Hatoon Al Ali

TitleGraduate Student
InstitutionBaylor College of Medicine
DepartmentGenetics & Genomics
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Kulmanov M, Tawfiq R, Liu Y, Al Ali H, Abdelhakim M, Alarawi M, Aldakhil H, Alhattab D, Alsolme EA, Althagafi A, Angelov A, Bougouffa S, Driguez P, Park C, Putra A, Reyes-Ramos AM, Hauser CAE, Cheung MS, Abedalthagafi MS, Hoehndorf R. A reference quality, fully annotated diploid genome from a Saudi individual. Sci Data. 2024 Nov 23; 11(1):1278. PMID: 39580486; PMCID: PMC11585617.
      Citations:    Fields:    Translation:Humans
    2. Alsaif HS, Al Ali H, Faqeih E, Ramadan SM, Barth M, Colin E, Prouteau C, Bonneau D, Ziegler A, Alkuraya FS. ZNF668 deficiency causes a recognizable disorder of DNA damage repair. Hum Genet. 2021 Sep; 140(9):1395-1401. PMID: 34313816.
      Citations:    
    3. Maddirevula S, Kuwahara H, Ewida N, Shamseldin HE, Patel N, Alzahrani F, AlSheddi T, AlObeid E, Alenazi M, Alsaif HS, Alqahtani M, AlAli M, Al Ali H, Helaby R, Ibrahim N, Abdulwahab F, Hashem M, Hanna N, Monies D, Derar N, Alsagheir A, Alhashem A, Alsaleem B, Alhebbi H, Wali S, Umarov R, Gao X, Alkuraya FS. Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics. Genome Biol. 2020 06 17; 21(1):145. PMID: 32552793; PMCID: PMC7298854.
      Citations:    
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