Hindy, G, Dornbos, P, Chaffin, M D, Liu, D J, Wang, M, Selvaraj, M S, Zhang, D, Park, J, Aguilar-Salinas, C A, Antonacci-Fulton, L, Ardissino, D, Arnett, D K, Aslibekyan, S, Atzmon, G, Ballantyne, C M, Barajas-Olmos, F, Barzilai, N, Becker, L C, Bielak, L F, Bis, J C, Blangero, J, Boerwinkle, E, Bonnycastle, L L, Bottinger, E, Bowden, D W, Bown, M J, Brody, J A, Broome, J G, Burtt, N P, Cade, B E, Centeno-Cruz, F, Chan, E, Chang, Y C, Chen, Y D I, Cheng, C Y, Choi, W J, Chowdhury, R, Contreras-Cubas, C, Córdova, E J, Correa, A, Cupples, L A, Curran, J E, Danesh, J, de Vries, P S, Grarup, N, Hansen, T, Linneberg, A, Loos, R J F, Pedersen, O, Witte, D R, AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & NHLBI TOPMed Lipids Working Group 2022, ' Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes ', American Journal of Human Genetics, vol. 109, no. 1, pp. 81-96 . https://doi.org/10.1016/j.ajhg.2021.11.021 Am J Hum Genet Hindy, G, Dornbos, P, Chaffin, M D, Liu, D J, Wang, M, Selvaraj, M S, Zhang, D, Park, J, Aguilar-Salinas, C A, Antonacci-Fulton, L, Ardissino, D, Arnett, D K, Aslibekyan, S, Atzmon, G, Ballantyne, C M, Barajas-Olmos, F, Barzilai, N, Becker, L C, Bielak, L F, Bis, J C, Blangero, J, Boerwinkle, E, Bonnycastle, L L, Bottinger, E, Bowden, D W, Bown, M J, Brody, J A, Broome, J G, Burtt, N P, Cade, B E, Centeno-Cruz, F, Chan, E, Chang, Y C, Chen, Y D I, Cheng, C Y, Choi, W J, Chowdhury, R, Contreras-Cubas, C, Córdova, E J, Correa, A, Cupples, L A, Curran, J E, Danesh, J, de Vries, P S, DeFronzo, R A, Grarup, N, Hansen, T, Pedersen, O, Wang, F F, Witte, D R, AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & NHLBI TOPMed Lipids Working Group 2022, ' Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes ', American Journal of Human Genetics, vol. 109, no. 1, pp. 81-96 . https://doi.org/10.1016/j.ajhg.2021.11.021 Hindy, G, Dornbos, P, Chaffin, M D, Liu, D J, Wang, M, Selvaraj, M S, Zhang, D, Park, J, Aguilar-Salinas, C A, Antonacci-Fulton, L, Ardissino, D, Arnett, D K, Aslibekyan, S, Atzmon, G, Ballantyne, C M, Barajas-Olmos, F, Barzilai, N, Becker, L C, Bielak, L F, Bis, J C, Blangero, J, Boerwinkle, E, Bonnycastle, L L, Bottinger, E, Bowden, D W, Bown, M J, Brody, J A, Broome, J G, Burtt, N P, Cade, B E, Centeno-Cruz, F, Chan, E, Chang, Y-C, Chen, Y-D I, Cheng, C-Y, Choi, W J, Chowdhury, R, Contreras-Cubas, C, Córdova, E J, Correa, A, Cupples, L A, Curran, J E, Danesh, J, de Vries, P S, DeFronzo, R A, Doddapaneni, H, Duggirala, R, Dutcher, S K, Ellinor, P T, Grarup, N, Hansen, T, Pedersen, O, Linneberg, A, Witte, D R & AMP-T2D-GENES, Myocardial Infarction Genetics Consortium 2022, ' Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes ', American Journal of Human Genetics, vol. 109, no. 1, pp. 81-96 . https://doi.org/10.1016/j.ajhg.2021.11.021
Cell Genomics Hayward, C, Campbell, A, Porteous, D J, Richmond, A & Marioni, R E 2022, ' Global Biobank Meta-analysis Initiative: powering genetic discovery across human disease ', Cell Genomics . https://doi.org/10.1016/j.xgen.2022.100192 Cell Genomics, 2(10):100192 Zhou, W, Kanai, M, Wu, K H H, Rasheed, H, Tsuo, K, Hirbo, J B, Wang, Y, Bhattacharya, A, Zhao, H, Namba, S, Surakka, I, Wolford, B N, Lo Faro, V, Lopera-Maya, E A, Läll, K, Favé, M J, Partanen, J J, Chapman, S B, Karjalainen, J, Kurki, M, Maasha, M, Brumpton, B M, Chavan, S, Chen, T T, Daya, M, Ding, Y, Feng, Y C A, Guare, L A, Gignoux, C R, Graham, S E, Hornsby, W E, Ingold, N, Ismail, S I, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, I Y, Moreno-Grau, S, Nam, K, Palta, P, Pandit, A, Preuss, M H, Saad, C, Setia-Verma, S, Thorsteinsdottir, U, Uzunovic, J, Verma, A, Zawistowski, M, Loos, R J F, deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, Genes & Health Research Team, LifeLines, Mass General Brigham Biobank, Michigan Genomics Initiative, National Biobank of Korea, Penn Medicine BioBank, Qatar Biobank, The QSkin Sun and Health Study, Taiwan Biobank, The HUNT Study, UCLA ATLAS Community Health Initiative, Uganda Genome Resource, UK Biobank, Biobank of the Americas, BioBank Japan Project, BioMe, BioVU, CanPath-Ontario Health Study, China Kadoorie Biobank Collaborative Group & Colorado Center for Personalized Medicine 2022, ' Global Biobank Meta-analysis Initiative : Powering genetic discovery across human disease ', Cell Genomics, vol. 2, no. 10, 100192 . https://doi.org/10.1016/j.xgen.2022.100192
Moksnes, M R, Røsjø, H, Richmond, A, Lyngbakken, M N, Graham, S E, Hansen, A F, Wolford, B N, Gagliano Taliun, S A, Lefaive, J, Rasheed, H, Thomas, L F, Zhou, W, Aung, N, Surakka, I, Douville, N J, Campbell, A, Porteous, D J, Petersen, S E, Munroe, P B, Welsh, P, Sattar, N, Smith, G D, Fritsche, L G, Nielsen, J B, Åsvold, B O, Hveem, K, Hayward, C, Willer, C J, Brumpton, B M & Omland, T 2021, ' Genome-wide association study of cardiac troponin i in the general population ', Human Molecular Genetics, vol. 30, no. 21, pp. 2027-2039 . https://doi.org/10.1093/hmg/ddab124 Moksnes, M, Røsjø, H, Richmond, A, Lyngbakken, M N, Graham, S E, Falkmo Hansen, A, Wolford, B N, Gagliano Taliun, S A, LeFaive, J, Rasheed, H, Thomas, L, Zhou, W, Aung, N, Surakka, I, Douville, N J, Campbell, A, Porteous, D J, Petersen, S E, Munroe, P B, Welsh, P, Sattar, N, Davey Smith, G, Fritsche, L G, Nielsen, J B, Åsvold, B O, Hveem, K, Hayward, C, Willer, C J, Brumpton, B M & Omland, T 2021, ' Genome-wide association study of cardiac troponin I in the general population ', Human Molecular Genetics, vol. 30, no. 21, ddab124, pp. 2027–2039 . https://doi.org/10.1093/hmg/ddab124 Human Molecular Genetics