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

Cost-effectiveness of an app-based treatment for urinary incontinence in comparison with care-as-usual in Dutch general practice: a pragmatic randomised controlled trial over 12 months

在荷兰全科医疗中，基于应用程序的尿失禁治疗与常规护理相比的成本效益：一项为期 12 个月的实用性随机对照试验

期刊:Bjog-An International Journal of Obstetrics and Gynaecology
影响因子:4.3
doi:10.1111/1471-0528.17191
Loohuis, Anne M M; Van Der Worp, Henk; Wessels, Nienke J; Dekker, Janny H; Slieker-Ten Hove, Marijke C Ph; Berger, Marjolein Y; Vermeulen, Karin M; Blanker, Marco H
发表日期：2022
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Value of infarct location in the prediction of functional outcome in patients with an anterior large vessel occlusion: results from the HERMES study

梗死部位在预测前壁大血管闭塞患者功能预后中的价值：HERMES 研究的结果

期刊:Neuroradiology
影响因子:2.6
doi:10.1007/s00234-021-02784-x
Tolhuisen, Manon L; Ernst, Marielle; Boers, Anne M M; Brown, Scott; Beenen, Ludo F M; Guillemin, Francis; Roos, Yvo B W E M; Saver, Jeffrey L; van Oostenbrugge, Robert; Demchuck, Andrew M; van Zwam, Wim; Jovin, Tudor G; Berkhemer, Olvert A; Muir, Keith W; Bracard, Serge; Campbell, Bruce C V; van der Lugt, Aad; White, Phill; Hill, Michael D; Dippel, Diederik W J; Mitchell, Peter J; Goyal, Mayank; Caan, Matthan W A; Marquering, Henk A; Majoie, Charles B L M
发表日期：2022
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Barriers and Facilitators Associated With App-Based Treatment for Female Urinary Incontinence: Mixed Methods Evaluation

基于应用程序的女性尿失禁治疗的障碍和促进因素：混合方法评估

期刊:Jmir Mhealth and Uhealth
影响因子:6.2
doi:10.2196/25878
Wessels, Nienke J; Loohuis, Anne M M; van der Worp, Henk; Abbenhuis, Linde; Dekker, Janny; Berger, Marjolein Y; van Gemert-Pijnen, Julia E W C; Blanker, Marco H
发表日期：2021
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User Experiences and Preferences Regarding an App for the Treatment of Urinary Incontinence in Adult Women: Qualitative Study

针对成年女性尿失禁治疗应用程序的用户体验和偏好：一项定性研究

期刊:Jmir Mhealth and Uhealth
影响因子:6.2
doi:10.2196/17114
Wessels, Nienke J; Hulshof, Lisa; Loohuis, Anne M M; van Gemert-Pijnen, Lisette; Jellema, Petra; van der Worp, Henk; Blanker, Marco H
发表日期：2020
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Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells

与非综合征性耳聋相关的新型和复发性CIB2变异体并不影响毛细胞中的钙缓冲和定位。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2015.157
Seco, Celia Zazo; Giese, Arnaud P; Shafique, Sobia; Schraders, Margit; Oonk, Anne M M; Grossheim, Mike; Oostrik, Jaap; Strom, Tim; Hegde, Rashmi; van Wijk, Erwin; Frolenkov, Gregory I; Azam, Maleeha; Yntema, Helger G; Free, Rolien H; Riazuddin, Saima; Verheij, Joke B G M; Admiraal, Ronald J; Qamar, Raheel; Ahmed, Zubair M; Kremer, Hannie
细胞生物学
发表日期：2016
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Distinct α- and β-band rhythms over rat somatosensory cortex with similar properties as in humans

大鼠体感皮层上存在明显的α波段和β波段节律，其特性与人类相似。

期刊:Journal of Neurophysiology
影响因子:2.1
doi:10.1152/jn.00507.2015
Fransen, Anne M M; Dimitriadis, George; van Ede, Freek; Maris, Eric
Rat
发表日期：2016
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Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

CLIC5基因纯合无义突变导致进行性听力丧失和前庭功能障碍

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2014.83
Seco, Celia Zazo; Oonk, Anne M M; Domínguez-Ruiz, María; Draaisma, Jos M T; Gandía, Marta; Oostrik, Jaap; Neveling, Kornelia; Kunst, Henricus P M; Hoefsloot, Lies H; del Castillo, Ignacio; Pennings, Ronald J E; Kremer, Hannie; Admiraal, Ronald J C; Schraders, Margit
发表日期：2015
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Development and validation of a single-tube multiple-locus variable number tandem repeat analysis for Klebsiella pneumoniae

肺炎克雷伯菌单管多位点可变数目串联重复分析的开发和验证

期刊:PLoS One
影响因子:2.9
doi:10.1371/journal.pone.0091209
Antoinette A T P Brink, Christian J H von Wintersdorff, Christina F M van der Donk, Anne M M W Peeters, Patrick S Beisser, Ellen E Stobberingh, Petra F G Wolffs
免疫
肺炎
发表日期：2014
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Similar phenotypes caused by mutations in OTOG and OTOGL

OTOG 和 OTOGL 基因突变引起的表型相似

期刊:Ear and Hearing
影响因子:2.8
doi:10.1097/AUD.0000000000000008
Oonk, Anne M M; Leijendeckers, Joop M; Huygen, Patrick L M; Schraders, Margit; del Campo, Miguel; del Castillo, Ignacio; Tekin, Mustafa; Feenstra, Ilse; Beynon, Andy J; Kunst, Henricus P M; Snik, Ad F M; Kremer, Hannie; Admiraal, Ronald J C; Pennings, Ronald J E
发表日期：2014
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Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment

编码耳凝蛋白的基因突变是常染色体隐性遗传性非综合征型中度听力障碍的病因。

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2012.09.012
Schraders, Margit; Ruiz-Palmero, Laura; Kalay, Ersan; Oostrik, Jaap; del Castillo, Francisco J; Sezgin, Orhan; Beynon, Andy J; Strom, Tim M; Pennings, Ronald J E; Zazo Seco, Celia; Oonk, Anne M M; Kunst, Henricus P M; Domínguez-Ruiz, María; García-Arumi, Ana M; del Campo, Miguel; Villamar, Manuela; Hoefsloot, Lies H; Moreno, Felipe; Admiraal, Ronald J C; del Castillo, Ignacio; Kremer, Hannie
发表日期：2012
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