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Clinical utility of polygenic scores for cardiometabolic disease in Arabs Shim, Injeong; Kuwahara, Hiroyuki; Chen, NingNing; Hashem, Mais O.; AlAbdi, Lama; Abouelhoda, Mohamed; Won, Hong-Hee; Natarajan, Pradeep; Ellinor, Patrick T.; Khera, Amit V.; Gao, Xin; Alkuraya, Fowzan S.; Fahed, Akl C. 分享 收藏
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Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk Alkhamis, Fahad A.; Alabdali, Majed M.; Alsulaiman, Abdulla A.; Alamri, Abdullah S.; Alali, Rudaynah; Akhtar, Mohammed S.; Alsalman, Sadiq A.; Cyrus, Cyril; Albakr, Aishah I.; Alduhalan, Anas S.; Gandla, Divya; Al-Romaih, Khaldoun; Abouelhoda, Mohamed; Loza, Bao-Li; Keating, Brendan; Al-Ali, Amein K. 分享 收藏
Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients Al-Hamed, Mohamed H.; Hussein, Maged H.; Shah, Yaser; Al-Mojalli, Hamad; Alsabban, Essam; Alshareef, Turki; Altayyar, Ali; Elshouny, Samir; Ali, Wafaa; Abduljabbar, Mai; AlOtaibi, Afaf; AlShammasi, Amal; Akili, Rana; Abouelhoda, Mohamed; Sayer, John A.; Dasouki, Majed J.; Imtiaz, Faiqa 分享 收藏
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes Al-Hamed, Mohamed; Kurdi, Wesam; Khan, Rubina; Tulbah, Maha; AlNemer, Maha; AlSahan, Nada; AlMugbel, Maisoon; Rafiullah, Rafiullah; Assoum, Mirna; Monies, Dorota; Shah, Zeeshan; Rahbeeni, Zuhair; Derar, Nada; Hakami, Fahad; Almutairi, Gawaher; AlOtaibi, Afaf; Ali, Wafaa; AlShammasi, Amal; AlMubarak, Wardah; AlDawoud, Samia; AlAmri, Saja; Saeed, Bashayer; Bukhari, Hanifa; Ali, Mohannad; Akili, Rana; Alquayt, Laila; Nagos, Samia; Elbardisy, Hadeel; Akilan, Asma; Almuhana, Nora; AlKhalifah, Abrar; Abouelhoda, Mohamed; Ramzan, Khushnooda; Sayer, John A.; Imtiaz, Faiqa 分享 收藏
Characterization of the SARS-CoV-2 genomes in Egypt in first and second waves of infection Zekri, Abdel-Rahman N.; Bahnasy, Abeer A.; Hafez, Mohamed M.; Hassan, Zeinab K.; Ahmed, Ola S.; Soliman, Hany K.; El-Sisi, Enas R.; El Dine, Mona H. Salah; Solimane, May S.; Latife, Lamyaa S. Abdel; Seadawy, Mohamed G.; Elsafty, Ahmed S.; Abouelhoda, Mohamed 分享 收藏
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Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss 全基因组测序揭示ASIC5基因的外显子变异导致复发性妊娠丢失 Al Qahtani, Nourah H.; AbdulAzeez, Sayed; Almandil, Noor B.; Alhur, Norah Fahad; Alsuwat, Hind Saleh; Al Taifi, Hatoon Ahmed; Al-Ghamdi, Ahlam A.; Jermy, B. Rabindran; Abouelhoda, Mohamed; Subhani, Shazia; Al Asoom, Lubna; Borgio, J. Francis 分享 收藏
Genomic characterization of SARS-CoV-2 in Egypt Zekri, Abdel-Rahman N.; Amer, Khaled Easa; Hafez, Mohammed M.; Hassan, Zeinab K.; Ahmed, Ola S.; Soliman, Hany K.; Bahnasy, Abeer A.; Hamid, Wael Abdel; Gad, Ahmad; Ali, Mahmoud; Hassan, Wael Ali; Madboly, Mahmoud Samir; Raouf, Ahmad Abdel; Khattab, Ayman A.; Hamdy, Mona Salah El Din; Soliman, May Sherif; El Sissy, Maha Hamdi; El Khateeb, Sara Mohamed; Ezzelarab, Moushira Hosny; Fathalla, Lamiaa A.; Abouelhoda, Mohamed 分享 收藏
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Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients 靶向下一代测序鉴定埃及乳腺癌患者队列中的体细胞突变 Nassar, Auhood; Abouelhoda, Mohamed; Mansour, Osman; Loutfy, Samah A.; Hafez, Mohamed M.; Gomaa, M.; Bahnassy, Abeer; Youssef, Amira Salah El-Din; Lotfy, Mai M.; Ismail, Hoda; Ahmed, Ola S.; Abou-Bakr, Amany Abd-Elhameed; Zekri, Abdel-Rahman N. 分享 收藏
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Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission Al-Mubarak, Bashayer R.; Omar, Aisha; Baz, Batoul; Al-Abdulaziz, Basma; Magrashi, Amna, I; Al-Yemni, Eman; Jabaan, Amjad; Monies, Dorota; Abouelhoda, Mohamed; Abebe, Dejene; Ghaziuddin, Mohammad; Al-Tassan, Nada A. 分享 收藏
Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans Shaheen, Ranad; Alsahli, Saud; Ewida, Nour; Alzahrani, Fatema; Shamseldin, Hanan E.; Patel, Nisha; Al Qahtani, Awad; Alhebbi, Homoud; Alhashem, Amal; Al-Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Abouelhoda, Mohamed; Monies, Dorota; Al-Hussaini, Abdulrahman; Alzouman, Muneerah A.; Shagrani, Mohammad; Faqeih, Eissa; Alkuraya, Fowzan S. 分享 收藏
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease Al Yemni, Eman; Monies, Dorota; Alkhairallah, Thamer; Bohlega, Saeed; Abouelhoda, Mohamed; Magrashi, Amna; Mustafa, Abeer; AlAbdulaziz, Basma; Alhamed, Mohamed; Baz, Batoul; Goljan, Ewa; Albar, Renad; Jabaan, Amjad; Faquih, Tariq; Subhani, Shazia; Ali, Wafa; Shinwari, Jameela; Al-Mubarak, Bashayer; Al-Tassan, Nada 分享 收藏
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Autozygome and high throughput confirmation of disease genes candidacy Maddirevula, Sateesh; Alzahrani, Fatema; Al-Owain, Mohammed; Al Muhaizea, Mohammad A.; Kayyali, Husam R.; AlHashem, Amal; Rahbeeni, Zuhair; Al-Otaibi, Maha; Alzaidan, Hamad I.; Balobaid, Ameera; El Khashab, Heba Y.; Bubshait, Dalal K.; Faden, Maha; Al Yamani, Suad; Dabbagh, Omar; Al-Mureikhi, Mariam; Al Jasser, Abdulla; Alsaif, Hessa S.; Alluhaydan, Iram; Seidahmed, Mohammed Zain; Alabbasi, Bashair Hamza; Almogarri, Ibrahim; Kurdi, Wesam; Akleh, Hana; Qari, Alya; Al Tala, Saeed M.; Alhomaidi, Suzan; Kentab, Amal Y.; Salih, Mustafa A.; Chedrawi, Aziza; Alameer, Seham; Tabarki, Brahim; Shamseldin, Hanan E.; Patel, Nisha; Ibrahim, Niema; Abdulwahab, Firdous; Samira, Menasria; Goljan, Ewa; Abouelhoda, Mohamed; Meyer, Brian F.; Hashem, Mais; Shaheen, Ranad; AlShahwan, Saad; Alfadhel, Majid; Ben-Omran, Tawfeg; Al-Qattan, Mohammad M.; Monies, Dorota; Alkuraya, Fowzan S. 分享 收藏
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