Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: WNT5A[original query] |
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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 |
Lack of association of WNT5A mutations with Müllerian duct abnormalities. Reproductive biomedicine online 2012 Oct . Wu K, Chang X, Wei D, Xu C, Qin Y, Chen ZJ |
Exploring the genetic basis of chronic periodontitis: a genome-wide association study.
Human molecular genetics 2013 Jun 22 (11): 2312-24. Divaris Kimon, Monda Keri L, North Kari E, Olshan Andrew F, Reynolds Lindsay M, Hsueh Wen-Chi, Lange Ethan M, Moss Kevin, Barros Silvana P, Weyant Robert J, Liu Yongmei, Newman Anne B, Beck James D, Offenbacher Stev |
Hepatic interferon-stimulated genes are differentially regulated in the liver of chronic hepatitis C patients with different interleukin-28B genotypes. Hepatology (Baltimore, Md.) 2013 Oct . Honda M, Shirasaki T, Shimakami T, Sakai A, Horii R, Arai K, Yamashita T, Sakai Y, Yamashita T, Okada H, Murai K, Nakamura M, Mizukoshi E, Kaneko S |
Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population. Scientific reports 2015 5 13120. Li Peiqiang, Li Haijie, Zheng Yufang, Qiao Bin, Duan Wenyuan, Huang Lijuan, Liu Weiqi, Wang Hongy |
MiR-217 mediates the protective effects of the dopamine D2 receptor on fibrosis in human renal proximal tubule cells. Hypertension 2015 May 65 (5): 1118-25. Han Fei, Konkalmatt Prasad, Chen Jianghua, Gildea John, Felder Robin A, Jose Pedro A, Armando In |
Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios. Genetic epidemiology 2015 Jul 39 (5): 385-94. Li Qing, Kim Yoonhee, Suktitipat Bhoom, Hetmanski Jacqueline B, Marazita Mary L, Duggal Priya, Beaty Terri H, Bailey-Wilson Joan |
Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.
PloS one 2016 11 (8): e0160335. Bacelis Jonas, Juodakis Julius, Sengpiel Verena, Zhang Ge, Myhre Ronny, Muglia Louis J, Nilsson Staffan, Jacobsson |
SNP-SNP interactions between WNT4 and WNT5A were associated with obesity related traits in Han Chinese Population. Scientific reports 2017 Mar 7 43939. Dong Shan-Shan, Hu Wei-Xin, Yang Tie-Lin, Chen Xiao-Feng, Yan Han, Chen Xiang-Ding, Tan Li-Jun, Tian Qing, Deng Hong-Wen, Guo Y |
Role of wnt5a in Metabolic Inflammation in Humans. The Journal of clinical endocrinology and metabolism 2018 8 103 (11): 4253-4264. Relling Isabelle, Akcay Gül, Fangmann Daniela, Knappe Carina, Schulte Dominik Maria, Hartmann Katharina, Müller Nike, Türk Kathrin, Dempfle Astrid, Franke Andre, Schreiber Stefan, Laudes Matthi |
Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2019 7 57 (1): 80-87. Shibano Masayasu, Watanabe Akira, Takano Nobuo, Mishima Hiroyuki, Kinoshita Akira, Yoshiura Koh-Ichiro, Shibahara Takahi |
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 |
Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response. Journal for immunotherapy of cancer 2020 5 8 (1): . Roelands Jessica, Hendrickx Wouter, Zoppoli Gabriele, Mall Raghvendra, Saad Mohamad, Halliwill Kyle, Curigliano Giuseppe, Rinchai Darawan, Decock Julie, Delogu Lucia G, Turan Tolga, Samayoa Josue, Chouchane Lotfi, Ballestrero Alberto, Wang Ena, Finetti Pascal, Bertucci Francois, Miller Lance D, Galon Jerome, Marincola Francesco M, Kuppen Peter J K, Ceccarelli Michele, Bedognetti Davi |
Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia. Biological psychiatry 2020 Jan . Evgrafov Oleg V, Armoskus Chris, Wrobel Bozena B, Spitsyna Valeria N, Souaiaia Tade, Herstein Jennifer S, Walker Christopher P, Nguyen Joseph D, Camarena Adrian, Weitz Jonathan R, Kim Jae Mun Hugo, Lopez Duarte Edder, Wang Kai, Simpson George M, Sobell Janet L, Medeiros Helena, Pato Michele T, Pato Carlos N, Knowles James |
Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use. The European respiratory journal 2020 Dec . Hernandez-Pacheco Natalia, Vijverberg Susanne J, Herrera-Luis Esther, Li Jiang, Sio Yang Yie, Granell Raquel, Corrales Almudena, Maroteau Cyrielle, Lethem Ryan, Perez-Garcia Javier, Farzan Niloufar, Repnik Katja, Gorenjak Mario, Soares Patricia, Karimi Leila, Schieck Maximilian, Pérez-Méndez Lina, Berce Vojko, Tavendale Roger, Eng Celeste, Sardon Olaia, Kull Inger, Mukhopadhyay Somnath, Pirmohamed Munir, Verhamme Katia Mc, Burchard Esteban G, Kabesch Michael, Hawcutt Daniel B, Melén Erik, Potocnik Uroš, Chew Fook Tim, Tantisira Kelan G, Turner Steve, Palmer Colin N, Flores Carlos, Pino-Yanes Maria, Maitland-van der Zee Anke H, |
IGLV3-21R110 identifies an aggressive biological subtype of chronic lymphocytic leukemia with intermediate epigenetics. Blood 2020 11 137 (21): 2935-2946. Nadeu Ferran, Royo Romina, Clot Guillem, Duran-Ferrer Martí, Navarro Alba, Martín Silvia, Lu Junyan, Zenz Thorsten, Baumann Tycho, Jares Pedro, Puente Xose S, Martín-Subero José I, Delgado Julio, Campo Elí |
Association of Wnt9B rs1530364 and Wnt5A rs566926 Gene Polymorphisms with Nonsyndromic Cleft lip and Palate in South Indian Population using Deoxyribonucleic Acid Sequencing. Contemporary clinical dentistry 0 11 (1): 60-66. Jain Rohit, Dharma R M, Dinesh M R, Amarnath B C, Hegde Manjunath, Pramod K |
[Evaluating the effect of WNT pathway genes considering interactions on the risk of non-syndromic oral clefts among Chinese populations]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2020 Oct 52 (5): 815-820. Wang M Y, Li W Y, Zhou R, Wang S Y, Liu D J, Zheng H C, Li J, Li N, Zhou Z B, Zhu H P, Wu T, Hu Y |
Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. American journal of medical genetics. Part A 2020 Oct . Zhang Chaofan, Mazzeu Juliana F, Eisfeldt Jesper, Grochowski Christopher M, White Janson, Akdemir Zeynep C, Jhangiani Shalini N, Muzny Donna M, Gibbs Richard A, Lindstrand Anna, Lupski James R, Sutton V Reid, Carvalho Claudia M |
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 |
Determinants of Lung Fissure Completeness. American journal of respiratory and critical care medicine 2021 6 204 (7): 807-816. van der Molen Marieke C, Hartman Jorine E, Vermeulen Cornelis J, van den Berge Maarten, Faiz Alen, Kerstjens Huib A M, Charbonnier Jean-Paul, Vanfleteren Lowie E G W, Slebos Dirk-J |
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Journal of the American Society of Nephrology : JASN 2021 Feb . Verbitsky Miguel, Krithivasan Priya, Batourina Ekaterina, Khan Atlas, Graham Sarah E, Marasà Maddalena, Kim Hyunwoo, Lim Tze Y, Weng Patricia L, Sánchez-Rodríguez Elena, Mitrotti Adele, Ahram Dina F, Zanoni Francesca, Fasel David A, Westland Rik, Sampson Matthew G, Zhang Jun Y, Bodria Monica, Kil Byum Hee, Shril Shirlee, Gesualdo Loreto, Torri Fabio, Scolari Francesco, Izzi Claudia, van Wijk Joanna A E, Saraga Marijan, Santoro Domenico, Conti Giovanni, Barton David E, Dobson Mark G, Puri Prem, Furth Susan L, Warady Bradley A, Pisani Isabella, Fiaccadori Enrico, Allegri Landino, Degl'Innocenti Maria Ludovica, Piaggio Giorgio, Alam Shumyle, Gigante Maddalena, Zaza Gianluigi, Esposito Pasquale, Lin Fangming, Simões-E-Silva Ana Cristina, Brodkiewicz Andrzej, Drozdz Dorota, Zachwieja Katarzyna, Miklaszewska Monika, Szczepanska Maria, Adamczyk Piotr, Tkaczyk Marcin, Tomczyk Daria, Sikora Przemyslaw, Mizerska-Wasiak Malgorzata, Krzemien Grazyna, Szmigielska Agnieszka, Zaniew Marcin, Lozanovski Vladimir J, Gucev Zoran, Ionita-Laza Iuliana, Stanaway Ian B, Crosslin David R, Wong Craig S, Hildebrandt Friedhelm, Barasch Jonathan, Kenny Eimear E, Loos Ruth J F, Levy Brynn, Ghiggeri Gian Marco, Hakonarson Hakon, Latos-Biele?ska Anna, Materna-Kiryluk Anna, Darlow John M, Tasic Velibor, Willer Cristen, Kiryluk Krzysztof, Sanna-Cherchi Simone, Mendelsohn Cathy L, Gharavi Ali |
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms. Pediatric research 2021 Dec . Akat Ayberk, Yilmaz Semerci Seda, Ugurel Osman Mutluhan, Erdemir Aysegul, Danhaive Olivier, Cetinkaya Merih, Turgut-Balik Dil |
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 |
Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Molecular genetics and genomics : MGG 2022 Jul . D?browska Justyna, Biedziak Barbara, Szponar-?urowska Anna, Budner Margareta, Jagodzi?ski Pawe? P, P?oski Rafa?, Mostowska Adrian |
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 |
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 |
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. HGG advances 2022 1 3 (1): 100074. Zhang Chaofan, Jolly Angad, Shayota Brian J, Mazzeu Juliana F, Du Haowei, Dawood Moez, Soper Patricia Celestino, Ramalho de Lima Ariadne, Ferreira Bárbara Merfort, Coban-Akdemir Zeynep, White Janson, Shears Deborah, Thomson Fraser Robert, Douglas Sarah Louise, Wainwright Andrew, Bailey Kathryn, Wordsworth Paul, Oldridge Mike, Lester Tracy, Calder Alistair D, Dumic Katja, Banka Siddharth, Donnai Dian, Jhangiani Shalini N, Potocki Lorraine, Chung Wendy K, Mora Sara, Northrup Hope, Ashfaq Myla, Rosenfeld Jill A, Mason Kati, Pollack Lynda C, McConkie-Rosell Allyn, Kelly Wei, McDonald Marie, Hauser Natalie S, Leahy Peter, Powell Cynthia M, Boy Raquel, Honjo Rachel Sayuri, Kok Fernando, Martelli Lucia R, Filho Vicente Odone, Genomics England Research Consortium , Muzny Donna M, Gibbs Richard A, Posey Jennifer E, Liu Pengfei, Lupski James R, Sutton V Reid, Carvalho Claudia M |
Multifactor dimensionality reduction method identifies novel SNP interactions in the WNT protein interaction networks that are associated with recurrence risk in colorectal cancer. Frontiers in oncology 2023 3 13 1122229. Curtis Aaron A, Yu Yajun, Carey Megan, Parfrey Patrick, Yilmaz Yildiz E, Savas Sevt |
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- Page last updated:Apr 22, 2024
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