日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
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2026
影响因子:
–

Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia

复杂性先天性膈疝中新生预测有害变异负担增加

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddv196
Yu, Lan; Sawle, Ashley D; Wynn, Julia; Aspelund, Gudrun; Stolar, Charles J; Arkovitz, Marc S; Potoka, Douglas; Azarow, Kenneth S; Mychaliska, George B; Shen, Yufeng; Chung, Wendy K
发表日期：2015
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The association between congenital diaphragmatic hernia and undescended testes

先天性膈疝与隐睾之间的关联

期刊:Journal of Pediatric Surgery
影响因子:2.5
doi:10.1016/j.jpedsurg.2015.02.025
Azarow, Kenneth S; Cusick, Robert; Wynn, Julia; Chung, Wendy; Mychaliska, George B; Crombleholme, Timothy M; Chung, Dai H; Lim, Foong Yen; Potoka, Douglas; Warner, Brad W; Aspelund, Gundrun; Arkovitz, Marc S
发表日期：2015
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Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

全外显子组测序鉴定出与先天性膈疝相关的GATA6基因新生突变

期刊:Journal of Medical Genetics
影响因子:3.7
doi:10.1136/jmedgenet-2013-101989
Yu, Lan; Bennett, James T; Wynn, Julia; Carvill, Gemma L; Cheung, Yee Him; Shen, Yufeng; Mychaliska, George B; Azarow, Kenneth S; Crombleholme, Timothy M; Chung, Dai H; Potoka, Douglas; Warner, Brad W; Bucher, Brian; Lim, Foong-Yen; Pietsch, John; Stolar, Charles; Aspelund, Gudrun; Arkovitz, Marc S; Mefford, Heather; Chung, Wendy K
GATA
发表日期：2014
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Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

GATA4基因变异是家族性和散发性先天性膈疝的罕见病因。

期刊:Human Genetics
影响因子:3.6
doi:10.1007/s00439-012-1249-0
Yu, Lan; Wynn, Julia; Cheung, Yee Him; Shen, Yufeng; Mychaliska, George B; Crombleholme, Timothy M; Azarow, Kenneth S; Lim, Foong Yen; Chung, Dai H; Potoka, Douglas; Warner, Brad W; Bucher, Brian; Stolar, Charles; Aspelund, Gudrun; Arkovitz, Marc S; Chung, Wendy K
GATA
发表日期：2013
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Outcomes of congenital diaphragmatic hernia in the modern era of management

现代治疗时代先天性膈疝的预后

期刊:Journal of Pediatrics
影响因子:3.5
doi:10.1016/j.jpeds.2012.12.036
Wynn, Julia; Krishnan, Usha; Aspelund, Gudrun; Zhang, Yuan; Duong, Jimmy; Stolar, Charles J H; Hahn, Eunice; Pietsch, John; Chung, Dai; Moore, Donald; Austin, Eric; Mychaliska, George; Gajarski, Robert; Foong, Yen-Lim; Michelfelder, Erik; Potolka, Douglas; Bucher, Brian; Warner, Brad; Grady, Mark; Azarow, Ken; Fletcher, Scott E; Kutty, Shelby; Delaney, Jeff; Crombleholme, Timothy; Rosenzweig, Erika; Chung, Wendy; Arkovitz, Marc S
发表日期：2013
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Timing and expression of the angiopoietin-1-Tie-2 pathway in murine lung development and congenital diaphragmatic hernia

血管生成素-1-Tie-2通路在小鼠肺发育和先天性膈疝中的时序和表达

期刊:Disease Models & Mechanisms
影响因子:3.3
doi:10.1242/dmm.008821
Grzenda, Adrienne; Shannon, John; Fisher, Jason; Arkovitz, Marc S
信号转导
发育与干细胞
血管生成
Tie-2
发表日期：2013
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Developmental outcomes of children with congenital diaphragmatic hernia: a multicenter prospective study

先天性膈疝患儿的发育结局：一项多中心前瞻性研究

期刊:Journal of Pediatric Surgery
影响因子:2.5
doi:10.1016/j.jpedsurg.2013.02.041
Wynn, Julia; Aspelund, Gudrun; Zygmunt, Annette; Stolar, Charles J H; Mychaliska, George; Butcher, Jennifer; Lim, Foong-Yen; Gratton, Teresa; Potoka, Douglas; Brennan, Kate; Azarow, Ken; Jackson, Barbara; Needelman, Howard; Crombleholme, Timothy; Zhang, Yuan; Duong, Jimmy; Arkovitz, Marc S; Chung, Wendy K; Farkouh, Christiana
发育与干细胞
发表日期：2013
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Multivariate model for predicting recurrence in congenital diaphragmatic hernia

用于预测先天性膈疝复发的多变量模型

期刊:Journal of Pediatric Surgery
影响因子:2.5
doi:10.1016/j.jpedsurg.2009.02.043
Fisher, Jason C; Haley, Mary Jo; Ruiz-Elizalde, Alejandro; Stolar, Charles J H; Arkovitz, Marc S
发表日期：2009
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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

脊髓性肌萎缩症小鼠模型中，SMN 蛋白减少会损害神经肌肉接头的成熟

期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddn156
Shingo Kariya, Gyu-Hwan Park, Yuka Maeno-Hikichi, Olga Leykekhman, Cathleen Lutz, Marc S Arkovitz, Lynn T Landmesser, Umrao R Monani
神经
心力衰竭
肌萎缩症
Mouse
发表日期：2008
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