Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes

Por Almoguera, Berta, Vazquez, Lyam, Connolly, John J., Bradfield, Jonathan, Sleiman, Patrick, Keating, Brendan, Hakonarson, Hakon
Publicado em 2014

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Por Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon
Publicado em 2014

Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic ass...

Por Jackson, Kathryn L., Mbagwu, Michael, Pacheco, Jennifer A., Baldridge, Abigail S., Viox, Daniel J., Linneman, James G., Shukla, Sanjay K., Peissig, Peggy L., Borthwick, Kenneth M., Carrell, David A., Bielinski, Suzette J., Kirby, Jacqueline C., Denny, Joshua C., Mentch, Frank D., Vazquez, Lyam M., Rasmussen-Torvik, Laura J., Kho, Abel N.
Publicado no BMC Infect Dis (2016)

AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

Por Falk, Marni J., Li, Dong, Gai, Xiaowu, McCormick, Elizabeth, Place, Emily, Lasorsa, Francesco M., Otieno, Frederick G., Hou, Cuiping, Kim, Cecilia E., Abdel-Magid, Nada, Vazquez, Lyam, Mentch, Frank D., Chiavacci, Rosetta, Liang, Jinlong, Liu, Xuanzhu, Jiang, Hui, Giannuzzi, Giulia, Marsh, Eric D., Yiran, Guo, Tian, Lifeng, Palmieri, Ferdinando, Hakonarson, Hakon
Publicado em 2014

Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

Por Falk, Marni J., Li, Dong, Gai, Xiaowu, McCormick, Elizabeth, Place, Emily, Lasorsa, Francesco M., Otieno, Frederick G., Hou, Cuiping, Kim, Cecilia E., Abdel-Magid, Nada, Vazquez, Lyam, Mentch, Frank D., Chiavacci, Rosetta, Liang, Jinlong, Liu, Xuanzhu, Jiang, Hui, Giannuzzi, Giulia, Marsh, Eric D., Guo, Yiran, Tian, Lifeng, Palmieri, Ferdinando, Hakonarson, Hakon
Publicado em 2014

Identification of Four Novel Loci in Asthma in European American and African American Populations

Por Almoguera, Berta, Vazquez, Lyam, Mentch, Frank, Connolly, John, Pacheco, Jennifer A., Sundaresan, Agnes S., Peissig, Peggy L., Linneman, James G., McCarty, Catherine A., Crosslin, David, Carrell, David S., Lingren, Todd, Namjou-Khales, Bahram, Harley, John B., Larson, Eric, Jarvik, Gail P., Brilliant, Murray, Williams, Marc S., Kullo, Iftikhar J., Hysinger, Erik B., Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado no Am J Respir Crit Care Med (2017)

Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder

Por Lingren, Todd, Chen, Pei, Bochenek, Joseph, Doshi-Velez, Finale, Manning-Courtney, Patty, Bickel, Julie, Wildenger Welchons, Leah, Reinhold, Judy, Bing, Nicole, Ni, Yizhao, Barbaresi, William, Mentch, Frank, Basford, Melissa, Denny, Joshua, Vazquez, Lyam, Perry, Cassandra, Namjou, Bahram, Qiu, Haijun, Connolly, John, Abrams, Debra, Holm, Ingrid A., Cobb, Beth A., Lingren, Nataline, Solti, Imre, Hakonarson, Hakon, Kohane, Isaac S., Harley, John, Savova, Guergana
Publicado no PLoS One (2016)