日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome

22q11.2缺失综合征患者的缺失大小和背景遗传变异影响先天性心脏病表型,共纳入3016例患者。

Lin, Jhih-Rong; Miller, Daniella; Luong, Dana; Nelson, Tanner; Crowley, T Blaine; Tran, Oanh T; Thiruvahindrapuram, Bhooma; Hajianpour, Amirhossein; Campbell, Linda; Busa, Tiffany; Heine-Suñer, Damian; García-Miñaúr, Sixto; Fernández, Luis; Murphy, Kieran C; Murphy, Declan; Hawula, Wanda; Angkustsiri, Kathleen; Shashi, Vandana; Schoch, Kelly; Bearden, Carrie E; Tomita Mitchell, Aoy; Mitchell, Michael E; Carmel, Miri; Weizman, Abraham; Michaelovsky, Elena; Gothelf, Doron; van den Bree, Marianne B M; Owen, Michael J; Vorstman, Jacob A S; Boot, Erik; Vingerhoets, Claudia; van Amelsvoort, Therese; Swillen, Ann; Breckpot, Jeroen; Vermeesch, Joris R; Devriendt, Koen; Schneider, Maude; Eliez, Stephan; Digilio, M Cristina; Unolt, Marta; Putotto, Carolina; Marino, Bruno; Pontillo, Maria; Armando, Marco; Vicari, Stefano; Repetto, Gabriela M; Kates, Wendy R; Shprintzen, Robert J; Gur, Raquel E; Zackai, Elaine H; Goldmuntz, Elizabeth; Wang, Tao; Raj, Srilakshmi; Emanuel, Beverly S; McDonald-McGinn, Donna M; Scherer, Stephen C; Bassett, Anne S; Zhang, Zhengdong D; Morrow, Bernice E

Advancing cell-free DNA as a biomarker of damage to heart caused by ionizing radiation

将游离DNA作为电离辐射造成心脏损伤的生物标志物进行研究

Wallisch, Erin; Tomita-Mitchell, Aoy; Liang, Huan-Ling; Szabo, Aniko; Lenarczyk, Marek; Kwitek, Anne; Smith, Jennifer R; Tutaj, Monika; Baker, John E

MYH6 Variants Are Associated with Atrial Dysfunction in Neonates with Hypoplastic Left Heart Syndrome

MYH6 变异与左心发育不全综合征新生儿的心房功能障碍相关

Quintanilla Anfinson, Melissa; Creighton, Sara; Simpson, Pippa M; James, Jeanne M; Lim, Phoebe; Frommelt, Peter C; Tomita-Mitchell, Aoy; Mitchell, Michael E

Evaluating threshold for donor fraction cell-free DNA using clinically available assay for rejection in pediatric and adult heart transplantation

利用临床可用的检测方法评估供体细胞游离DNA阈值,以用于儿科和成人心脏移植排斥反应的诊断

Deshpande, Shriprasad R; Zangwill, Steven D; Richmond, Marc E; Kindel, Steven J; Schroder, Jacob N; Gaglianello, Nunzio; Bichell, David P; Wigger, Mark A; Knecht, Kenneth R; Thrush, Phillip T; Mahle, William T; North, Paula E; Simpson, Pippa M; Zhang, Liyun; Dasgupta, Mahua; Tomita-Mitchell, Aoy; Mitchell, Michael E

Validation of donor fraction cell-free DNA with biopsy-proven cardiac allograft rejection in children and adults

验证供体组分游离DNA在儿童和成人心脏同种异体移植排斥反应中的有效性(经活检证实)

Richmond, Marc E; Deshpande, Shriprasad R; Zangwill, Steven D; Bichell, David P; Kindel, Steven J; Mahle, William T; Schroder, Jacob N; Wigger, Mark A; Knecht, Kenneth R; Pahl, Elfriede; Gaglianello, Nunzio A; Goetsch, Mary A; Simpson, Pippa; Dasgupta, Mahua; Zhang, Liyun; North, Paula E; Tomita-Mitchell, Aoy; Mitchell, Michael E

Altered contractility, Ca2+ transients, and cell morphology seen in a patient-specific iPSC-CM model of Ebstein's anomaly with left ventricular noncompaction

在患有左心室致密化不全的 Ebstein 畸形患者特定 iPSC-CM 模型中观察到收缩力、Ca2+ 瞬变和细胞形态的改变

Suma K Thareja, Melissa Anfinson, Matthew Cavanaugh, Min-Su Kim, Peter Lamberton, Jackson Radandt, Ryan Brown, Huan-Ling Liang, Karl Stamm, Muhammad Zeeshan Afzal, Jennifer Strande, Michele A Frommelt, John W Lough, Robert H Fitts, Michael E Mitchell, Aoy Tomita-Mitchell

3D-bioprinting of patient-derived cardiac tissue models for studying congenital heart disease

3D 生物打印患者心脏组织模型用于研究先天性心脏病

Jayne T Wolfe, Wei He, Min-Su Kim, Huan-Ling Liang, Akankshya Shradhanjali, Hilda Jurkiewicz, Bonnie P Freudinger, Andrew S Greene, John F LaDisa Jr, Lobat Tayebi, Michael E Mitchell, Aoy Tomita-Mitchell, Brandon J Tefft

Sinus of Valsalva Aneurysm in a Preschooler With Schuurs-Hoeijmakers Syndrome

患有 Schuurs-Hoeijmakers 综合征的学龄前儿童的 Valsalva 动脉瘤

Thalner, Sharadhi M; Chaszczewski, Kasey J; Melamed, Joshua; Hambrook, John T; Tomita-Mitchell, Aoy; Mitchell, Michael E

A Systematic Review of Ebstein's Anomaly with Left Ventricular Noncompaction

对伴有左心室致密化不全的埃布斯坦畸形进行系统性综述

Thareja, Suma K; Frommelt, Michele A; Lincoln, Joy; Lough, John W; Mitchell, Michael E; Tomita-Mitchell, Aoy

Significance of α-Myosin Heavy Chain (MYH6) Variants in Hypoplastic Left Heart Syndrome and Related Cardiovascular Diseases

α-肌球蛋白重链(MYH6)变异在左心发育不全综合征及相关心血管疾病中的意义

Anfinson, Melissa; Fitts, Robert H; Lough, John W; James, Jeanne M; Simpson, Pippa M; Handler, Stephanie S; Mitchell, Michael E; Tomita-Mitchell, Aoy