Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 38 Records) |
Query Trace: WNT3A[original query] |
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Polygenic prediction of preeclampsia and gestational hypertension.
Nature medicine 2023 5 29 (6): 1540-1549. Honigberg Michael C, Truong Buu, Khan Raiyan R, Xiao Brenda, Bhatta Laxmi, Vy Ha My T, Guerrero Rafael F, Schuermans Art, Selvaraj Margaret Sunitha, Patel Aniruddh P, Koyama Satoshi, Cho So Mi Jemma, Vellarikkal Shamsudheen Karuthedath, Trinder Mark, Urbut Sarah M, Gray Kathryn J, Brumpton Ben M, Patil Snehal, Zöllner Sebastian, Antopia Mariah C, Saxena Richa, Nadkarni Girish N, Do Ron, Yan Qi, Pe'er Itsik, Verma Shefali Setia, Gupta Rajat M, Haas David M, Martin Hilary C, van Heel David A, Laisk Triin, Natarajan Prade |
[Association study of WNT3A gene polymorphisms with the susceptibility to congenital scoliosis in a Chinese Han population]. Zhonghua yi xue za zhi 2011 Mar 91 (11): 746-51. Fei Qi, Wu Zhi-hong, Wang Yi-peng, Zhou Xi, Wang Hai, Wang Nai-guo, Li Xiang, Qiu Gui-xi |
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene. International journal of molecular medicine 2012 Dec 30 (6): 1459-64. Draaken Markus, Prins Wiebke, Zeidler Claudia, Hilger Alina, Mughal Sadaf S, Latus Jeanette, Boemers Thomas M, Schmidt Dominik, Schmiedeke Eberhard, Spychalski Nicole, Bartels Enrika, Nöthen Markus M, Reutter Heiko, Ludwig Micha |
Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate. European journal of oral sciences 2012 Feb 120 (1): 1. Mostowska A, Hozyasz KK, Biedziak B, Wojcicki P, Lianeri M, Jagodzinski PP |
WNT3A gene expression is associated with isolated Hirschsprung disease polymorphism and disease status. International journal of clinical and experimental pathology 2014 7 (4): 1359-68. Chen Dong, Mi Jie, Liu Xiaomei, Zhang Juan, Wang Weilin, Gao Ho |
WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening. Age (Dordrecht, Netherlands) 2014 Jun 36 (3): 9635. Velázquez-Cruz Rafael, García-Ortiz Humberto, Castillejos-López Manuel, Quiterio Manuel, Valdés-Flores Margarita, Orozco Lorena, Villarreal-Molina Teresa, Salmerón Jor |
Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma. PLoS genetics 2016 May 12 (5): e1006051. Lin Yung-Feng, Li Ling-Hui, Lin Chih-Hung, Tsou Mei-Hua, Chuang Ming-Tai Kiffer, Wu Keh-Ming, Liao Tsai-Lien, Li Jian-Chiuan, Wang Wei-Jie, Tomita Angela, Tomita Beverly, Huang Shiu-Feng, Tsai Shih-Fe |
Genetic 3'UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight. Experimental dermatology 2017 Mar . Hernando Barbara, Peña-Chilet Maria, Ibarrola-Villava Maider, Martin-Gonzalez Manuel, Gomez-Fernandez Cristina, Ribas Gloria, Martinez-Cadenas Conra |
Polymorphisms associated with oral clefts as potential susceptibility markers for oral and breast cancer. Archives of oral biology 2019 Mar 99 9-14. de Freitas Edimilson Martins, Machado Renato Assis, de Moura Santos Edilmar, de Matos Felipe Rodrigues, Galvão Hébel Cavalcanti, Miranda Soares Priscila Bernardina, Freitas Roseana de Almeida, Martelli-Júnior Hercíl |
Association of single nucleotide polymorphisms in WNT genes with the risk of nonsyndromic cleft lip with or without cleft palate. Congenital anomalies 2018 Jan . Rafighdoost Houshang, Hashemi Mohammad, Asadi Hossein, Bahari Gholamre |
WNT gene polymorphisms and predisposition to apical periodontitis. Scientific reports 2019 Dec 9 (1): 18980. de Souza Letícia Chaves, Cavalla Franco, Maili Lorena, Garlet Gustavo P, Vieira Alexandre R, Silva Renato M, Letra Ariad |
Left-right asymmetry in palatal rugae is associated with genetic variants in WNT signaling pathway. Archives of oral biology 2019 Nov 110 104604. Silva-Sousa Alice Corrêa, Marañón-Vásquez Guido Artemio, Gerber Jennifer Tsi, Judachesci Claudia S, Stuani Maria Bernadete Sasso, Nakane Matsumoto Mírian Aiko, Coletta Ricardo D, Scariot Rafaela, Küchler Erika Calva |
A gene co-expression network analysis of the candidate genes and molecular pathways associated with feather follicle traits of chicken skin. Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie 2020 5 138 (1): 122-134. Ji Gai-Ge, Zhang Ming, Liu Yi-Fan, Shan Yan-Ju, Tu Yun-Jie, Ju Xiao-Jun, Zou Jian-Min, Shu Jing-Ting, Wu Jun-Feng, Xie Jin-Fa |
Potential interactions among single nucleotide polymorphisms in bone- and cartilage-related genes in skeletal malocclusions. Orthodontics & craniofacial research 2020 Oct . Küchler Erika Calvano, Reis Caio Luiz Bitencourt, Carelli Julia, Scariot Rafaela, Nelson-Filho Paulo, Coletta Ricardo D, Paza Aleysson Olimpio, Matsumoto Mírian Aiko Nakane, Proff Peter, Kirschneck Christi |
Identification of the prognostic value of a 2-gene signature of the WNT gene family in UCEC using bioinformatics and real-world data. Cancer cell international 2021 Sep 21 (1): 516. Hu Yuexin, Zheng Mingjun, Zhang Dandan, Gou Rui, Liu Ouxuan, Wang Shuang, Lin B |
The effect of genetic polymorphisms on treatment duration following premolar extraction. Scientific reports 2021 Aug 11 (1): 15942. Yu Jiyon, Choi Yoon Jeong, Choi Sung-Hwan, Jung Han-Sung, Lee Ji Hyun, Cha Jung-Y |
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. Frontiers in cardiovascular medicine 2021 7 8 675222. Ren Huan, Luo Jian-Quan, Ouyang Fan, Cheng Li, Chen Xiao-Ping, Zhou Hong-Hao, Huang Wei-Hua, Zhang W |
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A. Molecular genetics & genomic medicine 2021 5 9 (6): e1681. Caetano da Silva Caroline, Ricquebourg Manon, Orcel Philippe, Fabre Stéphanie, Funck-Brentano Thomas, Cohen-Solal Martine, Collet Corin |
Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study.
The Lancet. Oncology 2021 12 23 (1): 161-171. Trépo Eric, Caruso Stefano, Yang Jie, Imbeaud Sandrine, Couchy Gabrielle, Bayard Quentin, Letouzé Eric, Ganne-Carrié Nathalie, Moreno Christophe, Oussalah Abderrahim, Féray Cyrille, Blanc Jean Frédéric, Clément Bruno, Hillon Patrick, Boursier Jérôme, Paradis Valérie, Calderaro Julien, Gnemmi Viviane, Nault Jean-Charles, Guéant Jean-Louis, Devière Jacques, Archambeaud Isabelle, Vitellius Carole, Turlin Bruno, Bronowicki Jean-Pierre, Gustot Thierry, Sutton Angela, , Ziol Marianne, Nahon Pierre, Zucman-Rossi Jessi |
Genetic and Epigenetic Impact of Chronic Inflammation on Colon Mucosa Cells. Frontiers in genetics 2021 11 12 722835. He Jia, Han Jimin, Liu Jia, Yang Ronghua, Wang Jingru, Wang Xusheng, Chen Xiaodo |
Ghrelin modulates dopaminergic neuron formation and attention deficit hyperactivity disorder-like behaviors: From animals to human models. Brain, behavior, and immunity 2021 1 94 327-337. Shi Xulai, Guan Kaiyu, Peng Xuyan, Xu Bingru, Zhou Xianyong, Wang Shao, Xu Shengnan, Zheng Miaomiao, Huang Jing, Wan Xiaoyang, Guan Wanchun, Su Kuan-Pin, Ye Minjie, Gao Xiang, Yin Zhan, Li |
Dissecting Molecular Heterogeneity of Circulating Tumor Cells (CTCs) from Metastatic Breast Cancer Patients through Copy Number Aberration (CNA) and Single Nucleotide Variant (SNV) Single Cell Analysis. Cancers 2022 8 14 (16): . Rossi Tania, Angeli Davide, Tebaldi Michela, Fici Pietro, Rossi Elisabetta, Rocca Andrea, Palleschi Michela, Maltoni Roberta, Martinelli Giovanni, Fabbri Francesco, Gallerani Giul |
Dysregulation of Wnt signaling in bone of type 2 diabetes mellitus and diabetic Charcot arthropathy. BMC musculoskeletal disorders 2022 4 23 (1): 365. Gassel Laurens Christian, Schneider Sandra, Banke Ingo Jörg, Braun Karl Friedrich, Volkering Christoph, Zeeb Leonie, Burgkart Rainer Hans Hermann, von Eisenhart-Rothe Rüdiger, Biberthaler Peter, van Griensven Martijn, Haug Alexander Tobi |
Clinical relevance of genetic polymorphisms in WNT signaling pathway (SFRP1, WNT3A, CTNNB1, WIF-1, DKK-1, LRP5, LRP6) on pulmonary tuberculosis in a Chinese population. Frontiers in immunology 2022 12 13 1011700. Huang Qian, Wang Chao-Cai, Liu Yun-Guang, Zhao Chang-Ming, Zhang Tian-Ping, Liu Yan, Wang H |
Integrating genetic variants into clinical models for hepatocellular carcinoma risk stratification in cirrhosis. Journal of hepatology 2022 11 . Nahon Pierre, Bamba-Funck Jessica, Layese Richard, Trépo Eric, Zucman-Rossi Jessica, Cagnot Carole, Ganne-Carrié Nathalie, Chaffaut Cendrine, Guyot Erwan, Ziol Marianne, Sutton Angela, Audureau Etienne, |
Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis. Scientific reports 2022 1 12 (1): 1214. Slavec Lara, Karas Kuželi?ki Nataša, Locatelli Igor, Geršak Kseni |
Pharmacogenetic study of phosphatase and tensin homolog polymorphism (rs701848) in childhood epilepsy: relation to circulating Wnt signaling. Neurological research 2023 9 1-12. Mohammed H Hassan, Ahmed Y Nassar, Abdel-Raheim M A Meki, Shimaa A Nasser, Ali Helmi Bakri, Eman Radw |
The role of TOP2A in immunotherapy and vasculogenic mimicry in non-small cell lung cancer and its potential mechanism. Scientific reports 2023 7 13 (1): 10906. Jiatao Wu, Lei Zhang, Wenjuan Li, Luyao Wang, Qianhao Jia, Fan Shi, Kairui Li, Lingli Liao, Yuqi Shi, Shiwu |
Impact of genetic variations in the WNT family members and RUNX2 on dental and skeletal maturation: a cross-sectional study. Head & face medicine 2023 7 19 (1): 26. Caio Luiz Bitencourt Reis, Mirian Aiko Nakane Matsumoto, Flares Baratto-Filho, Rafaela Scariot, Maria Bernadete Sasso Stuani, Fábio Lourenço Romano, Ricardo Della Coletta, Daniela Silva Barroso de Oliveira, Peter Proff, Christian Kirschneck, Erika Calvano Küchl |
TGF?1, SMAD2, CTNN?1, and Wnt3a gene mutational status and serum concentrations in individuals with non-small cell lung cancer. Cellular and molecular biology (Noisy-le-Grand, France) 2023 11 69 (11): 81-91. Hemn Abdalla Omer, Kawa Am |
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- Page last updated:Apr 22, 2024
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