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

A Novel Echocardiography Feature-Tracking Algorithm for Stabilized Frame-to-Frame Extraction of Aortic Root Diameters in the Parasternal Long Axis

一种用于稳定逐帧提取胸骨旁长轴主动脉根部直径的新型超声心动图特征跟踪算法

Damen, Frederick W; Ghajar-Rahimi, Elnaz; Lai, Dongbing; Goergen, Craig J; Landis, Benjamin J

Dysmorphology-Based Prediction Model for Genetic Disorders in Infants With Congenital Heart Disease

基于畸形学的先天性心脏病患儿遗传疾病预测模型

Helm, Benjamin M; Wetherill, Leah; Landis, Benjamin J; Ware, Stephanie M

Identification of Long Noncoding RNA Candidate Disease Genes Associated With Clinically Reported Copy Number Variants in Congenital Heart Disease

鉴定与先天性心脏病临床报告的拷贝数变异相关的长链非编码RNA候选疾病基因

Penaloza, Jacqueline S; Moreland, Blythe; Gaither, Jeffrey B; Landis, Benjamin J; Ware, Stephanie M; McBride, Kim L; White, Peter

Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome.

基因组和转录组联合分析揭示了马凡综合征患者主动脉疾病的分子特征

Stanley Katherine B, Mederos Alexa V, Barksdale Ethan H, Corvera Joel S, Davis Joshua L, Fang Fang, Gao Hongyu, Vujakovich Courtney E, Liu Yunlong, Ware Stephanie M, Landis Benjamin J

Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery

早期确定基因诊断有助于明确其对新生儿先天性心脏病手术后中期生存率的影响

Landis, Benjamin J; Helm, Benjamin M; Durbin, Matthew D; Helvaty, Lindsey R; Herrmann, Jeremy L; Johansen, Michael; Geddes, Gabrielle C; Ware, Stephanie M

Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing

基于畸形学特征的遗传疾病筛查在儿童先天性心脏病中的应用表现良好,支持扩大基因检测范围。

Helm, Benjamin M; Helvaty, Lindsey R; Conboy, Erin; Geddes, Gabrielle C; Graham, Brett H; Lah, Melissa; Wetherill, Leah; Landis, Benjamin J; Ware, Stephanie M

Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects

快速基因组测序在先天性心脏病患儿的诊断中显示出应用价值

Durbin, Matthew D; Helvaty, Lindsey R; Posorske, Alyx; Zhang, Samuel; Huang, Manyan; Li, Ming; Abreu, Daniel; Fairman, Korre; Geddes, Gabrielle C; Helm, Benjamin M; Landis, Benjamin J; McEntire, Alexis; Mitchell, Dana K; Ware, Stephanie M

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

先天性心脏病异常染色体微阵列结果的多中心分析

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

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

临床外显子组测序的有效性及涉及异常肺静脉回流的表型扩展

Huth, Emily A; Zhao, Xiaonan; Owen, Nichole; Luna, Pamela N; Vogel, Ida; Dorf, Inger L H; Joss, Shelagh; Clayton-Smith, Jill; Parker, Michael J; Louw, Jacoba J; Gewillig, Marc; Breckpot, Jeroen; Kraus, Alison; Sasaki, Erina; Kini, Usha; Burgess, Trent; Tan, Tiong Y; Armstrong, Ruth; Neas, Katherine; Ferrero, Giovanni B; Brusco, Alfredo; Kerstjens-Frederikse, Wihelmina S; Rankin, Julia; Helvaty, Lindsey R; Landis, Benjamin J; Geddes, Gabrielle C; McBride, Kim L; Ware, Stephanie M; Shaw, Chad A; Lalani, Seema R; Rosenfeld, Jill A; Scott, Daryl A

Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects

基因检测指南对先天性心脏病新生儿的护理产生影响

Durbin, Matthew D; Fairman, Korre; Helvaty, Lindsey R; Huang, Manyan; Li, Ming; Abreu, Daniel; Geddes, Gabrielle C; Helm, Benjamin M; Landis, Benjamin J; McEntire, Alexis; Mitchell, Dana K; Ware, Stephanie M