Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: IRX1[original query] |
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A genome-wide scan maps a novel high myopia locus to 5p15. Investigative ophthalmology & visual science 2008 Sep 49 (9): 3768-78. Lam Ching Yan, Tam Pancy O S, Fan Dorothy S P, Fan Bao Jian, Wang Dan Yi, Lee Coral W S, Pang Chi Pui, Lam Dennis S |
Identifying novel biomarkers of gastric cancer through integration analysis of single nucleotide polymorphisms and gene expression profile. The International journal of biological markers 2015 30 (3): e321-6. Wang Tao, Xu Yan, Hou Pe |
Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome-Wide Association Study.
Arthritis & rheumatology (Hoboken, N.J.) 2016 Jan . Julià Antonio, Blanco Francisco, Fernández-Gutierrez Benjamín, González Antonio, Cañete Juan D, Maymó Joan, Alperi-López Mercedes, Olivè Alex, Corominas Héctor, Martínez-Taboada Víctor, González Isidoro, Fernandez-Nebro Antonio, Erra Alba, Sánchez-Fernández Simón, Alonso Arnald, López-Lasanta María, Tortosa Raül, Codó Laia, Lluis Gelpi Josep, García-Montero Andrés C, Bertranpetit Jaume, Absher Devin, Myers Richard M, Tornero Jesús, Marsal Sa |
Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies.
Placenta 2018 Jun 66 8-16. Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Sanchez Sixto E, Garcia Pedro J, Tekola-Ayele Fasil, Hajat Anjum, Thornton Timothy A, Ananth Cande V, Williams Michelle |
Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 Mar e3698. Hsu Yi-Hsiang, Estrada Karol, Evangelou Evangelos, Ackert-Bicknell Cheryl, Akesson Kristina, Beck Thomas, Brown Suzanne J, Capellini Terence, Carbone Laura, Cauley Jane, Cheung Ching-Lung, Cummings Steven R, Czerwinski Stefan, Demissie Serkalem, Econs Michael, Evans Daniel, Farber Charles, Gautvik Kaare, Harris Tamara, Kammerer Candace, Kemp John, Koller Daniel L, Kung Annie, Lawlor Debbie, Lee Miryoung, Lorentzon Mattias, McGuigan Fiona, Medina-Gomez Carolina, Mitchell Braxton, Newman Anne, Nielson Carrie, Ohlsson Claes, Peacock Munro, Reppe Sjur, Richards J Brent, Robbins John, Sigurdsson Gunnar, Spector Timothy D, Stefansson Kari, Streeten Elizabeth, Styrkarsdottir Unnur, Tobias Jonathan, Trajanoska Katerina, Uitterlinden André, Vandenput Liesbeth, Wilson Scott G, Yerges-Armstrong Laura, Young Mariel, Zillikens M Carola, Rivadeneira Fernando, Kiel Douglas P, Karasik Dav |
Investigating Role of IRX Family in Development of Female Adolescent Idiopathic Scoliosis: Which One Is Real Cause? World neurosurgery 2019 Mar . Xia Chao, Xue Bingchuan, Wang Yuwen, Qin Xiaodong, Qiu Yong, Zhu Zezhang, Xu Leil |
IRX1 is a novel gene, overexpressed in high-grade IDH-mutant astrocytomas. Pathology, research and practice 2023 4 245 154464. Harsha S Sugur, Shilpa Rao, Palavalasa Sravya, K Athul Menon, Arimappamagan Arivazhagan, Bhupesh Mehta, Vani Santo |
ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon. Nature communications 2023 10 14 (1): 6156. Sylvia Hartmann, Summaira Yasmeen, Benjamin M Jacobs, Spiros Denaxas, Munir Pirmohamed, Eric R Gamazon, Mark J Caulfield, , Harry Hemingway, Maik Pietzner, Claudia Langenbe |
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- Page last updated:Apr 22, 2024
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