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EMILY BLAND

TitleInstructor
InstitutionBaylor College of Medicine
DepartmentDepartment of Molecular & Human Genetics
Address6701 FANNIN
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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. Boyd CA, Novy TJ, Beecroft-Dawson TA, Bell CA, Bland EM, Miyake CY. When targeted gene testing falls short: Case report of a novel SLC4A3 F347S genetic variant associated with short QT syndrome. HeartRhythm Case Rep. 2026 Jan; 12(1):48-51. PMID: 41732448; PMCID: PMC12925700.
      Citations:    
    2. Williams A, Weisz-Hubshman M, Rossi V, Bland E, Mizerik E, Luo X, Hillman PR, Shields K, Scaglia F. TPI deficiency: A case report and review of the literature. Mol Genet Metab. 2025 Sep-Oct; 146(1-2):109227. PMID: 40897044.
      Citations: 1     Fields:    Translation:HumansAnimals
    3. Duarte R, Vossaert L, Darilek SA, Rose C, Schauer E, Parobek C, Bland E, Machol K, Mizerik E, Murali CN. Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Nov; 196(2-3):e32117. PMID: 39428697; PMCID: PMC12619969.
      Citations:    Fields:    Translation:Humans
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