Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: TNR[original query] |
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Absence of association of androgen receptor trinucleotide expansion and poor semen quality. International journal of andrology 2003 1 26 (1): 46-51. Erasmuson Tanya, Sin Iris L, Sin Frank Y |
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases. Journal of neural transmission (Vienna, Austria : 1996) 2005 Apr 112 (4): 539-46. Wu Y R, Fung H C, Lee-Chen G J, Gwinn-Hardy K, Ro L S, Chen S T, Hsieh-Li H M, Lin H Y, Lin C Y, Li S N, Chen C |
TNR/11q#1 trinucleotide (GCC)n repeat alleles and predisposition to acute and chronic leukemia. Annals of human genetics 2004 Jul 68 (Pt 4): 362-6. Klinkov A A, Nikitin E A, Maiorova O V, Ivanov M A, Strelnikov V V, Babenko O V, Zemlyakova V V, Kuznetsova E B, Zaletayev D |
Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia. Schizophrenia research 2005 Oct 78 (2-3): 131-6. Chen Chiung-Mei, Lane Hsien-Yuan, Wu Yih-Ru, Ro Long-Sun, Chen Fen-Lin, Hung Wei-Ling, Hou Yi-Ting, Lin Cheng-Yueh, Huang Shu-Yi, Chen I-Cheng, Soong Bing-Wen, Li Ming-Liang, Hsieh-Li Hsiu-Mei, Su Ming-Tsan, Lee-Chen Guey-J |
Chronic beryllium disease and glutathione biosynthesis genes. Journal of occupational and environmental medicine / American College of Occupational and Environmental Medicine 2006 Jun 48 (6): 599-606. Bekris Lynn M, Viernes Hannah-Malia A, Farin Federico M, Maier Lisa A, Kavanagh Terrance J, Takaro Tim |
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. Neuroscience letters 2006 Apr 397 (3): 234-9. Lorenz Susanne, Heils Armin, Taylor Kirsten P, Gehrmann Anne, Muhle Hiltrud, Gresch Meike, Becker Tim, Tauer Ulrike, Stephani Ulrich, Sander Thom |
Glutamate cysteine ligase catalytic subunit promoter polymorphisms and associations with type 1 diabetes age-at-onset and GAD65 autoantibody levels. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2007 Apr 115 (4): 221-8. Bekris L M, Shephard C, Janer M, Graham J, McNeney B, Shin J, Zarghami M, Griffith W, Farin F, Kavanagh T J, Lernmark |
Impaired glutathione synthesis in schizophrenia: convergent genetic and functional evidence. Proceedings of the National Academy of Sciences of the United States of America 2007 Oct 104 (42): 16621-6. Gysin René, Kraftsik Rudolf, Sandell Julie, Bovet Pierre, Chappuis Céline, Conus Philippe, Deppen Patricia, Preisig Martin, Ruiz Viviane, Steullet Pascal, Tosic Mirjana, Werge Thomas, Cuénod Michel, Do Kim |
Somatic mutations at the trinucleotide repeats of androgen receptor gene in male hepatocellular carcinoma. International journal of cancer. Journal international du cancer 2007 Apr 120 (8): 1610-7. Yeh Shiou-Hwei, Chiu Chi-Ming, Chen Chi-Ling, Lu Shu-Fen, Hsu Hey-Chi, Chen Ding-Shinn, Chen Pei-J |
Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study. Molecular psychiatry 2009 Aug 14 (8): 804-19. Lavedan C, Licamele L, Volpi S, Hamilton J, Heaton C, Mack K, Lannan R, Thompson A, Wolfgang C D, Polymeropoulos M |
Lung function loss, smoking, vitamin C intake, and polymorphisms of the glutamate-cysteine ligase genes. American journal of respiratory and critical care medicine 2008 Jul 178 (1): 13-9. Siedlinski Mateusz, Postma Dirkje S, van Diemen Cleo C, Blokstra Anneke, Smit Henriette A, Boezen H Mari |
Parallel genotyping of 10,204 single nucleotide polymorphisms to screen for susceptible genes for IgA nephropathy. Annals of the Academy of Medicine, Singapore 2009 Oct 38 (10): 894-9. Woo Keng Thye, Lau Yeow Kok, Wong Kok Seng, Zhao Yi, Chan Choong Me |
Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area. Biological psychiatry 2011 Jan 69 (1): 90-6. Kähler Anna K, Djurovic Srdjan, Rimol Lars M, Brown Andrew Anand, Athanasiu Lavinia, Jönsson Erik G, Hansen Thomas, Gústafsson Omar, Hall Håkan, Giegling Ina, Muglia Pierandrea, Cichon Sven, Rietschel Marcella, Pietiläinen Olli P H, Peltonen Leena, Bramon Elvira, Collier David, St Clair David, Sigurdsson Engilbert, Petursson Hannes, Rujescu Dan, Melle Ingrid, Werge Thomas, Steen Vidar M, Dale Anders M, Matthews Russell T, Agartz Ingrid, Andreassen Ole |
Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2012 Jan 37 (2): 557-66. Zuo Lingjun, Gelernter Joel, Zhang Clarence K, Zhao Hongyu, Lu Lingeng, Kranzler Henry R, Malison Robert T, Li Chiang-Shan R, Wang Fei, Zhang Xiang-Yang, Deng Hong-Wen, Krystal John H, Zhang Fengyu, Luo Xinggua |
Trinucleotide Repeat Expansion in the TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy in Japanese. Investigative ophthalmology & visual science 2015 Jul 56 (8): 4865-9. Nakano Masakazu, Okumura Naoki, Nakagawa Hiroko, Koizumi Noriko, Ikeda Yoko, Ueno Morio, Yoshii Kengo, Adachi Hiroko, Aleff Ross A, Butz Malinda L, Highsmith W Edward, Tashiro Kei, Wieben Eric D, Kinoshita Shigeru, Baratz Keith |
A cross-species genetic analysis identifies candidate genes for mouse anxiety and human bipolar disorder. Frontiers in behavioral neuroscience 2015 9 171. Ashbrook David G, Williams Robert W, Lu Lu, Hager Reinm |
Functional enrichment analysis of three Alzheimer's disease genome-wide association studies identities DAB1 as a novel candidate liability/protective gene. Biochemical and biophysical research communications 2015 Aug 463 (4): 490-5. Gao Hui, Tao Yu, He Qin, Song Fan, Saffen Dav |
Genetic Polymorphism Associated Prefrontal Glutathione and Its Coupling With Brain Glutamate and Peripheral Redox Status in Early Psychosis. Schizophrenia bulletin 2016 09 42 (5): 1185-96. Xin Lijing, Mekle Ralf, Fournier Margot, Baumann Philipp S, Ferrari Carina, Alameda Luis, Jenni Raoul, Lu Huanxiang, Schaller Benoit, Cuenod Michel, Conus Philippe, Gruetter Rolf, Do Kim |
Mutation analysis of 6 spinocerebellar ataxia (SCA) types in patients from southern Turkey. Turkish journal of medical sciences 2015 45 (6): 1228-33. Pazarci Perçin, Kasap Halil, Koç Ay?e Filiz, Altunba?ak Sakir, Erkoç Mehmet A |
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 |
A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene.
Translational psychiatry 2018 12 8 (1): 284. Hawi Ziarih, Yates Hannah, Pinar Ari, Arnatkeviciute Aurina, Johnson Beth, Tong Janette, Pugsley Kealan, Dark Callum, Pauper Marc, Klein Marieke, Heussler Helen S, Hiscock Harriet, Fornito Alex, Tiego Jeggan, Finlay Amy, Vance Alasdair, Gill Michael, Kent Lindsey, Bellgrove Mark |
Genome-wide analysis of disease progression in age-related macular degeneration.
Human molecular genetics 2018 Mar 27 (5): 929-940. Yan Qi, Ding Ying, Liu Yi, Sun Tao, Fritsche Lars G, Clemons Traci, Ratnapriya Rinki, Klein Michael L, Cook Richard J, Liu Yu, Fan Ruzong, Wei Lai, Abecasis Gonçalo R, Swaroop Anand, Chew Emily Y, , Weeks Daniel E, Chen W |
Trinucleotide repeat expansion in the transcription factor 4 (TCF4) gene in Thai patients with Fuchs endothelial corneal dystrophy. Eye (London, England) 2019 Sep . Okumura Naoki, Puangsricharern Vilavun, Jindasak Raina, Koizumi Noriko, Komori Yuya, Ryousuke Hayashi, Nakahara Makiko, Nakano Masakazu, Adachi Hiroko, Tashiro Kei, Yoshii Kengo, Chantaren Patchima, Ittiwut Rungnapa, Shotelersuk Vorasuk, Suphapeetiporn Kan |
Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy. Cornea 2019 Apr . Okumura Naoki, Hayashi Ryousuke, Nakano Masakazu, Tashiro Kei, Yoshii Kengo, Aleff Ross, Butz Malinda, Highsmith Edward W, Wieben Eric D, Fautsch Michael P, Baratz Keith H, Komori Yuya, Ueda Emi, Nakahara Makiko, Weller Julia, Tourtas Theofilos, Schlötzer-Schrehardt Ursula, Kruse Friedrich, Koizumi Nori |
Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal Dystrophy. Investigative ophthalmology & visual science 2019 2 60 (2): 779-786. Okumura Naoki, Hayashi Ryosuke, Nakano Masakazu, Yoshii Kengo, Tashiro Kei, Sato Takahiko, Blake Derek J, Aleff Ross, Butz Malinda, Highsmith Edward W, Wieben Eric D, Fautsch Michael P, Baratz Keith H, Komori Yuya, Nakahara Makiko, Tourtas Theofilos, Schlötzer-Schrehardt Ursula, Kruse Friedrich, Koizumi Nori |
Role of ATG16LI (rs2241880) and Interleukin 10 (rs1800872) Polymorphisms in Breast Cancer Among Egyptian Patients. The Egyptian journal of immunology 2020 Jan 27 (1): 65-76. El-Amir Mostafa I, Wahman Mohammed M, Khaled Hanan A, El-Feky Mohamed |
Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort.
Molecular brain 2021 Jan 14 (1): 3. Liang Xiao, Cheng ShiQiang, Ye Jing, Chu XiaoMeng, Wen Yan, Liu Li, Qi Xin, Jia YuMeng, Zhang Fe |
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients. Clinical neurology and neurosurgery 2021 Jan 202 106487. Albuz Burcu, Ozdemir Ozturk, Silan Fat |
Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Frontiers in cardiovascular medicine 2022 2 8 811156. Zhou Yue, Bai Kai, Wang Yu, Meng Zhuo, Zhou Shuang, Jiang Shiwei, Wang Hualin, Wang Jian, Yang Mei, Wang Qingjie, Sun Kun, Chen S |
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort. Neurogenetics 2023 11 . Nishu Tyagi, Bharathram Uppili, Pooja Sharma, Shaista Parveen, Sheeba Saifi, Abhinav Jain, Akhilesh Sonakar, Istaq Ahmed, Shweta Sahni, Uzma Shamim, Avni Anand, Varun Suroliya, Vivekanand Asokachandran, Achal Srivastava, Sridhar Sivasubbu, Vinod Scaria, Mohammed Far |
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- Page last updated:Mar 25, 2024
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