Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: GPR126[original query] |
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Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.
PLoS genetics 2009 Apr 5 (4): e1000445. Soranzo Nicole, Rivadeneira Fernando, Chinappen-Horsley Usha, Malkina Ida, Richards J Brent, Hammond Naomi, Stolk Lisette, Nica Alexandra, Inouye Michael, Hofman Albert, Stephens Jonathan, Wheeler Eleanor, Arp Pascal, Gwilliam Rhian, Jhamai P Mila, Potter Simon, Chaney Amy, Ghori Mohammed J R, Ravindrarajah Radhi, Ermakov Sergey, Estrada Karol, Pols Huibert A P, Williams Frances M, McArdle Wendy L, van Meurs Joyce B, Loos Ruth J F, Dermitzakis Emmanouil T, Ahmadi Kourosh R, Hart Deborah J, Ouwehand Willem H, Wareham Nicholas J, Barroso Inês, Sandhu Manjinder S, Strachan David P, Livshits Gregory, Spector Timothy D, Uitterlinden André G, Deloukas Pan |
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
Nature genetics 2010 Jan 42 (1): 45-52. Hancock Dana B, Eijgelsheim Mark, Wilk Jemma B, Gharib Sina A, Loehr Laura R, Marciante Kristin D, Franceschini Nora, van Durme Yannick M T A, Chen Ting-Hsu, Barr R Graham, Schabath Matthew B, Couper David J, Brusselle Guy G, Psaty Bruce M, van Duijn Cornelia M, Rotter Jerome I, Uitterlinden André G, Hofman Albert, Punjabi Naresh M, Rivadeneira Fernando, Morrison Alanna C, Enright Paul L, North Kari E, Heckbert Susan R, Lumley Thomas, Stricker Bruno H C, O'Connor George T, London Stephanie |
The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature. BMC medical genetics 2010 11 (1): 96. Zhao Jianhua, Li Mingyao, Bradfield Jonathan P, Zhang Haitao, Mentch Frank D, Wang Kai, Sleiman Patrick M, Kim Cecilia E, Glessner Joseph T, Hou Cuiping, Keating Brendan J, Thomas Kelly A, Garris Maria L, Deliard Sandra, Frackelton Edward C, Otieno F George, Chiavacci Rosetta M, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
Genome-wide association study of height and body mass index in Australian twin families.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2010 Apr 13 (2): 179-93. Liu Jimmy Z, Medland Sarah E, Wright Margaret J, Henders Anjali K, Heath Andrew C, Madden Pamela A F, Duncan Alexis, Montgomery Grant W, Martin Nicholas G, McRae Allan |
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis.
Nature genetics 2013 Jun 45 (6): 676-9. Kou Ikuyo, Takahashi Yohei, Johnson Todd A, Takahashi Atsushi, Guo Long, Dai Jin, Qiu Xusheng, Sharma Swarkar, Takimoto Aki, Ogura Yoji, Jiang Hua, Yan Huang, Kono Katsuki, Kawakami Noriaki, Uno Koki, Ito Manabu, Minami Shohei, Yanagida Haruhisa, Taneichi Hiroshi, Hosono Naoya, Tsuji Taichi, Suzuki Teppei, Sudo Hideki, Kotani Toshiaki, Yonezawa Ikuho, Londono Douglas, Gordon Derek, Herring John A, Watanabe Kota, Chiba Kazuhiro, Kamatani Naoyuki, Jiang Qing, Hiraki Yuji, Kubo Michiaki, Toyama Yoshiaki, Tsunoda Tatsuhiko, Wise Carol A, Qiu Yong, Shukunami Chisa, Matsumoto Morio, Ikegawa Shi |
Association of GPR126 gene polymorphism with adolescent idiopathic scoliosis in Chinese populations. Genomics 2015 Feb 105 (2): 101-7. Xu Ji-Feng, Yang Guang-hai, Pan Xiao-Hong, Zhang Shui-Jun, Zhao Chen, Qiu Bin-Song, Gu Hai-Feng, Hong Jian-Fei, Cao Li, Chen Yu, Xia Bing, Bi Qin, Wang Ya-Pi |
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Human molecular genetics 2015 Feb 24 (4): 1155-68. van der Valk Ralf J P, Kreiner-Møller Eskil, Kooijman Marjolein N, Guxens Mònica, Stergiakouli Evangelia, Sääf Annika, Bradfield Jonathan P, Geller Frank, Hayes M Geoffrey, Cousminer Diana L, Körner Antje, Thiering Elisabeth, Curtin John A, Myhre Ronny, Huikari Ville, Joro Raimo, Kerkhof Marjan, Warrington Nicole M, Pitkänen Niina, Ntalla Ioanna, Horikoshi Momoko, Veijola Riitta, Freathy Rachel M, Teo Yik-Ying, Barton Sheila J, Evans David M, Kemp John P, St Pourcain Beate, Ring Susan M, Davey Smith George, Bergström Anna, Kull Inger, Hakonarson Hakon, Mentch Frank D, Bisgaard Hans, Chawes Bo, Stokholm Jakob, Waage Johannes, Eriksen Patrick, Sevelsted Astrid, Melbye Mads, , van Duijn Cornelia M, Medina-Gomez Carolina, Hofman Albert, de Jongste Johan C, Taal H Rob, Uitterlinden André G, , Armstrong Loren L, Eriksson Johan, Palotie Aarno, Bustamante Mariona, Estivill Xavier, Gonzalez Juan R, Llop Sabrina, Kiess Wieland, Mahajan Anubha, Flexeder Claudia, Tiesler Carla M T, Murray Clare S, Simpson Angela, Magnus Per, Sengpiel Verena, Hartikainen Anna-Liisa, Keinanen-Kiukaanniemi Sirkka, Lewin Alexandra, Da Silva Couto Alves Alexessander, Blakemore Alexandra I, Buxton Jessica L, Kaakinen Marika, Rodriguez Alina, Sebert Sylvain, Vaarasmaki Marja, Lakka Timo, Lindi Virpi, Gehring Ulrike, Postma Dirkje S, Ang Wei, Newnham John P, Lyytikäinen Leo-Pekka, Pahkala Katja, Raitakari Olli T, Panoutsopoulou Kalliope, Zeggini Eleftheria, Boomsma Dorret I, Groen-Blokhuis Maria, Ilonen Jorma, Franke Lude, Hirschhorn Joel N, Pers Tune H, Liang Liming, Huang Jinyan, Hocher Berthold, Knip Mikael, Saw Seang-Mei, Holloway John W, Melén Erik, Grant Struan F A, Feenstra Bjarke, Lowe William L, Widén Elisabeth, Sergeyev Elena, Grallert Harald, Custovic Adnan, Jacobsson Bo, Jarvelin Marjo-Riitta, Atalay Mustafa, Koppelman Gerard H, Pennell Craig E, Niinikoski Harri, Dedoussis George V, Mccarthy Mark I, Frayling Timothy M, Sunyer Jordi, Timpson Nicholas J, Rivadeneira Fernando, Bønnelykke Klaus, Jaddoe Vincent W V, |
Current progress in genetic research of adolescent idiopathic scoliosis. Annals of translational medicine 2015 May 3 (Suppl 1): S19. Zhu Zezhang, Xu Leilei, Qiu Yo |
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. Thorax 2016 Feb . Jackson Victoria E, Ntalla Ioanna, Sayers Ian, Morris Richard, Whincup Peter, Casas Juan-Pablo, Amuzu Antoinette, Choi Minkyoung, Dale Caroline, Kumari Meena, Engmann Jorgen, Kalsheker Noor, Chappell Sally, Guetta-Baranes Tamar, McKeever Tricia M, Palmer Colin N A, Tavendale Roger, Holloway John W, Sayer Avan A, Dennison Elaine M, Cooper Cyrus, Bafadhel Mona, Barker Bethan, Brightling Chris, Bolton Charlotte E, John Michelle E, Parker Stuart G, Moffat Miriam F, Wardlaw Andrew J, Connolly Martin J, Porteous David J, Smith Blair H, Padmanabhan Sandosh, Hocking Lynne, Stirrups Kathleen E, Deloukas Panos, Strachan David P, Hall Ian P, Tobin Martin D, Wain Louise |
Genetic Variant of GPR126 Gene is Functionally Associated With Adolescent Idiopathic Scoliosis in Chinese Population. Spine 2017 Feb . Qin Xiaodong, Xu Leilei, Xia Chao, Zhu Weiguo, Sun Weixiang, Liu Zhen, Qiu Yong, Zhu Zezha |
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
American journal of human genetics 2017 Dec 101 (6): 913-924. Shaffer John R, Li Jinxi, Lee Myoung Keun, Roosenboom Jasmien, Orlova Ekaterina, Adhikari Kaustabh, , Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Rothhammer Francisco, Bedoya Gabriel, González-José Rolando, Pfeffer Paige E, Wollenschlaeger Christopher A, Hecht Jacqueline T, Wehby George L, Moreno Lina M, Ding Anan, Jin Li, Yang Yajun, Carlson Jenna C, Leslie Elizabeth J, Feingold Eleanor, Marazita Mary L, Hinds David A, Cox Timothy C, Wang Sijia, Ruiz-Linares Andrés, Weinberg Seth |
Copy Number Profiling of MammaPrint™ Genes Reveals Association with the Prognosis of Breast Cancer Patients. Journal of breast cancer 2017 10 20 (3): 246-253. Fatima Areej, Tariq Fomaz, Malik Muhammad Faraz Arshad, Qasim Muhammad, Haq Farh |
Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population. Cancer biomarkers : section A of Disease markers 2017 Oct . Lu Nanhang, Wang Jinzeng, Zhu Bijun, Zhang Miaomiao, Qi Fazhi, Wang Xiangdong, Gu Jianyi |
Evidence of Early-Stage Selection on EPAS1 and GPR126 Genes in Andean High Altitude Populations. Scientific reports 2017 10 7 (1): 13042. Eichstaedt Christina A, Pagani Luca, Antao Tiago, Inchley Charlotte E, Cardona Alexia, Mörseburg Alexander, Clemente Florian J, Sluckin Timothy J, Metspalu Ene, Mitt Mario, Mägi Reedik, Hudjashov Georgi, Metspalu Mait, Mormina Maru, Jacobs Guy S, Kivisild Toom |
Replication Study for the Association of GWAS-associated Loci With Adolescent Idiopathic Scoliosis Susceptibility and Curve Progression in a Chinese Population. Spine 2018 Sep . Man Gene Chi-Wai, Tang Nelson Leung-Sang, Chan Ting Fung, Lam Tsz Ping, Li Jing Woei, Ng Bobby Kin-Wah, Zhu Zezhang, Qiu Yong, Cheng Jack Chun-Y |
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis. Scientific reports 2018 Aug 8 (1): 11575. Kou Ikuyo, Watanabe Kota, Takahashi Yohei, Momozawa Yukihide, Khanshour Anas, Grauers Anna, Zhou Hang, Liu Gang, Fan Yan-Hui, Takeda Kazuki, Ogura Yoji, Zhou Taifeng, Iwasaki Yusuke, Kubo Michiaki, Wu Zhihong, Matsumoto Morio, , , Einarsdottir Elisabet, Kere Juha, Huang Dongsheng, Qiu Guixing, Qiu Yong, Wise Carol A, Song You-Qiang, Wu Nan, Su Peiqiang, Gerdhem Paul, Ikegawa Shi |
High Prevalence of a Hotspot of Noncoding Somatic Mutations in Intron 6 of GPR126 in Bladder Cancer. Molecular cancer research : MCR 2018 11 17 (2): 469-475. Garinet Simon, Pignot Géraldine, Vacher Sophie, Le Goux Constance, Schnitzler Anne, Chemlali Walid, Sirab Nanor, Barry Delongchamps Nicolas, Zerbib Marc, Sibony Mathilde, Allory Yves, Damotte Diane, Bieche Iv |
Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population. Journal of cellular and molecular medicine 2018 Jan . Liu Gang, Liu Sen, Lin Mao, Li Xiaoxin, Chen Weisheng, Zuo Yuzhi, Liu Jiaqi, Niu Yuchen, Zhao Sen, Long Bo, Wu Zhihong, Wu Nan, Qiu Guixi |
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 |
A Genetic Variant in GPR126 Causing a Decreased Inclusion of Exon 6 Is Associated with Cartilage Development in Adolescent Idiopathic Scoliosis Population. BioMed research international 2019 2019 4678969. Xu Enjie, Shao Wei, Jiang Heng, Lin Tao, Gao Rui, Zhou Xuh |
Regulation of body length and bone mass by Gpr126/Adgrg6. Science advances 2020 Mar 6 (12): eaaz0368. Sun Peng, He Liang, Jia Kunhang, Yue Zhiying, Li Shichang, Jin Yunyun, Li Zhenxi, Siwko Stefan, Xue Feng, Su Jiacan, Liu Mingyao, Luo Ji |
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 |
Genomic Instability Signature of Palindromic Non-Coding Somatic Mutations in Bladder Cancer. Cancers 2020 Oct 12 (10): . Vacher Sophie, Suybeng Voreak, Girard Elodie, Masliah Planchon Julien, Thomson Grégory, Le Goux Constance, Garinet Simon, Schnitzler Anne, Chemlali Walid, Firlej Virginie, Damotte Diane, Allory Yves, Kamal Maud, Pignot Géraldine, Bieche Iv |
Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Scientific reports 2021 Sep 11 (1): 19365. Yang Tianzhong, Jackson Victoria E, Smith Albert V, Chen Han, Bartz Traci M, Sitlani Colleen M, Psaty Bruce M, Gharib Sina A, O'Connor George T, Dupuis Josée, Xu Jiayi, Lohman Kurt, Liu Yongmei, Kritchevsky Stephen B, Cassano Patricia A, Flexeder Claudia, Gieger Christian, Karrasch Stefan, Peters Annette, Schulz Holger, Harris Sarah E, Starr John M, Deary Ian J, Manichaikul Ani, Oelsner Elizabeth C, Barr R G, Taylor Kent D, Rich Stephen S, Bonten Tobias N, Mook-Kanamori Dennis O, Noordam Raymond, Li-Gao Ruifang, Jarvelin Marjo-Riitta, Wielscher Matthias, Terzikhan Natalie, Lahousse Lies, Brusselle Guy, Weiss Stefan, Ewert Ralf, Gläser Sven, Homuth Georg, Shrine Nick, Hall Ian P, Tobin Martin, London Stephanie J, Wei Peng, Morrison Alanna |
Regulatory region mutations of TERT, PLEKHS1 and GPR126 genes as urinary biomarkers in upper tract urothelial carcinomas. Journal of Cancer 2021 6 12 (13): 3853-3861. Xing Xiangling, Yuan Xiaotian, Liu Tiantian, Dai Mingkai, Fan Yidong, Liu Cheng, Strååt Klas, Björkholm Magnus, Xu Daw |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
Association between genetic polymorphisms and risk of adolescent idiopathic scoliosis in case-control studies: a systematic review. Journal of medical genetics 2023 9 . Elizabeth Terhune, Patricia Heyn, Christi Piper, Cambria Wethey, Anna Monley, Melissa Cuevas, Nancy Hadley Mill |
Analysis of GPR126 polymorphisms and their relationship with scoliosis in Marfan syndrome and Marfan-like syndrome in Mexican patients. Biomolecules and biomedicine 2023 6 . Maria Elena Soto, Giovanny Fuentevilla-Alvarez, Solange Gabriela Koretzky, Gilberto Vargas-Alarcón, Yazmín Estela Torres-Paz, Sergio Enrique Meza-Toledo, Israel Pérez-Torres, Claudia Huesca-Gómez, Ricardo Gamb |
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