Endocytic Protein Defects in the Neural Crest Cell Lineage and Its Pathway Are Associated with Congenital Heart Defects

por Arrigo, Angelo B., Lin, Jiuann-Huey Ivy
Publicado 2021

Contribution of LRP1 in Human Congenital Heart Disease Correlates with Its Roles in the Outflow Tract and Atrioventricular Cushion Development

por Arrigo, Angelo B., Zhu, Wenjuan, Williams, Kylia A., Guzman-Moreno, Carla, Lo, Cecilia, Lin, Jiuann-Huey I.
Publicado 2023

Mucociliary Clearance Scans Show Infants Undergoing Congenital Cardiac Surgery Have Poor Airway Clearance Function

por Adams, Phillip S., Corcoran, Timothy E., Lin, Jiuann-Huey, Weiner, Daniel J., Sanchez-de-Toledo, Joan, Lo, Cecilia W.
Publicado 2021

Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease

por Xu, Xinxiu, Lin, Jiuann-Huey Ivy, Bais, Abha S., Reynolds, Michael John, Tan, Tuantuan, Gabriel, George C., Kondos, Zoie, Liu, Xiaoqin, Shiva, Sruti S., Lo, Cecilia W.
Publicado 2021

Double outlet right ventricle

por Bell-Cheddar, Yolandee, Devine, William A., Diaz-Castrillon, Carlos-Eduardo, Seese, Laura, Castro-Medina, Mario, Morales, Raymond, Follansbee, Christopher W., Alsaied, Tarek, Lin, Jiuann-Huey I.
Publicado 2023

Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening

por Lin, Jiuann-Huey I., Feinstein, Timothy N., Jha, Anupma, McCleary, Jacob T., Xu, Juan, Arrigo, Angelo B., Rong, Grace, Maclay, Lindsey M., Ridge, Taylor, Xu, XinXiu, Lo, Cecilia W.
Publicado 2020

A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

por Landis, Benjamin J., Helvaty, Lindsey R., Geddes, Gabrielle C., Lin, Jiuann‐Huey Ivy, Yatsenko, Svetlana A., Lo, Cecilia W., Border, William L., Wechsler, Stephanie Burns, Murali, Chaya N., Azamian, Mahshid S., Lalani, Seema R., Hinton, Robert B., Garg, Vidu, McBride, Kim L., Hodge, Jennelle C., Ware, Stephanie M.
Publicado 2023

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

por Teekakirikul, Polakit, Zhu, Wenjuan, Xu, Xinxiu, Young, Cullen B., Tan, Tuantuan, Smith, Amanda M., Wang, Chengdong, Peterson, Kevin A., Gabriel, George C., Ho, Sebastian, Sheng, Yi, Moreau de Bellaing, Anne, Sonnenberg, Daniel A., Lin, Jiuann-huey, Fotiou, Elisavet, Tenin, Gennadiy, Wang, Michael X., Wu, Yijen L., Feinstein, Timothy, Devine, William, Gou, Honglan, Bais, Abha S., Glennon, Benjamin J., Zahid, Maliha, Wong, Timothy C., Ahmad, Ferhaan, Rynkiewicz, Michael J., Lehman, William J., Keavney, Bernard, Alastalo, Tero-Pekka, Freckmann, Mary-Louise, Orwig, Kyle, Murray, Steve, Ware, Stephanie M., Zhao, Hui, Feingold, Brian, Lo, Cecilia W.
Publicado 2022

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

por Teekakirikul, Polakit, Zhu, Wenjuan, Gabriel, George C., Young, Cullen B., Williams, Kylia, Martin, Lisa J., Hill, Jennifer C., Richards, Tara, Billaud, Marie, Phillippi, Julie A., Wang, Jianbin, Wu, Yijen, Tan, Tuantuan, Devine, William, Lin, Jiuann-huey, Bais, Abha S., Klonowski, Jonathan, de Bellaing, Anne Moreau, Saini, Ankur, Wang, Michael X., Emerel, Leonid, Salamacha, Nathan, Wyman, Samuel K., Lee, Carrie, Li, Hung Sing, Miron, Anastasia, Zhang, Jingyu, Xing, Jianhua, McNamara, Dennis M., Fung, Erik, Kirshbom, Paul, Mahle, William, Kochilas, Lazaros K., He, Yihua, Garg, Vidu, White, Peter, McBride, Kim L., Benson, D. Woodrow, Gleason, Thomas G., Mital, Seema, Lo, Cecilia W.
Publicado 2021