Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 46 Records) |
| Query Trace: Disease and TCF4[original query] |
|---|
| Correlation of Severity of Fuchs Endothelial Corneal Dystrophy With Triplet Repeat Expansion in TCF4. JAMA ophthalmology 2015 Sep 1-6. Soliman Ahmed Z, Xing Chao, Radwan Salma H, Gong Xin, Mootha V Vin |
| Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India. Molecular vision 2015 21 1252-60. Gupta Ranjan, Kumawat Babu Lal, Paliwal Preeti, Tandon Radhika, Sharma Namrata, Sen Seema, Kashyap Seema, Nag Tapas Chandra, Vajpayee Rasik B, Sharma Arundha |
| Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level. BioMed research international 2015 2015 640234. O?dak Monika, Ruszkowska Ewelina, Udziela Monika, Ozi?b?o Dominika, Bi?czyk Ewelina, ?cie?y?ska Aneta, P?oski Rafa?, Szaflik Jacek |
| Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia. Translational psychiatry 2016 6 e724. Wright C, Gupta C N, Chen J, Patel V, Calhoun V D, Ehrlich S, Wang L, Bustillo J R, Perrone-Bizzozero N I, Turner J |
| Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy. Investigative ophthalmology & visual science 2017 Sep 58 (11): 4579-4585. Mootha V Vinod, Hansen Brock, Rong Ziye, Mammen Pradeep P, Zhou Zhengyang, Xing Chao, Gong X |
| TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases. PloS one 2017 12 (8): e0183719. Kuot Abraham, Hewitt Alex W, Snibson Grant R, Souzeau Emmanuelle, Mills Richard, Craig Jamie E, Burdon Kathryn P, Sharma Shiwa |
| Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response. Schizophrenia research 2017 Dec . Quednow Boris B, Ejebe Kenechi, Wagner Michael, Giakoumaki Stella G, Bitsios Panos, Kumari Veena, Roussos Pan |
| Association of polymorphisms in the intron of TCF4 gene to late-onset Fuchs endothelial corneal dystrophy: An Indian cohort study. Indian journal of ophthalmology 2017 Oct 65 (10): 931-935. Rao Bhavna S, Tharigopala Arokiasamy, Rachapalli Sudhir R, Rajagopal Rama, Soumittra Nagasa |
| Instability of TCF4 Triplet Repeat Expansion With Parent-Child Transmission in Fuchs' Endothelial Corneal Dystrophy. Investigative ophthalmology & visual science 2018 8 59 (10): 4065-4070. Saade Joanna S, Xing Chao, Gong Xin, Zhou Zhengyang, Mootha V Vin |
| Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4. PloS one 2018 13 (7): e0200005. Wieben Eric D, Aleff Ross A, Tang Xiaojia, Kalari Krishna R, Maguire Leo J, Patel Sanjay V, Baratz Keith H, Fautsch Michael |
| Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1. Investigative ophthalmology & visual science 2018 Jun 59 (7): 3053-3057. Winkler Nelson S, Milone Margherita, Martinez-Thompson Jennifer M, Raja Harish, Aleff Ross A, Patel Sanjay V, Fautsch Michael P, Wieben Eric D, Baratz Keith |
| Analysis of candidate genes ZEB1 and LOXHD1 in late-onset Fuchs' endothelial corneal dystrophy in an Indian cohort. Ophthalmic genetics 2018 May 1-7. Rao Bhavna S, Ansar Samdani, Arokiasamy Tharigopala, Sudhir Rachapalli R, Umashankar Vetrivel, Rajagopal Rama, Soumittra Nagasa |
| Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. European journal of human genetics : EJHG 2018 Apr . Mary Laura, Piton Amélie, Schaefer Elise, Mattioli Francesca, Nourisson Elsa, Feger Claire, Redin Claire, Barth Magali, El Chehadeh Salima, Colin Estelle, Coubes Christine, Faivre Laurence, Flori Elisabeth, Geneviève David, Capri Yline, Perrin Laurence, Fabre-Teste Jennifer, Timbolschi Dana, Verloes Alain, Olaso Robert, Boland Anne, Deleuze Jean-François, Mandel Jean-Louis, Gerard Bénédicte, Giurgea Iri |
| Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy. PloS one 2019 7 14 (7): e0219446. Wieben Eric D, Aleff Ross A, Basu Shubham, Sarangi Vivekananda, Bowman Brett, McLaughlin Ian J, Mills John R, Butz Malinda L, Highsmith Edward W, Ida Cristiane M, Ekholm Jenny M, Baratz Keith H, Fautsch Michael |
| Dataset on transcriptome profiling of corneal endothelium from patients with Fuchs endothelial corneal dystrophy. Data in brief 2019 6 25 104047. Nikitina Anastasia S, Belodedova Alexandra V, Malyugin Boris E, Sharova Elena I, Kostryukova Elena S, Larin Andrey K, Veselovsky Vladimir A, Antonova Olga P, Skorodumova Liubov |
| Genetic variants and cognitive functions in patients with brain tumors. Neuro-oncology 2019 May . Correa Denise D, Satagopan Jaya, Martin Axel, Braun Erica, Kryza-Lacombe Maria, Cheung Kenneth, Sharma Ajay, Dimitriadoy Sofia, O'Connell Kelli, Leong Siok, Karimi Sasan, Lyo John, DeAngelis Lisa M, Orlow Ire |
| Evaluation of Single-Nucleotide Polymorphisms of Transcription Factor 7-Like 2 and ATP2B1 Genes as Cardiovascular Risk Predictors in Chronic Kidney Disease. International journal of applied & basic medical research 0 9 (4): 221-225. Kulkarni Sweta, Lenin M, Ramesh R, Delphine Silvia Cr Wilma, Velu Kuzhand |
| Genotype Variations of rs13381800 in TCF4 Gene and rs17039988 in NRXN1 Gene among a Sample of Iranian Patients with Schizophrenia. Iranian journal of psychiatry 2020 2 14 (4): 265-273. Agahi Mohadeseh, Noormohammadi Zahra, Salahshourifar Iman, Mahdavi Hezaveh Nilouf |
| [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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Increased Risk of Glaucoma in Fuchs Endothelial Corneal Dystrophy Is Independent of TCF4 Trinucleotide Repeat Expansion. Cornea 2024 9 . Chao Xing, Sara Schultis, Vladyslav Bondar, Xin Gong, Jess T Whitson, V Vinod Moot |
| Prevalence of Transcription Factor 4 Gene Triplet Repeat Expansion Associated with Fuchs' Endothelial Corneal Dystrophy in the United States and Global Populations. Ophthalmology science 2024 12 5 (1): 100611. Xunzhi Zhang, Ashwani Kumar, Xin Gong, Chao Xing, V Vinod Moot |
- Page last reviewed:Feb 1, 2024
- Content source: