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

Suitable Evaluation Frameworks for Disease-Agnostic Platforms for Remote Patient Monitoring: Scoping Review

适用于疾病无关型远程患者监护平台的评估框架:范围界定综述

Yassaee, Arrash; Reed, Angus Bruno; Swanson, Ben; Neves, Ana Luísa; Hargreaves, Dougal

Association Between Genetic Variants in DEFB1 Gene and Dental Caries Susceptibility

DEFB1基因遗传变异与龋齿易感性的关联

Mokhtari, Mohammad Javad; Koohpeima, Fatemeh; Hashemi-Gorji, Farzad; Mirfakhraie, Reza; Yassaee, Vahid Reza; Marjani, Majid; Varahram, Mohammad; Rezaei-Tavirani, Mostafa; Omidifar, Navid; Rezaei, Mitra

Engagement With mHealth COVID-19 Digital Biomarker Measurements in a Longitudinal Cohort Study: Mixed Methods Evaluation

在纵向队列研究中,参与移动医疗 COVID-19 数字生物标志物测量的情况:混合方法评估

Rennie, Kirsten L; Lawlor, Emma R; Yassaee, Arrash; Booth, Adam; Westgate, Kate; Sharp, Stephen J; Tyrrell, Carina S B; Aral, Mert; Wareham, Nicholas J

BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients

BRAT1相关疾病:97例患者的表型谱和表型-基因型相关性

Engel, Camille; Valence, Stéphanie; Delplancq, Geoffroy; Maroofian, Reza; Accogli, Andrea; Agolini, Emanuele; Alkuraya, Fowzan S; Baglioni, Valentina; Bagnasco, Irene; Becmeur-Lefebvre, Mathilde; Bertini, Enrico; Borggraefe, Ingo; Brischoux-Boucher, Elise; Bruel, Ange-Line; Brusco, Alfredo; Bubshait, Dalal K; Cabrol, Christelle; Cilio, Maria Roberta; Cornet, Marie-Coralie; Coubes, Christine; Danhaive, Olivier; Delague, Valérie; Denommé-Pichon, Anne-Sophie; Di Giacomo, Marilena Carmela; Doco-Fenzy, Martine; Engels, Hartmut; Cremer, Kirsten; Gérard, Marion; Gleeson, Joseph G; Heron, Delphine; Goffeney, Joanna; Guimier, Anne; Harms, Frederike L; Houlden, Henry; Iacomino, Michele; Kaiyrzhanov, Rauan; Kamien, Benjamin; Karimiani, Ehsan Ghayoor; Kraus, Dror; Kuentz, Paul; Kutsche, Kerstin; Lederer, Damien; Massingham, Lauren; Mignot, Cyril; Morris-Rosendahl, Déborah; Nagarajan, Lakshmi; Odent, Sylvie; Ormières, Clothilde; Partlow, Jennifer Neil; Pasquier, Laurent; Penney, Lynette; Philippe, Christophe; Piccolo, Gianluca; Poulton, Cathryn; Putoux, Audrey; Rio, Marlène; Rougeot, Christelle; Salpietro, Vincenzo; Scheffer, Ingrid; Schneider, Amy; Srivastava, Siddharth; Straussberg, Rachel; Striano, Pasquale; Valente, Enza Maria; Venot, Perrine; Villard, Laurent; Vitobello, Antonio; Wagner, Johanna; Wagner, Matias; Zaki, Maha S; Zara, Federizo; Lesca, Gaetan; Yassaee, Vahid Reza; Miryounesi, Mohammad; Hashemi-Gorji, Farzad; Beiraghi, Mehran; Ashrafzadeh, Farah; Galehdari, Hamid; Walsh, Christopher; Novelli, Antonio; Tacke, Moritz; Sadykova, Dinara; Maidyrov, Yerdan; Koneev, Kairgali; Shashkin, Chingiz; Capra, Valeria; Zamani, Mina; Van Maldergem, Lionel; Burglen, Lydie; Piard, Juliette

Association of HOTAIR rs2366152 and rs1899663 polymorphisms with colorectal cancer susceptibility in Iranian population: A case-control study

HOTAIR rs2366152 和 rs1899663 多态性与伊朗人群结直肠癌易感性的关联:一项病例对照研究

Eivazi, Nasim; Mirfakhraie, Reza; Nazemalhosseini Mojarad, Ehsan; Behroozi, Javad; Yassaee, Vahid Reza; Tahmaseb, Mohammad; Sadeghi, Hossein

Use of Telemedicine in Pediatric Services for 4 Representative Clinical Conditions: Scoping Review

远程医疗在儿科服务中针对四种典型临床疾病的应用:范围界定综述

Southgate, Genevieve; Yassaee, Arrash A; Harmer, Matthew J; Livesey, Helen; Pryde, Kate; Roland, Damian

Autophagy ATG16L1 rs2241880 impacts the colorectal cancer risk: A case-control study

自噬 ATG16L1 rs2241880 影响结直肠癌风险:一项病例对照研究

Jamali, Leila; Sadeghi, Hossein; Ghasemi, Mohammad-Reza; Mohseni, Roohollah; Nazemalhosseini-Mojarad, Ehsan; Yassaee, Vahid Reza; Larki, Pegah; Zali, Mohammad Reza; Mirfakhraie, Reza

Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran

伊朗一个大家族中发现一种新的基因变异,导致颌骨干发育不良

Yassaee, Vahid Reza; Khojasteh, Arash; Hashemi-Gorji, Farzad; Sadeghi, Hossein; Safiaghdam, Hannaneh; Mirfakhraie, Reza

Ectopic expression of CYP24A1 circular RNA hsa_circ_0060927 in uterine leiomyomas

子宫平滑肌瘤中CYP24A1环状RNA hsa_circ_0060927的异位表达

Fazeli, Elnaz; Piltan, Samira; Sadeghi, Hossein; Gholami, Milad; Azizi-Tabesh, Ghasem; Yassaee, Fakhrolmolook; Mirfakhraie, Reza

Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi-Bickel Syndrome

全外显子组测序揭示了三名患有VI型糖原贮积症和范可尼-比克尔综合征患者的新致病变异及其他发现

Eghbali, Maryam; Fatemi, Kiyana Sadat; Salehpour, Shadab; Abiri, Maryam; Saei, Hassan; Talebi, Saeed; Olyaei, Nasrin Alipour; Yassaee, Vahid Reza; Modarressi, Mohammad Hossein