SEQMINER: An R‐Package to Facilitate the Functional Interpretation of Sequence‐Based Associations

by Zhan, Xiaowei, Liu, Dajiang J.
Published 2015

A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data

by Liu, Dajiang J., Leal, Suzanne M.
Published 2012

RAREMETAL: fast and powerful meta-analysis for rare variants

by Feng, Shuang, Liu, Dajiang, Zhan, Xiaowei, Wing, Mary Kate, Abecasis, Gonçalo R.
Published 2014

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data

by Zhan, Xiaowei, Hu, Youna, Li, Bingshan, Abecasis, Goncalo R., Liu, Dajiang J.
Published 2016

Meta-Analysis of Gene Level Tests for Rare Variant Association

by Liu, Dajiang J., Peloso, Gina M., Zhan, Xiaowei, Holmen, Oddgeir L., Zawistowski, Matthew, Feng, Shuang, Nikpay, Majid, Auer, Paul L., Goel, Anuj, Zhang, He, Peters, Ulrike, Farrall, Martin, Orho-Melander, Marju, Kooperberg, Charles, McPherson, Ruth, Watkins, Hugh, Willer, Cristen J., Hveem, Kristian, Melander, Olle, Kathiresan, Sekar, Abecasis, Gonçalo R.
Published 2013

Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration

by Zhan, Xiaowei, Larson, David E., Wang, Chaolong, Koboldt, Daniel C., Sergeev, Yuri V., Fulton, Robert S., Fulton, Lucinda L., Fronick, Catrina C., Branham, Kari E., Bragg-Gresham, Jennifer, Jun, Goo, Hu, Youna, Kang, Hyun Min, Liu, Dajiang, Othman, Mohammad, Brooks, Matthew, Ratnapriya, Rinki, Boleda, Alexis, Grassmann, Felix, von Strachwitz, Claudia, Olson, Lana M., Buitendijk, Gabriëlle H.S., Hofman, Albert, van Duijn, Cornelia M., Cipriani, Valentina, Moore, Anthony T., Shahid, Humma, Jiang, Yingda, Conley, Yvette P., Morgan, Denise J., Kim, Ivana K., Johnson, Matthew P., Cantsilieris, Stuart, Richardson, Andrea J., Guymer, Robyn H., Luo, Hongrong, Ouyang, Hong, Licht, Christoph, Pluthero, Fred G., Zhang, Mindy M., Zhang, Kang, Baird, Paul N., Blangero, John, Klein, Michael L., Farrer, Lindsay A., DeAngelis, Margaret M., Weeks, Daniel E., Gorin, Michael B., Yates, John R.W., Klaver, Caroline C.W., Pericak-Vance, Margaret A., Haines, Jonathan L., Weber, Bernhard H.F., Wilson, Richard K., Heckenlively, John R., Chew, Emily Y., Stambolian, Dwight, Mardis, Elaine R., Swaroop, Anand, Abecasis, Goncalo R.
Published 2013

Genetic variants in CETP increase risk of intracerebral hemorrhage

by Anderson, Christopher D., Falcone, Guido J., Phuah, Chia‐Ling, Radmanesh, Farid, Brouwers, H. Bart, Battey, Thomas W. K., Biffi, Alessandro, Peloso, Gina M., Liu, Dajiang J., Ayres, Alison M., Goldstein, Joshua N., Viswanathan, Anand, Greenberg, Steven M., Selim, Magdy, Meschia, James F., Brown, Devin L., Worrall, Bradford B., Silliman, Scott L., Tirschwell, David L., Flaherty, Matthew L., Kraft, Peter, Jagiella, Jeremiasz M., Schmidt, Helena, Hansen, Björn M., Jimenez‐Conde, Jordi, Giralt‐Steinhauer, Eva, Elosua, Roberto, Cuadrado‐Godia, Elisa, Soriano, Carolina, van Nieuwenhuizen, Koen M., Klijn, Catharina J. M., Rannikmae, Kristiina, Samarasekera, Neshika, Salman, Rustam Al‐Shahi, Sudlow, Catherine L., Deary, Ian J., Morotti, Andrea, Pezzini, Alessandro, Pera, Joanna, Urbanik, Andrzej, Pichler, Alexander, Enzinger, Christian, Norrving, Bo, Montaner, Joan, Fernandez‐Cadenas, Israel, Delgado, Pilar, Roquer, Jaume, Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Kidwell, Chelsea S., Kittner, Steven J., Waddy, Salina P., Langefeld, Carl D., Abecasis, Goncalo, Willer, Cristen J., Kathiresan, Sekar, Woo, Daniel, Rosand, Jonathan
Published 2016