Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and MED12[original query] |
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| MED12 is frequently mutated in breast phyllodes tumours: a study of 112 cases. Journal of clinical pathology 2015 Sep 68 (9): 685-91. Ng Cedric Chuan Young, Tan Jing, Ong Choon Kiat, Lim Weng Khong, Rajasegaran Vikneswari, Nasir Nur Diyana Md, Lim Jeffrey Chun Tatt, Thike Aye Aye, Salahuddin Syed Ahmed, Iqbal Jabed, Busmanis Inny, Chong Angela Phek Yoon, Teh Bin Tean, Tan Puay Ho |
| Next-Gen Sequencing Exposes Frequent MED12 Mutations and Actionable Therapeutic Targets in Phyllodes Tumors. Molecular cancer research : MCR 2015 Apr 13 (4): 613-9. Cani Andi K, Hovelson Daniel H, McDaniel Andrew S, Sadis Seth, Haller Michaela J, Yadati Venkata, Amin Anmol M, Bratley Jarred, Bandla Santhoshi, Williams Paul D, Rhodes Kate, Liu Chia-Jen, Quist Michael J, Rhodes Daniel R, Grasso Catherine S, Kleer Celina G, Tomlins Scott |
| Frequency of MED12 mutations in phyllodes tumors: Inverse correlation with histologic grade. Genes, chromosomes & cancer 2016 Feb . Yoon Nara, Bae Go Eun, Kang So Young, Choi Mi Sun, Hwang Hye Won, Kim Seok Won, Lee Jeong Eon, Nam Seok Jin, Gong Gyungyub, Lee Hee Jin, Bae Young Kyung, Lee Ahwon, Cho Eun Yo |
| Genetic analysis of microglandular adenosis and acinic cell carcinomas of the breast provides evidence for the existence of a low-grade triple-negative breast neoplasia family. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 Oct . Geyer Felipe C, Berman Samuel H, Marchiò Caterina, Burke Kathleen A, Guerini-Rocco Elena, Piscuoglio Salvatore, Ng Charlotte Ky, Pareja Fresia, Wen Hannah Y, Hodi Zoltan, Schnitt Stuart J, Rakha Emad A, Ellis Ian O, Norton Larry, Weigelt Britta, Reis-Filho Jorge |
| Somatic Genetic Variation in Solid Pseudopapillary Tumor of the Pancreas by Whole Exome Sequencing. International journal of molecular sciences 2017 1 18 (1): . Guo Meng, Luo Guopei, Jin Kaizhou, Long Jiang, Cheng He, Lu Yu, Wang Zhengshi, Yang Chao, Xu Jin, Ni Quanxing, Yu Xianjun, Liu Ch |
| Germline BRCA2 mutations drive prostate cancers with distinct evolutionary trajectories. Nature communications 2017 1 8 13671. Taylor Renea A, Fraser Michael, Livingstone Julie, Espiritu Shadrielle Melijah G, Thorne Heather, Huang Vincent, Lo Winnie, Shiah Yu-Jia, Yamaguchi Takafumi N, Sliwinski Ania, Horsburgh Sheri, Meng Alice, Heisler Lawrence E, Yu Nancy, Yousif Fouad, Papargiris Melissa, Lawrence Mitchell G, Timms Lee, Murphy Declan G, Frydenberg Mark, Hopkins Julia F, Bolton Damien, Clouston David, McPherson John D, van der Kwast Theodorus, Boutros Paul C, Risbridger Gail P, Bristow Robert |
| SET domain containing 1B gene is mutated in primary hepatic neuroendocrine tumors. International journal of cancer 2019 4 145 (11): 2986-2995. Yang Penghui, Huang Xuanlin, Lai Chengcai, Li Lin, Li Tieling, Huang Peide, Ouyang Songying, Yan Jin, Cheng Sijie, Lei Guanglin, Wang Zhaohai, Yu Linxiang, Hong Zhixian, Li Ruisheng, Dong Hui, Wang Cheng, Yu Yinghao, Wang Xuan, Li Xianghong, Wang Liming, Lv Fudong, Yin Ye, Yang Huanming, Song Jianxun, Gao Qiang, Wang Xiliang, Zhang Shaoge |
| Complex karyotype in de novo acute myeloid leukemia: typical and atypical subtypes differ molecularly and clinically. Leukemia 2019 2 33 (7): 1620-1634. Mrózek Krzysztof, Eisfeld Ann-Kathrin, Kohlschmidt Jessica, Carroll Andrew J, Walker Christopher J, Nicolet Deedra, Blachly James S, Bill Marius, Papaioannou Dimitrios, Wang Eunice S, Uy Geoffrey L, Kolitz Jonathan E, Powell Bayard L, Blum William, Stone Richard M, Byrd John C, Bloomfield Clara |
| Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women. Frontiers in genetics 2019 1 9 552. Ajabnoor Ghada M A, Mohammed Nesma Amin, Banaganapalli Babajan, Abdullah Layla Saleh, Bondagji Ola Nabeel, Mansouri Nisma, Sahly Nora Naif, Vaidyanathan Venkatesh, Bondagji Nabeel, Elango Ramu, Shaik Noor Ahm |
| Genomic profiling of primary and recurrent adult granulosa cell tumors of the ovary. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 Mar . Da Cruz Paula Arnaud, da Silva Edaise M, Segura Sheila E, Pareja Fresia, Bi Rui, Selenica Pier, Kim Sarah H, Ferrando Lorenzo, Vahdatinia Mahsa, Soslow Robert A, Vidal August, Gatius Sonia, Przybycin Christopher G, Abu-Rustum Nadeem R, Matias-Guiu Xavier, Rubin Brian P, Reis-Filho Jorge S, DeLair Deborah F, Weigelt Brit |
| Predictive significance of selected gene mutations in relapsed and refractory chronic lymphocytic leukemia patients treated with ibrutinib. European journal of haematology 2020 Nov . Machnicki Marcin M, Górniak Patryk, P?pek Monika, Szymczyk Agnieszka, Iskierka-Ja?d?ewska El?bieta, Steckiewicz Pawe?, Bluszcz Aleksandra, Rydzanicz Ma?gorzata, Hus Marek, P?oski Rafa?, Makuch-?asica Hanna, Nowak Gra?yna, Juszczy?ski Przemys?aw, Jamroziak Krzysztof, Stok?osa Tomasz, Pu?a Barto |
| Somatic mutations in benign breast disease tissues and association with breast cancer risk. BMC medical genomics 2021 7 14 (1): 185. Winham Stacey J, Wang Chen, Heinzen Ethan P, Bhagwate Aditya, Liu Yuanhang, McDonough Samantha J, Stallings-Mann Melody L, Frost Marlene H, Vierkant Robert A, Denison Lori A, Carter Jodi M, Sherman Mark E, Radisky Derek C, Degnim Amy C, Cunningham Julie |
| High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing. NPJ breast cancer 2022 6 8 (1): 76. Kostecka Anna, Nowikiewicz Tomasz, Olszewski Pawe?, Koczkowska Magdalena, Horbacz Monika, Heinzl Monika, Andreou Maria, Salazar Renato, Mair Theresa, Madanecki Piotr, Gucwa Magdalena, Davies Hanna, Skokowski Jaros?aw, Buckley Patrick G, P?ksa Rafa?, ?rutek Ewa, Szylberg ?ukasz, Hartman Johan, Jankowski Micha?, Zegarski Wojciech, Tiemann-Boege Irene, Dumanski Jan P, Piotrowski Arkadiu |
| High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects. American journal of medical genetics. Part A 2022 4 188 (7): 2082-2095. Munabi Naikhoba C O, Mikhail Shady, Toubat Omar, Webb Michelle, Auslander Allyn, Sanchez-Lara Pedro A, Manojlovic Zarko, Schmidt Ryan J, Craig David, Magee William P, Kumar Subramanyan R |
| Frequently mutated genes in predicting the relapse of stage I lung adenocarcinoma. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 2 . Rao Wen, Yang Lujie, Dai Nan, Zhang Liang, Liu Jie, Yang Bo, Li Mengxia, Shan Jinlu, Wang Qiushi, Wang Do |
| Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas. American journal of human genetics 2023 2 110 (3): 460-474. Välimäki Niko, Jokinen Vilja, Cajuso Tatiana, Kuisma Heli, Taira Aurora, Dagnaud Olivia, Ilves Sini, Kaukomaa Jaana, Pasanen Annukka, Palin Kimmo, Heikinheimo Oskari, Bützow Ralf, Aaltonen Lauri A, Karhu Au |
| Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable KDR Variants, Recurrent MED12 Mutations and a High Burden of Germline POT1Alterations. Clinical cancer research : an official journal of the American Association for Cancer Research 2025 1 . Igor Odintsov, David J Papke, Suzanne George, Robert F Padera, Jason L Hornick, Stephanie E Siegmu |
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