PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

Por Nato, Alejandro Q., Chapman, Nicola H., Sohi, Harkirat K., Nguyen, Hiep D., Brkanac, Zoran, Wijsman, Ellen M.
Publicado no Bioinformatics (2015)

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

Por Chapman, Nicola H., Nato, Alejandro Q., Bernier, Raphael, Ankeman, Katy, Sohi, Harkirat, Munson, Jeff, Patowary, Ashok, Archer, Marilyn, Blue, Elizabeth M., Webb, Sara Jane, Coon, Hilary, Raskind, Wendy H., Brkanac, Zoran, Wijsman, Ellen M.
Publicado no Hum Genet (2015)

Analysis of Pedigree Data in Populations with Multiple Ancestries: Strategies for Dealing with Admixture in Caribbean Hispanic Families from the ADSP

Por Nafikov, Rafael A., Nato, Alejandro Q., Sohi, Harkirat, Wang, Bowen, Brown, Lisa, Horimoto, Andrea R., Vardarajan, Badri N., Barral, Sandra M., Tosto, Giuseppe, Mayeux, Richard P., Thornton, Timothy A., Blue, Elizabeth, Wijsman, Ellen M.
Publicado no Genet Epidemiol (2018)

Solving Interoperability in Translational Health: Perspectives of Students from the International Partnership in Health Informatics Education (IPHIE) 2016 Master Class

Por Turner, Anne M., Facelli, Julio C., Jaspers, Monique, Wetter, Thomas, Pfeifer, Daniel, Gatewood, Laël Cranmer, Adam, Terry, Li, YuChuan, Lin, Ming-Chin, Evans, R. Scott, Beukenhorst, Anna, Theodoore van Mens, Hugo Johan, Tensen, Esmée, Bock, Christian, Fendrich, Laura, Seitz, Peter, Suleder, Julian, Aldekhyyel, Ranyah, Bridgeman, Kent, Hu, Zhen, Sattler, Aaron, Guo, Shin-Yi, Mohaimenul, Islam Md., Anggraini Ningrum, Dina Nur, Tung, Hsin-Ru, Bian, Jiantao, Plasek, Joseph M., Rommel, Casey, Burke, Juandalyn, Sohi, Harkirat
Publicado no Appl Clin Inform (2017)

Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer’s Disease Sequencing Project

Por Naj, Adam C., Lin, Honghuang, Vardarajan, Badri N., White, Simon, Lancour, Daniel, Ma, Yiyi, Schmidt, Michael, Sun, Fangui, Butkiewicz, Mariusz, Bush, William S., Kunkle, Brian W., Malamon, John, Amin, Najaf, Choi, Seung Hoan, Hamilton-Nelson, Kara L., van der Lee, Sven J., Gupta, Namrata, Koboldt, Daniel C., Saad, Mohamad, Wang, Bowen, Nato, Alejandro Q., Sohi, Harkirat K., Kuzma, Amanda, Wang, Li-San, Adrienne Cupples, L., van Duijn, Cornelia, Seshadri, Sudha, Schellenberg, Gerard D., Boerwinkle, Eric, Bis, Joshua C., Dupuis, Josée, Salerno, William J, Wijsman, Ellen M., Martin, Eden R., DeStefano, Anita L.
Publicado no Genomics (2018)

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

Por 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.
Publicado no Dement Geriatr Cogn Disord (2018)