Loss of RNA expression and allele-specific expression associated with congenital heart disease

by McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Ware, James S., DePalma, Steven R., Gorham, Joshua, Zaidi, Samir, Ma, Wenji, Patel, Nihir, Shen, Yufeng, Chung, Wendy K., Lifton, Richard P., Kim, Richard, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.
Published 2016

CANOES: detecting rare copy number variants from whole exome sequencing data

by Backenroth, Daniel, Homsy, Jason, Murillo, Laura R., Glessner, Joe, Lin, Edwin, Brueckner, Martina, Lifton, Richard, Goldmuntz, Elizabeth, Chung, Wendy K., Shen, Yufeng
Published 2014

Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

by Hinson, John Travis, Chopra, Anant, Nafissi, N., Polacheck, William, Benson, Craig Carlyle, Swist, S., Gorham, Joshua McClean, Yang, Luhan, Schafer, S., Sheng, Calvin Chen, Haghighi, Alireza, Homsy, Jason George, Hubner, N., Church, George McDonald, Cook, S. A., Linke, Wolfgang, Chen, Christopher, Seidman, Jonathan G., Seidman, Christine Edry
Published 2017

Loss of RNA expression and allele-specific expression associated with congenital heart disease

by McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Gorham, Joshua, DePalma, Steven R., Ware, James S., Zaidi, Samir, Ma, Wenji, Patel, Nihir, Lifton, Richard P., Chung, Wendy K., Kim, Richard, Shen, Yufeng, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.
Published 2016

Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells

by Yang, Luhan, Grishin, Dennis, Wang, Gang, Aach, John, Zhang, Cheng-Zhong, Chari, Raj, Homsy, Jason, Cai, Xuyu, Zhao, Yue, Fan, Jian-Bing, Seidman, Christine, Seidman, Jonathan, Pu, William, Church, George
Published 2015

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

by Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R, Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C, Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D, Castaldi, Christopher, Tikhonoa, Irina R, Bilguvar, Kaya, Mane, Shrikant M, Sanders, Stephan J, Mital, Seema, Russell, Mark W, Gaynor, J William, Deanfield, John, Giardini, Alessandro, Porter, George A, Srivastava, Deepak, Lo, Cecelia W, Shen, Yufeng, Watkins, W Scott, Yandell, Mark, Yost, H Joseph, Tristani-Firouzi, Martin, Newburger, Jane W, Roberts, Amy E, Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R, Goldmuntz, Elizabeth, Chung, Wendy K, Seidman, Jonathan G, Gelb, Bruce D, Seidman, Christine E, Lifton, Richard P, Brueckner, Martina
Published 2017

Genomic analyses implicate noncoding de novo variants in congenital heart disease.

by Richter, Felix, Morton, Sarah U, Kim, Seong Won, Kitaygorodsky, Alexander, Wasson, Lauren K, Chen, Kathleen M, Zhou, Jian, Qi, Hongjian, Patel, Nihir, DePalma, Steven R, Parfenov, Michael, Homsy, Jason, Gorham, Joshua M, Manheimer, Kathryn B, Velinder, Matthew, Farrell, Andrew, Marth, Gabor, Schadt, Eric E, Kaltman, Jonathan R, Newburger, Jane W, Giardini, Alessandro, Goldmuntz, Elizabeth, Brueckner, Martina, Kim, Richard, Porter, George A, Bernstein, Daniel, Chung, Wendy K, Srivastava, Deepak, Tristani-Firouzi, Martin, Troyanskaya, Olga G, Dickel, Diane E, Shen, Yufeng, Seidman, Jonathan G, Seidman, Christine E, Gelb, Bruce D
Published 2020

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

by Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R., Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C., Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D., Castaldi, Christopher, Tikhonoa, Irina R., Bilguvar, Kaya, Mane, Shrikant M., Sanders, Stephan J., Mital, Seema, Russell, Mark, Gaynor, William, Deanfield, John, Giardini, Alessandro, Porter, George A., Srivastava, Deepak, Lo, Cecelia W., Shen, Yufeng, Watkins, W. Scott, Yandell, Mark, Yost, H. Joseph, Tristani-Firouzi, Martin, Newburger, Jane W., Roberts, Amy E., Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R., Goldmuntz, Elizabeth, Chung, Wendy K., Seidman, Jonathan G., Gelb, Bruce D., Seidman, Christine E., Lifton, Richard P., Brueckner, Martina
Published 2018