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

Urine cf-nucleosomes: A non-invasive window into human physiology and disease

尿液cf-核小体:一种无创观察人类生理和疾病的窗口

Lotem, Matan; Sharkia, Israa; Azria, Batia; Harpenas, Esther; Ormianer, Maayan; Rosen, Hadar; Falick-Michaeli, Tal; Friedman, Nir

Morning vs. evening growth hormone injections and their impact on sleep-wake patterns and daytime alertness

早晨注射生长激素与晚上注射生长激素及其对睡眠-觉醒模式和日间警觉性的影响

Levshtein, Aglaya; Sharkia, Mohamad; Shimshi-Barash, Maya; Almagor, Tal; Albertsson-Wikland, Kerstin; Hochberg, Zeev; Pillar, Giora; German, Alina

Epigenetic liquid biopsies reveal endothelial turnover and erythropoiesis in asymptomatic COVID-19

表观遗传学液体活检揭示无症状 COVID-19 患者的内皮细胞更新和红细胞生成

Ben-Ami, Roni; Loyfer, Netanel; Cohen, Eden; Fialkoff, Gavriel; Sharkia, Israa; Piyanzin, Sheina; Bogot, Naama; Kochan, Danit; Kalak, George; Jarjoui, Amir; Chen-Shuali, Chen; Azulai, Hava; Barhoum, Hezi; Arish, Nissim; Greenberger, Moshe M; Velleman, David; Kurd, Ramzi; Ben-Chetrit, Eli; Bohm, Davina; Wolak, Talya; Quteineh, Ahmad; Cann, Gordon; Glaser, Benjamin; Friedman, Nir; Kaplan, Tommy; Shemer, Ruth; Rokach, Ariel; Dor, Yuval

SCAPER-Related Autosomal Recessive Retinitis Pigmentosa with Intellectual Disability: Confirming and Extending the Phenotypic Spectrum and Bioinformatics Analyses

SCAPER相关常染色体隐性遗传性视网膜色素变性伴智力障碍:表型谱的确认与扩展及生物信息学分析

Sharkia, Rajech; Zalan, Abdelnaser; Kessel, Amit; Al-Shareef, Wasif; Zahalka, Hazar; Hengel, Holger; Schöls, Ludger; Azem, Abdussalam; Mahajnah, Muhammad

An Update of Phenotypic-Genotypic IMNEPD Cases and a Bioinformatics Analysis of the New PTRH2 Gene Variants

IMNEPD 表型-基因型病例更新及新 PTRH2 基因变异的生物信息学分析

Sharkia, Rajech; Vuillaume, Marie-Laure; Jain, Sahil; Mahajnah, Muhammad; Stoeva, Radka; Guichet, Agnès; Colin, Estelle; Champ, Jérome; Derive, Nicolas; Chefdor, Arnaud; Zalan, Abdelnaser

Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes

运动后 cfDNA 升高主要来自成熟的多形核中性粒细胞,心肌细胞的贡献较小

Ori Fridlich, Ayelet Peretz, Ilana Fox-Fisher, Sheina Pyanzin, Ziv Dadon, Eilon Shcolnik, Ronen Sadeh, Gavriel Fialkoff, Israa Sharkia, Joshua Moss, Ludovica Arpinati, Shachar Nice, Christopher D Nogiec, Samuel Terkper Ahuno, Rui Li, Eddie Taborda, Sonia Dunkelbarger, Zvi G Fridlender, Paz Polak, To

PTRH2 Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis

PTRH2基因变异:表型特征及其生物信息学分析的最新综述

Sharkia, Rajech; Jain, Sahil; Mahajnah, Muhammad; Habib, Clair; Azem, Abdussalam; Al-Shareef, Wasif; Zalan, Abdelnaser

High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

儿童假性脑瘤综合征患者脑脊液中检测到高水平CCL2

Genizi, Jacob; Berger, Lotan; Mahajnah, Muhammad; Shlonsky, Yulia; Golan-Shany, Orit; Romem, Azriel; Halevy, Ayelet; Nathan, Keren; Sharkia, Rajech; Zalan, Abdelnaser; Kessel, Aharon; Cohen, Rony

Personal Growth and Life Satisfaction during Fertility Treatment-A Comparison between Arab and Jewish Women

生育治疗期间的个人成长和生活满意度——阿拉伯女性与犹太女性的比较

Abu-Sharkia, Salam; Taubman-Ben-Ari, Orit; Mofareh, Ali

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

更正:对患有神经系统疾病的巴勒斯坦和以色列阿拉伯人进行一线外显子组测序是有效的,并有助于发现致病基因。

Hengel, Holger; Buchert, Rebecca; Sturm, Marc; Haack, Tobias B; Schelling, Yvonne; Mahajnah, Muhammad; Sharkia, Rajech; Azem, Abdussalam; Balousha, Ghassan; Ghanem, Zaid; Falana, Mohammed; Balousha, Osama; Ayesh, Suhail; Keimer, Reinhard; Deigendesch, Werner; Zaidan, Jimmy; Marzouqa, Hiyam; Bauer, Peter; Schöls, Ludger