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Susan Hassed

TitleClinical Associate Professor
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
Address1200 N Phillips Ave
Oklahoma City OK 73104-4600
Phone405/271-8685
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    Collapse Bibliographic 
    Collapse selected publications
    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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    1. Hassed S, Li S, Mulvihill J, Aston C, Palmer S. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype. Am J Med Genet A. 2017 Mar; 173(3):790-800. PMID: 28160419.
      View in: PubMed
    2. Hassed SJ, Li S, Xu W, Taylor AC. A Novel Mutation in PITX2 in a Patient with Axenfeld-Rieger Syndrome. Mol Syndromol. 2017 Mar; 8(2):107-109. PMID: 28611552.
      View in: PubMed
    3. Hayes B, Hassed S, Chaloner JL, Aston CE, Guy C. Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family. J Genet Couns. 2016 Jun; 25(3):443-53. PMID: 26482744.
      View in: PubMed
    4. Hassed SJ, Wiley GB, Wang S, Lee JY, Li S, Xu W, Zhao ZJ, Mulvihill JJ, Robertson J, Warner J, Gaffney PM. RBPJ mutations identified in two families affected by Adams-Oliver syndrome. Am J Hum Genet. 2012 Aug 10; 91(2):391-5. PMID: 22883147; PMCID: PMC3415535.
    5. Purandare SM, Lee J, Hassed S, Steele MI, Blackett PR, Mulvihill JJ, Li S. Ring chromosome 9 [r(9)(p24q34)]: a report of two cases. Am J Med Genet A. 2005 Oct 15; 138A(3):229-35. PMID: 16158426.
      View in: PubMed
    6. Casas KA, Mononen TK, Mikail CN, Hassed SJ, Li S, Mulvihill JJ, Lin HJ, Falk RE. Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals. Am J Med Genet A. 2004 Nov 01; 130A(4):331-9. PMID: 15386475.
      View in: PubMed
    7. Hassed SJ, Hopcus-Niccum D, Zhang L, Li S, Mulvihill JJ. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet. 2004 May; 65(5):400-4. PMID: 15099348.
      View in: PubMed
    8. Li S, Hassed S, Mulvihill JJ, Nair AK, Hopcus DJ. Double trisomy. Am J Med Genet A. 2004 Jan 01; 124A(1):96-8. PMID: 14679595.
      View in: PubMed
    9. Hassed SJ. Genetic counseling. J Okla State Med Assoc. 2003 Oct; 96(10):495-7. PMID: 14619605.
      View in: PubMed
    10. Sawyer JR, Lukacs JL, Hassed SJ, Arnold GL, Mitchell HF, Muenke M. Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly. Am J Med Genet. 1996 Oct 16; 65(2):113-6. PMID: 8911601.
      View in: PubMed
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