Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 122 Records) |
Query Trace: TCF4[original query] |
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Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
Genetic variant rs613872 in transcription factor 4 (TCF4) is not associated with primary open-angle glaucoma. Eye (London, England) 2020 Apr . Kondkar Altaf A, Azad Taif A, Sultan Tahira, Osman Essam A, Almobarak Faisal A, Al-Obeidan Saleh |
Association between KCNQ2, TCF4 and RGS18 polymorphisms and silent brain infarction based on whole?exome sequencing. Molecular medicine reports 2020 Feb . Kim Jung Oh, Lee Kee Ook, Kim Hyun Woo, Park Han Sung, Kim Jinkwon, Sung Jung Hoon, Oh Doyeun, Kim Ok Joon, Kim Nam Ke |
Association between a TCF4 Polymorphism and Susceptibility to Schizophrenia. BioMed research international 2020 4 2020 1216303. Gao Jia-Yang, Ma Pan, Li Ying, Yan Chun-Xia, Zhang Qian, Yang Xi-Xi, Shi Qiang, Zhang Bao, Wen Xiao-Pe |
Genetic Determinants of Gating Functions: Do We Get Closer to Understanding Schizophrenia Etiopathogenesis? Frontiers in psychiatry 2020 12 11 550225. Rovný Rastislav, Besterciová Dominika, Rie?anský Ig |
Pro64His (rs4644) Polymorphism Within Galectin-3 Is a Risk Factor of Differentiated Thyroid Carcinoma and Affects the Transcriptome of Thyrocytes Engineered via CRISPR/Cas9 System. Thyroid : official journal of the American Thyroid Association 2020 Dec . Corrado Alda, Aceto Romina, Silvestri Roberto, Dell'Anno Irene, Ricci Benedetta, Miglietta Simona, Romei Cristina, Giovannoni Roberto, Poliseno Laura, Evangelista Monica, Vitiello Marianna, Cipollini Monica, Garritano Sonia, Giusti Laura, Zallocco Lorenzo, Elisei Rossella, Landi Stefano, Gemignani Federi |
[Genetic analysis of a case with Pitt-Hopkins syndrome due to variant of TCF4 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 11 37 (11): 1253-1256. Ma Jian, Zhang Huawei, Zhang Kaihui, Lyu Yuqiang, Gao Min, Wang Dong, Gai Zhongtao, Liu |
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 |
Causal links between major depressive disorder and insomnia: A Mendelian randomisation study. Gene 2020 10 768 145271. Cai Lei, Bao Yiran, Fu Xiaoqian, Cao Hongbao, Baranova Ancha, Zhang Xiangrong, Sun Jing, Zhang Fuqu |
Transcription factor 4 (TCF4) expression predicts clinical outcome in RUNX1 mutated and translocated acute myeloid leukemia. Haematologica 2020 10 105 (9): e454-457. In't Hout Florentien E M, Gerritsen Mylène, Bullinger Lars, Van der Reijden Bert A, Huls Gerwin, Vellenga Edo, Jansen Joop |
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 |
Causal influences of neuroticism on mental health and cardiovascular disease. Human genetics 2021 May . Zhang Fuquan, Baranova Ancha, Zhou Chao, Cao Hongbao, Chen Jiu, Zhang Xiangrong, Xu Mingqi |
Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer. International journal of molecular sciences 2021 3 22 (4): . Skopelitou Diamanto, Miao Beiping, Srivastava Aayushi, Kumar Abhishek, Kuswick Magdalena, Dymerska Dagmara, Paramasivam Nagarajan, Schlesner Matthias, Lubinski Jan, Hemminki Kari, Försti Asta, Bandapalli Obul Red |
Novel Genetic Variant Predicts Surgical Recurrence Risk in Crohn's Disease Patients.
Inflammatory bowel diseases 2021 . Wang Ming-Hsi, Friton Jessica J, Raffals Laura E, Leighton Jonathan A, Pasha Shabana F, Picco Michael F, Monroe Kelly, Nix Billy D, Newberry Rodney D, Faubion William |
Whole genome sequencing of 45 Japanese patients with intellectual disability. American journal of medical genetics. Part A 2021 2 185 (5): 1468-1480. Abe-Hatano Chihiro, Iida Aritoshi, Kosugi Shunichi, Momozawa Yukihide, Terao Chikashi, Ishikawa Keiko, Okubo Mariko, Hachiya Yasuo, Nishida Hiroya, Nakamura Kazuyuki, Miyata Rie, Murakami Chie, Takahashi Kan, Hoshino Kyoko, Sakamoto Haruko, Ohta Sayaka, Kubota Masaya, Takeshita Eri, Ishiyama Akihiko, Nakagawa Eiji, Sasaki Masayuki, Kato Mitsuhiro, Matsumoto Naomichi, Kamatani Yoichiro, Kubo Michiaki, Takahashi Yoshiyuki, Natsume Jun, Inoue Ken, Goto Yu-Ic |
Genomic Analysis of Korean Patient With Microcephaly. Frontiers in genetics 2021 2 11 543528. Lee Jiwon, Park Jong Eun, Lee Chung, Kim Ah Reum, Kim Byung Joon, Park Woong-Yang, Ki Chang-Seok, Lee Jeeh |
Impact of TCF4 Repeat Number on Resolution of Corneal Edema after Descemet's Stripping Only in Fuchs Dystrophy: A Pilot Study. Vision (Basel, Switzerland) 2021 Oct 5 (4): . Spiteri Natasha, Hirnschall Nino, van Bysterveldt Katherine, Hou Alec Lin, Moloney Gregory, Ball Matthew, Vincent Andrea |
TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy. Acta ophthalmologica 2021 10 100 (5): 541-548. Viberg Andreas, Westin Ida Maria, Golovleva Irina, Byström Ber |
Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. BMC genomics 2022 May 23 (1): 385. Feng Yen-Chen A, Stanaway Ian B, Connolly John J, Denny Joshua C, Luo Yuan, Weng Chunhua, Wei Wei-Qi, Weiss Scott T, Karlson Elizabeth W, Smoller Jordan |
TF and TCF4 gene polymorphisms are linked to autism spectrum disorder: a case-control study. The Journal of international medical research 2022 11 50 (11): 3000605221138492. Azmerin Maria, Hussain Md Saddam, Aziz Md Abdul, Barek Md Abdul, Begum Mobashera, Sen Niloy, Rahman Md Abdur, Shahriar Mohammad, Baeesa Saleh Salem, Ashraf Ghulam Md, Islam Mohammad Safiq |
Overlap between genetic variants associated with schizophrenia spectrum disorders and intelligence quotient: a systematic review. Journal of psychiatry & neuroscience : JPN 2022 11 47 (6): E393-E408. Murillo-García Nancy, Barrio-Martínez Sara, Setién-Suero Esther, Soler Jordi, Papiol Sergi, Fatjó-Vilas Mar, Ayesa-Arriola Ro |
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinics. American journal of medical genetics. Part A 2022 11 191 (2): 510-517. Mainali Apurba, Athey Taryn, Bahl Shalini, Hung Clara, Caluseriu Oana, Chan Alicia, Eaton Alison, Ghai Shailly Jain, Kannu Peter, MacPherson Melissa, Niederhoffer Karen Y, Siriwardena Komudi, Mercimek-Andrews Saad |
Loss of Corneal Nerves and Corneal Haze in Patients with Fuchs' Endothelial Corneal Dystrophy with the Transcription Factor 4 Gene Trinucleotide Repeat Expansion. Ophthalmology science 2022 10 3 (1): 100214. Gillings Matthew, Mastro Andrew, Zhang Xunzhi, Kiser Kelly, Gu Jane, Xing Chao, Robertson Danielle M, Petroll W Matthew, Mootha V Vin |
Sequence Analysis of Transcription Factor 7-like 2 Protein (TCF7L2) in Iraqi Patients with Diabetic Mellitus Type 2 Using Bioinformatics Methods. Archives of Razi Institute 2022 1 76 (4): 841-846. Kareem Queen B, Abdullah Al-Janabi |
Genetic Polymorphisms in miR-137 and Its Target Genes, TCF4 and CACNA1C, Contribute to the Risk of Bipolar Disorder: A Preliminary Case-Control Study and Bioinformatics Analysis. Disease markers 2022 2022 1886658. Mokhtari Mohammad Ali, Sargazi Saman, Saravani Ramin, Heidari Nia Milad, Mirinejad Shekoufeh, Hadzsiev Kinga, Bene Judit, Shakiba Manso |
Polygenic Risk Score and Rare Variant Burden Identified by Targeted Sequencing in a Group of Patients with Pigment Epithelial Detachment in Age-Related Macular Degeneration. Genes 2023 9 14 (9): . Anna W?sowska, Adam Sendecki, Anna Boguszewska-Chachulska, S?awomir Tep |
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. Research square 2023 5 . Neal Peachey, Bryan Gorman, Michael Francis, Cari Nealon, Christopher Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro Hysi, Hélène Choquet, Natalie Afshari, Yi-Ju Li, J Michael Gaziano, Adriana Hung, Wen-Chih Wu, Paul Greenberg, Saiju Pyarajan, Jonathan Lass, Sudha Iyeng |
Identification of endothelial-related molecular subtypes for bladder cancer patients. Frontiers in oncology 2023 4 13 1101055. Li Deng-Xiong, Feng De-Chao, Shi Xu, Wu Rui-Cheng, Chen Kai, Han Pi |
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 |
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation. Communications biology 2024 4 7 (1): 418. Bryan R Gorman, Michael Francis, Cari L Nealon, Christopher W Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro G Hysi, Hélène Choquet, Natalie A Afshari, Yi-Ju Li, , J Michael Gaziano, Adriana M Hung, Wen-Chih Wu, Paul B Greenberg, Saiju Pyarajan, Jonathan H Lass, Neal S Peachey, Sudha K Iyeng |
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- Page last updated:Apr 22, 2024
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