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

The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit

犹他州NeoSeq项目:一项旨在促进新生儿重症监护病房基因组诊断的多学科合作项目

Malone Jenkins, Sabrina; Palmquist, Rachel N; Moore, Barry; Boyden, Steven E; Nicholas, Thomas J; Bayrak-Toydemir, Pinar; Mao, Rong; Farrell, J Andrew R; Holt, Carson H; Rynearson, Shawn G; Solorzano, Chelsea M; Ward, Alistair; Best, D Hunter; Al-Sweel, Najla; Bentley, Dawn L; Brunelli, Luca; Chow, Clement Y; Close, Devin W; Cormier, Michael J; Deshotel, Malia J; Durtschi, Jacob; Eide, Erik J; Floyd, Luaiva; Fredrickson, Eric K; Fulmer, Makenzie L; Hernandez, Edgar J; Kapron, Ashley L; Karren, Mary Anne; Lewis, Robert G; Miller, Christine E; Murtaugh, L Charles; Nicholson, Kelsey E; Noble, Katherine; O'Fallon, Brendan D; O'Shea, John M; Pattison, David C; Pedersen, Brent S; Petersen, Brandy J; Peterson, Bennet D; Pizzo, Lucilla; Reynolds, Hayley M; Rindler, Paul; Torr, Carrie B; Wen, Ting; Yost, H Joseph; Zhao, Jian; Yandell, Mark; Marth, Gabor T; Quinlan, Aaron R; Carey, John C; Shayota, Brian J; Tristani-Firouzi, Martin; Bonkowsky, Joshua L

Assisted therapy optimizing module to improve physician adhErence with guideLine-directed medical heart failure therapy rationale and design of the AMPEL trial

辅助治疗优化模块旨在提高医生对指南指导的心力衰竭药物治疗方案的依从性,其原理和设计见AMPEL试验。

Brunelli, Luca; Hoch, Luiza; Pfeifer, Bernhard; Neururer, Sabrina; Kleinheinz, Elisabeth; Fetz, Bettina; Lauschensky, Aaron; Schreier, Günter; Modre-Osprian, Robert; Zaruba, Marc-Michael; Messner, Moritz; Ungericht, Maria; Wallner, Markus; Stark, Cosima; Pötz, Stefan; Taucher, Bernadette; Frank, Almut; Pölzl, Gerhard

The Role of Genetic Testing in Palliative Care Decisions for Critically Ill Newborns

基因检测在危重新生儿姑息治疗决策中的作用

Mowery, Ashley; Brunelli, Luca

A Rare Case of Neonatal Cholestasis Linked to FOCAD Gene Variants: Exploring the Variable Phenotypic Presentation and Its Implications

一例与FOCAD基因变异相关的罕见新生儿胆汁淤积症:探索其表型表现的多样性及其意义

Tarrell, Ariel; Weber, Jessika; Shawar, Reem; Brunelli, Luca; Morelli, Susan; Bayrak-Toydemir, Pinar; Doughty, Elizabeth; Akay, Gulsen; Botto, Lorenzo D; Flemming, Emily; Reading, N Scott; Jaramillo, Catalina

More Than a Decade of Rapid Genomic Sequencing: Where Are We Now?

快速基因组测序十余年:我们现在处于什么阶段?

Saunders, Carol J; Brunelli, Luca; Deem, Michael J; Farrow, Emily G; Hegde, Madhuri; Stark, Zornitza

Health data space nodes for privacy-preserving linkage of medical data to support collaborative secondary analyses

用于保护隐私的医疗数据链接的健康数据空间节点,以支持协作式二次分析

Baumgartner, Martin; Kreiner, Karl; Lauschensky, Aaron; Jammerbund, Bernhard; Donsa, Klaus; Hayn, Dieter; Wiesmüller, Fabian; Demelius, Lea; Modre-Osprian, Robert; Neururer, Sabrina; Slamanig, Gerald; Prantl, Sarah; Brunelli, Luca; Pfeifer, Bernhard; Pölzl, Gerhard; Schreier, Günter

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

利用临床自然语言处理和机器学习技术,自动确定患病新生儿全基因组测序的优先顺序

Peterson, Bennet; Hernandez, Edgar Javier; Hobbs, Charlotte; Malone Jenkins, Sabrina; Moore, Barry; Rosales, Edwin; Zoucha, Samuel; Sanford, Erica; Bainbridge, Matthew N; Frise, Erwin; Oriol, Albert; Brunelli, Luca; Kingsmore, Stephen F; Yandell, Mark

Newborn sequencing is only part of the solution for better child health

新生儿基因测序只是改善儿童健康解决方案的一部分

Brunelli, Luca; Sohn, Heeju; Brower, Amy

Promoting children's rights to health and well-being in the United States

促进美国儿童享有健康和福祉的权利

Chapman, Audrey R; Brunelli, Luca; Forman, Lisa; Kaempf, Joseph

Provision and availability of genomic medicine services in Level IV neonatal intensive care units

四级新生儿重症监护病房基因组医学服务的提供和可用性

Wojcik, Monica H; Callahan, Katharine P; Antoniou, Austin; Del Rosario, Maya C; Brunelli, Luca; ElHassan, Nahed O; Gogcu, Semsa; Murthy, Karna; Rumpel, Jennifer A; Wambach, Jennifer A; Suhrie, Kristen; Fishler, Kristen; Chaudhari, Bimal P