Harvard Catalyst Profiles

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Abdulrahman Aldeeri, M.B.,B.S.

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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. Aldeeri AA, Abu-El-Haija A. A typical variant in TCF4 exon 18 is not associated with Pitt-Hopkins syndrome but with a familial case of mild and nonspecific neurodevelopmental disorder. Am J Med Genet A. 2022 Dec 27. PMID: 36574749.
    Citations:    Fields:    
  2. Smith JS, Aldeeri AA, Elman SA, Krier JB, Merola JF. A novel variant in the GNAS complex locus causes Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism. JAAD Case Rep. 2022 Mar; 21:103-105. PMID: 35198712; PMCID: PMC8850575.
    Citations:    
  3. Aljohar A, Muayqil T, Aldeeri A, Jammah A, Hersi A, Alhabib K. Pure Autonomic Failure with Asymptomatic Hypertensive Urgency: A Case Report and Literature Review. Case Rep Neurol. 2018 Sep-Dec; 10(3):357-362. PMID: 30687067; PMCID: PMC6341310.
    Citations:    
  4. Shamseldin HE, Aldeeri A, Babay Z, Alsultan A, Hashem M, Alkuraya FS. A lethal phenotype associated with tissue plasminogen deficiency in humans. Hum Genet. 2016 10; 135(10):1209-11. PMID: 27417437.
    Citations: 1     Fields:    Translation:Humans
  5. Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, Hijazi H, Alshammari M, Aldahmesh MA, Salih MA, Faqeih E, Alhashem A, Bashiri FA, Al-Owain M, Kentab AY, Sogaty S, Al Tala S, Temsah MH, Tulbah M, Aljelaify RF, Alshahwan SA, Seidahmed MZ, Alhadid AA, Aldhalaan H, AlQallaf F, Kurdi W, Alfadhel M, Babay Z, Alsogheer M, Kaya N, Al-Hassnan ZN, Abdel-Salam GM, Al-Sannaa N, Al Mutairi F, El Khashab HY, Bohlega S, Jia X, Nguyen HC, Hammami R, Adly N, Mohamed JY, Abdulwahab F, Ibrahim N, Naim EA, Al-Younes B, Meyer BF, Hashem M, Shaheen R, Xiong Y, Abouelhoda M, Aldeeri AA, Monies DM, Alkuraya FS. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. Cell Rep. 2015 Jan 13; 10(2):148-61. PMID: 25558065.
    Citations: 168     Fields:    Translation:Humans
  6. Aldeeri AA, Alazami AM, Hijazi H, Alzahrani F, Alkuraya FS. Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome. Clin Genet. 2014 Nov; 86(5):469-72. PMID: 24773188.
    Citations: 5     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.