Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 72 Records) |
| Query Trace: Disease and TSHR[original query] |
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Genome-Wide Association Study of Male Sexual Orientation.
Scientific reports 2017 Dec 7 (1): 16950. Sanders Alan R, Beecham Gary W, Guo Shengru, Dawood Khytam, Rieger Gerulf, Badner Judith A, Gershon Elliot S, Krishnappa Ritesha S, Kolundzija Alana B, Duan Jubao, , Gejman Pablo V, Bailey J Michael, Martin Eden |
| The Role of Cytotoxic T-lymphocyte-associated Protein 4 (CTLA-4) Gene, Thyroid Stimulating Hormone Receptor (TSHR) Gene and Regulatory T-cells as Risk Factors for Relapse in Patients with Graves Disease. Acta medica Indonesiana 2017 Jul 49 (3): 195-204. Eliana Fatimah, Suwondo Pradana, Asmarinah Asmarinah, Harahap Alida, Djauzi Samsuridjal, Prihartono Joedo, Pemayun Tjokorda Gde Dal |
| High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism. PloS one 2018 13 (9): e0204323. Makretskaya Nina, Bezlepkina Olga, Kolodkina Anna, Kiyaev Alexey, Vasilyev Evgeny V, Petrov Vasily, Kalinenkova Svetlana, Malievsky Oleg, Dedov Ivan I, Tiulpakov Anato |
| Analysis of chosen polymorphisms rs2476601 a/G - PTPN22, rs1990760 C/T - IFIH1, rs179247 a/G - TSHR in pathogenesis of autoimmune thyroid diseases in children. Autoimmunity 2018 Jul 1-8. Rydzewska Marta, Góralczyk Aleksandra, Go?cik Joanna, Wawrusiewicz-Kurylonek Natalia, Bossowska Anna, Kr?towski Adam, Bossowski Art |
| Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer. Endocrinology and metabolism (Seoul, Korea) 2018 6 33 (2): 175-184. Hwangbo Yul, Park Young J |
| Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology. The Journal of clinical endocrinology and metabolism 2018 07 103 (7): 2640-2650. Nicolson Norman G, Murtha Timothy D, Dong Weilai, Paulsson Johan O, Choi Jungmin, Barbieri Andrea L, Brown Taylor C, Kunstman John W, Larsson Catharina, Prasad Manju L, Korah Reju, Lifton Richard P, Juhlin C Christofer, Carling Tobi |
| Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis. The Journal of clinical endocrinology and metabolism 2018 3 103 (5): 1889-1898. Zou Minjing, Alzahrani Ali S, Al-Odaib Ali, Alqahtani Mohammad A, Babiker Omer, Al-Rijjal Roua A, BinEssa Huda A, Kattan Walaa E, Al-Enezi Anwar F, Al Qarni Ali, Al-Faham Manar S A, Baitei Essa Y, Alsagheir Afaf, Meyer Brian F, Shi Yuf |
| CEP128 is a crucial risk locus for autoimmune thyroid diseases. Molecular and cellular endocrinology 2019 01 480 97-106. Wang Bin, Jia Xi, Yao Qiuming, Li Qian, He Weiwei, Li Ling, Song Ronghua, Zhang Jing, Zhang Jin- |
| Subclinical thyroid disease and single nucleotide polymorphisms in reproductive-age women in areas of Shanxi Province, China, where iodine exposure is excessive. Asia Pacific journal of clinical nutrition 0 27 (6): 1366-1373. Su Chang, Yu Tianlong, Zhao Rencheng, Wang Yunan, Jia Haihan, Jing Miao, Liu Pe |
| Utility of systematic TSHR gene testing in adults with hyperthyroidism lacking overt autoimmunity and diffuse uptake on thyroid scintigraphy. Clinical endocrinology 2019 Feb 90 (2): 328-333. Patel Kashyap A, Knight Bridget, Aziz Aftab, Babiker Tarig, Tamar Avades, Findlay Joanna, Cox Sue, Dimitropoulos Ioannis, Tysoe Carolyn, Panicker Vijay, Vaidya Bij |
| Clinical Significance of Thyroid-Stimulating Hormone Receptor Gene Mutations and/or Sodium-Iodine Symporter Gene Overexpression in Indeterminate Thyroid Fine Needle Biopsies. Frontiers in endocrinology 2018 10 9 566. Guan Haixia, Matonis Danielle, Toraldo Gianluca, Lee Stephanie |
| Regulation of TSHR Expression in the Thyroid and Thymus May Contribute to TSHR Tolerance Failure in Graves' Disease Patients via Two Distinct Mechanisms. Frontiers in immunology 2019 8 10 1695. Marín-Sánchez Ana, Álvarez-Sierra Daniel, González Oscar, Lucas-Martin Ana, Sellés-Sánchez Alicia, Rudilla Francesc, Enrich Emma, Colobran Roger, Pujol-Borrell Ricar |
| Mutation profiles of follicular thyroid tumors by targeted sequencing. Diagnostic pathology 2019 May 14 (1): 39. Duan Huanli, Liu Xiaoding, Ren Xinyu, Zhang Hui, Wu Huanwen, Liang Zhiyo |
| Correlation of TSHR and CTLA-4 Single Nucleotide Polymorphisms with Graves Disease. International journal of genomics 2019 2019 6982623. Sun Weihua, Zhang Xiaomei, Wu Jing, Zhao Wendi, Zhao Shuangxia, Li Minglo |
| Polymorphisms in TSHR gene and the risk and prognosis of autoimmune thyroid disease in Tunisian population. Acta endocrinologica (Bucharest, Romania : 2005) 0 16 (1): 1-8. Zaaber I, Mestiri S, Marmouch H, Bel Hadj Jrad Tensaout |
| Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism. The Journal of clinical endocrinology and metabolism 2020 Apr . Zhang Qian-Yue, Liu Wei, Li Lu, Du Wen-Hua, Zuo Chun-Lin, Ye Xiao-Ping, Zhou Zheng, Yuan Fei-Fei, Ma Yu-Ru, Sun Feng, Yu Sha-Sha, Xie Hui-Jun, Zhang Chang-Run, Ying Ying-Xia, Yuan Guo-Yue, Gao Guan-Qi, Liang Jun, Zhao Shuang-Xia, Song Huai-Do |
| Genome-wide association study identifies new loci for albuminuria in the Japanese population.
Clinical and experimental nephrology 2020 Apr . Okuda Hiroshi, Okamoto Koji, Abe Michiaki, Ishizawa Kota, Makino Satoshi, Tanabe Osamu, Sugawara Junichi, Hozawa Atsushi, Tanno Kozo, Sasaki Makoto, Tamiya Gen, Yamamoto Masayuki, Ito Sadayoshi, Ishii Tadas |
| DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients. Endocrine connections 2020 12 9 (11): 1121-1134. Sorapipatcharoen Kinnaree, Tim-Aroon Thipwimol, Mahachoklertwattana Pat, Chantratita Wasun, Iemwimangsa Nareenart, Sensorn Insee, Panthan Bhakbhoom, Jiaranai Poramate, Noojarern Saisuda, Khlairit Patcharin, Pongratanakul Sarunyu, Suprasongsin Chittiwat, Korwutthikulrangsri Manassawee, Sriphrapradang Chutintorn, Poomthavorn Preamrud |
| Human leucocyte antigen alleles confer susceptibility and progression to Graves' ophthalmopathy in a Southern Chinese population. The British journal of ophthalmology 2020 Nov . Huang Xiaosheng, Liu Guiqin, Mei Shaoyi, Cai Jiamin, Rao Jing, Tang Minzhong, Zhu Tianhui, Chen Wenchiew, Peng Shiming, Wang Yan, Ye Ye, Zhang Tong, Deng Zhihui, Zhao J |
| Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population. Frontiers in endocrinology 2021 12 695426. Huang Miao, Lu Xiyan, Dong Guoqing, Li Jianxu, Chen Chengcong, Yu Qiuxia, Li Mingzhu, Su Yuey |
| Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review. Inquiry : a journal of medical care organization, provision and financing 2021 12 58 469580211067943. Da Dong-Zhu, Wang Ye, Wang Min, Long Zhi, Wang Qian, Liu J |
| High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing. NPJ breast cancer 2022 6 8 (1): 76. Kostecka Anna, Nowikiewicz Tomasz, Olszewski Pawe?, Koczkowska Magdalena, Horbacz Monika, Heinzl Monika, Andreou Maria, Salazar Renato, Mair Theresa, Madanecki Piotr, Gucwa Magdalena, Davies Hanna, Skokowski Jaros?aw, Buckley Patrick G, P?ksa Rafa?, ?rutek Ewa, Szylberg ?ukasz, Hartman Johan, Jankowski Micha?, Zegarski Wojciech, Tiemann-Boege Irene, Dumanski Jan P, Piotrowski Arkadiu |
| Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis. Endocrine 2022 5 77 (1): 86-101. Molina Maricel F, Papendieck Patricia, Sobrero Gabriela, Balbi Viviana A, Belforte Fiorella S, Martínez Elena Bueno, Adrover Ezequiela, Olcese María C, Chiesa Ana, Miras Mirta B, González Verónica G, Pio Mauricio Gomes, González-Sarmiento Rogelio, Targovnik Héctor M, Rivolta Carina |
| Interactions between Polygenetic Variants and Lifestyle Factors in Hypothyroidism: A Hospital-Based Cohort Study. Nutrients 2023 9 15 (17): . Da Sol Kim, Sunmin Pa |
| Evaluation of the etiology of subclinical hypothyroidism in children. Journal of pediatric endocrinology & metabolism : JPEM 2024 8 . Ay?e Ya?ar, Esma Ebru Altun, Heves K?rm?z?bekmez, Fatma Durs |
| TSHR Gene (rs179247) Polymorphism and Susceptibility to Autoimmune Thyroid Disease: A Systematic Review and Meta-Analysis. Endocrinology and metabolism (Seoul, Korea) 2024 8 . Hendra Zufry, Timotius Ivan Hariyan |
| Prognostic Model for High-Grade Neuroendocrine Carcinoma of the Lung Incorporating Genomic Profiling and Poly (ADP-ribose) Polymerase-1 Expression. JCO precision oncology 2024 4 8 e2300495. Hye Sook Kim, Jong Kwang Kim, Jeong Hyeon Lee, Young Joo Lee, Geon-Kuk Lee, Ji-Youn H |
| Transcriptomic analysis reveals a critical role for activating G? mutations in spontaneous feline hyperthyroidism. Scientific reports 2024 11 14 (1): 28749. Thomas K Hiron, Joana Aguiar, Jonathan M Williams, Sara Falcone, Paul A Norman, Jonathan Elliott, Robert C Fowkes, Harriet M Syme, Lucy J Davis |
| STAT3 single-nucleotide variants in autoimmune thyroid disease in the Pakhtun population of Khyber Pakhtunkhwa, Pakistan. Gene reports 2024 10 36 . Khayyam Khan, Muhammad Zahid, Niaz Ali, Sobia Attaullah, Mujeeb Ullah, Khalid Khan, Ijaz Muhammad, Ali Abusharha, Michael Aschner, Haroon Kh |
| Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T knock-in model. JCI insight 2024 1 . Kristiina Makkonen, Meeri Jännäri, Luís Crisóstomo, Matilda Kuusi, Konrad Patyra, Vladyslav Melnyk, Veli M Linnossuo, Johanna O Ojala, Rowmika Ravi, Christoffer Löf, Juho-Antti Mäkelä, Päivi J Miettinen, Saila Laakso, Marja Ojaniemi, Jarmo Jääskeläinen, Markku Laakso, Filip Bossowski, Beata Sawicka, Karolina Sto?ek, Artur Bossowski, Gunnar Kleinau, Patrick Scheerer, Finngen Finngen, Mary Pat Reeve, Jukka Ke |
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