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

Photobiomodulation versus fractional carbon dioxide laser for stria alba in phototype III-IV: a randomized controlled study

光生物调节疗法与点阵二氧化碳激光治疗III-IV型皮肤白纹的随机对照研究

Hafez, Vanessa; Mahgoub, Doaa; Satour, Elsayed Mohamed Ali; Mikhail, Marina Mozeih Shaker; El-Kalioby, Mona

How does COVID-19 impact psoriasis practice, prescription patterns, and healthcare delivery for psoriasis patients? A cross-sectional survey study

COVID-19 如何影响银屑病诊疗实践、处方模式和银屑病患者的医疗保健服务?一项横断面调查研究

El-Komy, Mohamed H M; Abdelnaby, Asmaa; El-Kalioby, Mona

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

全外显子组测序揭示自闭症谱系障碍的遗传和新生变异:来自沙特家庭的三人研究

Bashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham AlDhalaan, Mohammed Aldosari, Michael Nester, Hussain A Alshamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma Tahir, Sultana Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies,

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

基于前1000个诊断样本和外显子组的沙特阿拉伯遗传疾病概况

Monies, Dorota; Abouelhoda, Mohamed; AlSayed, Moeenaldeen; Alhassnan, Zuhair; Alotaibi, Maha; Kayyali, Husam; Al-Owain, Mohammed; Shah, Ayaz; Rahbeeni, Zuhair; Al-Muhaizea, Mohammad A; Alzaidan, Hamad I; Cupler, Edward; Bohlega, Saeed; Faqeih, Eissa; Faden, Maha; Alyounes, Banan; Jaroudi, Dyala; Goljan, Ewa; Elbardisy, Hadeel; Akilan, Asma; Albar, Renad; Aldhalaan, Hesham; Gulab, Shamshad; Chedrawi, Aziza; Al Saud, Bandar K; Kurdi, Wesam; Makhseed, Nawal; Alqasim, Tahani; El Khashab, Heba Y; Al-Mousa, Hamoud; Alhashem, Amal; Kanaan, Imaduddin; Algoufi, Talal; Alsaleem, Khalid; Basha, Talal A; Al-Murshedi, Fathiya; Khan, Sameena; Al-Kindy, Adila; Alnemer, Maha; Al-Hajjar, Sami; Alyamani, Suad; Aldhekri, Hasan; Al-Mehaidib, Ali; Arnaout, Rand; Dabbagh, Omar; Shagrani, Mohammad; Broering, Dieter; Tulbah, Maha; Alqassmi, Amal; Almugbel, Maisoon; AlQuaiz, Mohammed; Alsaman, Abdulaziz; Al-Thihli, Khalid; Sulaiman, Raashda A; Al-Dekhail, Wajeeh; Alsaegh, Abeer; Bashiri, Fahad A; Qari, Alya; Alhomadi, Suzan; Alkuraya, Hisham; Alsebayel, Mohammed; Hamad, Muddathir H; Szonyi, Laszlo; Abaalkhail, Faisal; Al-Mayouf, Sulaiman M; Almojalli, Hamad; Alqadi, Khalid S; Elsiesy, Hussien; Shuaib, Taghreed M; Seidahmed, Mohammed Zain; Abosoudah, Ibraheem; Akleh, Hana; AlGhonaium, Abdulaziz; Alkharfy, Turki M; Al Mutairi, Fuad; Eyaid, Wafa; Alshanbary, Abdullah; Sheikh, Farrukh R; Alsohaibani, Fahad I; Alsonbul, Abdullah; Al Tala, Saeed; Balkhy, Soher; Bassiouni, Randa; Alenizi, Ahmed S; Hussein, Maged H; Hassan, Saeed; Khalil, Mohamed; Tabarki, Brahim; Alshahwan, Saad; Oshi, Amira; Sabr, Yasser; Alsaadoun, Saad; Salih, Mustafa A; Mohamed, Sarar; Sultana, Habiba; Tamim, Abdullah; El-Haj, Moayad; Alshahrani, Saif; Bubshait, Dalal K; Alfadhel, Majid; Faquih, Tariq; El-Kalioby, Mohamed; Subhani, Shazia; Shah, Zeeshan; Moghrabi, Nabil; Meyer, Brian F; Alkuraya, Fowzan S

Characterizing the morbid genome of ciliopathies

纤毛病致病基因组的特征分析

Shaheen, Ranad; Szymanska, Katarzyna; Basu, Basudha; Patel, Nisha; Ewida, Nour; Faqeih, Eissa; Al Hashem, Amal; Derar, Nada; Alsharif, Hadeel; Aldahmesh, Mohammed A; Alazami, Anas M; Hashem, Mais; Ibrahim, Niema; Abdulwahab, Firdous M; Sonbul, Rawda; Alkuraya, Hisham; Alnemer, Maha; Al Tala, Saeed; Al-Husain, Muneera; Morsy, Heba; Seidahmed, Mohammed Zain; Meriki, Neama; Al-Owain, Mohammed; AlShahwan, Saad; Tabarki, Brahim; Salih, Mustafa A; Faquih, Tariq; El-Kalioby, Mohamed; Ueffing, Marius; Boldt, Karsten; Logan, Clare V; Parry, David A; Al Tassan, Nada; Monies, Dorota; Megarbane, Andre; Abouelhoda, Mohamed; Halees, Anason; Johnson, Colin A; Alkuraya, Fowzan S

A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies.

肢带型肌营养不良症和其他肌病的一线诊断检测方法

Monies Dorota, Alhindi Hindi N, Almuhaizea Mohamed A, Abouelhoda Mohamed, Alazami Anas M, Goljan Ewa, Alyounes Banan, Jaroudi Dyala, AlIssa Abdulelah, Alabdulrahman Khalid, Subhani Shazia, El-Kalioby Mohamed, Faquih Tariq, Wakil Salma M, Altassan Nada A, Meyer Brian F, Bohlega Saeed

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

利用靶向肾脏基因检测组分析沙特阿拉伯产前囊性肾病和纤毛病表型患者的遗传谱

Al-Hamed, Mohamed H; Kurdi, Wesam; Alsahan, Nada; Alabdullah, Zainab; Abudraz, Rania; Tulbah, Maha; Alnemer, Maha; Khan, Rubina; Al-Jurayb, Haya; Alahmed, Ahmed; Tahir, Asma I; Khalil, Dania; Edwards, Noel; Al Abdulaziz, Basma; Binhumaid, Faisal S; Majid, Salma; Faquih, Tariq; El-Kalioby, Mohamed; Abouelhoda, Mohamed; Altassan, Nada; Monies, Dorota; Meyer, Brian; Sayer, John A; Albaqumi, Mamdouh

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

PLA2G6相关帕金森病的临床异质性:对两个沙特阿拉伯家族的分析

Bohlega, Saeed A; Al-Mubarak, Bashayer R; Alyemni, Eman A; Abouelhoda, Mohamed; Monies, Dorota; Mustafa, Abeer E; Khalil, Dania S; Al Haibi, Sara; Abou Al-Shaar, Hussam; Faquih, Tariq; El-Kalioby, Mohamed; Tahir, Asma I; Al Tassan, Nada A

Personalized cloud-based bioinformatics services for research and education: use cases and the elasticHPC package

面向科研和教育的个性化云端生物信息学服务:用例和 elasticHPC 软件包

El-Kalioby, Mohamed; Abouelhoda, Mohamed; Krüger, Jan; Giegerich, Robert; Sczyrba, Alexander; Wall, Dennis P; Tonellato, Peter

WAMI: a web server for the analysis of minisatellite maps

WAMI:用于分析微型卫星地图的网络服务器

Abouelhoda, Mohamed; El-Kalioby, Mohamed; Giegerich, Robert