Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 121 Records) |
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Clinical and mutational profiles of adult medulloblastoma groups. Acta neuropathologica communications 2020 Nov 8 (1): 191. Wong Gabriel Chun-Hei, Li Kay Ka-Wai, Wang Wei-Wei, Liu Anthony Pak-Yin, Huang Queenie Junqi, Chan Aden Ka-Yin, Poon Manix Fung-Man, Chung Nellie Yuk-Fei, Wong Queenie Hoi-Wing, Chen Hong, Chan Danny Tat Ming, Liu Xian-Zhi, Mao Ying, Zhang Zhen-Yu, Shi Zhi-Feng, Ng Ho-Keu |
Association of PD-L1 gene polymorphisms and circulating sPD-L1 levels with HBV infection susceptibility and related liver disease progression. Gene 2021 9 806 145935. Xuan Hoan Nghiem, Thi Minh Huyen Pham, Dinh Tung Bui, Phuong Giang Dao, Tat Trung Ngo, Tien Sy Bui, Thi Tuan Nguyen, Thi Ngoc Dung Dang, Reddy Pallerla Srinivas, Velavan Thirumalaisamy P, Hong Bang Mai, Huu Song |
Mismatch repair proteins PMS2 and MLH1 can further refine molecular stratification of IDH-mutant lower grade astrocytomas. Clinical neurology and neurosurgery 2021 8 208 106882. Yang Rui Ryan, Li Kay Ka-Wai, Zhang Zhen-Yu, Chan Aden Ka-Yin, Wang Wei-Wei, Chan Danny Tat-Ming, Li Wen-Cai, Liu Xian-Zhi, Li Fang-Cheng, Chen Hong, Ng Ho-Keung, Mao Ying, Shi Zhi-Fe |
Clinical utility of next-generation sequencing-based ctDNA testing for common and novel ALK fusions. Lung cancer (Amsterdam, Netherlands) 2021 Jul 159 66-73. Mondaca Sebastian, Lebow Emily S, Namakydoust Azadeh, Razavi Pedram, Reis-Filho Jorge S, Shen Ronglai, Offin Michael, Tu Hai-Yan, Murciano-Goroff Yonina, Xu Chongrui, Makhnin Alex, Martinez Andres, Pavlakis Nick, Clarke Stephen, Itchins Malinda, Lee Adrian, Rimner Andreas, Gomez Daniel, Rocco Gaetano, Chaft Jamie E, Riely Gregory J, Rudin Charles M, Jones David R, Li Mark, Shaffer Tristan, Hosseini Seyed Ali, Bertucci Caterina, Lim Lee P, Drilon Alexander, Berger Michael F, Benayed Ryma, Arcila Maria E, Isbell James M, Li Bob |
Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencing. BMC medical genomics 2021 6 14 (1): 165. Davila Jaime I, Chanana Pritha, Sarangi Vivekananda, Fogarty Zachary C, Weroha S John, Guo Ruifeng, Goode Ellen L, Huang Yajue, Wang Ch |
Genetic variants of programmed cell death 1 are associated with HBV infection and liver disease progression. Scientific reports 2021 Apr 11 (1): 7772. Hoan Nghiem Xuan, Huyen Pham Thi Minh, Binh Mai Thanh, Trung Ngo Tat, Giang Dao Phuong, Linh Bui Thuy, Dung Dang Thi Ngoc, Pallerla Srinivas Reddy, Kremsner Peter G, Velavan Thirumalaisamy P, Bang Mai Hong, Song Le H |
Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population. PLoS genetics 2021 Feb 17 (2): e1009323. Yu Mullin Ho Chung, Chan Marcus Chun Yin, Chung Claudia Ching Yan, Li Andrew Wang Tat, Yip Chara Yin Wa, Mak Christopher Chun Yu, Chau Jeffrey Fong Ting, Lee Mianne, Fung Jasmine Lee Fong, Tsang Mandy Ho Yin, Chan Joshua Chun Ki, Wong Wilfred Hing Sang, Yang Jing, Chui William Chun Ming, Chung Patrick Ho Yu, Yang Wanling, Lee So Lun, Chan Godfrey Chi Fung, Tam Paul Kwong Hang, Lau Yu Lung, Tang Clara Sze Man, Yeung Kit San, Chung Brian Hon Y |
Distinctive genomic characteristics in POLE/POLD1-mutant cancers can potentially predict beneficial clinical outcomes in patients who receive immune checkpoint inhibitor. Annals of translational medicine 2021 2 9 (2): 129. He Junjun, Ouyang Wei, Zhao Wugan, Shao Lin, Li Bing, Liu Bihao, Wang Dejuan, Han-Zhang Han, Zhang Zhou, Shao Liang, Li Wenc |
Association of HSD17B13 rs72613567: TA allelic variant with liver disease: review and meta-analysis. BMC gastroenterology 2021 12 21 (1): 490. Tang Shan, Zhang Jing, Mei Ting-Ting, Zhang Wen-Yan, Zheng Su-Jun, Yu Hai-B |
Circulating level of sPD-1 and PD-1 genetic variants are associated with hepatitis B infection and related liver disease progression. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2021 12 115 229-236. Huyen Pham Thi Minh, Dung Dang Thi Ngoc, Weiß Peter Johann, Hoan Phan Quoc, Giang Dao Phuong, Uyen Ngo Thi, Van Tuan Nguyen, Trung Ngo Tat, Velavan Thirumalaisamy P, Song Le Huu, Hoan Nghiem Xu |
Relationship between visceral adipose tissue and genetic mutations (VHL and KDM5C) in clear cell renal cell carcinoma. La Radiologia medica 2021 Jan . Greco Federico, Mallio Carlo Augus |
HIV-1C and HIV-1B Tat protein polymorphism in Southern Brazil. Journal of neurovirology 2021 Jan . de Almeida Sérgio Monteiro, Rotta Indianara, Vidal Luine Rosele Renaud, Dos Santos Jucelia Stadinicki, Nath Avindra, Johnson Kory, Letendre Scott, Ellis Ronald J, |
Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia. Journal of human genetics 2022 9 67 (12): 701-709. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Viana Marcos Borato, Luizon Marcelo Rizzat |
Combinations of Single-Gene Biomarkers Can Precisely Stratify 1,028 Adult Gliomas for Prognostication. Frontiers in oncology 2022 12 839302. Chan Aden Ka-Yin, Shi Zhi-Feng, Li Kay Ka-Wai, Wang Wei-Wei, Chen Hong, Chung Nellie Yuk-Fei, Chan Danny Tat-Ming, Poon Wai-Sang, Loong Herbert Ho-Fung, Liu Xian-Zhi, Zhang Zhen-Yu, Mao Ying, Ng Ho-Keu |
HIV-1 subtype C Tat exon-1 amino acid residue 24K is a signature for neurocognitive impairment. Journal of neurovirology 2022 4 28 (3): 392-403. Ruhanya Vurayai, Jacobs Graeme Brendon, Paul Robert H, Joska John A, Seedat Soraya, Nyandoro George, Glashoff Richard H, Engelbrecht Sus |
ABCB1 gene polymorphisms impact the effect of high-dose intravenous methylprednisolone therapy on optic neuritis associated with AQP4-IgG-positive neuromyelitis optica spectrum disorder. Journal of clinical pharmacy and therapeutics 2022 4 47 (9): 1379-1387. Dai Yuyang, Ni Siyang, Wu Feng, Guo Shaojie, Zhao Xiuli, Wang Jiaw |
Analysis of TNFSF13B polymorphisms and BAFF expression in rheumatoid arthritis and primary Sjögren's syndrome patients. Molecular genetics & genomic medicine 2022 4 10 (6): e1950. Santillán-López Enrique, Muñoz-Valle José Francisco, Oregon-Romero Edith, Espinoza-García Noemí, Treviño-Talavera Beatriz Alejandra, Salazar-Camarena Diana Celeste, Marín-Rosales Miguel, Cruz Alvaro, Alvarez-Gómez Jhonatan Antonio, Sagrero-Fabela Nefertari, Cerpa-Cruz Sergio, Palafox-Sánchez Claudia Azuce |
Molecular landscape of pediatric type IDH wildtype, H3 wildtype hemispheric glioblastomas. Laboratory investigation; a journal of technical methods and pathology 2022 3 102 (7): 731-740. Hong Liang, Shi Zhi-Feng, Li Kay Ka-Wai, Wang Wei-Wei, Yang Rui Ryan, Kwan Johnny Sheung-Him, Chen Hong, Li Fang-Cheng, Liu Xian-Zhi, Chan Danny Tat-Ming, Li Wen-Cai, Zhang Zhen-Yu, Mao Ying, Ng Ho-Keu |
Author Correction: Genetic variants of programmed cell death 1 are associated with HBV infection and liver disease progression. Scientific reports 2022 2 12 (1): 2034. Hoan Nghiem Xuan, Huyen Pham Thi Minh, Binh Mai Thanh, Trung Ngo Tat, Giang Dao Phuong, Linh Bui Thuy, Dung Dang Thi Ngoc, Pallerla Srinivas Reddy, Kremsner Peter G, Velavan Thirumalaisamy P, Bang Mai Hong, Song Le H |
Association between KRAS gene polymorphisms and genetic susceptibility to breast cancer in a Chinese population. Journal of clinical laboratory analysis 2022 12 37 (1): e24806. Jin Min, Lu Fengke, Li Xi, Zhou Wei, Li Sihui, Jiang Yanting, Wu Huiling, Wang Ji |
Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population. Medicine 2022 11 101 (46): e31653. Tran Nam Quang, Truong Steven D, Ma Phat Tung, Hoang Chi Khanh, Le Bao Hoang, Dinh Thang Tat Ngo, Van Tran Luong, Tran Thang Viet, Le Linh Hoang Gia, Le Khuong Thai, Nguyen Hien Thanh, Vu Hoang Anh, Mai Thao Phuong, Do Minh D |
Molecular landscape of IDH-wildtype, H3-wildtype glioblastomas of adolescents and young adults (AYA). Neuropathology and applied neurobiology 2022 Feb . Shi Zhi-Feng, Li Kay Ka-Wai, Huang Queenie Jun-Qi, Wang Wei-Wei, Kwan Johnny Sheung-Him, Chen Hong, Liu Xiang-Zhi, Li Wen-Cai, Chan Danny Tat-Ming, Zhang Zhen-Yu, Mao Ying, Ng Ho-Keu |
A prospective phase 2 study of expeditious EGFR genotyping and immediate therapeutic initiation through extracellular vesicles (EV)-based bronchoalveolar lavage fluid (BALF) liquid biopsy in advanced NSCLC patients. Translational lung cancer research 2023 8 12 (7): 1425-1435. In Ae Kim, Jae Young Hur, Hee Joung Kim, Wan Seop Kim, Kye Young L |
The genetic polymorphisms and activity of glyoxalase 1 as a risk factor for acute coronary syndrome in South Indians with type 2 diabetes mellitus. Gene 2023 8 885 147701. Sushmita Bora, Prashant Shankarrao Adole, Kolar Vishwanath Vinod, Ajith Ananthakrishna Pillai, Shaheer Ahm |
SCN1A Polymorphisms and Haplotypes Are Associated With Valproic Acid Treatment Outcomes in Chinese Children With Epilepsy. Pediatric neurology 2023 7 146 55-64. Jiahao Zhu, Jieluan Lu, Xianhuan Shen, Yaodong He, Hanbing Xia, Wenzhou Li, Huijuan Guo, Jianping Zhang, Xiaomei F |
Clinical application of the AMOY 9-in-1 panel to lung cancer patients. Lung cancer (Amsterdam, Netherlands) 2023 4 179 107190. Kunimasa Kei, Matsumoto Shingo, Kawamura Takahisa, Inoue Takako, Tamiya Motohiro, Kanzaki Ryu, Maniwa Tomohiro, Okami Jiro, Honma Keiichiro, Goto Koichi, Nishino Kazu |
Clinical impact of high platelet reactivity in patients with atrial fibrillation and concomitant percutaneous coronary intervention on dual or triple antithrombotic therapy. Journal of thrombosis and thrombolysis 2023 3 . Berteotti M, Gori A M, Giusti B, Fortini A, Grossi G, Ciardetti N, Migliorini A, Lotti E, Valenti R, Di Mario C, Marchionni N, Marcucci |
Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator.
Frontiers in immunology 2023 2 14 1101488. Cardinale Christopher J, Chang Xiao, Wei Zhi, Qu Hui-Qi, Bradfield Jonathan P, Polychronakos Constantin, Hakonarson Hak |
Factor XII deficiency: a clinical and molecular genetic study. International journal of hematology 2023 1 . Demidova Ekaterina, Salomashkina Valentina, Pshenichnikova Olesya, Selivanova Daria, Yakovleva Elena, Zozulya Nadezda, Gorgidze Lana, Surin Vad |
Rapid and reliable testing for clinically actionable EGFR mutations in non-small cell lung cancer using the Idylla platform: a real-world two-center experience in Greece. Expert review of molecular diagnostics 2024 1 1-10. Kleita Michaelidou, Ioannis Karniadakis, Varvara Pantelaion, Chara Koutoulaki, Eleni Boukla, Konstantinos Folinas, Pantelis Dimaras, Maria A Papadaki, Anastasios V Koutsopoulos, Dimitrios Mavroudis, Christine Vourlakou, Konstantinos Mavridis, Sofia Agela |
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- Page last updated:Apr 22, 2024
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