Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: WNT3[original query] |
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Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. Birth defects research. Part A, Clinical and molecular teratology 2010 Sep 88 (9): 748-56. Nikopensius Tiit, Jagomägi Triin, Krjutskov Kaarel, Tammekivi Veronika, Saag Mare, Prane Inga, Piekuse Linda, Akota Ilze, Barkane Biruta, Krumina Astrida, Ambrozaityte Laima, Matuleviciene Ausra, Kucinskiene Zita Ausrele, Lace Baiba, Kucinskas Vaidutis, Metspalu Andr |
Studies with Wnt genes and nonsyndromic cleft lip and palate. Birth defects research. Part A, Clinical and molecular teratology 2010 Nov 88 (11): 995-1000. Menezes Renato, Letra Ariadne, Kim Ana H, Küchler Erika C, Day Alicia, Tannure Patricia N, Gomes da Motta Luise, Paiva Katiucia B S, Granjeiro Jose M, Vieira Alexandre |
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
[Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]. Molekuliarnaia genetika, mikrobiologiia i virusologiia 2011 (2): 3-4. Filatova E V, Shadrina M I, Fedotova E Iu, Slominski? P A, Illarioshkin S N, Ivanova-Smolenskaia I A, Limborskaia S |
Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. Birth defects research. Part A, Clinical and molecular teratology 2011 Apr 91 (4): 218-25. Nikopensius Tiit, Kempa Inga, Ambrozaityt? Laima, Jagomägi Triin, Saag Mare, Matulevi?ien? Aušra, Utkus Algirdas, Krjutškov Kaarel, Tammekivi Veronika, Piekuse Linda, Akota Ilze, Barkane Biruta, Krumina Astrida, Klovins Janis, Lace Baiba, Ku?inskas Vaidutis, Metspalu Andr |
Insights from studies with oral cleft genes suggest associations between WNT-pathway genes and risk of oral cancer. Journal of dental research 2011 Jun 90 (6): 740-6. Andrade Filho P A, Letra A, Cramer A, Prasad J L, Garlet G P, Vieira A R, Ferris R L, Menezes |
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 |
[Association between single nucleotide polymorphism in Wnt3 and nonsyndromic cleft lip with or without cleft palate in Hui and Han population of Ningxia Autonomous Region]. Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology 2013 Aug 31 (4): 4. Xin Y, Ma L, Zhai K, Zhou Z, Yang X, Ma J, Wang Y, Zhu J, Jiang M, Huang Y |
A miR-151 binding site polymorphism in the 3'-untranslated region of the cyclin E1 gene associated with nasopharyngeal carcinoma. Biochemical and biophysical research communications 2013 Mar 432 (4): 660-5. Liu Ying, Cai Hongbing, Liu Jie, Fan Haoning, Wang Zhiyuan, Wang Qirui, Shao Meng, Sun Xuegang, Diao Jianxin, Liu Yuanliang, Shi Yusheng, Fan Q |
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Human molecular genetics 2014 Oct 23 (20): 5536-44. Reutter Heiko, Draaken Markus, Pennimpede Tracie, Wittler Lars, Brockschmidt Felix F, Ebert Anne-Karolin, Bartels Enrika, Rösch Wolfgang, Boemers Thomas M, Hirsch Karin, Schmiedeke Eberhard, Meesters Christian, Becker Tim, Stein Raimund, Utsch Boris, Mangold Elisabeth, Nordenskjöld Agneta, Barker Gillian, Kockum Christina Clementsson, Zwink Nadine, Holmdahl Gundula, Läckgren Göran, Jenetzky Ekkehart, Feitz Wouter F J, Marcelis Carlo, Wijers Charlotte H W, Van Rooij Iris A L M, Gearhart John P, Herrmann Bernhard G, Ludwig Michael, Boyadjiev Simeon A, Nöthen Markus M, Mattheisen Manu |
Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension. American journal of human genetics 2015 Jan 96 (1): 21-36. Zhu Xiaofeng, Feng Tao, Tayo Bamidele O, Liang Jingjing, Young J Hunter, Franceschini Nora, Smith Jennifer A, Yanek Lisa R, Sun Yan V, Edwards Todd L, Chen Wei, Nalls Mike, Fox Ervin, Sale Michele, Bottinger Erwin, Rotimi Charles, , Liu Yongmei, McKnight Barbara, Liu Kiang, Arnett Donna K, Chakravati Aravinda, Cooper Richard S, Redline Sus |
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predisposition. International journal of cancer. Journal international du cancer 2015 May 136 (9): 2109-19. Ibarrola-Villava Maider, Kumar Rajiv, Nagore Eduardo, Benfodda Meriem, Guedj Mickael, Gazal Steven, Hu Hui-Han, Guan Jian, Rachkonda P Sivaramakishna, Descamps Vincent, Basset-Seguin Nicole, Bensussan Armand, Bagot Martine, Saiag Philippe, Schadendorf Dirk, Martin-Gonzalez Manuel, Mayor Matias, Grandchamp Bernard, Ribas Gloria, Soufir Nad |
Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2015 Jan 52 (1): 44-8. Fontoura Clarissa, Silva Renato M, Granjeiro José M, Letra Ariad |
Association Between Genes Involved in Craniofacial Development and Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2015 Sep . Machado Renato Assis, Messetti Ana Camila, de Aquino Sibele Nascimento, Martelli-Júnior Hercílio, Swerts Mário Sérgio Oliveira, de Almeida Reis Silvia Regina, Moreira Helenara Salvati Bertolossi, Persuhn Darlene Camati, Coletta Ricardo |
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Human molecular genetics 2015 Sep 24 (18): 5069-78. Baranowska Körberg Izabella, Hofmeister Wolfgang, Markljung Ellen, Cao Jia, Nilsson Daniel, Ludwig Michael, Draaken Markus, Holmdahl Gundela, Barker Gillian, Reutter Heiko, Vukojevi? Vladana, Clementson Kockum Christina, Lundin Johanna, Lindstrand Anna, Nordenskjöld Agne |
Variations in WNT3 gene are associated with incidence of non-syndromic cleft lip with or without cleft palate in a northeast Chinese population. Genetics and molecular research : GMR 2015 14 (4): 12646-53. Lu Y P, Han W T, Liu Q, Li J X, Li Z J, Jiang M, Xu |
Association of the WNT3 Variations and the Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants. Avicenna journal of medical biotechnology 0 10 (3): 168-172. Farrokhi Karibozorg Homa, Masoudian Nahid, Saliminejad Kioomars, Ebadifar Asghar, Kamali Koorosh, Khorram Khorshid Hamid Re |
Association of the WNT3 polymorphisms and non-syndromic cleft lip with or without cleft palate: evidence from a meta-analysis. Bioscience reports 2018 12 38 (6): . Wang Bing-Qian, Gao Shu-Tao, Chen Kun, Xu Zhu-Qiu, Sun Jia-Ming, Xia Yun, Lv Zheng-T |
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 |
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.
Brain : a journal of neurology 2019 Oct 142 (10): 2938-2947. Wiberg Akira, Ng Michael, Al Omran Yasser, Alfaro-Almagro Fidel, McCarthy Paul, Marchini Jonathan, Bennett David L, Smith Stephen, Douaud Gwenaëlle, Furniss Domin |
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 |
Congenital heart disease risk loci identified by genome-wide association study in European patients.
The Journal of clinical investigation 2020 Nov . Lahm Harald, Jia Meiwen, Dreßen Martina, Wirth Felix, Puluca Nazan, Gilsbach Ralf, Keavney Bernard D, Cleuziou Julie, Beck Nicole, Bondareva Olga, Dzilic Elda, Burri Melchior, König Karl C, Ziegelmüller Johannes A, Abou-Ajram Claudia, Neb Irina, Zhang Zhong, Doppler Stefanie A, Mastantuono Elisa, Lichtner Peter, Eckstein Gertrud, Hörer Jürgen, Ewert Peter, Priest James R, Hein Lutz, Lange Rüdiger, Meitinger Thomas, Cordell Heather J, Müller-Myhsok Bertram, Krane Mark |
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 |
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 |
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.
Frontiers in cell and developmental biology 2021 4 9 621482. Mukhopadhyay Nandita, Feingold Eleanor, Moreno-Uribe Lina, Wehby George, Valencia-Ramirez Luz Consuelo, Muñeton Claudia P Restrepo, Padilla Carmencita, Deleyiannis Frederic, Christensen Kaare, Poletta Fernando A, Orioli Ieda M, Hecht Jacqueline T, Buxó Carmen J, Butali Azeez, Adeyemo Wasiu L, Vieira Alexandre R, Shaffer John R, Murray Jeffrey C, Weinberg Seth M, Leslie Elizabeth J, Marazita Mary |
Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson's Disease and Multiple System Atrophy. Frontiers in genetics 2021 12 12 765833. Su Wei-Ming, Gu Xiao-Jing, Hou Yan-Bing, Zhang Ling-Yu, Cao Bei, Ou Ru-Wei, Wu Ying, Chen Xue-Ping, Song Wei, Zhao Bi, Shang Hui-Fang, Chen Yong-Pi |
Unraveling the genomic basis of congenital heart disease. The Journal of clinical investigation 2021 Jan 131 (2): . Darbar Dawo |
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes. Genetic epidemiology 2022 Feb . Mukhopadhyay Nandita, Feingold Eleanor, Moreno-Uribe Lina, Wehby George, Valencia-Ramirez Luz Consuelo, Restrepo Muñeton Claudia P, Padilla Carmencita, Deleyiannis Frederic, Christensen Kaare, Poletta Fernando A, Orioli Ieda M, Hecht Jacqueline T, Buxó Carmen J, Butali Azeez, Adeyemo Wasiu L, Vieira Alexandre R, Shaffer John R, Murray Jeffrey C, Weinberg Seth M, Leslie Elizabeth J, Marazita Mary |
Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities. Neurobiology of disease 2022 10 174 105880. Katsumata Yuriko, Shade Lincoln M, Hohman Timothy J, Schneider Julie A, Bennett David A, Farfel Jose M, , Kukull Walter A, Fardo David W, Nelson Peter |
eQTL colocalization analysis highlights novel susceptibility genes in Autism Spectrum Disorders (ASD). Translational psychiatry 2023 11 13 (1): 336. S Dominguez-Alonso, A Carracedo, C Rodriguez-Fonten |
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- Page last updated:Apr 22, 2024
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