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Items where Author is "Narita, A"
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Number of items: 3.
Graham, SE, Clarke, SL, Wu, KHH, Kanoni, S, Zajac, GJM, Ramdas, S, Surakka, I, Ntalla, I, Vedantam, S, Winkler, TW, Locke, AE, Marouli, E, Hwang, MY, Han, S, Narita, A, Choudhury, A, Bentley, AR, Ekoru, K, Verma, A, Trivedi, B, Martin, HC, Hunt, KA, Hui, Q, Klarin, D, Zhu, X, Thorleifsson, G, Helgadottir, A, Gudbjartsson, DF, Holm, H, Olafsson, I, Akiyama, M, Sakaue, S, Terao, C, Kanai, M, Zhou, W, Brumpton, BM, Rasheed, H, Ruotsalainen, SE, Havulinna, AS, Veturi, Y, Feng, QP, Rosenthal, EA, Lingren, T, Pacheco, JA, Pendergrass, SA, Haessler, J, Giulianini, F, Bradford, Y, Miller, JE, Campbell, A, Lin, K, Millwood, IY, Hindy, G, Rasheed, A, Faul, JD, Zhao, W, Weir, DR, Turman, C, Huang, H, Graff, M, Mahajan, A, Brown, MR, Zhang, W, Yu, K, Schmidt, EM, Pandit, A, Gustafsson, S, Yin, S, Luan, J, Zhao, JH, Matsuda, F, Jang, HM, Yoon, K, Medina-Gomez, C, Pitsillides, A, Hottenga, JJ, Willemsen, G, Wood, AR, Ji, Y, Gao, Z, Haworth, S, Mitchell, RE, Chai, JF, Aadahl, M, Yao, J, Manichaikul, A, Warren, HR, Ramirez, J, Bork-Jensen, J, Karhus, LL, Goel, A, Sabater-Lleal, M, Noordam, R, Sidore, C, Fiorillo, E, McDaid, AF, Marques-Vidal, P, Wielscher, M, Trompet, S and Hewitt, AW 
ORCID: 0000-0002-5123-5999 2021
, 'The power of genetic diversity in genome wide association studies of lipids'
, Nature, vol. 600, no. 7890
, pp. 675-679
, doi: https://doi.org/10.1038/s41586-021-04064-3.
ORCID: 0000-0002-5123-5999 2021
, 'The power of genetic diversity in genome wide association studies of lipids'
, Nature, vol. 600, no. 7890
, pp. 675-679
, doi: https://doi.org/10.1038/s41586-021-04064-3.
Siggs, OM, Souzeau, E, Pasutto, F, Dubowsky, A, Smith, JEH, Taranath, D, Pater, J, Rait, JL, Narita, A, Mauri, L, Del Longo, A, Reis, A, Chappell, A, Kearns, LS, Staffieri, SE, Elder, JE, Ruddle, JB, Hewitt, AW ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA and Craig, JE 2019
, 'Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma'
, JAMA Ophthalmology, no. Januar
, E1-E8
, doi: https://doi.org/10.1001/jamaophthalmol.2018.5646.
ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA and Craig, JE 2019
, 'Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma'
, JAMA Ophthalmology, no. Januar
, E1-E8
, doi: https://doi.org/10.1001/jamaophthalmol.2018.5646.
Siggs, OM, Souzeau, E, Taranath, DA, Dubowsky, A, Chappell, A, Zhou, T, Javadiyan, S, Nicholl, J, Kearns, LS, Staffieri, SE, Narita, A, Smith, JEH, Pater, J, Hewitt, AW ORCID: 0000-0002-5123-5999, Ruddle, JB, Elder, JE, Mackey, DA, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2020
, 'Biallelic CPAMD8 variants are a frequent cause of childhood and juvenile open-angle glaucoma'
, Ophthalmology, vol. 127, no. 6
, pp. 758-766
, doi: https://doi.org/10.1016/j.ophtha.2019.12.024.
ORCID: 0000-0002-5123-5999, Ruddle, JB, Elder, JE, Mackey, DA, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2020
, 'Biallelic CPAMD8 variants are a frequent cause of childhood and juvenile open-angle glaucoma'
, Ophthalmology, vol. 127, no. 6
, pp. 758-766
, doi: https://doi.org/10.1016/j.ophtha.2019.12.024.