Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 65 Records) |
Query Trace: ARID1B[original query] |
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Comprehensive Immunohistochemical Study of the SWI/SNF Complex Expression Status in Gastric Cancer Reveals an Adverse Prognosis of SWI/SNF Deficiency in Genomically Stable Gastric Carcinomas. Cancers 2021 8 13 (15): . Glückstein Marie-Isabelle, Dintner Sebastian, Arndt Tim Tobias, Vlasenko Dmytro, Schenkirsch Gerhard, Agaimy Abbas, Müller Gernot, Märkl Bruno, Grosser Bian |
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS genetics 2021 Jul 17 (7): e1009679. Audain Enrique, Wilsdon Anna, Breckpot Jeroen, Izarzugaza Jose M G, Fitzgerald Tomas W, Kahlert Anne-Karin, Sifrim Alejandro, Wünnemann Florian, Perez-Riverol Yasset, Abdul-Khaliq Hashim, Bak Mads, Bassett Anne S, Benson D Woodrow, Berger Felix, Daehnert Ingo, Devriendt Koenraad, Dittrich Sven, Daubeney Piers Ef, Garg Vidu, Hackmann Karl, Hoff Kirstin, Hofmann Philipp, Dombrowsky Gregor, Pickardt Thomas, Bauer Ulrike, Keavney Bernard D, Klaassen Sabine, Kramer Hans-Heiner, Marshall Christian R, Milewicz Dianna M, Lemaire Scott, Coselli Joseph S, Mitchell Michael E, Tomita-Mitchell Aoy, Prakash Siddharth K, Stamm Karl, Stewart Alexandre F R, Silversides Candice K, Siebert Reiner, Stiller Brigitte, Rosenfeld Jill A, Vater Inga, Postma Alex V, Caliebe Almuth, Brook J David, Andelfinger Gregor, Hurles Matthew E, Thienpont Bernard, Larsen Lars Allan, Hitz Marc-Phill |
Genotype-Phenotype Correlations in 208 Individuals with Coffin-Siris Syndrome. Genes 2021 7 12 (6): . Vasko Ashley, Drivas Theodore G, Schrier Vergano Samantha |
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies. Journal of human genetics 2021 5 66 (11): 1061-1068. Miyamoto Sachiko, Kato Mitsuhiro, Hiraide Takuya, Shiohama Tadashi, Goto Tomohide, Hojo Akira, Ebata Akio, Suzuki Manabu, Kobayashi Kozue, Chong Pin Fee, Kira Ryutaro, Matsushita Hiroko Baber, Ikeda Hiroko, Hoshino Kyoko, Matsufuji Mayumi, Moriyama Nobuko, Furuyama Masayuki, Yamamoto Tatsuya, Nakashima Mitsuko, Saitsu Hiroto |
Novel LRRK2 mutations and other rare, non-BAP1-related candidate tumor predisposition gene variants in high-risk cancer families with mesothelioma and other tumors. Human molecular genetics 2021 5 30 (18): 1750-1761. Cheung Mitchell, Kadariya Yuwaraj, Sementino Eleonora, Hall Michael J, Cozzi Ilaria, Ascoli Valeria, Ohar Jill A, Testa Joseph |
SMARCA4 and Other SWItch/Sucrose NonFermentable Family Genomic Alterations in NSCLC: Clinicopathologic Characteristics and Outcomes to Immune Checkpoint Inhibition. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2021 Apr . Alessi Joao V, Ricciuti Biagio, Spurr Liam F, Gupta Hersh, Li Yvonne Y, Glass Carolyn, Nishino Mizuki, Cherniack Andrew D, Lindsay James, Sharma Bijaya, Felt Kristen D, Rodig Scott J, Cheng Michael L, Sholl Lynette M, Awad Mark |
Meta-Analysis and Systematic Review of the Genomics of Mucosal Melanoma. Molecular cancer research : MCR 2021 3 19 (6): 991-1004. Broit Natasa, Johansson Peter A, Rodgers Chloe B, Walpole Sebastian T, Newell Felicity, Hayward Nicholas K, Pritchard Antonia |
Genetic and molecular subtype heterogeneity in newly diagnosed early- and advanced-stage endometrial cancer. Gynecologic oncology 2021 2 161 (2): 535-544. Da Cruz Paula Arnaud, DeLair Deborah F, Ferrando Lorenzo, Fix Daniel J, Soslow Robert A, Park Kay J, Chiang Sarah, Reis-Filho Jorge S, Zehir Ahmet, Donoghue Mark T A, Wu Michelle, Brown David N, Murali Rajmohan, Friedman Claire F, Zamarin Dmitriy, Makker Vicky, Mueller Jennifer J, Leitao Mario M, Abu-Rustum Nadeem R, Aghajanian Carol, Weigelt Brit |
Whole-Exome Sequencing Reveals Recurrent but Heterogeneous Mutational Profiles in Sporadic WHO Grade 1 Meningiomas. Frontiers in oncology 2021 11 740782. González-Tablas María, Prieto Carlos, Arandia Daniel, Jara-Acevedo María, Otero Álvaro, Pascual Daniel, Ruíz Laura, Álvarez-Twose Iván, García-Montero Andrés Celestino, Orfao Alberto, Tabernero María Dolor |
Somatic Mutational Profile of High-Grade Serous Ovarian Carcinoma and Triple-Negative Breast Carcinoma in Young and Elderly Patients: Similarities and Divergences. Cells 2021 12 10 (12): . Serio Pedro Adolpho de Menezes Pacheco, de Lima Pereira Gláucia Fernanda, Katayama Maria Lucia Hirata, Roela Rosimeire Aparecida, Maistro Simone, Folgueira Maria Aparecida Azevedo Koi |
Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea. BMC medical genomics 2021 10 14 (1): 254. Lee Yena, Choi Yunha, Seo Go Hun, Kim Gu-Hwan, Keum Changwon, Kim Yoo-Mi, Do Hyo-Sang, Choi Jeongmin, Choi In Hee, Yoo Han-Wook, Lee Beom H |
Genomic alterations in tumor tissue and ctDNA from Chinese pancreatic cancer patients. American journal of cancer research 2021 10 11 (9): 4551-4567. Xiong Anwen, Ma Ning, Wei Guo, Li Chunhua, Li Kainan, Wang B |
The clinicopathological significance of SWI/SNF alterations in gastric cancer is associated with the molecular subtypes. PloS one 2021 16 (1): e0245356. Huang Shih-Chiang, Ng Kwai-Fong, Chang Ian Yi-Feng, Chang Chee-Jen, Chao Yi-Chun, Chang Shu-Chen, Chen Min-Chi, Yeh Ta-Sen, Chen Tse-Chi |
Comprehensive analysis of genomic alterations of Chinese hilar cholangiocarcinoma patients. International journal of clinical oncology 2021 Jan . Feng Feiling, Wu Xiaobing, Shi Xiaoliang, Gao Qingxiang, Wu Yue, Yu Yong, Cheng Qingbao, Li Bin, Yi Bin, Liu Chen, Hao Qing, Zhang Lin, Gao Chunfang, Jiang Xiaoqi |
An additional whole-exome sequencing study in 102 panel-undiagnosed patients: A retrospective study in a Chinese craniosynostosis cohort. Frontiers in genetics 2022 13 967688. Chen Jieyi, Zhang Ping, Peng Meifang, Liu Bo, Wang Xiao, Du Siyuan, Lu Yao, Mu Xiongzheng, Lu Yulan, Wang Sijia, Wu Yingz |
Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population. International review of psychiatry (Abingdon, England) 2022 Feb 34 (2): 154-167. Lo Tzuyao, Kushima Itaru, Aleksic Branko, Kato Hidekazu, Nawa Yoshihiro, Hayashi Yu, Otgonbayar Gantsooj, Kimura Hiroki, Arioka Yuko, Mori Daisuke, Ozaki Nor |
Analysis of recurrent molecular alterations in phyllodes tumour of breast: insights into prognosis and pathogenesis. Pathology 2022 Jun . Tsang Julia Y, Shao Yan, Poon Ivan K, Ni Yun-Bi, Kwan Johnny S, Chow Chit, Shea Ka-Ho, Tse Gary |
A Somatic Mutation Signature Predicts the Best Overall Response to Anti-programmed Cell Death Protein-1 Treatment in Epidermal Growth Factor Receptor/Anaplastic Lymphoma Kinase-Negative Non-squamous Non-small Cell Lung Cancer. Frontiers in medicine 2022 9 808378. Peng Jie, Xiao Lushan, Zou Dan, Han Lij |
Identification of distinct genomic features reveals frequent somatic AHNAK and PTEN mutations predominantly in primary malignant melanoma presenting in the ureter. Japanese journal of clinical oncology 2022 5 52 (8): 930-943. Huang Yan, Wei Lai, Huang Yuanbin, Wen Shuang, Liu Tianqing, Duan Xu, Wang Yutong, Zhang Hongshuo, Fan Bo, Hu B |
[Analysis of ARID1B gene variants in two Chinese pedigrees with Coffin-Siris syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 3 39 (3): 282-285. Xiang Yanbao, Wan Ru, Li Huanzheng, Xu Chenyang, Xu Yunzhi, Tang Shaoh |
SWI/SNF complex gene variations are associated with a higher tumor mutational burden and a better response to immune checkpoint inhibitor treatment: a pan-cancer analysis of next-generation sequencing data corresponding to 4591 cases. Cancer cell international 2022 11 22 (1): 347. Li Yue, Yang Xinhua, Zhu Weijie, Xu Yuxia, Ma Jiangjun, He Caiyun, Wang Fa |
Landscape of Genomic Alterations in IDH Wild-Type Glioblastoma Identifies PI3K as a Favorable Prognostic Factor. JCO precision oncology 2022 1 4 575-584. Yan Yuanqing, Takayasu Takeshi, Hines Gabriella, Dono Antonio, Hsu Sigmund H, Zhu Jay-Jiguang, Riascos-Castaneda Roy F, Kamali Arash, Bhattacharjee Meenakshi B, Blanco Angel I, Tandon Nitin, Kim Dong H, Ballester Leomar Y, Esquenazi And Yosh |
Acute myeloid leukemia with NUP98::RARG resembling acute promyelocytic leukemia accompanying ARID1B gene mutation. Hematology (Amsterdam, Netherlands) 2023 6 28 (1): 2227495. Danyang Wu, Ran G |
Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. The Journal of molecular diagnostics : JMD 2023 4 . Se Hee Kim, Soon Sung Kwon, Mi Ri Park, Hyeon Ah Lee, Ji Hun Kim, JiHoon Cha, Sangwoo Kim, Seung Tae Baek, Se Hoon Kim, Joon Soo Lee, Heung Dong Kim, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Ka |
Landscape of chromatin remodeling gene alterations in endometrial carcinoma. Gynecologic oncology 2023 3 172 54-64. Momeni-Boroujeni Amir, Vanderbilt Chad, Yousefi Elham, Abu-Rustum Nadeem R, Aghajanian Carol, Soslow Robert A, Ellenson Lora H, Weigelt Britta, Murali Rajmoh |
Identification of tumor mutation burden-associated molecular and clinical features in cancer by analyzing multi-omics data. Frontiers in immunology 2023 3 14 1090838. Li Mengyuan, Gao Xuejiao, Wang Xiaoshe |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders. EBioMedicine 2023 12 99 104928. Kuokuo Li, Jifang Xiao, Zhengbao Ling, Tengfei Luo, Jingyu Xiong, Qian Chen, Lijie Dong, Yijing Wang, Xiaomeng Wang, Zhaowei Jiang, Lu Xia, Zhen Yu, Rong Hua, Rui Guo, Dongdong Tang, Mingrong Lv, Aojie Lian, Bin Li, GuiHu Zhao, Xiaojin He, Kun Xia, Yunxia Cao, Jinchen |
Genetic variants in African-American and Hispanic patients with breast cancer. Oncology letters 2023 1 25 (2): 51. Dutta Pranabananda, Keung Man Y, Wu Yanyuan, Vadgama Jaydutt |
Clinical utility of plasma cell-free DNA in pancreatic neuroendocrine neoplasms. Endocrine-related cancer 2024 1 . Darren Cowzer, Ronak H Shah, Joanne F Chou, Ritika Kundra, Sippy Punn, Laura Fiedler, April DeMore, Marinela Capanu, Michael F Berger, Diane Reidy-Lagunes, Nitya R |
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- Page last updated:Apr 22, 2024
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