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

Modeling cerebral palsy in animals

动物脑瘫模型

Quinlan, Katharina A; Reedich, Emily J; Mena Avila, Elvia; Moline, Brendan C; Genry, Landon T; Detloff, Megan R; Katholi, Benjamin R; Gaebler-Spira, Deborah; Aravamuthan, Bhooma R

Characteristics of Cerebral Palsy in the Midwestern US

美国中西部地区脑瘫的特征

Kim, Susie; Steffen, Kelsey; Gottschalk-Henneberry, Lauren; Miros, Jennifer; Robichaux-Viehoever, Amy; Taca, Karen; Aravamuthan, Bhooma R

GWAS SVatalog: a visualization tool to aid fine-mapping of GWAS loci with structural variations

GWAS SVatalog:一种可视化工具,用于辅助对具有结构变异的 GWAS 位点进行精细定位

Chirmade, Shalvi; Wang, Zhuozhi; Mastromatteo, Scott; Sanders, Eric; Thiruvahindrapuram, Bhooma; Nalpathamkalam, Thomas; Pellecchia, Giovanna; Lin, Fan; Keenan, Katherine; Patel, Rohan V; Sung, Wilson Wl; Roshandel, Delnaz; Whitney, Joe; Allana, Sana; Avolio, Julie; Eckford, Paul Dw; Ratjen, Felix; Strug, Lisa J

Human chorionic gonadotropin decreases cerebral cystic encephalomalacia and parvalbumin interneuron degeneration in a pro-inflammatory model of mouse neonatal hypoxia-ischemia

人绒毛膜促性腺激素可降低小鼠新生儿缺氧缺血促炎模型中的脑囊性脑软化和小白蛋白中间神经元变性

Miller, Benjamin; Crider, Alexander; Aravamuthan, Bhooma; Galindo, Rafael

Pediatric Constraint-Induced Movement Therapy: Current Practices and Implementation Barriers

儿童约束诱导运动疗法:现状与实施障碍

Larson, Sophia C; Smith, Alyssa E; Aravamuthan, Bhooma R; Moore, Hunter G; Antonoff, Kaylin A; Ramey, Sharon; Hoyt, Catherine R

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

Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-Analysis

脑瘫基因检测结果的临床应用价值:系统评价和荟萃分析

Lewis, Sara A; Chopra, Maya; Cohen, Julie S; Bain, Jennifer M; Aravamuthan, Bhooma; Carmel, Jason B; Fahey, Michael C; Segel, Reeval; Wintle, Richard F; Zech, Michael; May, Halie; Haque, Nahla; Fehlings, Darcy; Srivastava, Siddharth; Kruer, Michael C

Chromosome X-wide common variant association study in autism spectrum disorder

自闭症谱系障碍中X染色体常见变异关联研究

Mendes, Marla; Chen, Desmond Zeya; Engchuan, Worrawat; Leal, Thiago Peixoto; Thiruvahindrapuram, Bhooma; Trost, Brett; Howe, Jennifer L; Pellecchia, Giovanna; Nalpathamkalam, Thomas; Alexandrova, Roumiana; Salazar, Nelson Bautista; McKee, Ethan A; Rivera-Alfaro, Natalia; Lai, Meng-Chuan; Bandres-Ciga, Sara; Roshandel, Delnaz; Bradley, Clarrisa A; Anagnostou, Evdokia; Sun, Lei; Scherer, Stephen W

Optimized gene transduction in human lung organoids: A high-efficiency method for advanced research applications

人类肺类器官中基因转导的优化:一种用于高级研究应用的高效方法

Jasmin Khateeb #, Jady Liang #, Yuchong Li, Thenuka Thanabalasingam, Julie Khang, Mirjana Jerkic, Giovanna Pellecchia, Bhooma Thiruv, Ya-Wen Chen, Ori Rotstein, Arthur S Slutsky, Haibo Zhang2

UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literature

UBR5功能缺失变异与自闭症谱系障碍和智力障碍:病例系列及文献综述

Reuter, Miriam S; Salazar, Nelson Bautista; Howe, Jennifer L; Hoang, Ny; Sarikaya, Ege; Selvanayagam, Thanuja; Mendes de Aquino, Marla; Vicente, Astrid M; Oliveira, Guiomar; Freitag, Christine M; Thiruvahindrapuram, Bhooma; Trost, Brett; Scherer, Stephen W