دورية أكاديمية

Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.

التفاصيل البيبلوغرافية
العنوان: Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
المؤلفون: Hindy, George, Dornbos, Peter, Chaffin, Mark D, Liu, Dajiang J, Wang, Minxian, Selvaraj, Margaret Sunitha, Zhang, David, Park, Joseph, Aguilar-Salinas, Carlos A, Antonacci-Fulton, Lucinda, Ardissino, Diego, Arnett, Donna K, Aslibekyan, Stella, Atzmon, Gil, Ballantyne, Christie M, Barajas-Olmos, Francisco, Barzilai, Nir, Becker, Lewis C, Bielak, Lawrence F, Bis, Joshua C, Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L, Bottinger, Erwin, Bowden, Donald W, Bown, Matthew J, Brody, Jennifer A, Broome, Jai G, Burtt, Noël P, Cade, Brian E, Centeno-Cruz, Federico, Chan, Edmund, Chang, Yi-Cheng, Chen, Yii-Der I, Cheng, Ching-Yu, Choi, Won Jung, Chowdhury, Rajiv, Contreras-Cubas, Cecilia, Córdova, Emilio J, Correa, Adolfo, Cupples, L Adrienne, Curran, Joanne E, Danesh, John, de Vries, Paul S, DeFronzo, Ralph A, Doddapaneni, Harsha, Duggirala, Ravindranath, Dutcher, Susan K, Ellinor, Patrick T, Emery, Leslie S, Florez, Jose C, Fornage, Myriam, Freedman, Barry I, Fuster, Valentin, Garay-Sevilla, Ma Eugenia, García-Ortiz, Humberto, Germer, Soren, Gibbs, Richard A, Gieger, Christian, Glaser, Benjamin, Gonzalez, Clicerio, Gonzalez-Villalpando, Maria Elena, Graff, Mariaelisa, Graham, Sarah E, Grarup, Niels, Groop, Leif C, Guo, Xiuqing, Gupta, Namrata, Han, Sohee, Hanis, Craig L, Hansen, Torben, He, Jiang, Heard-Costa, Nancy L, Hung, Yi-Jen, Hwang, Mi Yeong, Irvin, Marguerite R, Islas-Andrade, Sergio, Jarvik, Gail P, Kang, Hyun Min, Kardia, Sharon L R, Kelly, Tanika, Kenny, Eimear E, Khan, Alyna T, Kim, Bong-Jo, Kim, Ryan W, Kim, Young Jin, Koistinen, Heikki A, Kooperberg, Charles, Kuusisto, Johanna, Kwak, Soo Heon, Laakso, Markku, Lange, Leslie A, Lee, Jiwon, Lee, Juyoung, Lee, Seonwook, Lehman, Donna M, Lemaitre, Rozenn N, Linneberg, Allan, Liu, Jianjun, Loos, Ruth J F, Lubitz, Steven A, Lyssenko, Valeriya, Ma, Ronald C W, Martin, Lisa Warsinger, Martínez-Hernández, Angélica, Mathias, Rasika A, McGarvey, Stephen T, McPherson, Ruth, Meigs, James B, Meitinger, Thomas, Melander, Olle, Mendoza-Caamal, Elvia, Metcalf, Ginger A, Mi, Xuenan, Mohlke, Karen L, Montasser, May E, Moon, Jee-Young, Moreno-Macías, Hortensia, Morrison, Alanna C, Muzny, Donna M, Nelson, Sarah C, Nilsson, Peter M, O'Connell, Jeffrey R, Orho-Melander, Marju, Orozco, Lorena, Palmer, Colin N A, Palmer, Nicholette D, Park, Cheol Joo, Park, Kyong Soo, Pedersen, Oluf, Peralta, Juan M, Peyser, Patricia A, Post, Wendy S, Preuss, Michael, Psaty, Bruce M, Qi, Qibin, Rao, D C, Redline, Susan, Reiner, Alexander P, Revilla-Monsalve, Cristina, Rich, Stephen S, Samani, Nilesh, Schunkert, Heribert, Schurmann, Claudia, Seo, Daekwan, Seo, Jeong-Sun, Sim, Xueling, Sladek, Rob, Small, Kerrin S, So, Wing Yee, Stilp, Adrienne M, Tai, E Shyong, Tam, Claudia H T, Taylor, Kent D, Teo, Yik Ying, Thameem, Farook, Tomlinson, Brian, Tsai, Michael Y, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Teresa, Udler, Miriam S, van Dam, Rob M, Vasan, Ramachandran S, Viaud Martinez, Karine A, Wang, Fei Fei, Wang, Xuzhi, Watkins, Hugh, Weeks, Daniel E, Wilson, James G, Witte, Daniel R, Wong, Tien-Yin, Yanek, Lisa R, Kathiresan, Sekar, Rader, Daniel J, Rotter, Jerome I, Boehnke, Michael, McCarthy, Mark I, Willer, Cristen J, Natarajan, Pradeep, Flannick, Jason A, Khera, Amit V, Peloso, Gina M
المصدر: Medicine Faculty Publications
بيانات النشر: Health Sciences Research Commons
سنة النشر: 2022
المجموعة: George Washington University: Health Sciences Research Commons (HSRC)
مصطلحات موضوعية: 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, Medicine and Health Sciences
نوع الوثيقة: text
اللغة: unknown
العلاقة: https://hsrc.himmelfarb.gwu.edu/smhs_medicine_facpubs/5212Test; http://dx.doi.org/10.1016/j.ajhg.2021.11.021Test
DOI: 10.1016/j.ajhg.2021.11.021
الإتاحة: https://doi.org/10.1016/j.ajhg.2021.11.021Test
https://hsrc.himmelfarb.gwu.edu/smhs_medicine_facpubs/5212Test
رقم الانضمام: edsbas.924D26BC
قاعدة البيانات: BASE