Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Wendy Chung"'
Autor:
Thomas A. Miller, Edgar J. Hernandez, J. William Gaynor, Mark W. Russell, Jane W. Newburger, Wendy Chung, Elizabeth Goldmuntz, James F. Cnota, Sinai C. Zyblewski, William T. Mahle, Victor Zak, Chitra Ravishankar, Jonathan R. Kaltman, Brian W. McCrindle, Shanelle Clarke, Jodie K. Votava-Smith, Eric M. Graham, Mike Seed, Nancy Rudd, Daniel Bernstein, Teresa M. Lee, Mark Yandell, Martin Tristani-Firouzi
Publikováno v:
Communications Medicine, Vol 3, Iss 1, Pp 1-9 (2023)
Abstract Background Recent large-scale sequencing efforts have shed light on the genetic contribution to the etiology of congenital heart defects (CHD); however, the relative impact of genetics on clinical outcomes remains less understood. Outcomes a
Externí odkaz:
https://doaj.org/article/c560dc3733ce40c0907a0447f485a366
Autor:
Michelle Kowanda, Katina Calakos, LeeAnne Green Snyder, Catherine Kentros, Jennifer Bain, Siddharth Srivastava, Tristan Sands, Gerhard Schratt, Cora Taylor, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101049- (2024)
Externí odkaz:
https://doaj.org/article/df9cc68298bf493eac0b7efab51198e6
Autor:
Alexandra Goler, Jessica Wright, Sarah Barns, Jacob Hall, Bing Han, Irina Astrovskaya, SPARK Consortium, Natalia Volfovsky, Aaron Wong, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101084- (2024)
Externí odkaz:
https://doaj.org/article/2408e6cb4de947f9b08ae00b95ab44bf
Autor:
Sarah Barns, Jessica Wright, Alexandra Goler, Jacob Hall, Irina Astrovskaya, Bing Han, SPARK Consortium, Natalia Volfovsky, Aaron Wong, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101096- (2024)
Externí odkaz:
https://doaj.org/article/5694561c406a420a8c974d0226c1a8f5
Autor:
Wendy Chung, Alban Ziegler, Carrie Koval-Burt, Denise Kay, Sharon Suchy, Amber Bergtrup, Katherine Langley, Laura Amendola, Brenna Boyd, Jennifer Bradley, Tracy Brandt, Lilian Cohen, Alison Coffey, Joseph Devaney, Beata Dygulska, Bethany Friedman, Ramsey Fuleihan, Awura Gyimah, Rebecca Hernan, Sean Hofherr, Kathleen Hruska, Zhanzhi Hu, Mederic Jeanne, Guanjun Jin, Aaron Johnson, Haluk Kavus, Rudolph Leibel, Kirsty McWalter, Kristin Monaghan, Nicole Pimentel Soler, Yeyson Quevedo, Samantha Ratner, Kyle Retterer, Natasha Shapiro, Robert Sicko, Samuel Storm, Rebecca Torene, Olatundun Williams, Julia Wynn, Ryan Taft, Paul Kruszka, Michele Caggana
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101369- (2024)
Externí odkaz:
https://doaj.org/article/77189ae45b2c491f99280943989bfb4f
Autor:
Michelle Kowanda, Rebecca Sheedy Smith, Jamie Lundy, Catherine Kentros, Elisheva Kleinman, Lauren Kasparson Walsh, Gerhard Schratt, Cora Taylor, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101518- (2024)
Externí odkaz:
https://doaj.org/article/570f11715d344aaa950ecaa728751034
Autor:
Alexandra Goler, Jessica Wright, Sarah Barns, Jacob Hall, Bing Han, Irina Astrovskaya, Natalia Volfovsky, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100076- (2023)
Externí odkaz:
https://doaj.org/article/cf24b3acceaa42288a92579968480d34
Autor:
Sarah Barns, Chang Shu, Jessica Wright, Alexandra Goler, Jacob Hall, Bing Han, Irina Astrovskaya, Natalia Volfovsky, Yufeng Shen, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100140- (2023)
Externí odkaz:
https://doaj.org/article/09a2007415554ee283f42765878a8bd4
Autor:
Betina Idnay, Yilu Fang, Alex Butler, Joyce Moran, Ziran Li, Junghwan Lee, Casey Ta, Cong Liu, Chi Yuan, Huanyao Chen, Edward Stanley, George Hripcsak, Elaine Larson, Karen Marder, Wendy Chung, Brenda Ruotolo, Chunhua Weng
Publikováno v:
Journal of Clinical and Translational Science, Vol 7 (2023)
Abstract Background: Randomized clinical trials (RCT) are the foundation for medical advances, but participant recruitment remains a persistent barrier to their success. This retrospective data analysis aims to (1) identify clinical trial features a
Externí odkaz:
https://doaj.org/article/4380736b6103418dbdb03affab828b78
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102711- (2022)
Esophageal atresia/tracheoesophageal fistula (EA/TEF) is the most common congenital anomaly of the upper gastrointestinal tract affecting 1 in 3,000 which could stem from a developmental anomaly of the foregut. The cause is not fully understood. We g
Externí odkaz:
https://doaj.org/article/32c59c83e2f4460c83b41b6c01f17372