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

Perinatal genetic diagnostic yield in a population of fetuses with the phenotype arthrogryposis multiplex congenita: a cohort study 2007-2021

先天性多发性关节挛缩症胎儿群体围产期遗传诊断率：一项2007-2021年的队列研究

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-025-01848-3
Arduç, Arda; De Vries, Johanna I P; B Tan-Sindhunata, Maria; Waisfisz, Quinten; Pajkrt, Eva; Linskens, Ingeborg H
发表日期：2026
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Genetic analysis in fetuses with isolated clubfoot: diagnostic insights and added value

对孤立性马蹄内翻足胎儿进行基因分析：诊断见解和附加价值

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-025-01982-y
de Vries, Jana M; Arduç, Arda; Waisfisz, Quinten; B Tan-Sindhunata, Maria; Faas, Brigitte Hw; van Leeuwen, Elisabeth; Linskens, Ingeborg H; Pajkrt, Eva
发表日期：2026
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Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non-Isolated Clubfoot?

产前超声和基因检测能否可靠地排除非孤立性马蹄内翻足？

期刊:Prenatal Diagnosis
影响因子:2.7
doi:10.1002/pd.70055
de Vries, Jana M; Arduc, Arda; van Leeuwen, Elisabeth; Tan-Sindhunata, Maria B; Struijs, Peter; Witbreuk, Melinda; Linskens, Ingeborg H; Pajkrt, Eva
发表日期：2026
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Mortality in prenatally detected congenital small bowel obstructions: systematic review and meta-analysis

产前诊断的先天性小肠梗阻的死亡率：系统评价和荟萃分析

期刊:AJOG Global Reports
影响因子:
doi:10.1016/j.xagr.2026.100619
Heinrich, Hanna; Koorn, Ian; Denswil, Nerissa P; van Leeuwen, Elisabeth; Linskens, Ingeborg H; Pajkrt, Eva
肠梗阻
发表日期：2026
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Maternal, fetal and neonatal outcomes among pregnant women with arthrogryposis multiplex congenita: a scoping review

先天性多发性关节挛缩症孕妇的母体、胎儿和新生儿结局：一项范围界定综述

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03631-5
Arduç, Arda; De Vries, Johanna I P; Tan-Sindhunata, Maria B; Stoelinga, Femke; Jansen, Remco; Linskens, Ingeborg H
发表日期：2025
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Arthrogryposis Multiplex Congenita (AMC) and counselling before and during pregnancy: a questionnaire study

先天性多发性关节挛缩症 (AMC) 与孕前及孕期咨询：一项问卷调查研究

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03913-y
Arduç, Arda; Slootbeek, Julia; de Vries, Johanna I P; Tan-Sindhunata, Maria B; Stoelinga, Femke; Sawatzky, Bonita; Filges, Isabel; Linskens, Ingeborg H
发表日期：2025
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The Influence of the Introduction of Fetal Anomaly Scans on Pregnancy Terminations in Cases of Upper Limb Anomalies: A Retrospective Cohort Study From 2000 to 2023

引入胎儿畸形筛查对上肢畸形病例妊娠终止的影响：一项2000年至2023年的回顾性队列研究

期刊:Prenatal Diagnosis
影响因子:2.7
doi:10.1002/pd.6882
Arduç, Arda; Huiberts, Eline; van Doesburg, Margriet H M; Linskens, Ingeborg H; van Leeuwen, Elisabeth; Maarle, Merel C Van; Pajkrt, Eva
发表日期：2025
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A Practical Prenatal Ultrasound Classification System for Lower Limb Anomalies-PRELLIM Classification

下肢畸形的实用产前超声分类系统——PRELLIM分类

期刊:Prenatal Diagnosis
影响因子:2.7
doi:10.1002/pd.6885
Arduç, Arda; van Doesburg, Margriet H M; Witbreuk, Melinda M E H; Van Maarle, Merel C; van Leeuwen, Elisabeth; Pajkrt, Eva; Linskens, Ingeborg H
发表日期：2025
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Postnatal outcomes of sonographically suspected isolated congenital lung anomalies

超声检查怀疑为孤立性先天性肺部畸形的出生后结局

期刊:Pediatric Surgery International
影响因子:1.6
doi:10.1007/s00383-025-06047-1
Heinrich, Hanna; Linskens, Ingeborg H; Gorter, Ramon R; Oomen, Matthijs W N; van Leeuwen, Elisabeth; Pajkrt, Eva
发表日期：2025
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The Prognostic Role of Global Longitudinal Strain and NT-proBNP in Heart Failure Patients Receiving Cardiac Resynchronization Therapy

全球纵向应变和NT-proBNP在接受心脏再同步治疗的心力衰竭患者中的预后作用

期刊:Journal of Personalized Medicine
影响因子:3
doi:10.3390/jpm14020188
Kadoglou, Nikolaos P E; Bouwmeester, Sjoerd; de Lepper, Anouk G W; de Kleijn, Marloes C; Herold, Ingeborg H F; Bouwman, Arthur R A; Korakianitis, Ioannis; Simmers, Tim; Bracke, Franke A L E; Houthuizen, Patrick
心力衰竭
心血管
发表日期：2024
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