Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 104 Records) |
Query Trace: PAX8[original query] |
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GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
Human molecular genetics 2023 3 32 (12): 2103-2116. Koel Mariann, Võsa Urmo, Jõeloo Maarja, Läll Kristi, Gualdo Natàlia P, Laivuori Hannele, Lemmelä Susanna, , Daly Mark, Palta Priit, Mägi Reedik, Laisk Tri |
Diagnostic and prognostic value of a 7-panel mutation testing in thyroid nodules with indeterminate cytology: the SWEETMAC study. Endocrine 2020 Jul . Bardet Stéphane, Goardon Nicolas, Lequesne Justine, Vaur Dominique, Ciappuccini Renaud, Leconte Alexandra, Monpeyssen Hervé, Saguet-Rysanek Virginie, Clarisse Bénédicte, Lasne-Cardon Audrey, Ménégaux Fabrice, Leenhardt Laurence, Buffet Camil |
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 |
Genetic differences in follicular thyroid carcinoma between Asian and Western countries: a systematic review. Gland surgery 2020 11 9 (5): 1813-1826. Odate Toru, Oishi Naoki, Vuong Huy Gia, Mochizuki Kunio, Kondo Tets |
Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing. Endocrine journal 2021 7 68 (12): 1411-1419. Watanabe Daisuke, Yagasaki Hideaki, Narusawa Hiromune, Saito Tomohiro, Mitsui Yumiko, Miyake Kunio, Ohta Masanori, Inukai Takes |
High Prevalence of DICER1 Mutations and Low Frequency of Gene Fusions in Pediatric Follicular-Patterned Tumors of the Thyroid. Endocrine pathology 2021 7 32 (3): 336-346. Bae Ja-Seong, Jung Seung-Hyun, Hirokawa Mitsuyoshi, Bychkov Andrey, Miyauchi Akira, Lee Sohee, Chung Yeun-Jun, Jung Chan Kw |
HMGA2 rs968697 T?>?C polymorphism is associated with the risk of colorectal cancer. Nucleosides, nucleotides & nucleic acids 2021 7 40 (8): 821-828. Gao Xueren, Wang Xiaoti |
Total thyroidectomy can still remain the method of choice in some Bethesda III cases. Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2021 Jul . Lukas Jindrich, Hintnausova Barbora, Sykorova Vlasta, Syrucek Martin, Maly Marek, Duskova Jarosla |
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Scientific reports 2021 7 11 (1): 14633. Foo Heidi, Thalamuthu Anbupalam, Jiang Jiyang, Koch Forrest C, Mather Karen A, Wen Wei, Sachdev Perminder |
Testing of mutations on thyroid nodules with indeterminate cytology: A prospective study of 112 patients in Argentina. Endocrinologia, diabetes y nutricion 2021 6 . Tolaba Norma, Spedaletti Yamila, Bazzoni Paola, Galindez Macarena, Cerioni Valeria, Santillan Cecilia, Richter Gilda, Herrera Cecilia, Sanchez Laura, Van Cauwlaert Leopoldo, Toscano Marta A, Nallar Marcelo, Monteros Alvi Marcelo, Moya Christian Mart |
Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children (Basel, Switzerland) 2021 6 8 (6): . Alcántara-Ortigoza Miguel Angel, Sánchez-Verdiguel Iraís, Fernández-Hernández Liliana, Enríquez-Flores Sergio, González-Núñez Aidy, Hernández-Martínez Nancy Leticia, Sánchez Carmen, González-Del Angel Ariad |
PAX8/PAX8-AS1 DNA methylation levels are associated with objective sleep duration in persons with unexplained hypersomnolence using a deep phenotyping approach. Sleep 2021 6 44 (10): . Plante David T, Papale Ligia A, Madrid Andy, Cook Jesse D, Prairie Michael L, Alisch Reid |
NTRK Fusion Genes in Thyroid Carcinomas: Clinicopathological Characteristics and Their Impacts on Prognosis. Cancers 2021 4 13 (8): . Pekova Barbora, Sykorova Vlasta, Mastnikova Karolina, Vaclavikova Eliska, Moravcova Jitka, Vlcek Petr, Lastuvka Petr, Taudy Milos, Katra Rami, Bavor Petr, Kodetova Daniela, Chovanec Martin, Drozenova Jana, Astl Jaromir, Hrabal Petr, Vcelak Josef, Bendlova Be |
Association of genomic variants at PAX8 and PBX2 with cervical cancer risk. International journal of cancer 2021 4 . Ramachandran Dhanya, Wang Yingying, Schürmann Peter, Hülse Fabienne, Mao Qianqian, Jentschke Matthias, Böhmer Gerd, Strauß Hans-Georg, Hirchenhain Christine, Schmidmayr Monika, Müller Florian, Runnebaum Ingo, Hein Alexander, Koch Martin, Ruebner Matthias, Beckmann Matthias W, Fasching Peter A, Luyten Alexander, Dürst Matthias, Hillemanns Peter, Dörk Thi |
Genetic Variability of the Paired Box Transcription Factor; PAX8 Gene: Guidance Towards Treatment Strategies in a Cohort of Congenital Hypothyroidism. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2021 4 53 (5): 311-318. El-Ella Sohier S Abou, Khattab Essam Shawky A E H, Beddah Rehab K, Barseem Naglaa Fat |
Combination of ultrasound and molecular testing in malignancy risk estimate of Bethesda category IV thyroid nodules: results from a single-institution prospective study. Journal of endocrinological investigation 2021 Apr . Marina M, Zatelli M C, Goldoni M, Del Rio P, Corcione L, Martorana D, Percesepe A, Bonatti F, Mozzoni P, Crociara A, Ceresini |
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.
The Lancet. Oncology 2021 04 22 (4): 548-557. Bowden Sarah J, Bodinier Barbara, Kalliala Ilkka, Zuber Verena, Vuckovic Dragana, Doulgeraki Triada, Whitaker Matthew D, Wielscher Matthias, Cartwright Rufus, Tsilidis Konstantinos K, Bennett Phillip, Jarvelin Marjo-Riitta, Flanagan James M, Chadeau-Hyam Marc, Kyrgiou Maria, |
Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in Henan. Clinica chimica acta; international journal of clinical chemistry 2021 3 518 162-169. Li Liangshan, Jia Chenlu, Li Xiaole, Wang Fang, Wang Yangang, Chen Yanping, Liu Shiguo, Zhao Deh |
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome. American journal of human genetics 2021 Jan . Chen Na, Zhao Sen, Jolly Angad, Wang Lianlei, Pan Hongxin, Yuan Jian, Chen Shaoke, Koch André, Ma Congcong, Tian Weijie, Jia Ziqi, Kang Jia, Zhao Lina, Qin Chenglu, Fan Xin, Rall Katharina, Coban-Akdemir Zeynep, Chen Zefu, Jhangiani Shalini, Liang Ze, Niu Yuchen, Li Xiaoxin, Yan Zihui, Wu Yong, Dong Shuangshuang, Song Chengcheng, Qiu Guixing, Zhang Shuyang, Liu Pengfei, Posey Jennifer E, Zhang Feng, Luo Guangnan, Wu Zhihong, , Su Jianzhong, Zhang Jianguo, Chen Eugenia Y, Rouskas Konstantinos, Glentis Stavros, Bacopoulou Flora, Deligeoroglou Efthymios, Chrousos George, Lyonnet Stanislas, Polak Michel, Rosenberg Carla, Dingeldein Irene, Bonilla Ximena, Borel Christelle, Gibbs Richard A, Dietrich Jennifer E, Dimas Antigone S, Antonarakis Stylianos E, Brucker Sara Y, Lupski James R, Wu Nan, Zhu L |
Association between PAX8AS1 (rs4848320 C?>?T, rs1110839?G?>?T, and rs6726151 T?>?G) and MEG3 (rs7158663) gene polymorphisms and non-Hodgkin lymphoma risk. Nucleosides, nucleotides & nucleic acids 2022 Aug 1-13. Mirzazadeh Samaneh, Sarani Hosna, Nakhaee Alireza, Hashemi Seyed-Mehdi, Taheri Mohsen, Hashemi Mohammad, Bahari Gholamre |
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 |
Mutational analysis using next generation sequencing in pediatric thyroid cancer reveals BRAF and fusion oncogenes are common. International journal of pediatric otorhinolaryngology 2022 4 157 111121. Newfield Ron S, Jiang Wen, Sugganth Daniel X, Hantash Feras M, Lee Euyhyun, Newbury Robert |
Genome Sequencing and Transcriptome Profiling in Twins Discordant for Mayer-Rokitansky-Küster-Hauser Syndrome. Journal of clinical medicine 2022 10 11 (19): . Buchert Rebecca, Schenk Elisabeth, Hentrich Thomas, Weber Nico, Rall Katharina, Sturm Marc, Kohlbacher Oliver, Koch André, Riess Olaf, Brucker Sara Y, Schulze-Hentrich Julia |
Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis.
BMC genomics 2022 3 23 (1): 227. Fang Fang, Hazegh Kelsey, Mast Alan E, Triulzi Darrell J, Spencer Bryan R, Gladwin Mark T, Busch Michael P, Kanias Tamir, Page Grier |
Molecular pathology and clinical treatment of independent HPV primary serous carcinoma of the uterine cervix (USCC): A case report. Clinical case reports 2023 9 11 (9): e7833. Lina Niu, Fangying Ruan, Qisheng Yang, Chaoran Xia, Tao Xu, Fei Dong, Lizhen Zhang, Sheng Guo, Weiqin Lv, Junxia Wang, Yun Sha |
A Case-Control Study of the Relationship Between Genetic Polymorphism and Cretinism in Xinjiang. Pharmacogenomics and personalized medicine 2023 8 16 785-794. Jia Huang, Haiyan Wu, Guiqiang Zhao, Yan Ma, Yunping An, Li Sun, Fuye Li, Shengling Wa |
Immunohistochemical and Molecular Characteristics of Anogenital Papillary Hidradenomas. The American Journal of dermatopathology 2023 12 . Georgia Karpathiou, Angela Sim, Tiphanie Picot, Khaoula Mekhzoumi, Celine Chauleur, Michel Péoc |
Relationship between PIWIL1 gene polymorphisms and epithelial ovarian cancer susceptibility among southern Chinese woman: a three-center case-control study. BMC cancer 2023 11 23 (1): 1149. Shanshan Liu, Yaping Yan, Zhizhong Cui, Haipeng Feng, Fengmei Zhong, Ziguang Liu, Yan Li, Xiang Ou, Wenjuan |
Association of LncRNA-PAX8-AS1 and LAIR-2 polymorphisms along with their expression with clinical and subclinical hypothyroidism. Scientific reports 2023 1 13 (1): 6. Elsayed Omar M, Abdelazim Samy A, Darwish Hebatallah A, Shaker Olfat G, Senousy Mahmoud |
Initial screening of the rs104893657 variant of the PAX8 gene in women with hypothyroidism from Northeastern Slovakia. Central European journal of public health 2024 1 31 (Suppl 1): S89-S94. Marta Mydlárová Blaš?áková, Barbora Homjáková, Melinda Nagy, Janka Porá?ová, Zuzana Lörinczová, Pavol Makovický, Tatiana Kimáková, Vincent Sedlák, Mária Kone? |
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- Page last updated:Apr 22, 2024
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