Search

You searched for: Author Shen, Yufeng Start Over

1. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study

Griffin, Emily Leann; Nees, Shannon N.; Morton, Sarah U.; Wynn, Julia; Patel, Nihir; Jobanputra, Vaidehi; Robinson, Scott; Kochav, Stephanie M.; Tao, Alice May; Andrews, Carli; Cross, Nancy; Geva, Judith; Lanzilotta, Kristen; Ritter, Alyssa; Taillie, Eileen; Thompson, Alexandra; Meyer, Chris; Akers, Rachel; King, Eileen C.; Cnota, James F.; Kim, Richard W.; Porter, Jr., George A.; Brueckner, Martina; Seidman, Christine E.; Shen, Yufeng; Gelb, Bruce D.; Goldmuntz, Elizabeth; Newburger, Jane W.; Roberts, Amy E.; Chung, Wendy K.
2023
Articles
Congenital heart diseaseGeneticsGenetic screeningMedicine

3. Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Zhu, Na; Swietlik, Emilia M.; Welch, Carrie L.; Pauciulo, Michael W.; Hagen, Jacob J.; Zhou, Xueya; Guo, Yicheng; Karten, Johannes; Pandya, Divya; Tilly, Tobias; Lutz, Katie A.; Martin, Jennifer M.; Treacy, Carmen M.; Rosenzweig, Erika B.; Krishnan, Usha; Coleman, Anna W.; Gonzaga-Jauregui, Claudia; Lawrie, Allan; Trembath, Richard C.; Wilkins, Martin R.; Morrell, Nicholas W.; Shen, Yufeng; Gräf, Stefan; Nichols, William C.; Chung, Wendy K.
2021
Articles
Lungs--DiseasesHypertensionLungs--Diseases--Research

5. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Zhu, Na; Swietlik, Emilia M.; Welch, Carrie L.; Pauciulo, Michael W.; Hagen, Jacob J.; Zhou, Xueya; Guo, Yicheng; Karten, Johannes; Pandya, Divya; Tilly, Tobias; Lutz, Katie A.; Martin, Jennifer M.; Treacy, Carmen M.; Rosenzweig, Erika B.; Krishnan, Usha; Coleman, Anna W.; Gonzaga-Juaregui, Claudia; Lawrie, Allan; Trembath, Richard C.; Wilkins, Martin R.; Morrell, Nicholas W.; Shen, Yufeng; Gräf, Stefan; Nichols, William C.; Chung, Wendy K.
2021
Articles
GeneticsLungs--DiseasesHypertensionClinical trials

6. EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

Hsieh, Alexander; Morton, Sarah U.; Willcox, Jon A. L.; Gorham, Joshua M.; Tai, Angela C.; Qi, Hongjian; DePalma, Steven; McKean, David; Griffin, Emily; Manheimer, Kathryn B.; Bernstein, Daniel; Kim, Richard W.; Newburger, Jane W.; Porter, George A.; Srivastava, Deepak; Tristani-Firouzi, Martin; Brueckner, Martina; Lifton, Richard P.; Goldmuntz, Elizabeth; Gelb, Bruce D.; Chung, Wendy K.; Seidman, Christine E.; Seidman, J. G.; Shen, Yufeng
2020
Articles
Coronary heart disease--EtiologyMosaicismCoronary heart disease--Genetic aspectsExomesCongenital heart disease

10. De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Qi, Hongjian; Yu, Lan; Zhou, Xueya; Wynn, Julia; Zhao, Haoquan; Guo, Yicheng; Zhu, Na; Kitaygorodsky, Alexander; Hernan, Rebecca Rose; 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
2018
Articles
Diaphragmatic herniaGenetic disordersMyelin genes--Expression

11. Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease

Zhu, Na; Welch, Carrie L.; Wang, Jiayao; Allen, Philip M.; Gonzaga-Jauregui, Claudia; Ma, Lijiang; King, Alejandra K.; Krishnan, Usha; Rosenzweig, Erika B.; Ivy, D. Dunbar; Austin, Eric D.; Hamid, Rizwan; Pauciulo, Michael W.; Lutz, Katie A.; Nichols, William C.; Reid, Jeffrey G.; Overton, John D.; Baras, Aris; Dewey, Frederick E.; Shen, Yufeng; Chung, Wendy K.
2018
Articles
Pulmonary hypertensionCongenital heart diseaseExomesGeneticsGenomics

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

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.
2016
Articles
Gene expressionAbnormalities, HumanRNACongenital heart diseaseGenetics

20. Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes

Behr, Elijah R.; Ritchie, Marylyn D.; Tanaka, Toshihiro; Kääb, Stefan; Crawford, Dana C.; Nicoletti, Paola; Floratos, Aristidis; Kannankeril, Prince J.; Sinner, Moritz F.; M. Wilde, Arthur A.; Bezzina, Connie R.; Schulze-Bahr, Eric; Zumhagen, Sven; Guicheney, Pascale; Bishopric, Nanette H.; Marshall, Vanessa; Shakir, Saad; Dalageorgou, Chrysoula; Jamshidi, Yalda; Bevan, Steve; Bastiaenen, Rachel; Myerburg, Robert J.; Schott, Jean-Jacques; Camm, A. John; Steinbeck, Gerhard; Norris, Kris; Altman, Russ B.; Tatonetti, Nicholas P.; Jeffery, Steve; Kubo, Michiaki; Nakamura, Yusuke; Shen, Yufeng; George Jr, Alfred L.; Roden, Dan M.
2013
Articles
Medical geneticsVentricular tachycardiaDrug interactionsGenomics