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

Patient passports for rare diseases: results of a pilot study

罕见病患者护照：一项试点研究的结果

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-025-01930-w
Balfour, Jo; Morrison, Vaila; Seed, Lydia; Clymer, Joseph; Warnants, Emma; Lampkin, Abigail; Leiter, Sarah M; Chandratillake, Gemma
发表日期：2026
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A systematic literature review of the impact and measurement of mobility impairment in rare bone diseases

对罕见骨病中行动障碍的影响和测量方法进行系统性文献综述

期刊:Therapeutic Advances in Musculoskeletal Disease
影响因子:4.1
doi:10.1177/1759720X251369963
Alves, Inês; Westerheim, Ingunn; Hsiao, Edward C; Upadhyay, Jaymin; Sangiorgi, Luca; Artyomenko, Alexander; Croskery, Kim; Johns, Juliet; Warnants, Emma; Barton, Gabor
发表日期：2025
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Identifying global trends from case reports of fibrodysplasia ossificans progressiva: a scoping review

从进行性骨化性纤维发育不良病例报告中识别全球趋势：一项范围界定综述

期刊:Therapeutic Advances in Musculoskeletal Disease
影响因子:4.1
doi:10.1177/1759720X251407060
Scott, Christiaan; Al Mukaddam, Mona; Davis, Michelle; De Cunto, Carmen L; Hsiao, Edward C; Pignolo, Robert J; Schwegler, Odette; Artyomenko, Alexander; Croskery, Kim; Hanman, Kate; Sanchot, Boris; Warnants, Emma; Kaplan, Frederick S
发育与干细胞
发表日期：2025
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Vitamin D insufficiency in infants with increased risk of developing type 1 diabetes: a secondary analysis of the POInT Study

维生素D不足与婴儿罹患1型糖尿病风险增加相关：POInT研究的二次分析

期刊:Bmj Paediatrics Open
影响因子:2.3
doi:10.1136/bmjpo-2023-002212
Jacobs, An; Warnants, Maarten; Vollmuth, Veronika; Winkler, Christiane; Weiss, Andreas; Ziegler, Anette-Gabriele; Lundgren, Markus; Elding Larsson, Helena; Kordonouri, Olga; von dem Berge, Thekla; Zielmann, Marie-Luise; Bonifacio, Ezio; Hommel, Angela; Ołtarzewski, Mariusz; Szypowska, Agnieszka; Besser, Rachel; Todd, John A; Casteels, Kristina
糖尿病
代谢
发表日期：2024
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