Celia Delozier
Associate Clinical Professor
Pediatrics - Fresno
School of Medicine

Publications (8)

Top publication keywords:
Germ-Line MutationEhlers-Danlos SyndromeGenes, APCColorectal Neoplasms, Hereditary NonpolyposisPeriodontitisAdenomatous Polyposis ColiDNA-Binding ProteinsRNA HelicasesFrameshift MutationMutS Homolog 2 ProteinCarcinomaChoroid Plexus NeoplasmsConnective TissueColonic NeoplasmsFanconi Anemia Complementation Group Proteins

• BRIP-1 germline mutation and its role in colon cancer: presentation of two case reports and review of literature.
  BMC medical genetics 2019 Ali M, Delozier CD, Chaudhary U
• A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer).
  Clinical neurology and neurosurgery 2017 Zhu VW, Hinduja S, Knezevich SR, Silveira WR, DeLozier CD
• Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features.
  European journal of human genetics : EJHG 2012 Reinstein E, DeLozier CD, Simon Z, Bannykh S, Rimoin DL, Curry CJ
• Risk factors for perinatal arterial stroke: a study of 60 mother-child pairs.
  Pediatric neurology 2007 Curry CJ, Bhullar S, Holmes J, Delozier CD, Roeder ER, Hutchison HT
• Non-disjunction of chromosome 13.
  Human molecular genetics 2007 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 …
• ABCA12 is the major harlequin ichthyosis gene.
  The Journal of investigative dermatology 2006 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…
• Double frameshift mutations in APC and MSH2 in the same individual.
  International journal of colorectal disease 2006 Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Bründler MA, Blouin JL, Foulkes WD, Hutter P
• Double frameshift mutations in APC and MSH2 in the same individual.
  International journal of colorectal disease 2005 Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Bründler MA, Blouin JL, Foulkes WD, Hutter P