Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: PAX1[original query] |
---|
[Association of PAX1 gene polymorphisms with susceptibility to congenital scoliosis in Chinese Han population]. Zhonghua yi xue za zhi 2008 Oct 88 (37): 2597-602. Fei Qi, Wu Zhi-Hong, Yuan Suo-Mao, Wang Hai, Zhou Xi, Liu Zheng, Song Hai-Feng, Yin Ruo-Feng, Wang Yi-Peng, Qiu Gui-Xi |
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.
The British journal of dermatology 2011 Dec 165 (6): 1293-302. Brockschmidt F F, Heilmann S, Ellis J A, Eigelshoven S, Hanneken S, Herold C, Moebus S, Alblas M A, Lippke B, Kluck N, Priebe L, Degenhardt F A, Jamra R A, Meesters C, Jöckel K-H, Erbel R, Harrap S, Schumacher J, Fröhlich H, Kruse R, Hillmer A M, Becker T, Nöthen M |
Genetic architecture of carotid artery intima-media thickness in Mexican Americans. Circulation. Cardiovascular genetics 2013 Mar . Melton PE, Carless MA, Curran JE, Dyer TD, Göring HH, Kent JW, Drigalenko E, Johnson MP, Maccluer JW, Moses EK, Comuzzie AG, Mahaney MC, O'Leary DH, Blangero J, Almasy L |
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.
Nature communications 2015 6 6452. Sharma Swarkar, Londono Douglas, Eckalbar Walter L, Gao Xiaochong, Zhang Dongping, Mauldin Kristen, Kou Ikuyo, Takahashi Atsushi, Matsumoto Morio, Kamiya Nobuhiro, Murphy Karl K, Cornelia Reuel, , , Herring John A, Burns Dennis, Ahituv Nadav, Ikegawa Shiro, Gordon Derek, Wise Carol |
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.
PLoS genetics 2016 Aug 12 (8): e1006149. Shaffer John R, Orlova Ekaterina, Lee Myoung Keun, Leslie Elizabeth J, Raffensperger Zachary D, Heike Carrie L, Cunningham Michael L, Hecht Jacqueline T, Kau Chung How, Nidey Nichole L, Moreno Lina M, Wehby George L, Murray Jeffrey C, Laurie Cecelia A, Laurie Cathy C, Cole Joanne, Ferrara Tracey, Santorico Stephanie, Klein Ophir, Mio Washington, Feingold Eleanor, Hallgrimsson Benedikt, Spritz Richard A, Marazita Mary L, Weinberg Seth |
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.
Nature communications 2016 May 7 11616. Adhikari Kaustubh, Fuentes-Guajardo Macarena, Quinto-Sánchez Mirsha, Mendoza-Revilla Javier, Camilo Chacón-Duque Juan, Acuña-Alonzo Victor, Jaramillo Claudia, Arias William, Lozano Rodrigo Barquera, Pérez Gastón Macín, Gómez-Valdés Jorge, Villamil-Ramírez Hugo, Hunemeier Tábita, Ramallo Virginia, Silva de Cerqueira Caio C, Hurtado Malena, Villegas Valeria, Granja Vanessa, Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Salzano Francisco M, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Cheeseman Michael, Rosique Javier, Bedoya Gabriel, Rothhammer Francisco, Headon Denis, González-José Rolando, Balding David, Ruiz-Linares Andr |
Genetic Variant of PAX1 Gene Is Functionally Associated With Adolescent Idiopathic Scoliosis in the Chinese Population. Spine 2017 Oct . Xu Leilei, Sheng Fei, Xia Chao, Qin Xiaodong, Tang Nelson Leung-Sang, Qiu Yong, Cheng Jack Chun-Yiu, Zhu Zezha |
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population. Gene 2019 Mar 688 215-220. Liu Gang, Liu Sen, Li Xiaoxin, Chen Jia, Chen Weisheng, Zuo Yuzhi, Liu Jiaqi, Niu Yuchen, Lin Mao, Zhao Sen, Long Bo, Zhao Yanxue, Ye Yongyu, Zhang Jianguo, Shen Jianxiong, Qiu Guixing, Wu Zhihong, Wu N |
Association of Susceptibility Genes for Adolescent Idiopathic Scoliosis and Intervertebral Disc Degeneration With Adult Spinal Deformity. Spine 2019 Jul . Takeda Kazuki, Kou Ikuyo, Hosogane Naobumi, Otomo Nao, Yagi Mitsuru, Kaneko Shinjiro, Kono Hitoshi, Ishikawa Masayuki, Takahashi Yohei, Ikegami Takeshi, Nojiri Kenya, Okada Eijiro, Funao Haruki, Okuyama Kunimasa, Tsuji Takashi, Fujita Nobuyuki, Nagoshi Narihito, Tsuji Osahiko, Ogura Yoji, Ishii Ken, Nakamura Masaya, Matsumoto Morio, Ikegawa Shiro, Watanabe Ko |
Genetic Variant of TBX1 Gene Is Functionally Associated With Adolescent Idiopathic Scoliosis in the Chinese Population. Spine 2020 Sep . Li Yang, Wu Zhichong, Xu LeiLei, Feng Zhenhua, Wang Yuwen, Dai Zhicheng, Liu Zhen, Sun Xu, Qiu Yong, Zhu Zezha |
A Genetic Predictive Model Estimating the Risk of Developing Adolescent Idiopathic Scoliosis. Current genomics 2019 May 20 (4): 246-251. Xu Leilei, Wu Zhichong, Xia Chao, Tang Nelson, Cheng Jack C Y, Qiu Yong, Zhu ZeZha |
Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder. Journal of child psychology and psychiatry, and allied disciplines 2021 Jul . Peyre Hugo, Schoeler Tabea, Liu Chaoyu, Williams Camille Michèle, Hoertel Nicolas, Havdahl Alexandra, Pingault Jean-Baptis |
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.
HGG advances 2021 4 2 (2): . Curtis Sarah W, Chang Daniel, Lee Myoung Keun, Shaffer John R, Indencleef Karlijne, Epstein Michael P, Cutler David J, Murray Jeffrey C, Feingold Eleanor, Beaty Terri H, Claes Peter, Weinberg Seth M, Marazita Mary L, Carlson Jenna C, Leslie Elizabeth |
Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population.
Frontiers in genetics 2022 13 967684. Wang Peiqi, Sun Xinghan, Miao Qiang, Mi Hao, Cao Minyuan, Zhao Shan, Wang Yiyi, Shu Yang, Li Wei, Xu Heng, Bai Ding, Zhang Y |
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes. Human genetics 2023 9 . Sarah W Curtis, Jenna C Carlson, Terri H Beaty, Jeffrey C Murray, Seth M Weinberg, Mary L Marazita, Justin L Cotney, David J Cutler, Michael P Epstein, Elizabeth J Lesl |
Rare genetic variants in SEC24D modify orofacial cleft phenotypes. medRxiv : the preprint server for health sciences 2023 4 . Curtis Sarah W, Carlson Jenna C, Beaty Terri H, Murray Jeffrey C, Weinberg Seth M, Marazita Mary L, Cotney Justin L, Cutler David J, Epstein Michael P, Leslie Elizabeth |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: