Kirsten Allyson Blanco

Title(s)Assistant Health Sciences Professor, Pediatrics
SchoolSchool of Medicine
Address1001 Health Sciences Road
Irvine CA 92697-3950
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Characterizing a rare neurogenetic disease, SLC13A5 citrate transporter disorder, utilizing clinical data in a cloud-based medical record collection system. Front Genet. 2023; 14:1109547. Spelbrink EM, Brown TL, Brimble E, Blanco KA, Nye KL, Porter BE. PMID: 37025451; PMCID: PMC10072280.
      View in: PubMed   Mentions: 2  
    2. Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations. JNCI Cancer Spectr. 2022 03 02; 6(2). Horton C, Blanco K, Lo MT, Speare V, LaDuca H, Dolinsky JS, Kurian AW. PMID: 35603838; PMCID: PMC8904928.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    3. Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices. J Genet Couns. 2022 06; 31(3):631-640. Stefka J, El-Khechen D, Cain T, Blanco K, Feldmann B, Towne MC, Hagman KDF. PMID: 34826357.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. When moments matter: Finding answers with rapid exome sequencing. Mol Genet Genomic Med. 2020 02; 8(2):e1027. Powis Z, Farwell Hagman KD, Blanco K, Au M, Graham JM, Singh K, Gallant N, Randolph LM, Towne M, Hunter J, Shinde DN, Palmaer E, Schoenfeld B, Tang S. PMID: 31872981; PMCID: PMC7005623.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    5. Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions. Clin Genet. 2020 02; 97(2):305-311. Powis Z, Towne MC, Hagman KDF, Blanco K, Palmaer E, Castro A, Sajan SA, Radtke K, Feyma TJ, Juliette K, Tang S, Sidiropoulos C. PMID: 31628766.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    6. A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses. Genet Med. 2019 10; 21(10):2199-2207. Smith ED, Blanco K, Sajan SA, Hunter JM, Shinde DN, Wayburn B, Rossi M, Huang J, Stevens CA, Muss C, Alcaraz W, Hagman KDF, Tang S, Radtke K. PMID: 30894705; PMCID: PMC6774997.
      View in: PubMed   Mentions: 36     Fields:    Translation:Humans
    7. Quality of Clinician-Reported Cancer History When Ordering Genetic Testing. JCO Clin Cancer Inform. 2018 12; 2:1-11. LaDuca H, McFarland R, Gutierrez S, Yussuf A, Ho N, Pepper J, Reineke P, Cain T, Blanco K, Horton C, Dolinsky JS. PMID: 30652589.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    8. Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis. Genet Med. 2018 11; 20(11):1468-1471. Powis Z, Farwell Hagman KD, Speare V, Cain T, Blanco K, Mowlavi LS, Mayerhofer EM, Tilstra D, Vedder T, Hunter JM, Tsang M, Gonzalez L, Vockley G, Tang S. PMID: 29565416.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
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