Search Results - Azarow, Kenneth
- Showing 1 - 10 results of 10
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1
Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia by Yu, Lan, Sawle, Ashley D., Wynn, Julia, Aspelund, Gudrun, Stolar, Charles J., Arkovitz, Marc S., Potoka, Douglas, Azarow, Kenneth S., Mychaliska, George B., Shen, Yufeng, Chung, Wendy K.
Published 2015Text -
2
The association between congenital diaphragmatic hernia and undescended testes by Azarow, Kenneth S, Cusick, Robert, Wynn, Julia, Chung, Wendy, Mychaliska, George B, Crombleholme, Timothy M, Chung, Dai H, Lim, Foong Yen, Potolka, Douglas, Warner, Brad W, Aspelund, Gundrun, Arkovitz, Marc S
Published 2015Text -
3
Variants in GATA4 Are a Rare Cause of Familial and Sporadic Congenital Diaphragmatic Hernia by Yu, Lan, Wynn, Julia, Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Chung, Wendy K.
Published 2012Text -
4
De novo copy number variants are associated with congenital diaphragmatic hernia by Yu, Lan, Wynn, Julia, Ma, Lijiang, Guha, Saurav, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, LeDuc, Charles A., Costa, Katherine, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc, Chung, Wendy K.
Published 2012Text -
5
Whole Exome Sequencing Identifies de Novo Mutations in GATA6 Associated with Congenital Diaphragmatic Hernia by Yu, Lan, Bennett, James T., Wynn, Julia, Carvill, Gemma L., Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Azarow, Kenneth S., Crombleholme, Timothy M., Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Lim, Foong-Yen, Pietsch, John, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Mefford, Heather, Chung, Wendy K.
Published 2014Text -
6
The Need for Early Kasai Portoenterostomy: A Western Pediatric Surgery Research Consortium Study by Kelley-Quon, Lorraine I., Shue, Eveline, Burke, Rita V., Smith, Caitlin, Kling, Karen, Mahdi, Elaa, Ourshalimian, Shadassa, Fenlon, Michael, Dellinger, Matthew, Shew, Stephen B., Lee, Justin, Padilla, Benjamin, Inge, Thomas, Roach, Jonathan, Marwan, Ahmed I., Russell, Katie W., Ignacio, Romeo, Fialkowski, Elizabeth, Nijagal, Amar, Im, Cecilia, Azarow, Kenneth S., Ostlie, Daniel J., Wang, Kasper
Published 2021Text -
7
Guidelines for Opioid Prescribing in Children and Adolescents After Surgery: An Expert Panel Opinion by Kelley-Quon, Lorraine I., Kirkpatrick, Matthew G., Ricca, Robert L., Baird, Robert, Harbaugh, Calista M., Brady, Ashley, Garrett, Paula, Wills, Hale, Argo, Jonathan, Diefenbach, Karen A., Henry, Marion C.W., Sola, Juan E., Mahdi, Elaa M., Goldin, Adam B., St Peter, Shawn D., Downard, Cynthia D., Azarow, Kenneth S., Shields, Tracy, Kim, Eugene
Published 2021Text -
8
Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes by Qiao, Lu, Wynn, Julia, Yu, Lan, Hernan, Rebecca, Zhou, Xueya, Duron, Vincent, Aspelund, Gudrun, Farkouh-Karoleski, Christiana, Zygumunt, Annette, Krishnan, Usha S., Nees, Shannon, Khlevner, Julie, Lim, Foong Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa Ellen, Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., Soffer, Samuel, Schindel, David, McCulley, David J., Shen, Yufeng, Chung, Wendy K.
Published 2020Text -
9
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders by Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E., Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., ElFiky, Mahmoud, Wilson, Jay M., Nickerson, Debbie, Bamshad, Michael, High, Frances A., Longoni, Mauro, Donahoe, Patricia K., Chung, Wendy K., Shen, Yufeng
Published 2018Text -
10
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene by Qiao, Lu, Xu, Le, Yu, Lan, Wynn, Julia, Hernan, Rebecca, Zhou, Xueya, Farkouh-Karoleski, Christiana, Krishnan, Usha S., Khlevner, Julie, De, Aliva, Zygmunt, Annette, Crombleholme, Timothy, Lim, Foong-Yen, Needelman, Howard, Cusick, Robert A., Mychaliska, George B., Warner, Brad W., Wagner, Amy J., Danko, Melissa E., Chung, Dai, Potoka, Douglas, Kosiński, Przemyslaw, McCulley, David J., Elfiky, Mahmoud, Azarow, Kenneth, Fialkowski, Elizabeth, Schindel, David, Soffer, Samuel Z., Lyon, Jane B., Zalieckas, Jill M., Vardarajan, Badri N., Aspelund, Gudrun, Duron, Vincent P., High, Frances A., Sun, Xin, Donahoe, Patricia K., Shen, Yufeng, Chung, Wendy K.
Published 2021Text