Single variant and multi-variant trend tests for genetic association with next generation sequencing that are robust to sequencing error

Autor Kim, Wonkuk, Londono, Douglas, Zhou, Lisheng, Xing, Jinchuan, Nato, Andrew, Musolf, Anthony, Matise, Tara C., Finch, Stephen J., Gordon, Derek
Vydáno 2013

Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemi...

Autor Fesinmeyer, Megan D, Meigs, James B, North, Kari E, Schumacher, Fredrick R, Bůžková, Petra, Franceschini, Nora, Haessler, Jeffrey, Goodloe, Robert, Spencer, Kylee L, Voruganti, Venkata Saroja, Howard, Barbara V, Jackson, Rebecca, Kolonel, Laurence N, Liu, Simin, Manson, JoAnn E, Monroe, Kristine R, Mukamal, Kenneth, Dilks, Holli H, Pendergrass, Sarah A, Nato, Andrew, Wan, Peggy, Wilkens, Lynne R, Marchand, Loic Le, Ambite, José Luis, Buyske, Steven, Florez, Jose C, Crawford, Dana C, Hindorff, Lucia A, Haiman, Christopher A, Peters, Ulrike, Pankow, James S
Vydáno 2013

Genetic variation in genes underlying diverse dementias may explain a small proportion of cases in the Alzheimer’s Disease Sequencing Project

Autor Blue, Elizabeth E., Bis, Joshua C., Dorschner, Michael O., Tsuang, Debby, Barral, Sandra M., Beecham, Gary, Below, Jennifer E., Bush, William S., Butkiewicz, Mariusz, Cruchaga, Carlos, DeStefano, Anita, Farrer, Lindsay A., Goate, Alison, Haines, Jonathan, Jaworski, Jim, Jun, Gyungah, Kunkle, Brian, Kuzma, Amanda, Lee, Jenny J., Lunetta, Kathryn, Ma, Yiyi, Martin, Eden, Naj, Adam, Nato, Andrew Q., Navas, Patrick, Nguyen, Hiep, Reitz, Christiane, Reyes, Dolly, Salerno, William, Schellenberg, Gerard D., Seshadri, Sudha, Sohi, Harkirat, Thornton, Timothy A., Valladares, Otto, van Duijn, Cornelia, Vardarajan, Badri N., Wang, Li-San, Boerwinkle, Eric, Dupuis, Joseé, Pericak-Vance, Margaret A., Mayeux, Richard, Wijsman, Ellen M.
Vydáno v Dement Geriatr Cogn Disord (2018)