Moyra Smith

Title(s)Professor Emeritus, Pediatrics
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(949) 824-0211
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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. Mitochondrial and ion channel gene alterations in autism. Biochim Biophys Acta. 2012 Oct; 1817(10):1796-802. Smith M, Flodman PL, Gargus JJ, Simon MT, Verrell K, Haas R, Reiner GE, Naviaux R, Osann K, Spence MA, Wallace DC. PMID: 22538295.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCellsCTClinical Trials
    2. Preface. The year in human and medical genetics. Ann N Y Acad Sci. 2009 Jan; 1151:ix-x. Smith M. PMID: 19154513.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    3. The year in human and medical genetics. Highlights of 2007-2008. Ann N Y Acad Sci. 2009 Jan; 1151:1-21. Smith M. PMID: 19154514.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    4. Nuclear and mitochondrial genome defects in autisms. Ann N Y Acad Sci. 2009 Jan; 1151:102-32. Smith M, Spence MA, Flodman P. PMID: 19154520.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    5. Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits. Cytogenet Genome Res. 2002; 98(4):233-9. Smith M, Woodroffe A, Smith R, Holguin S, Martinez J, Filipek PA, Modahl C, Moore B, Bocian ME, Mays L, Laulhere T, Flodman P, Spence MA. PMID: 12826745.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    6. Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR. Cytogenet Cell Genet. 2001; 94(1-2):15-22. Smith M, Escamilla JR, Filipek P, Bocian ME, Modahl C, Flodman P, Spence MA. PMID: 11701947.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    7. Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13. Am J Med Genet. 2000 Dec 04; 96(6):765-70. Smith M, Filipek PA, Wu C, Bocian M, Hakim S, Modahl C, Spence MA. PMID: 11121177.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
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