, Chung Hye-Jung, Lee Ina, Raffeld Mark, Gilbert Mark R, Armstrong Terri S, Pytel Peter, Borys Ewa, Klonoski Joshua M, McCord Matthew, Horbinski Craig, Brat Daniel, Perry Arie, Solomon David, Eberhart Charles, Giannini Caterina, Quezado Martha, Aldape Kenne |
| Identifying tumor immunity-associated molecular features in liver hepatocellular carcinoma by multi-omics analysis. Frontiers in molecular biosciences 2022 11 9 960457. Shen Qianyun, He Yin, Qian Jiajie, Wang Xiaoshe |
| Low expression of INMT is associated with poor prognosis but favorable immunotherapy response in lung adenocarcinoma. Frontiers in genetics 2022 11 13 946848. Zhou Xincheng, Zou Bing, Wang Jian, Wu Lihong, Tan Qiang, Ji Chun |
| Profiling the male germline genome to unravel its reproductive potential. Fertility and sterility 2022 11 119 (2): 196-206. Cheung Stephanie, Xie Philip, Rosenwaks Zev, Palermo Gianpiero |
| Association of TP53 rs1042522 G?>?C, MDM2 rs2279744 T?>?G, and miR-34b/c rs4938723 T?>?C polymorphisms with aneuploidy pregnancy susceptibility. BMC pregnancy and childbirth 2023 8 23 (1): 624. Ying Chan, Weiming Xu, Yan Feng, Yan Zhang, Suyun Li, Zibiao Geng, Zhijiao Liu, Qingfen Zhao, Jinman Zhang, Baosheng Z |
| Clinical Characteristics and Outcomes of Patients with Primary and Secondary Myelofibrosis According to the Genomic Classification Using Targeted Next-Generation Sequencing. Cancers 2023 8 15 (15): . Marta Garrote, Mónica López-Guerra, Eduardo Arellano-Rodrigo, María Rozman, Sara Carbonell, Francesca Guijarro, Marta Santaliestra, Ana Triguero, Dolors Colomer, Francisco Cervantes, Alberto Álvarez-Larr |
| Genomic landscape of TP53-mutated myeloid malignancies. Blood advances 2023 6 . Haley J Abel, Karolyn A Oetjen, Christopher A Miller, Sai M Ramakrishnan, Ryan B Day, Nichole M Helton, Catrina C Fronick, Robert S Fulton, Sharon E Heath, Stefan P Tarnawsky, Sridhar Nonavinkere Srivatsan, Eric J Duncavage, Molly C Schroeder, Jacqueline E Payton, David H Spencer, Matthew J Walter, Peter Westervelt, John F DiPersio, Timothy J Ley, Daniel C Li |
| Association of Chromosome 17 Aneuploidy, TP53 Deletion, Expression and Its rs1042522 Variant with Multiple Myeloma Risk and Response to Thalidomide/Bortezomib Treatment. Cancers 2023 10 15 (19): . Sylwia Popek-Marciniec, Wojciech Styk, Magdalena Wojcierowska-Litwin, Sylwia Chocholska, Aneta Szudy-Szczyrek, Marzena Samardakiewicz, Grazyna Swiderska-Kolacz, Joanna Czerwik-Marcinkowska, Szymon Zmorzyns |
| Impact of somatic mutations and transcriptomic alterations on cancer aneuploidy. Biomedical research (Tokyo, Japan) 2023 10 44 (5): 187-197. Keiichi Hatakeyama, Takeshi Nagashima, Keiichi Ohshima, Sumiko Ohnami, Shumpei Ohnami, Yuji Shimoda, Akane Naruoka, Koji Maruyama, Akira Iizuka, Tadashi Ashizawa, Hirotsugu Kenmotsu, Tohru Mochizuki, Kenichi Urakami, Yasuto Akiyama, Ken Yamaguc |
| Genomic landscape of TP53 -mutated myeloid malignancies. medRxiv : the preprint server for health sciences 2023 1 . Abel Haley J, Oetjen Karolyn A, Miller Christopher A, Ramakrishnan Sai M, Day Ryan B, Helton Nichole M, Fronick Catrina C, Fulton Robert S, Heath Sharon E, Tarnawsky Stefan P, Srivatsan Sridhar Nonavinkere, Duncavage Eric J, Schroeder Molly C, Payton Jacqueline E, Spencer David H, Walter Matthew J, Westervelt Peter, DiPersio John F, Ley Timothy J, Link Daniel |
| Adult Low-Hypodiploid Acute Lymphoblastic Leukemia Emerges from Preleukemic TP53-Mutant Clonal Hematopoiesis. Blood cancer discovery 2023 1 4 (2): 134-149. Kim Rathana, Bergugnat Hugo, Larcher Lise, Duchmann Matthieu, Passet Marie, Gachet Stéphanie, Cuccuini Wendy, Lafage-Pochitaloff Marina, Pastoret Cédric, Grardel Nathalie, Asnafi Vahid, Schäfer Beat W, Delabesse Eric, Itzykson Raphaël, Adès Lionel, Hicheri Yosr, Chalandon Yves, Graux Carlos, Chevallier Patrice, Hunault Mathilde, Leguay Thibaut, Huguet Françoise, Lhéritier Véronique, Dombret Hervé, Soulier Jean, Rousselot Philippe, Boissel Nicolas, Clappier Emmanuel |
| Molecular and Clinicopathologic Impact of GNAS Variants Across Solid Tumors. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2024 8 JCO2400186. Paul Johannet, Somer Abdelfattah, Callahan Wilde, Shrey Patel, Henry Walch, Benoit Rousseau, Guillem Argiles, Oliver Artz, Miteshkumar Patel, Andrea Arfe, Andrea Cercek, Rona Yaeger, Karuna Ganesh, Nikolaus Schultz, Luis A Diaz, Michael B Foo |
| Pediatric therapy-related hematologic neoplasms show enrichment for KMT2A rearrangement and lymphoblastic phenotype. Leukemia & lymphoma 2024 8 1-13. Alexandra E Kovach, Daria Komova, Albert Itov, Maria Gaskova, Irina Kalinina, Kirill Voronin, Yulia Rumiantseva, Alexander Karachunskii, Michael Maschan, Alexey Maschan, Galina Novichkova, Yulia Olshanskaya, Deepa Bhojwani, Gordana Raca, Elena Zerkalenko |
| Genome-wide loss of heterozygosity predicts aggressive, treatment-refractory behavior in pituitary neuroendocrine tumors. Acta neuropathologica 2024 5 147 (1): 85. Andrew L Lin, Vasilisa A Rudneva, Allison L Richards, Yanming Zhang, Hyung Jun Woo, Marc Cohen, Jamie Tisnado, Nazanin Majd, Sharon L Wardlaw, Gabrielle Page-Wilson, Soma Sengupta, Frances Chow, Bernard Goichot, Byram H Ozer, Jorg Dietrich, Lisa Nachtigall, Arati Desai, Tina Alano, Shahiba Ogilive, David B Solit, Tejus A Bale, Marc Rosenblum, Mark T A Donoghue, Eliza B Geer, Viviane Tab |
- Page last reviewed:Feb 1, 2024
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