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Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families.
Genome Biol. 2015 Jun 3;16(1):116. doi: 10.1186/s13059-015-0681-6.
Genome Biol. 2015.
PMID: 26036949
Free PMC article.
Identification of a novel MKS locus defined by TMEM107 mutation.
Shaheen R, Almoisheer A, Faqeih E, Babay Z, Monies D, Tassan N, Abouelhoda M, Kurdi W, Al Mardawi E, Khalil MM, Seidahmed MZ, Alnemer M, Alsahan N, Sogaty S, Alhashem A, Singh A, Goyal M, Kapoor S, Alomar R, Ibrahim N, Alkuraya FS.
Shaheen R, et al. Among authors: al mardawi e.
Hum Mol Genet. 2015 Sep 15;24(18):5211-8. doi: 10.1093/hmg/ddv242. Epub 2015 Jun 29.
Hum Mol Genet. 2015.
PMID: 26123494
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The genetic landscape of familial congenital hydrocephalus.
Shaheen R, Sebai MA, Patel N, Ewida N, Kurdi W, Altweijri I, Sogaty S, Almardawi E, Seidahmed MZ, Alnemri A, Madirevula S, Ibrahim N, Abdulwahab F, Hashem M, Al-Sheddi T, Alomar R, Alobeid E, Sallout B, AlBaqawi B, AlAali W, Ajaji N, Lesmana H, Hopkin RJ, Dupuis L, Mendoza-Londono R, Al Rukban H, Yoon G, Faqeih E, Alkuraya FS.
Shaheen R, et al.
Ann Neurol. 2017 Jun;81(6):890-897. doi: 10.1002/ana.24964.
Ann Neurol. 2017.
PMID: 28556411
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Molecular autopsy in maternal-fetal medicine.
Shamseldin HE, Kurdi W, Almusafri F, Alnemer M, Alkaff A, Babay Z, Alhashem A, Tulbah M, Alsahan N, Khan R, Sallout B, Al Mardawi E, Seidahmed MZ, Meriki N, Alsaber Y, Qari A, Khalifa O, Eyaid W, Rahbeeni Z, Kurdi A, Hashem M, Alshidi T, Al-Obeid E, Abdulwahab F, Ibrahim N, Ewida N, El-Akouri K, Al Mulla M, Ben-Omran T, Pergande M, Cirak S, Al Tala S, Shaheen R, Faqeih E, Alkuraya FS.
Shamseldin HE, et al. Among authors: al mardawi e.
Genet Med. 2018 Apr;20(4):420-427. doi: 10.1038/gim.2017.111. Epub 2017 Jul 20.
Genet Med. 2018.
PMID: 28749478
Free article.
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The morbid genome of ciliopathies: an update.
Shamseldin HE, Shaheen R, Ewida N, Bubshait DK, Alkuraya H, Almardawi E, Howaidi A, Sabr Y, Abdalla EM, Alfaifi AY, Alghamdi JM, Alsagheir A, Alfares A, Morsy H, Hussein MH, Al-Muhaizea MA, Shagrani M, Al Sabban E, Salih MA, Meriki N, Khan R, Almugbel M, Qari A, Tulba M, Mahnashi M, Alhazmi K, Alsalamah AK, Nowilaty SR, Alhashem A, Hashem M, Abdulwahab F, Ibrahim N, Alshidi T, AlObeid E, Alenazi MM, Alzaidan H, Rahbeeni Z, Al-Owain M, Sogaty S, Seidahmed MZ, Alkuraya FS.
Shamseldin HE, et al.
Genet Med. 2020 Jun;22(6):1051-1060. doi: 10.1038/s41436-020-0761-1. Epub 2020 Feb 14.
Genet Med. 2020.
PMID: 32055034
Free article.
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The morbid genome of ciliopathies: an update.
Shamseldin HE, Shaheen R, Ewida N, Bubshait DK, Alkuraya H, Almardawi E, Howaidi A, Sabr Y, Abdalla EM, Alfaifi AY, Mohammed Alghamdi J, Alsagheir A, Alfares A, Morsy H, Hussein MH, Al-Muhaizea MA, Shagrani M, Al Sabban E, Salih MA, Meriki N, Khan R, Almugbel M, Qari A, Tulba M, Mahnashi M, Alhazmi K, Alsalamah AK, Nowilaty SR, Alhashem A, Hashem M, Abdulwahab F, Ibrahim N, Alshidi T, AlObeid E, Alenazi MM, Alzaidan H, Rahbeeni Z, Al-Owain M, Sogaty S, Zain Seidahmed M, Alkuraya FS.
Shamseldin HE, et al.
Genet Med. 2022 Apr;24(4):966. doi: 10.1016/j.gim.2022.01.019.
Genet Med. 2022.
PMID: 35394428
Free article.
No abstract available.
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Genetic, chromosomal, and syndromic causes of neural tube defects.
Seidahmed MZ, Abdelbasit OB, Shaheed MM, Alhussein KA, Miqdad AM, Samadi AS, Khalil MI, Al-Mardawi E, Salih MA.
Seidahmed MZ, et al. Among authors: al mardawi e.
Saudi Med J. 2014 Dec;35 Suppl 1(Suppl 1):S49-56.
Saudi Med J. 2014.
PMID: 25551112
Free PMC article.
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Postnatal outcome of isolated antenatal hydronephrosis.
Darwish HS, Habash YH, AlMardawi EA, AlHag SS.
Darwish HS, et al.
Saudi Med J. 2014 May;35(5):477-81.
Saudi Med J. 2014.
PMID: 24825809
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Misoprostol-Induced Fever and Unnecessary Antibiotic Prescribing: A Retrospective Study.
Abu Esba LC, Al Mardawi G, Al Mardawi E, Almadhi FM, Ardah HI.
Abu Esba LC, et al. Among authors: al mardawi e.
Infect Dis Ther. 2023 Sep;12(9):2259-2268. doi: 10.1007/s40121-023-00865-3. Epub 2023 Sep 13.
Infect Dis Ther. 2023.
PMID: 37704800
Free PMC article.
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