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Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R, Kjaer, Troels R, Fine, Rebecca S, Lu, Yingchang, Schurmann, Claudia, Highland, Heather M
et al (show 363 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). pp. 186-190.


Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William
et al (show 233 more authors) (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. NATURE GENETICS, 50 (4). 559-571+.


Hicks, Blanaid, Veronesi, Giovanni, Ferrario, Marco M, Forrest, Hannah, Whitehead, Margaret ORCID: 0000-0001-5614-6576, Diderichsen, Finn, Tunstall-Pedoe, Hugh, Kuulasmaa, Kari, Sans, Susana, Salomaa, Veikko
et al (show 11 more authors) (2021) Roles of allostatic load, lifestyle and clinical risk factors in mediating the association between education and coronary heart disease risk in Europe. JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 75 (12). pp. 1147-1154.

This list was generated on Sat Mar 9 08:47:53 2024 GMT.