Browsing by Author "n 2015008043"
Now showing items 1-2 of 2
-
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Li, Xihao; Li, Zilin; Zhou, Hufeng; Gaynor, Sheila M.; Liu, Yaowu; Chen, Han; Sun, Ryan; Dey, Rounak; Arnett, Donna K.; Aslibekyan, Stella; Ballantyne, Christie M.; Bielak, Lawrence F.; Blangero, John; Boerwinkle, Eric; Bowden, Donald W.; Broome, Jai G.; Conomos, Matthew P.; Correa, Adolfo; Cupples, L. Adrienne; Curran, Joanne E.; Freedman, Barry I.; Guo, Xiuqing; Hindy, George; Irvin, Marguerite R.; Kardia, Sharon L.R.; Kathiresan, Sekar; Khan, Alyna T.; Kooperberg, Charles L.; Laurie, Cathy C.; Liu, X. Shirley; Mahaney, Michael C.; Manichaikul, Ani W.; Martin, Lisa W.; Mathias, Rasika A.; McGarvey, Stephen T.; Mitchell, Braxton D.; Montasser, May E.; Moore, Jill E.; Morrison, Alanna C.; O’Connell, Jeffrey R.; Palmer, Nicholette D.; Pampana, Akhil; Peralta, Juan M.; Peyser, Patricia A.; Psaty, Bruce M.; Redline, Susan; Rice, Kenneth M.; Rich, Stephen S.; Smith, Jennifer A.; Tiwari, Hemant K.; Tsai, Michael Y.; Vasan, Ramachandran S.; Wang, Fei Fei; Weeks, Daniel E.; Weng, Zhiping; Wilson, James G.; Yanek, Lisa R.; Abe, Namiko; Abecasis, Gonçalo R.; Aguet, Francois; Albert, Christine; Almasy, Laura; Alonso, Alvaro; Ament, Seth; Anderson, Peter; Anugu, Pramod; Applebaum-Bowden, Deborah; Ardlie, Kristin; Arking, Dan; Ashley-Koch, Allison; Assimes, Tim; Auer, Paul; Avramopoulos, Dimitrios; Barnard, John; Barnes, Kathleen; Barr, R. Graham; Barron-Casella, Emily; Barwick, Lucas; Beaty, Terri; Beck, Gerald; Becker, Diane; Becker, Lewis; Beer, Rebecca; Beitelshees, Amber; Benjamin, Emelia; Benos, Takis; Bezerra, Marcos; Bis, Joshua; Blackwell, Thomas; Bowler, Russell; Brody, Jennifer; Broeckel, Ulrich; Bunting, Karen... more authors ... less authors ( Nature Research , 2020 , Article)Large-scale whole-genome sequencing studies have enabled the analysis of rare variants (RVs) associated with complex phenotypes. Commonly used RV association tests have limited scope to leverage variant functions. We propose ... -
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
George, Hindy; 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.... more authors ... less authors ( Elsevier , 2022 , Article)Large-scale gene sequencing studies for complex traits have the potential to identify causal genes with therapeutic implications. We performed gene-based association testing of blood lipid levels with rare (minor allele ...