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

A Collection of Patient-Derived Intestinal Organoid Lines Reveals Epithelial Phenotypes Associated with Genetic Drivers of Pediatric Inflammatory Bowel Disease.

一系列患者来源的肠道类器官系揭示了与儿童炎症性肠病遗传驱动因素相关的上皮表型。

Shojaei Jeshvaghani Zahra, Argmann Carmen, de Vries Maaike H, van Es Johan H, Collen Lauren V, Kotlarz Daniel, Sveen Mia, Comella Phillip H, Snapper Scott B, Klein Christoph, Schadt Eric E, Clevers Hans, Mokry Michal, Kuijk Ewart, Nieuwenhuis Edward

Gene signature linked to inhaled corticosteroid-induced lung function improvement in COPD: insights from the GLUCOLD Study

基因特征与吸入皮质类固醇诱导的慢性阻塞性肺疾病肺功能改善相关:来自 GLUCOLD 研究的启示

Zhang, Jing; van den Berge, Maarten; Brandsma, Corry-Anke; Timens, Wim; Faiz, Alen; Hylkema, Machteld N; de Vries, Maaike

General population-based lung function trajectories over the life course: an accelerated cohort study

基于一般人群的生命历程肺功能轨迹:一项加速队列研究

Garcia-Aymerich, Judith; de Las Heras, Martí; Carsin, Anne-Elie; Accordini, Simone; Agustí, Alvar; Bui, Dinh; Dharmage, Shyamali C; Dodd, James W; Eze, Ikenna; Gehring, Ulrike; Gislason, Thorarinn; Granell, Raquel; Imboden, Medea; Íñiguez, Carmen; Jeong, Ayoung; Koch, Sarah; Koppelman, Gerard H; Leynaert, Bénédicte; Melén, Erik; Perret, Jennifer; Probst-Hensch, Nicole; Santa-Marina, Loreto; Torrent, Maties; Vicendese, Don; Vonk, Judith M; de Vries, Maaike; Walters, E Haydn; Wang, Gang; Wedzicha, Jadwiga A; Jarvis, Deborah; Faner, Rosa

Respiratory symptoms associated with a new lobe-based bronchial scoring system in an urban Chinese low-dose CT screening population

在中国城市低剂量CT筛查人群中,一种新的基于肺叶的支气管评分系统与呼吸道症状的相关性

Nie, Zhenhui; de Bock, Geertruida H; Vliegenthart, Rozemarijn; Yang, Xiaofei; Oudkerk, Matthijs; Slebos, Dirk-Jan; Ye, Zhaoxiang; de Vries, Maaike; Dorrius, Monique D

Screening Tool Improves Recognition of Movement Disorders by Internists and Paediatricians in Patients With Inherited Metabolic Diseases

筛查工具可提高内科医生和儿科医生对遗传性代谢疾病患者运动障碍的识别率

Hulshof, Ellen M; Lantinga, Hugo P; Alkemade, Gonnie; Bosch, Annet M; Brands, Marion M; Vliet, Danique Draaisma-van; Haijer-Schreuder, Andrea B; Hoytema van Konijnenburg, Eva M M; Janssen, Mirian C H; van der Klauw, Melanie M; Langeveld, Mirjam; Lubout, Charlotte M A; van Ockenburg, Sonja L; Oussoren, Esmeralda; Panis, Bianca; Sjouke, Barbara; de Vries, Maaike; Wagenmakers, Margreet A E M; Wijnen, Mark; Sival, Deborah A; Tijssen, Marina A J; de Koning, Tom J; Koens, Lisette H

Evaluation of Newborn Screening for Diseases Using C5-OH as a Marker: Systematic Review of the Literature and Evaluation of 17 Years of C5-OH Screening in the Netherlands

以C5-OH为标志物评估新生儿疾病筛查:文献系统综述及荷兰17年C5-OH筛查评估

Aukes, Ryan; Albersen, Monique; Boelen, Anita; Kluijtmans, Leo A J; Visser, Wouter F; de Vries, Maaike C; Bosch, Annet M

Unveiling hidden connections: How social networks impact diversion in hospital emergency departments: An exploratory social network analysis

揭示隐藏的联系:社交网络如何影响医院急诊科的转诊:一项探索性社交网络分析

Francis, Troy; de Vries, Maaike; Fan, Mark; Yousefi-Nooraie, Reza; Ouimet, Mathieu; Rac, Valeria E; Trbovich, Patricia

Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism

WASHC3基因(WASH复合体的一个组成部分)的变异会导致身材矮小、不同程度的神经发育异常和独特的面部畸形。

Jee, Youn Hee; Lui, Julian C; Marafi, Dana; Xia, Zhi-Jie; Bhatia, Ruchika; Zhou, Elaine; Herman, Isabella; Temnycky, Adrian; Whalen, Philip; Elliot, Gene; Leschek, Ellen W; Wijngaard, Robin; van Beek, Ronald; de Vreugd, Annemarie; de Vries, Maaike C; van Karnebeek, Clara D M; Oud, Machteld M; Markello, Thomas C; Barnes, Kevin M; Alrohaif, Hadil; Freeze, Hudson H; Gahl, William A; Malicdan, May Christine V; Posey, Jennifer E; Lupski, James R; Baron, Jeffrey

A collection of patient-derived intestinal organoid lines reveals epithelial phenotypes associated with genetic drivers of pediatric inflammatory bowel disease.

一系列源自患者的肠道类器官系揭示了与儿童炎症性肠病遗传驱动因素相关的上皮表型

Jeshvaghani Zahra Shojaei, Argmann Carmen, Mokry Michal, van Es Johan H, de Vries Maaike H, Collen Lauren V, Kotlarz Daniel, Sveen Mia, Comella Phillip, Snapper Scott B, Klein Christoph, Schadt Eric, Clevers Hans, Kuijk Ewart, Nieuwenhuis Edward

Genome-wide association study of preserved ratio impaired spirometry (PRISm)

全基因组关联研究:保留比率受损的肺功能测定(PRISm)

Higbee, Daniel H; Lirio, Alvin; Hamilton, Fergus; Granell, Raquel; Wyss, Annah B; London, Stephanie J; Bartz, Traci M; Gharib, Sina A; Cho, Michael H; Wan, Emily; Silverman, Edwin; Crapo, James D; Lominchar, Jesus V T; Hansen, Torben; Grarup, Niels; Dantoft, Thomas; Kårhus, Line; Linneberg, Allan; O'Connor, George T; Dupuis, Josée; Xu, Hanfie; De Vries, Maaike M; Hu, Xiaowei; Rich, Stephen S; Barr, R Graham; Manichaikul, Ani; Wijnant, Sara R A; Brusselle, Guy G; Lahousse, Lies; Li, Xuan; Hernández Cordero, Ana I; Obeidat, Ma'en; Sin, Don D; Harris, Sarah E; Redmond, Paul; Taylor, Adele M; Cox, Simon R; Williams, Alexander T; Shrine, Nick; John, Catherine; Guyatt, Anna L; Hall, Ian P; Davey Smith, George; Tobin, Martin D; Dodd, James W