Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 49 Records) |
| Query Trace: Disease and ERBB4[original query] |
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Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI insight 2022 2 7 (3): . Yu Mengyao, Tcheandjieu Catherine, Georges Adrien, Xiao Ke, Tejeda Helio, Dina Christian, Le Tourneau Thierry, Fiterau Madalina, Judy Renae, Tsao Noah L, Amgalan Dulguun, Munger Chad J, Engreitz Jesse M, Damrauer Scott M, Bouatia-Naji Nabila, Priest James |
| Associations of high altitude polycythemia with polymorphisms in EPAS1, ITGA6 and ERBB4 in Chinese Han and Tibetan populations. Oncotarget 2017 Oct 8 (49): 86736-86746. Zhao Yiduo, Zhang Zhiying, Liu Lijun, Zhang Yao, Fan Xiaowei, Ma Lifeng, Li Jing, Zhang Yuan, He Haijin, Kang Long |
| Landscape of somatic mutations in gastric cancer assessed using next-generation sequencing analysis. Oncology letters 2018 Oct 16 (4): 4863-4870. Pan Xuan, Ji Xiaozhi, Zhang Renmin, Zhou Zhaofei, Zhong Yuejiao, Peng Wei, Sun Ning, Xu Xinyu, Xia Lei, Li Pansong, Lu Jianwei, Tu Ji |
| Detection of circulating tumour cell clusters in human glioblastoma. British journal of cancer 2018 8 119 (4): 487-491. Krol Ilona, Castro-Giner Francesc, Maurer Martina, Gkountela Sofia, Szczerba Barbara Maria, Scherrer Ramona, Coleman Niamh, Carreira Suzanne, Bachmann Felix, Anderson Stephanie, Engelhardt Marc, Lane Heidi, Evans Thomas Ronald Jeffry, Plummer Ruth, Kristeleit Rebecca, Lopez Juanita, Aceto Nico |
| Concomitant driver mutations in advanced EGFR-mutated non-small-cell lung cancer and their impact on erlotinib treatment. Oncotarget 2018 May 9 (40): 26195-26208. Jakobsen Jan Nyrop, Santoni-Rugiu Eric, Grauslund Morten, Melchior Linea, Sørensen Jens Be |
| Germline genetic variants in somatically significantly mutated genes in tumors are associated with renal cell carcinoma risk and outcome. Carcinogenesis 2018 Apr . Shu Xiang, Gu Jianchun, Huang Maosheng, Tannir Nizar M, Matin Surena F, Karam Jose A, Wood Christopher G, Wu Xifeng, Ye Yuanqi |
| A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
| Tumor Mutation Load: A Novel Independent Prognostic Factor in Stage IIIA-N2 Non-Small-Cell Lung Cancer. Disease markers 2019 2019 3837687. Kang Jingjing, Luo Yang, Wang Di, Men Yu, Wang Jianyang, Che Yi-Qun, Hui Zhougua |
| Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis. Aging and disease 2019 Dec 10 (6): 1199-1206. Liu Zhi-Jun, Lin Hui-Xia, Wei Qiao, Zhang Qi-Jie, Chen Cong-Xin, Tao Qing-Qing, Liu Gong-Lu, Ni Wang, Gitler Aaron D, Li Hong-Fu, Wu Zhi-Yi |
| Genome-wide conditional association study reveals the influences of lifestyle cofactors on genetic regulation of body surface area in MESA population. PloS one 2021 6 16 (6): e0253167. Khatun Mita, Monir Md Mamun, Xu Ting, Xu Haiming, Zhu J |
| Clonal Architectures Predict Clinical Outcome in Gastric Adenocarcinoma Based on Genomic Variation, Tumor Evolution, and Heterogeneity. Cell transplantation 0 30 963689721989606. Ren Chenxia, Wu Cuiling, Wang Niuniu, Lian Changhong, Yang Changqi |
| Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing. Frontiers in aging neuroscience 2021 11 13 745407. Sun Lin, Zhang Jianye, Su Ning, Zhang Shaowei, Yan Feng, Lin Xiang, Yu Jie, Li Wei, Li Xia, Xiao Shi |
| Genetic analysis of ALS cases in the isolated island population of Malta. European journal of human genetics : EJHG 2021 1 29 (4): 604-614. Borg Rebecca, Farrugia Wismayer Maia, Bonavia Karl, Farrugia Wismayer Andrew, Vella Malcolm, van Vugt Joke J F A, Kenna Brendan J, Kenna Kevin P, Vassallo Neville, Veldink Jan H, Cauchi Ruben |
| Genomic Landscape Alterations in Primary Tumor and Matched Lymph Node Metastasis in Hormone-Naïve Prostate Cancer Patients. Cancers 2022 Aug 14 (17): . Russo Giorgio Ivan, Bonacci Paolo, Bivona Dalida, Privitera Grete Francesca, Broggi Giuseppe, Caltabiano Rosario, Vella Jessica, Lo Giudice Arturo, Asmundo Maria Giovanna, Cimino Sebastiano, Morgia Giuseppe, Stefani Stefania, Musso Nico |
| Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population.
Cancers 2022 Aug 14 (17): . Garcia-Etxebarria Koldo, Etxart Ane, Barrero Maialen, Nafria Beatriz, Segues Merino Nerea Miren, Romero-Garmendia Irati, Franke Andre, D'Amato Mauro, Bujanda Lu |
| Comparative study on the mutation spectrum of tissue DNA and blood ctDNA in patients with non-small cell lung cancer. Translational cancer research 2022 May 11 (5): 1245-1254. Zhang Meichun, Wu Jing, Zhong Weinong, Zhao Ziwen, Guo Weiho |
| Analysis of ERBB4 Variants in Amyotrophic Lateral Sclerosis Within a Chinese Cohort. Frontiers in neurology 2022 4 13 865264. Wang Fan, Liu Xiangyi, He Ji, Zhang Nan, Chen Lu, Tang Lu, Fan Dongshe |
| Genomic profiling of gallbladder carcinoma: Targetable mutations and pathways involved. Pathology, research and practice 2022 3 232 153806. Mishra Sridhar, Kumari Swati, Srivastava Pallavi, Pandey Anshuman, Shukla Saumya, Husain Nuzh |
| Genetic association study of ERBB4 SNP rs1351592 with polycystic ovary syndrome in Pakistani population. JPMA. The Journal of the Pakistan Medical Association 2021 Jan 71 (1(B)): 332-335. Afzal Tayyaba, Raja Ghazala Kaukab, Afzal Maimoona, Ahmad Shakeel, Sultana Nighat, Kalsoom Umm |
| Genomic characterization reveals distinct mutation landscapes and therapeutic implications in neuroendocrine carcinomas of the gastrointestinal tract. Cancer communications (London, England) 2022 Oct . Wu Huanwen, Yu Zicheng, Liu Yueping, Guo Lei, Teng Lianghong, Guo Lingchuan, Liang Li, Wang Jing, Gao Jie, Li Ruiyu, Yang Ling, Nie Xiu, Su Dan, Liang Zhiyo |
| Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis. NPJ genomic medicine 2022 1 7 (1): 8. Al Khleifat Ahmad, Iacoangeli Alfredo, van Vugt Joke J F A, Bowles Harry, Moisse Matthieu, Zwamborn Ramona A J, van der Spek Rick A A, Shatunov Aleksey, Cooper-Knock Johnathan, Topp Simon, Byrne Ross, Gellera Cinzia, López Victoria, Jones Ashley R, Opie-Martin Sarah, Vural Atay, Campos Yolanda, van Rheenen Wouter, Kenna Brendan, Van Eijk Kristel R, Kenna Kevin, Weber Markus, Smith Bradley, Fogh Isabella, Silani Vincenzo, Morrison Karen E, Dobson Richard, van Es Michael A, McLaughlin Russell L, Vourc'h Patrick, Chio Adriano, Corcia Philippe, de Carvalho Mamede, Gotkine Marc, Panades Monica P, Mora Jesus S, Shaw Pamela J, Landers John E, Glass Jonathan D, Shaw Christopher E, Basak Nazli, Hardiman Orla, Robberecht Wim, Van Damme Philip, van den Berg Leonard H, Veldink Jan H, Al-Chalabi Amm |
| Genome-wide Detection of Chimeric Transcripts in Early-stage Non-small Cell Lung Cancer. Cancer genomics & proteomics 2023 8 20 (5): 417-432. Yaroslav Ilnytskyy, Lars Petersen, John B McIntyre, Mie Konno, Adrijana D'Silva, Michelle Dean, Anifat Elegbede, Andrey Golubov, Olga Kovalchuk, Igor Kovalchuk, Gwyn Be |
| Molecular features and clinical implications of the heterogeneity in Chinese patients with HER2-low breast cancer. Nature communications 2023 8 14 (1): 5112. Lei-Jie Dai, Ding Ma, Yu-Zheng Xu, Ming Li, Yu-Wei Li, Yi Xiao, Xi Jin, Song-Yang Wu, Ya-Xin Zhao, Han Wang, Wen-Tao Yang, Yi-Zhou Jiang, Zhi-Ming Sh |
| Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population. Frontiers in genetics 2023 6 14 1155211. Priyanka Srivastava, Chitra Bamba, Seema Chopra, Minakshi Rohilla, Chakshu Chaudhry, Anupriya Kaur, Inusha Panigrahi, Kausik Mand |
| A variant in the 5'UTR of ERBB4 is associated with lifespan in Golden Retrievers. GeroScience 2023 10 . Robert B Rebhun, Daniel York, Flora M D De Graaf, Paula Yoon, Kevin L Batcher, Madison E Luker, Stephanie Ryan, Jamie Peyton, Michael S Kent, Joshua A Stern, Danika L Bannas |
| "Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment". Journal of diabetes and its complications 2024 9 38 (11): 108833. Ferda Evin, Tar?k K?rkgöz, Tahir Atik, Güne? Ak, Timur Köse, Caner Kabasakal, Behzat Özkan, Samim Özen, ?ükran Darcan, Damla Gök? |
| [Amyotrophic lateral sclerosis associated with a new pathogenic variant of the ERBB4 gene]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2024 8 124 (7): 165-168. E V Pervushina, M A Kutlubaev, E V Saifullina, E V Gaisina, L A Smakova, I M Khidiyato |
| Integrative analysis of causal associations between neurodegenerative diseases and colorectal cancer. Heliyon 2024 8 10 (15): e35432. Feifan Wang, Lu Chen, Mengke Nie, Zhongxin |
| CDX2-Suppressed Colorectal Cancers Possess Potentially Targetable Alterations in Receptor Tyrosine Kinases and Other Colorectal-Cancer-Associated Pathways. Diseases (Basel, Switzerland) 2024 10 12 (10): . Ioannis A Voutsadak |
| Targeted Genetic Sequencing Analysis of 223 Cases of Pseudomyxoma Peritonei Treated by Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy Shows Survival Related to GNAS and KRAS Status. Cancer medicine 2024 10 13 (20): e70340. Jane Gibson, Reuben J Pengelly, Amatta Mirandari, Konstantinos Boukas, Sophia Stanford, Thomas Desmond Cecil, Faheez Mohamed, Sanjeev Paul Dayal, Alexios Tzivanakis, Brendan John Moran, Alex Mirnezami, Norman John Carr, Sarah Enn |
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