Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Document Type
Journal Article
Publication Date
1-6-2022
Journal
American Journal of Human Genetics
Volume
109
Issue
1
Inclusive Pages
81-96
DOI
10.1016/j.ajhg.2021.11.021
Keywords
Alleles; Blood Glucose; Case-Control Studies; Computational Biology; Databases, Genetic; Diabetes Mellitus, Type 2; Exome; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Genome-Wide Association Study; Humans; Lipid Metabolism; Lipids; Liver; Molecular Sequence Annotation; Multifactorial Inheritance; Open Reading Frames; Phenotype; Polymorphism, Single Nucleotide
APA Citation
Hindy, G., Dornbos, P., Chaffin, M., Liu, D., Wang, M., Selvaraj, M., Zhang, D., Park, J., Aguilar-Salinas, C., Antonacci-Fulton, L., Ardissino, D., Arnett, D., Aslibekyan, S., Atzmon, G., Ballantyne, C., Barajas-Olmos, F., Barzilai, N., Becker, L., Bielak, L., Bis, J., Blangero, J., Boerwinkle, E., Bonnycastle, L., Bottinger, E., Bowden, D., Bown, M., Brody, J., Broome, J., Burtt, N., Cade, B., Centeno-Cruz, F., Chan, E., Chang, Y., Chen, Y., Cheng, C., Choi, W., Chowdhury, R., Contreras-Cubas, C., Córdova, E., Correa, A., Cupples, L., Curran, J., Danesh, J., de Vries, P., DeFronzo, R., Doddapaneni, H., Duggirala, R., Dutcher, S., Ellinor, P., Emery, L., Florez, J., Fornage, M., Freedman, B., Fuster, V., Garay-Sevilla, M., García-Ortiz, H., Germer, S., Gibbs, R., Gieger, C., Glaser, B., Gonzalez, C., Gonzalez-Villalpando, M., Graff, M., Graham, S., Grarup, N., Groop, L., Guo, X., Gupta, N., Han, S., Hanis, C., Hansen, T., He, J., Heard-Costa, N., Hung, Y., Hwang, M., Irvin, M., Islas-Andrade, S., Jarvik, G., Kang, H., Kardia, S., Kelly, T., Kenny, E., Khan, A., Kim, B., Kim, R., Kim, Y., Koistinen, H., Kooperberg, C., Kuusisto, J., Kwak, S., Laakso, M., Lange, L., Lee, J., Lee, J., Lee, S., Lehman, D., Lemaitre, R., Linneberg, A., Liu, J., Loos, R., Lubitz, S., Lyssenko, V., Ma, R., Martin, L. W., Martínez-Hernández, A., Mathias, R., McGarvey, S., McPherson, R., Meigs, J., Meitinger, T., Melander, O., Mendoza-Caamal, E., Metcalf, G., Mi, X., Mohlke, K., Montasser, M., Moon, J., Moreno-Macías, H., Morrison, A., Muzny, D., Nelson, S., Nilsson, P., O'Connell, J., Orho-Melander, M., Orozco, L., Palmer, C., Palmer, N., Park, C., Park, K., Pedersen, O., Peralta, J., Peyser, P., Post, W., Preuss, M., Psaty, B., Qi, Q., Rao, D., Redline, S., Reiner, A., Revilla-Monsalve, C., Rich, S., Samani, N., Schunkert, H., Schurmann, C., Seo, D., Seo, J., Sim, X., Sladek, R., Small, K., So, W., Stilp, A., Tai, E., Tam, C., Taylor, K., Teo, Y., Thameem, F., Tomlinson, B., Tsai, M., Tuomi, T., Tuomilehto, J., Tusié-Luna, T., Udler, M., van Dam, R., Vasan, R., Viaud Martinez, K., Wang, F., Wang, X., Watkins, H., Weeks, D., Wilson, J., Witte, D., Wong, T., Yanek, L., Kathiresan, S., Rader, D., Rotter, J., Boehnke, M., McCarthy, M., Willer, C., Natarajan, P., Flannick, J., Khera, A., & Peloso, G. (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, 109 (1). http://dx.doi.org/10.1016/j.ajhg.2021.11.021
Peer Reviewed
1
Comments
Epub 2021 Dec 20