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

Interstitial Lung Disease and Lung Cancer Associated with a Monoallelic Novel Variant in SFTPB

间质性肺病和肺癌与SFTPB基因中的单等位基因新变异相关

Wambach, Jennifer A; Nogee, Lawrence M; Spielberg, David R; Cole, F Sessions; Roberts, Dion M; Murphy, Scarlett; Garcia, Christine K

Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases

美国儿童间质性和弥漫性肺疾病登记中基因检测的应用

Voss, Laura A; Nevel, Rebekah J; Wambach, Jennifer A; Nogee, Lawrence M; Deterding, Robin R; Casey, Alicia M; O'Connor, Michael G; Craven, Daniel I; Taylor, Jane B; Deutsch, Gail H; Tam-Williams, Jade B; Steffes, Lea C; Brennan, Steven K; Santiago, Maria T; Sadreameli, Sara C; Heras, Andrea F; Powers, Michael R; Popova, Antonia P; Bansal, Manvi; Hamvas, Aaron; Gower, William A; Urrego, Fernando; Young, Lisa R

The US national registry for childhood interstitial and diffuse lung disease: Report of study design and initial enrollment cohort

美国儿童间质性和弥漫性肺疾病国家登记处:研究设计和初始入组队列报告

Nevel, Rebekah J; Deutsch, Gail H; Craven, Daniel; Deterding, Robin; Fishman, Martha P; Wambach, Jennifer A; Casey, Alicia; Krone, Katie; Liptzin, Deborah R; O'Connor, Michael G; Kurland, Geoffrey; Taylor, Jane B; Gower, William A; Hagood, James S; Conrad, Carol; Tam-Williams, Jade B; Fiorino, Elizabeth K; Goldfarb, Samuel; Sadreameli, Sara C; Nogee, Lawrence M; Montgomery, Gregory; Hamvas, Aaron; Laguna, Theresa A; Bansal, Manvi; Lew, Cheryl; Santiago, Maria; Popova, Antonia; De, Aliva; Chan, Marilynn; Powers, Michael R; Josephson, Maureen B; Camburn, Devaney; Voss, Laura; Li, Yun; Young, Lisa R

Rare to "Ubiquitinous": Alveolar Capillary Dysplasia, FOXF1, and a Sly Approach to Angiogenesis

从罕见到“普遍”:肺泡毛细血管发育不良、FOXF1 和血管生成的巧妙机制

Cornfield, David N; Nogee, Lawrence M

Accurate assignment of disease liability to genetic variants using only population data

仅使用人群数据即可准确地将疾病易感性与基因变异联系起来

Collaco, Joseph M; Raraigh, Karen S; Betz, Joshua; Aksit, Melis Atalar; Blau, Nenad; Brown, Jordan; Dietz, Harry C; MacCarrick, Gretchen; Nogee, Lawrence M; Sheridan, Molly B; Vernon, Hilary J; Beaty, Terri H; Louis, Thomas A; Cutting, Garry R

First Steps toward Personalized Therapies for ABCA3 Deficiency

ABCA3 缺乏症个性化治疗的第一步

Wambach, Jennifer A; Nogee, Lawrence M; Cole, F Sessions

Community-Onset Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Young Infants: A Systematic Review

社区获得性严重急性呼吸综合征冠状病毒2感染在婴幼儿中的系统评价

Mark, Elyse G; Golden, W Christopher; Gilmore, Maureen M; Sick-Samuels, Anna; Curless, Melanie S; Nogee, Lawrence M; Milstone, Aaron M; Johnson, Julia

Coronavirus Disease 2019 in Pregnancy and Outcomes Among Pregnant Women and Neonates: A Literature Review

2019冠状病毒病在妊娠期及对孕妇和新生儿结局的影响:文献综述

Mark, Elyse G; McAleese, Samuel; Golden, W Christopher; Gilmore, Maureen M; Sick-Samuels, Anna; Curless, Melanie S; Nogee, Lawrence M; Milstone, Aaron M; Johnson, Julia

Genetic Testing for Neonatal Respiratory Disease

新生儿呼吸系统疾病的基因检测

Nogee, Lawrence M; Ryan, Rita M

The common K333Q polymorphism in long-chain acyl-CoA dehydrogenase (LCAD) reduces enzyme stability and function

长链酰基辅酶A脱氢酶(LCAD)中常见的K333Q多态性会降低酶的稳定性和功能。

Beck, Megan E; Zhang, Yuxun; Bharathi, Sivakama S; Kosmider, Beata; Bahmed, Karim; Dahmer, Mary K; Nogee, Lawrence M; Goetzman, Eric S