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

Shared and distinct phenotypic profiles among neurodevelopmental disorder genes

神经发育障碍基因的共同和独特表型特征

Shimelis, Hermela; Oetjens, Matthew T; McGivern, Bobbi; Zhang, Zhancheng; Stanton, Janelle E; McSalley, Ian; Ganesan, Shiva; Finucane, Brenda M; Helbig, Ingo; Martin, Christa L; Myers, Scott M; Ledbetter, David H

Factors associated with externalized anger among early adolescents in rural Appalachia: A conceptual proposition with implications for violence prevention

阿巴拉契亚农村地区青少年早期外化愤怒的相关因素:一个对预防暴力具有启示意义的概念性命题

Mills, Rosalina; Lilly, Christa L; Pollini, Robin A; Zullig, Keith J; Jarrett, Traci; Tebes, Jacob K; Kristjansson, Alfgeir L

Odds of Developing Overweight or Obesity Increase with Height Decile in Tall Healthy Weight Kindergarteners: Longitudinal Results from the West Virginia Coronary Artery Risk Detection In Appalachian Communities (WV CARDIAC) Project

在身材高挑、体重健康的幼儿园儿童中,超重或肥胖的几率随身高十分位数的增加而增加:来自西弗吉尼亚州阿巴拉契亚社区冠状动脉风险检测(WV CARDIAC)项目的纵向研究结果

Serrat, Maria A; Elliott, Eloise; Pyles, Lee A; Lilly, Christa L

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

遗传修饰因子和检测结果驱动复杂疾病的变异性表达

Jensen, Matthew; Smolen, Corrine; Tyryshkina, Anastasia; Pizzo, Lucilla; Sun, Jiawan; Noss, Serena; Banerjee, Deepro; Oetjens, Matthew; Shimelis, Hermela; Taylor, Cora M; Pounraja, Vijay Kumar; Song, Hyebin; Rohan, Laura; Huber, Emily; El Khattabi, Laila; van de Laar, Ingrid; Tadros, Rafik; Bezzina, Connie R; van Slegtenhorst, Marjon; Kammeraad, Janneke; Prontera, Paolo; Caberg, Jean-Hubert; Fraser, Harry; Banka, Siddharth; Van Dijck, Anke; Schwartz, Charles; Voorhoeve, Els; Callier, Patrick; Mosca-Boidron, Anne-Laure; Marle, Nathalie; Lefebvre, Mathilde; Pope, Kate; Snell, Penny; Boys, Amber; Lockhart, Paul J; Ashfaq, Myla; McCready, Elizabeth; Nowacyzk, Margaret; Castiglia, Lucia; Galesi, Ornella; Avola, Emanuela; Mattina, Teresa; Fichera, Marco; Bruccheri, Maria Grazia; Mandarà, Giuseppa Maria Luana; Mari, Francesca; Privitera, Flavia; Longo, Ilaria; Curró, Aurora; Renieri, Alessandra; Keren, Boris; Charles, Perrine; Cuinat, Silvestre; Nizon, Mathilde; Pichon, Olivier; Bénéteau, Claire; Stoeva, Radka; Martin-Coignard, Dominique; Blesson, Sophia; Le Caignec, Cedric; Mercier, Sandra; Vincent, Marie; Martin, Christa L; Mannik, Katrin; Reymond, Alexandre; Faivre, Laurence; Sistermans, Erik; Kooy, R Frank; Amor, David J; Romano, Corrado; Andrieux, Joris; Girirajan, Santhosh

Dexamethasone-loaded platelet-inspired nanoparticles improve intracortical microelectrode recording performance

载有地塞米松的仿血小板纳米颗粒可提高皮层内微电极记录性能

Li, Longshun; Hartzler, Aniya; Menendez-Lustri, Dhariyat M; Zhang, Jichu; Chen, Alex; Lam, Danny V; Traylor, Baylee; Quill, Emma; Nethery, David E; Hoeferlin, George F; Pawlowski, Christa L; Bruckman, Michael A; Sen Gupta, Anirban; Capadona, Jeffrey R; Shoffstall, Andrew J

Anatomical and behavioural correlates of auditory perception in developmental dyslexia

发展性阅读障碍中听觉感知的解剖学和行为学相关性

Qi, Ting; Mandelli, Maria Luisa; Watson Pereira, Christa L; Wellman, Emma; Bogley, Rian; Licata, Abigail E; Miller, Zachary A; Tee, Boon Lead; de Leon, Jessica; Chang, Edward F; Oganian, Yulia; Gorno-Tempini, Maria Luisa

Genomic Screening at a Single Health System

单一医疗系统基因组筛查

Savatt, Juliann M; Kelly, Melissa A; Sturm, Amy C; McCormick, Cara Z; Williams, Marc S; Nixon, Michelle Pistner; Rolston, David D; Strande, Natasha T; Wain, Karen E; Willard, Huntington F; Faucett, W Andrew; Ledbetter, David H; Buchanan, Adam H; Martin, Christa L

X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height

X 和 Y 基因剂量效应是人类性二态性的主要因素:以身高为例

Berry, Alexander S F; Finucane, Brenda M; Myers, Scott M; Martin, Christa L; Ledbetter, David H; Willard, Huntington F; Oetjens, Matthew T

Utilization of allogeneic hematopoietic stem cell transplantation among patients with newly diagnosed acute myeloid leukemia in California: a population-based linked dataset study

加州新诊断急性髓系白血病患者异基因造血干细胞移植的利用情况:一项基于人群关联数据集的研究

Meyer, Christa L; Keegan, Theresa H M; Brunson, Ann; Auletta, Jeffery J; Morton, Lindsay M; Wun, Ted; Schonfeld, Sara J; Valcarcel, Bryan; Abrahão, Renata; Yusuf, Rafeek A; Muffly, Lori

Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing

接受临床外显子组测序的儿童和青少年中与运动性言语表型相关的单基因疾病

Mitchel, Marissa W; Oetjens, Matthew; Berry, Alexander S F; Johns, Alicia; Moreno-De-Luca, Andrés; Torene, Rebecca I; Strande, Natasha T; DiStefano, Marina T; Dyer, Lindsay Havens; Brandt, Tracy; Finucane, Brenda M; Ledbetter, David H; Retterer, Kyle; Martin, Christa L; Myers, Scott M