Rare and low-frequency coding variants alter human adult height

EPIC-InterAct Consortium, ReproGen Consortium, CHD Exome+ Consortium, ExomeBP Consortium, T2D-Genes Consortium, GoT2D Genes Consortium, Global Lipids Genetics Consortium, The MAGIC Investigators, Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, Ken Sin Lo, Andrew R Wood, Troels R Kjaer, Rebecca S Fine, Yingchang Lu, Claudia Schurmann, Heather M Highland, Sina Rüeger, Gudmar ThorleifssonAnne E Justice, David Lamparter, Kathleen E Stirrups, Valérie Turcot, Kristin L Young, Thomas W Winkler, Tõnu Esko, Tugce Karaderi, Adam E Locke, Nicholas G D Masca, Maggie C Y Ng, Poorva Mudgal, Manuel A Rivas, Sailaja Vedantam, Anubha Mahajan, Xiuqing Guo, Goncalo Abecasis, Katja K Aben, Linda S Adair, Dewan S Alam, Linda Broer, Rajiv Chowdhury, Amanda J Cox, Mark C H de Groot, Anneke I den Hollander, Torben Hansen, Yongmei Liu, Roel A Ophoff, John R B Perry, Danielle Posthuma, Alexander Teumer, André G Uitterlinden, Sander W van der Laan, Cornelia M van Duijn, Jing Hua Zhao, Wei Zhao, Wei Zhou, Fernando Rivadeneira, Ruth J.F. Loos, Timothy Frayling, Joel N. Hirschorn*, Panos Deloukas*, Guillaume Lettre*

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

456 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology