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Year Number of Results
2015 2
2016 2
2018 2
2019 2
2020 2
2021 3
2022 2
2023 1
2024 0

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14 results

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Page 1
The role of HOX genes in head and neck squamous cell carcinoma.
Platais C, Hakami F, Darda L, Lambert DW, Morgan R, Hunter KD. Platais C, et al. Among authors: hakami f. J Oral Pathol Med. 2016 Apr;45(4):239-47. doi: 10.1111/jop.12388. Epub 2015 Dec 14. J Oral Pathol Med. 2016. PMID: 26661059 Review.
HLA-based banking of induced pluripotent stem cells in Saudi Arabia.
Alowaysi M, Lehmann R, Al-Shehri M, Baadhaim M, Alzahrani H, Aboalola D, Zia A, Malibari D, Daghestani M, Alghamdi K, Haneef A, Jawdat D, Hakami F, Gomez-Cabrero D, Tegner J, Alsayegh K. Alowaysi M, et al. Among authors: hakami f. Stem Cell Res Ther. 2023 Dec 18;14(1):374. doi: 10.1186/s13287-023-03612-0. Stem Cell Res Ther. 2023. PMID: 38111036 Free PMC article.
Clinical, molecular, and biochemical delineation of asparagine synthetase deficiency in Saudi cohort.
Alharby E, Faqeih EA, Saleh M, Alameer S, Almuntashri M, Pastore A, Samman MA, Alnawfal AM, Hashem M, Zaytuni D, Alharbi G, Almannai M, Alasmari A, Mahmoud AA, Alwadei AH, Jad L, AlOtaibi A, Al-Hakami F, Eyaid W, Alkuraya FS, Alfadhel M, Peake RWA, Almontashiri NAM. Alharby E, et al. Among authors: al hakami f. Genet Med. 2020 Dec;22(12):2071-2080. doi: 10.1038/s41436-020-0919-x. Epub 2020 Aug 3. Genet Med. 2020. PMID: 32741967 Free article.
Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I.
Alahmad A, Nasca A, Heidler J, Thompson K, Oláhová M, Legati A, Lamantea E, Meisterknecht J, Spagnolo M, He L, Alameer S, Hakami F, Almehdar A, Ardissone A, Alston CL, McFarland R, Wittig I, Ghezzi D, Taylor RW. Alahmad A, et al. Among authors: hakami f. EMBO Mol Med. 2020 Nov 6;12(11):e12619. doi: 10.15252/emmm.202012619. Epub 2020 Sep 24. EMBO Mol Med. 2020. PMID: 32969598 Free PMC article.
Cycle Threshold Value as a Predictor of Severity and Intensive Care Unit Admission for Children Presenting to the Emergency Department With COVID-19: A Single-Center Experience From Saudi Arabia.
Al-Shareef AS, Shirah B, Dabroom M, Ahmed MM, Aljohani KA, Al Dabbagh MA, Ramadan M, Hakami F. Al-Shareef AS, et al. Among authors: hakami f. Cureus. 2022 Jul 6;14(7):e26614. doi: 10.7759/cureus.26614. eCollection 2022 Jul. Cureus. 2022. PMID: 35936119 Free PMC article.
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 MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F. Al-Hamed MH, et al. Among authors: hakami f. Hum Genet. 2022 Jan;141(1):101-126. doi: 10.1007/s00439-021-02406-9. Epub 2021 Dec 1. Hum Genet. 2022. PMID: 34853893
14 results