Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: ROR2[original query] |
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Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis.
Nature communications 2023 5 14 (1): 2644. Sethi Anurag, Ruby J Graham, Veras Matthew A, Telis Natalie, Melamud Euge |
Family-based association study of ROR2 polymorphisms with an array of radiographic hand bone strength phenotypes. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2007 Dec 18 (12): 1683-92. Ermakov S, Malkin I, Keter M, Kobyliansky E, Livshits |
A significant association exists between receptor tyrosine kinase-like orphan receptor 2 gene variants and the OPG/RANKL ratio in human plasma. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2012 Jul 23 (7): 1899-907. Ermakov S, Trofimov S, Malkin I, Livshits |
ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population. Chinese medical journal 2012 Feb 125 (3): 476-80. Wang Hong, Hetmanski Jacqueline B, Ruczinski Ingo, Liang Kung Yee, Fallin M Daniele, Redett Richard J, Raymond Gerald V, Chou Yah-Huei Wu, Chen Philip Kuo-Ting, Yeow Vincent, Chong Samuel S, Cheah Felicia Sh, Jabs Ethylin Wang, Scott Alan F, Beaty Terri |
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 |
Prognostic value of receptor tyrosine kinase-like orphan receptor (ROR) family in cancer: A meta-analysis. Cancer treatment reviews 2019 6 77 11-19. Saleh Ramy R, Antrás Jesús Fuentes, Peinado Paloma, Pérez-Segura Pedro, Pandiella Atanasio, Amir Eitan, Ocaña Alber |
Whole-exome sequencing identified compound heterozygous variants in ROR2 gene in a fetus with Robinow syndrome. Journal of clinical laboratory analysis 2019 10 34 (2): e23074. Yang Kai, Zhu Jianjiang, Tan Ya, Sun Xiaofei, Zhao Huawei, Tang Guodong, Zhang Dongliang, Qi Ho |
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 |
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort.
Frontiers in dental medicine 2021 1 2 . Alotaibi Rasha N, Howe Brian J, Moreno Uribe Lina M, Ramirez Consuelo Valencia, Restrepo Claudia, Deleyiannis Frederic W B, Padilla Carmencita, Orioli Ieda M, Buxó Carmen J, Hecht Jacqueline T, Wehby George L, Neiswanger Katherine, Murray Jeffery C, Shaffer John R, Weinberg Seth M, Marazita Mary |
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human mutation 2022 3 43 (7): 900-918. Lima Ariadne R, Ferreira Barbara M, Zhang Chaofan, Jolly Angad, Du Haowei, White Janson J, Dawood Moez, Lins Tulio C, Chiabai Marcela A, van Beusekom Ellen, Cordoba Mara S, Caldas Rosa Erica C C, Kayserili Hulya, Kimonis Virginia, Wu Erica, Mellado Cecilia, Aggarwal Vineet, Richieri-Costa Antonio, Brunoni Décio, Canó Talyta M, Jorge Alexander A L, Kim Chong A, Honjo Rachel, Bertola Débora R, Dandalo-Girardi Raissa M, Bayram Yavuz, Gezdirici Alper, Yilmaz-Gulec Elif, Gumus Evren, Yilmaz Gülay C, Okamoto Nobuhiko, Ohashi Hirofumi, Coban-Akdemir Zeynep, Mitani Tadahiro, Jhangiani Shalini N, Muzny Donna M, Regattieri Neysa A P, Pogue Robert, Pereira Rinaldo W, Otto Paulo A, Gibbs Richard A, Ali Bassam R, van Bokhoven Hans, Brunner Han G, Sutton V Reid, Lupski James R, Vianna-Morgante Angela M, Carvalho Claudia M B, Mazzeu Juliana |
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 |
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- Page last updated:Apr 16, 2024
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