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

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis

FOCAD 的缺失(通过 SKI 信使 RNA 监视通路发挥作用)会导致一种伴有肝硬化的儿童综合征。

Ricardo Moreno Traspas,Tze Shin Teoh,Pui-Mun Wong,Michael Maier,Crystal Y Chia,Kenneth Lay,Nur Ain Ali,Austin Larson,Fuad Al Mutairi,Nouriya Abbas Al-Sannaa,Eissa Ali Faqeih,Majid Alfadhel,Huma Arshad Cheema,Juliette Dupont,Stéphane Bézieau,Bertrand Isidor,Dorrain Yanwen Low,Yulan Wang,Grace Tan,Poh San Lai,Hugues Piloquet,Madeleine Joubert,Hulya Kayserili,Kimberly A Kripps,Shareef A Nahas,Eric P Wartchow,Mikako Warren,Gandham SriLakshmi Bhavani,Majed Dasouki,Renata Sandoval,Elisa Carvalho,Luiza Ramos,Gilda Porta,Bin Wu,Harsha Prasada Lashkari,Badr AlSaleem,Raeda M BaAbbad,Anabela Natália Abreu Ferrão,Vasiliki Karageorgou,Natalia Ordonez-Herrera,Suliman Khan,Peter Bauer,Benjamin Cogne,Aida M Bertoli-Avella,Marie Vincent,Katta Mohan Girisha,Bruno Reversade

Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program

利用病毒测序技术鉴定SARS-CoV-2变异株,用于美国疾病控制与预防中心基因组监测计划

Goswami, Chirayu; Sheldon, Michael; Bixby, Christian; Keddache, Mehdi; Bogdanowicz, Alexander; Wang, Yihe; Schultz, Jonathan; McDevitt, Jessica; LaPorta, James; Kwon, Elaine; Buyske, Steven; Garbolino, Dana; Biloholowski, Glenys; Pastuszak, Alex; Storella, Mary; Bhalla, Amit; Charlier-Rodriguez, Florence; Hager, Russ; Grimwood, Robin; Nahas, Shareef A

Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome

基于快速测序的硫胺素代谢功能障碍综合征诊断

Owen, Mallory J; Niemi, Anna-Kaisa; Dimmock, David P; Speziale, Mark; Nespeca, Mark; Chau, Kevin K; Van Der Kraan, Luca; Wright, Meredith S; Hansen, Christian; Veeraraghavan, Narayanan; Ding, Yan; Lenberg, Jerica; Chowdhury, Shimul; Hobbs, Charlotte A; Batalov, Sergey; Zhu, Zhanyang; Nahas, Shareef A; Gilmer, Sheldon; Knight, Gail; Lefebvre, Sebastien; Reynders, John; Defay, Thomas; Weir, Jacqueline; Thomson, Vicki S; Fraser, Louise; Lajoie, Bryan R; McPhail, Tim K; Mehtalia, Shyamal S; Kunard, Chris M; Hall, Kevin P; Kingsmore, Stephen F

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

快速全基因组测序影响先天性心脏病患儿的护理和资源利用

Sweeney, Nathaly M; Nahas, Shareef A; Chowdhury, Shimul; Batalov, Sergey; Clark, Michelle; Caylor, Sara; Cakici, Julie; Nigro, John J; Ding, Yan; Veeraraghavan, Narayanan; Hobbs, Charlotte; Dimmock, David; Kingsmore, Stephen F

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

出版商更正:快速全基因组测序影响先天性心脏病患儿的护理和资源利用

Sweeney, Nathaly M; Nahas, Shareef A; Chowdhury, Shimul; Batalov, Sergey; Clark, Michelle; Caylor, Sara; Cakici, Julie; Nigro, John J; Ding, Yan; Veeraraghavan, Narayanan; Hobbs, Charlotte; Dimmock, David; Kingsmore, Stephen F

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

作者更正:快速全基因组测序影响先天性心脏病患儿的护理和资源利用

Sweeney, Nathaly M; Nahas, Shareef A; Chowdhury, Shimul; Batalov, Sergey; Clark, Michelle; Caylor, Sara; Cakici, Julie; Nigro, John J; Ding, Yan; Veeraraghavan, Narayanan; Hobbs, Charlotte; Dimmock, David; Kingsmore, Stephen F

Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU

快速全基因组测序在儿科重症监护室患儿中具有临床应用价值。

Sanford, Erica F; Clark, Michelle M; Farnaes, Lauge; Williams, Matthew R; Perry, James C; Ingulli, Elizabeth G; Sweeney, Nathaly M; Doshi, Ami; Gold, Jeffrey J; Briggs, Benjamin; Bainbridge, Matthew N; Feddock, Michele; Watkins, Kelly; Chowdhury, Shimul; Nahas, Shareef A; Dimmock, David P; Kingsmore, Stephen F; Coufal, Nicole G

The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin-Siris syndrome in an infant with left congenital diaphragmatic hernia, congenital heart disease, and recurrent infections

早期应用快速全基因组测序治疗危重症婴儿的案例:一名患有左侧先天性膈疝、先天性心脏病和反复感染的婴儿,其科芬-西里斯综合征诊断延迟。

Sweeney, Nathaly M; Nahas, Shareef A; Chowdhury, Shimul; Campo, Miguel Del; Jones, Marilyn C; Dimmock, David P; Kingsmore, Stephen F

Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome

快速全基因组测序发现了一种与韦斯特综合征相关的新型GABRA1变异。

Farnaes, Lauge; Nahas, Shareef A; Chowdhury, Shimul; Nelson, James; Batalov, Serge; Dimmock, David M; Kingsmore, Stephen F

Effectiveness and cost effectiveness of screening immigrants schemes for tuberculosis (TB) on arrival from high TB endemic countries to low TB prevalent countries

从结核病高流行国家抵达结核病低流行国家时,对移民进行结核病筛查方案的有效性和成本效益分析

Sanneh, A F N S; Al-Shareef, A M