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Marilyn Li, MD
Assistant Professor of Clinical Pediatrics
Director, Quality Improvement and Educational Activities For The Breathmobile Program
GLB 1-G14 1801 Marengo Street Off Campus Los Angeles
+1 323 226 3813


Scott L, Li M, Thobani S, Nichols B, Morphew T, Kwong KY. Factors affecting ability to achieve asthma control in adult patients with moderate to severe persistent asthma. J Asthma. 2016 Aug; 53(6):644-9. View in: PubMed

Scott L, Li M, Thobani S, Nichols B, Morphew T, Kwong KY. Asthma control and need for future asthma controller therapy among inner-city Hispanic asthmatic children engaged in a pediatric asthma disease management program (the Breathmobile program, Mobile Asthma Care for Kids Network). J Asthma. 2016 Aug; 53(6):629-34. View in: PubMed

Dunton G, Dzubur E, Li M, Huh J, Intille S, McConnell R. Momentary Assessment of Psychosocial Stressors, Context, and Asthma Symptoms in Hispanic Adolescents. Behav Modif. 2016 Jan; 40(1-2):257-80. View in: PubMed

Li MM, Monzon FA, Biegel JA, Jobanputra V, Laffin JJ, Levy B, Leon A, Miron P, Rossi MR, Toruner G, Alvarez K, Doho G, Dougherty MJ, Hu X, Kash S, Streck D, Znoyko I, Hagenkord JM, Wolff DJ. A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays. Cancer Genet. 2015 Nov; 208(11):525-36. View in: PubMed

Dzubur E, Li M, Kawabata K, Sun Y, McConnell R, Intille S, Dunton GF. Design of a smartphone application to monitor stress, asthma symptoms, and asthma inhaler use. Ann Allergy Asthma Immunol. 2015 Apr; 114(4):341-342. e2. View in: PubMed

Kapp JR, Diss T, Spicer J, Gandy M, Schrijver I, Jennings LJ, Li MM, Tsongalis GJ, de Castro DG, Bridge JA, Wallace A, Deignan JL, Hing S, Butler R, Verghese E, Latham GJ, Hamoudi RA. Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial. J Clin Pathol. 2015 Feb; 68(2):111-8. View in: PubMed

Schmit JM, Turner DJ, Hromas RA, Wingard JR, Brown RA, Li Y, Li MM, Slayton WB, Cogle CR. Two novel RUNX1 mutations in a patient with congenital thrombocytopenia that evolved into a high grade myelodysplastic syndrome. Leuk Res Rep. 2015; 4(1):24-7. View in: PubMed

Chang F, Li MM. Clinical application of amplicon-based next-generation sequencing in cancer. Cancer Genet. 2013 Dec; 206(12):413-9. View in: PubMed

Cooley LD, Lebo M, Li MM, Slovak ML, Wolff DJ. American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders. Genet Med. 2013 Jun; 15(6):484-94. View in: PubMed

Song J, Mercer D, Hu X, Liu H, Li MM. Common leukemia- and lymphoma-associated genetic aberrations in healthy individuals. J Mol Diagn. 2011 Mar; 13(2):213-9. View in: PubMed

Xiang B, Zhu H, Shen Y, Miller DT, Lu K, Hu X, Andersson HC, Narumanchi TM, Wang Y, Martinez JE, Wu BL, Li P, Li MM, Chen TJ, Fan YS. Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases. J Mol Diagn. 2010 Mar; 12(2):204-12. View in: PubMed

Li MM, Andersson HC. Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine. J Pediatr. 2009 Sep; 155(3):311-7. View in: PubMed

Freeman CE, Mercer DD, Ye Y, Van Brunt J, Li MM. Cytogenetic and molecular characterization of complex three-way translocations in acute promyelocytic leukemia. Beijing Da Xue Xue Bao. 2009 Aug 18; 41(4):477-9. View in: PubMed

Li MM, Nimmakayalu MA, Mercer D, Andersson HC, Emanuel BS. Characterization of a cryptic 3. 3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arrays. Am J Med Genet A. 2008 Feb 1; 146(3):368-75. View in: PubMed

Techakittiroj C, Kim KC, Andersson H, Li MM. 9p subtelomere deletion: pathogenic mutation or normal variant? Beijing Da Xue Xue Bao. 2006 Feb 18; 38(1):92-3. View in: PubMed

Kozon LK, Wesley DL, Van Brunt J, Li MM. A novel interstitial deletion on the long arm of chromosome 16 in a patient with chronic myelomonocytic leukemia. Cancer Genet Cytogenet. 2005 Oct 1; 162(1):92-4. View in: PubMed

Li MM. Advanced molecular and cytogenetic technologies in birth defect diagnosis and prevention. Beijing Da Xue Xue Bao. 2005 Feb 18; 37(1):14-9. View in: PubMed

Pochampally RR, Neville BT, Schwarz EJ, Li MM, Prockop DJ. Rat adult stem cells (marrow stromal cells) engraft and differentiate in chick embryos without evidence of cell fusion. Proc Natl Acad Sci U S A. 2004 Jun 22; 101(25):9282-5. View in: PubMed

Jones CA, Morphew T, Clement LT, Kimia T, Dyer M, Li M, Hanley-Lopez J. A school-based case identification process for identifying inner city children with asthma: the Breathmobile program. Chest. 2004 Mar; 125(3):924-34. View in: PubMed

Rivera AI, Li MM, Beltran G, Krause JR. Trisomy 4 as the sole cytogenetic abnormality in a Waldenström macroglobulinemia. Cancer Genet Cytogenet. 2002 Mar; 133(2):172-3. View in: PubMed

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