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Celia Delozier

Title(s)Associate Clinical Professor, Dean's Office
SchoolSchool of Medicine
Address155 N Fresno St
Fresno CA 93701
Phone--
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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. BRIP-1 germline mutation and its role in colon cancer: presentation of two case reports and review of literature. BMC Med Genet. 2019 05 07; 20(1):75. Ali M, Delozier CD, Chaudhary U. PMID: 31064327.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer). Clin Neurol Neurosurg. 2017 Jul; 158:46-48. Zhu VW, Hinduja S, Knezevich SR, Silveira WR, DeLozier CD. PMID: 28460341.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    3. Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features. Eur J Hum Genet. 2013 Feb; 21(2):233-6. Reinstein E, DeLozier CD, Simon Z, Bannykh S, Rimoin DL, Curry CJ. PMID: 22739343.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    4. Non-disjunction of chromosome 13. Hum Mol Genet. 2007 Aug 15; 16(16):2004-10. Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB. PMID: 17584770.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    5. ABCA12 is the major harlequin ichthyosis gene. J Invest Dermatol. 2006 Nov; 126(11):2408-13. Thomas AC, Cullup T, Norgett EE, Hill T, Barton S, Dale BA, Sprecher E, Sheridan E, Taylor AE, Wilroy RS, DeLozier C, Burrows N, Goodyear H, Fleckman P, Stephens KG, Mehta L, Watson RM, Graham R, Wolf R, Slavotinek A, Martin M, Bourn D, Mein CA, O'Toole EA, Kelsell DP. PMID: 16902423.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    6. Double frameshift mutations in APC and MSH2 in the same individual. Int J Colorectal Dis. 2006 Jan; 21(1):79-83. Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Br√ľndler MA, Blouin JL, Foulkes WD, Hutter P. PMID: 16676398.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    7. Double frameshift mutations in APC and MSH2 in the same individual. Int J Colorectal Dis. 2005 Sep; 20(5):466-470. Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Br√ľndler MA, Blouin JL, Foulkes WD, Hutter P. PMID: 15834612.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans