Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: MAML3[original query] |
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A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Nature genetics 2013 Jul 45 (7): 818-21. Hu Zhibin, Shi Yongyong, Mo Xuming, Xu Jing, Zhao Bijun, Lin Yuan, Yang Shiwei, Xu Zhengfeng, Dai Juncheng, Pan Shandong, Da Min, Wang Xiaowei, Qian Bo, Wen Yang, Wen Juan, Xing Jinliang, Guo Xuejiang, Xia Yankai, Ma Hongxia, Jin Guangfu, Yu Shiqiang, Liu Jiayin, Zhou Zuomin, Wang Xinru, Chen Yijiang, Sha Jiahao, Shen Hongbi |
Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD.
The European respiratory journal 2015 Jan 45 (1): 60-75. Dijkstra Akkelies E, Boezen H Marike, van den Berge Maarten, Vonk Judith M, Hiemstra Pieter S, Barr R Graham, Burkart Kirsten M, Manichaikul Ani, Pottinger Tess D, Silverman Edward K, Cho Michael H, Crapo James D, Beaty Terri H, Bakke Per, Gulsvik Amund, Lomas David A, Bossé Yohan, Nickle David C, Paré Peter D, de Koning Harry J, Lammers Jan-Willem, Zanen Pieter, Smolonska Joanna, Wijmenga Ciska, Brandsma Corry-Anke, Groen Harry J M, Postma Dirkje S, |
PTTG1IP and MAML3, novel genomewide association study genes for severity of hyperresponsiveness in adult asthma. Allergy 2016 Oct . Nieuwenhuis M A E, Vonk J M, Himes B E, Sarnowski C, Minelli C, Jarvis D, Bouzigon E, Nickle D C, Laviolette M, Sin D, Weiss S T, van den Berge M, Koppelman G H, Postma D |
Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2019 Jul . Golyan F F, Druley T E, Abbaszadegan M |
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
Whole-genome analysis identifies novel drivers and high-risk double-hit events in relapsed/refractory myeloma. Blood 2022 10 141 (6): 620-633. Ansari-Pour Naser, Samur Mehmet, Flynt Erin, Gooding Sarah, Towfic Fadi, Stong Nicholas, Estevez Maria Ortiz, Mavrommatis Konstantinos, Walker Brian, Morgan Gareth, Munshi Nikhil, Avet-Loiseau Herve, Thakurta Anj |
Genomic and immune landscape Of metastatic pheochromocytoma and paraganglioma. Nature communications 2023 2 14 (1): 1122. Calsina Bruna, Piñeiro-Yáñez Elena, Martínez-Montes Ángel M, Caleiras Eduardo, Fernández-Sanromán Ángel, Monteagudo María, Torres-Pérez Rafael, Fustero-Torre Coral, Pulgarín-Alfaro Marta, Gil Eduardo, Letón Rocío, Jiménez Scherezade, García-Martín Santiago, Martin Maria Carmen, Roldán-Romero Juan María, Lanillos Javier, Mellid Sara, Santos María, Díaz-Talavera Alberto, Rubio Ángeles, González Patricia, Hernando Barbara, Bechmann Nicole, Dona Margo, Calatayud María, Guadalix Sonsoles, Álvarez-Escolá Cristina, Regojo Rita M, Aller Javier, Del Olmo-Garcia Maria Isabel, López-Fernández Adrià, Fliedner Stephanie M J, Rapizzi Elena, Fassnacht Martin, Beuschlein Felix, Quinkler Marcus, Toledo Rodrigo A, Mannelli Massimo, Timmers Henri J, Eisenhofer Graeme, Rodríguez-Perales Sandra, Domínguez Orlando, Macintyre Geoffrey, Currás-Freixes Maria, Rodríguez-Antona Cristina, Cascón Alberto, Leandro-García Luis J, Montero-Conde Cristina, Roncador Giovanna, García-García Juan Fernando, Pacak Karel, Al-Shahrour Fátima, Robledo Merced |
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- Page last updated:Apr 22, 2024
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