Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Goiter and TPO[original query] |
---|
Interactions of HLA-DRB4 and CTLA-4 genes influence thyroid function in Hashimoto's thyroiditis in Japanese population. Journal of endocrinological investigation 2003 Dec 26 (12): 1208-12. Terauchi M, Yanagawa T, Ishikawa N, Ito K, Fukazawa T, Maruyama H, Saruta |
Functional analysis of thyroid peroxidase gene mutations detected in patients with thyroid dyshormonogenesis. International journal of endocrinology 2014 2014 390121. Guria Srikanta, Bankura Biswabandhu, Balmiki Nisha, Pattanayak Arup Kumar, Das Tapas Kumar, Sinha Anirban, Chakrabarti Sudipta, Chowdhury Subhankar, Das Madhusud |
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
PLoS genetics 2014 Feb 10 (2): e1004123. Medici Marco, Porcu Eleonora, Pistis Giorgio, Teumer Alexander, Brown Suzanne J, Jensen Richard A, Rawal Rajesh, Roef Greet L, Plantinga Theo S, Vermeulen Sita H, Lahti Jari, Simmonds Matthew J, Husemoen Lise Lotte N, Freathy Rachel M, Shields Beverley M, Pietzner Diana, Nagy Rebecca, Broer Linda, Chaker Layal, Korevaar Tim I M, Plia Maria Grazia, Sala Cinzia, Völker Uwe, Richards J Brent, Sweep Fred C, Gieger Christian, Corre Tanguy, Kajantie Eero, Thuesen Betina, Taes Youri E, Visser W Edward, Hattersley Andrew T, Kratzsch Jürgen, Hamilton Alexander, Li Wei, Homuth Georg, Lobina Monia, Mariotti Stefano, Soranzo Nicole, Cocca Massimiliano, Nauck Matthias, Spielhagen Christin, Ross Alec, Arnold Alice, van de Bunt Martijn, Liyanarachchi Sandya, Heier Margit, Grabe Hans Jörgen, Masciullo Corrado, Galesloot Tessel E, Lim Ee M, Reischl Eva, Leedman Peter J, Lai Sandra, Delitala Alessandro, Bremner Alexandra P, Philips David I W, Beilby John P, Mulas Antonella, Vocale Matteo, Abecasis Goncalo, Forsen Tom, James Alan, Widen Elisabeth, Hui Jennie, Prokisch Holger, Rietzschel Ernst E, Palotie Aarno, Feddema Peter, Fletcher Stephen J, Schramm Katharina, Rotter Jerome I, Kluttig Alexander, Radke Dörte, Traglia Michela, Surdulescu Gabriela L, He Huiling, Franklyn Jayne A, Tiller Daniel, Vaidya Bijay, de Meyer Tim, Jørgensen Torben, Eriksson Johan G, O'Leary Peter C, Wichmann Eric, Hermus Ad R, Psaty Bruce M, Ittermann Till, Hofman Albert, Bosi Emanuele, Schlessinger David, Wallaschofski Henri, Pirastu Nicola, Aulchenko Yurii S, de la Chapelle Albert, Netea-Maier Romana T, Gough Stephen C L, Meyer Zu Schwabedissen Henriette, Frayling Timothy M, Kaufman Jean-Marc, Linneberg Allan, Räikkönen Katri, Smit Johannes W A, Kiemeney Lambertus A, Rivadeneira Fernando, Uitterlinden André G, Walsh John P, Meisinger Christa, den Heijer Martin, Visser Theo J, Spector Timothy D, Wilson Scott G, Völzke Henry, Cappola Anne, Toniolo Daniela, Sanna Serena, Naitza Silvia, Peeters Robin |
[DIO2, TPO, CYP1A1 AND CYP1A2 gene polymorphism in women with thyroid disease]. Gigiena i sanitariia 0 (3): 52-6. Kochetova O V, Gaynullina M K, Viktorova T |
Interleukin 1 beta (IL1beta) gene polymorphisms (SNP-511 and SNP+3953) in Hashimoto's thyroiditis among the Polish population. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2014 Oct 122 (9): 544-7. Lacka K, Paradowska-Gorycka A, Maciejewski A, Kramer L, Herman W A, Lacki J |
A novel FoxD3 Variant Is Associated With Vitiligo and Elevated Thyroid Auto-Antibodies. The Journal of clinical endocrinology and metabolism 2015 Aug jc20152126. Schunter Jo Ana, Löffler Dennis, Wiesner Tobias, Kovacs Peter, Badenhoop Klaus, Aust Gabriela, Tönjes Anke, Müller Peter, Baber Ronny, Simon Jan C, Führer Dagmar, Pfäffle Roland W, Thiery Joachim, Stumvoll Michael, Kiess Wieland, Kratzsch Jürgen, Körner Ant |
Genotype-phenotype correlations of dyshormonogenetic goiter in children and adolescents from South India. Indian journal of endocrinology and metabolism 0 20 (6): 816-824. Ramesh Bangaraiah Gari, Bhargav Panchangam Ramakanth, Rajesh Bangaraiah Gari, Devi Nangedda Vimala, Vijayaraghavan Rajagopalan, Varma Bhongir Apar |
Genetic analyses in a cohort of Portuguese pediatric patients with congenital hypothyroidism. Journal of pediatric endocrinology & metabolism : JPEM 2019 8 32 (11): 1265-1273. Santos-Silva Rita, Rosário Marta, Grangeia Ana, Costa Carla, Castro-Correia Cíntia, Alonso Isabel, Leão Miguel, Fontoura Manu |
Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism. Molecular biology reports 2020 Sep . Kollati Yedukondalu, Akella Radha Rama Devi, Naushad Shaik Mohammad, Borkar Divya, Thalla Maunika, Nagalingam Swapna, Lingappa Lokesh, Patel Rajesh K, Reddy G Bhanuprakash, Dirisala Vijaya |
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism. Molecular and cellular endocrinology 2020 2 506 110761. Zhang Rui-Jia, Sun Feng, Chen Feng, Fang Ya, Yan Chen-Yan, Zhang Chang-Run, Ying Ying-Xia, Wang Zheng, Zhang Cao-Xu, Wu Feng-Yao, Han Bing, Liang Jun, Zhao Shuang-Xia, Song Huai-Do |
Antithyroid Antibody Status in Non-Pregnant Adult Bangladeshi Patients with Subclinical Hypothyroidism. Mymensingh medical journal : MMJ 2020 1 29 (1): 156-161. Rafiq-Uddin M, Kamrul-Hasan A B, Asaduzzaman M, Aminul-Islam A K, Islam M, Rauniyar B K, Hoque A, Mustari M, Fariduddin M, Hasanat M |
Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort. Frontiers in endocrinology 2021 9 12 705773. Long Wei, Guo Fang, Yao Ruen, Wang Ying, Wang Huaiyan, Yu Bin, Xue Pe |
Long-Term Outcome of Patients with TPO Mutations. Journal of clinical medicine 2021 9 10 (17): . Tobias Leraz, Elias-Assad Ghadir, Khayat Morad, Admoni Osnat, Almashanu Shlomo, Tenenbaum-Rakover Yarde |
Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis. Frontiers in endocrinology 2021 7 12 657913. Oliver-Petit Isabelle, Edouard Thomas, Jacques Virginie, Bournez Marie, Cartault Audrey, Grunenwald Solange, Savagner Frédériq |
Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. Journal of endocrinological investigation 2021 Nov . Acar S, Gürsoy S, Arslan G, Nalbanto?lu Ö, Hazan F, Köprülü Ö, Özkaya B, Özkan |
Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism. Endocrine 2022 9 79 (1): 125-134. Li Liangshan, Li Xiaole, Wang Xiaoyu, Han Mengmeng, Zhao Dehua, Wang Fang, Liu Shig |
Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China. Clinica chimica acta; international journal of clinical chemistry 2023 6 547 117459. Ting Zhang, Yaping Shen, Yanhua Xu, Dingwen Wu, Chi Chen, Rulai Ya |
Case Report - Multinodular goiter in a patient with Congenital Hypothyroidism and Bannayan-Riley-Ruvalcaba syndrome: the possible synergic role of TPO and PTEN mutation. Frontiers in endocrinology 2023 6 14 1205785. Gaia Vincenzi, Ilenia Teresa Petralia, Marco Abbate, Giulia Tarantola, Silvia Laura Carla Meroni, Riccardo Maggiore, Gilberto Mari, Maria Grazia Patricelli, Marco Schiavo Lena, Graziano Barera, Maria Cristina Vigo |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: