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

Identification of de novo variants from parent-proband duos via long-read sequencing

利用长读长测序技术从父母-先证者配对样本中鉴定新生变异。

Boukas, Leandros; Délot, Emmanuèle C; Pitsava, Georgia; Lambert, Christine; Fanslow, Cairbre; Baybayan, Primo; Belhadj, Sami; Losic, Bojan; Harting, John; Bluske, Krista; LoTempio, Jonathan; Al-Kouatly, Huda B; Karam, Rachid; Rowell, William J; Xiao, Changrui; Vilain, Eric; Berger, Seth I

Knowledge, attitude, and practice of self-medication among adults in the central region of Saudi Arabia: a cross-sectional study

沙特阿拉伯中部地区成年人自我用药的知识、态度和行为:一项横断面研究

Aldali, Rawand J; Elsokkary, Emadeldin M; Almousa, Huda B; Alzahrani, Yousef H; Elsokkary, Haneen E; Aldali, Jehad A

Acute Fatty Liver of Pregnancy and Fetal Fatty Acid Oxidation Disorders: A Systematic Review

妊娠期急性脂肪肝和胎儿脂肪酸氧化障碍:系统性综述

Varotsis, Dante; Araji, Sarah; Horgan, Rebecca; Powel, Jennifer E; McLaren, Rodney Jr; Kirmse, Brian; Makhamreh, Mona M; Al-Kouatly, Huda B

A Trihybrid Approach for Enhancing Crude Oil Recovery Using Effervescent-Tablet-Based Nanofluids

一种利用泡腾片基纳米流体提高原油采收率的三元混合方法

Ali, Naser; Bahzad, Husain; Aljuwayhel, Nawaf F; Ebrahim, Shikha A; Hamoud, Abbas T; Al-Mazidi, Hussain; Al-Naser, Huda B; Al-Attar, Mohammad A; Kholosy, Sohaib; Al-Zanki, Ayas; Banyan, Mohammad; Alenezi, Mumayaz

Lysosomal storage disorders in nonimmune hydrops fetalis diagnosed by exome sequencing

通过外显子组测序诊断非免疫性胎儿水肿中的溶酶体贮积症

Makhamreh, Mona M; Shivashankar, Kavya; Rice, Stephanie M; Wodoslawsky, Sascha; Grant, Christina; McLaren, Rodney Jr; Berger, Seth I; Al-Kouatly, Huda B

Recombinant erythropoietin for the treatment of iron deficiency anemia in pregnancy: A systematic review

重组人红细胞生成素治疗妊娠期缺铁性贫血:系统评价

Levy, Ariel T; Weingarten, Sarah J; Robinson, Keely; Suner, Talia; McLaren, Rodney A Jr; Saad, Antonio; Al-Kouatly, Huda B

Yield of RASopathy Gene Panel in Karyotype-Normal or Microarray-Normal Fetuses With Increased Nuchal Translucency: A Systematic Review and Meta-Analysis

RASopathy基因检测在核型正常或基因芯片检测正常的颈项透明层增厚胎儿中的检出率:系统评价和荟萃分析

Powel, Jennifer E; Barbera, Julie P; Raymond, Megan B; McLaren, Rodney Jr; Rice, Stephanie M; Russo, Melissa L; Makhamreh, Mona M; Al-Kouatly, Huda B

DNA methylation patterns in umbilical cord blood from infants of methadone maintained opioid dependent mothers

美沙酮维持的阿片类药物依赖母亲的婴儿脐带血中的 DNA 甲基化模式

Oluwatobi Adegboyega, Suhita Gayen Nee' Betal, Pedro Urday, Rachel Huang, Katherine Bodycot, Huda B Al-Kouatly, Kolawole Solarin, Joanna S Y Chan, Sankar Addya, Rupsa C Boelig, Zubair H Aghai

The genetic etiologies of bilateral renal agenesis

双侧肾脏发育不全的遗传病因

Kirschen, Gregory W; Blakemore, Karin; Al-Kouatly, Huda B; Fridkis, Gila; Baschat, Ahmet; Gearhart, John; Jelin, Angie C

Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review

葡萄糖-6-磷酸脱氢酶缺乏症是导致非免疫性胎儿水肿和严重胎儿贫血的原因:一项系统性综述

Iyer, Neel S; Mossayebi, Matthew H; Gao, Tracy J; Haizler-Cohen, Lylach; Di Mascio, Daniele; McLaren, Rodney A Jr; Al-Kouatly, Huda B