Marilyn Li, MD

Title(s)Clinical Associate Professor of Pediatrics (Clinician Educator)
SchoolKeck School of Medicine of Usc
AddressGLB 1-G14 1801 Marengo Street
Off Campus
Los Angeles CA 90033
Phone+1 323 409 3737
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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. AACR Project GENIE: 100,000 Cases and Beyond. Cancer Discov. 2022 09 02; 12(9):2044-2057. Pugh TJ, Bell JL, Bruce JP, Doherty GJ, Galvin M, Green MF, Hunter-Zinck H, Kumari P, Lenoue-Newton ML, Li MM, Lindsay J, Mazor T, Ovalle A, Sammut SJ, Schultz N, Yu TV, Sweeney SM, Bernard B, AACR Project GENIE Consortium, Genomics and Analysis Working Group. PMID: 35819403.
      View in: PubMed   Mentions:    Fields:    
    2. Rational drug combinations with CDK4/6 inhibitors in acute lymphoblastic leukemia. Haematologica. 2022 08 01; 107(8):1746-1757. Bride KL, Hu H, Tikhonova A, Fuller TJ, Vincent TL, Shraim R, Li MM, Carroll WL, Raetz EA, Aifantis I, Teachey DT. PMID: 34937317; PMCID: PMC9335101.
      View in: PubMed   Mentions: 3     Fields:    
    3. Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma. Acta Neuropathol Commun. 2022 07 14; 10(1):102. Xu F, Viaene AN, Ruiz J, Schubert J, Wu J, Chen J, Cao K, Fu W, Bagatell R, Fan Z, Long A, Pagliaroli L, Zhong Y, Luo M, Kreiger PA, Surrey LF, Wertheim GB, Cole KA, Li MM, Santi M, Storm PB. PMID: 35836290; PMCID: PMC9281131.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    4. Tiered Somatic Variant Classification Adoption Has Increased Worldwide With Some Practice Differences Based on Location and Institutional Setting. Arch Pathol Lab Med. 2022 07 01; 146(7):822-832. Bruehl FK, Kim AS, Li MM, Lindeman NI, Moncur JT, Souers RJ, Vasalos P, Voelkerding KV, Xian RR, Surrey LF. PMID: 34979564.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    5. Editorial. Cancer Genet. 2022 Aug; 266-267:37-38. Li MM, Drilon A, Laetsch TW. PMID: 35728328.
      View in: PubMed   Mentions:    Fields:    
    6. Multi-institutional study of the frequency, genomic landscape and outcome of IDH-mutant glioma in paediatrics. Neuro Oncol. 2022 May 23. Yeo KK, Alexandrescu S, Cotter JA, Vogelzang J, Bhave V, Li MM, Ji J, Benhamida JK, Rosenblum MK, Bale TA, Bouvier N, Kaneva K, Rosenberg T, Lim Fat MJ, Ghosh H, Martinez M, Aguilera D, Smith A, Goldman S, Diamond EL, Gavrilovic I, MacDonald TJ, Wood MD, Nazemi KJ, Truong AL, Cluster A, Ligon KL, Cole K, Bi WL, Margol AS, Karajannis MA, Wright KD. PMID: 35604410.
      View in: PubMed   Mentions:    Fields:    
    7. Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2022 07; 24(7):1392-1406. Li MM, Tayoun AA, DiStefano M, Pandya A, Rehm HL, Robin NH, Schaefer AM, Yoshinaga-Itano C, ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.net. PMID: 35802133.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. CancerVar: An artificial intelligence-empowered platform for clinical interpretation of somatic mutations in cancer. Sci Adv. 2022 05 06; 8(18):eabj1624. Li Q, Ren Z, Cao K, Li MM, Wang K, Zhou Y. PMID: 35544644; PMCID: PMC9075800.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. A novel TP53 tandem duplication in a child with Li-Fraumeni syndrome. Cold Spring Harb Mol Case Stud. 2022 04; 8(3). Xu F, Aref-Eshghi E, Wu J, Schubert J, Wertheim G, Bhatti T, Pogoriler J, Patel M, Cao K, Long A, Fan Z, Denenberg EH, Fanning EA, Wilmoth DM, Luo M, Conlin LK, Dain AS, Zelley K, Baldino S, Balamuth N, MacFarland S, Li MM, Zhong Y. PMID: 35232817; PMCID: PMC9059784.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions. Cancer Genet. 2022 06; 264-265:50-59. Saliba J, Church AJ, Rao S, Danos A, Furtado LV, Laetsch T, Zhang L, Nardi V, Lin WH, Ritter DI, Madhavan S, Li MM, Griffith OL, Griffith M, Raca G, Roy A. PMID: 35366592; PMCID: PMC9252326.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome. Pediatr Blood Cancer. 2022 10; 69(10):e29656. Leibowitz MS, Zelley K, Adams D, Brodeur GM, Fox E, Li MM, Mattei P, Pogoriler J, MacFarland SP. PMID: 35278038.
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    12. Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers. J Clin Oncol. 2022 04 01; 40(10):1081-1090. Franco AT, Ricarte-Filho JC, Isaza A, Jones Z, Jain N, Mostoufi-Moab S, Surrey L, Laetsch TW, Li MM, DeHart JC, Reichenberger E, Taylor D, Kazahaya K, Adzick NS, Bauer AJ. PMID: 35015563; PMCID: PMC8966969.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    13. Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1 Fusion in an Infant: A New Type of "Plagoma". Am J Dermatopathol. 2022 01 01; 44(1):54-57. Tomás-Velázquez A, Surrey LF, Miele E, Li MM, Alaggio R, Goitz RJ, Reyes-Múgica M, Salgado CM. PMID: 34291746.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    14. Atypical teratoid rhabdoid tumor in a child with neurofibromatosis type 2: A novel dual diagnosis. Cancer Genet. 2022 04; 262-263:1-4. Kotch C, Fisher MJ, Lin F, Zhong Y, Gallo D, Fan Z, Chen J, Santi M, Li MM. PMID: 34972035.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    15. The oncogenic roles of NTRK fusions and methods of molecular diagnosis. Cancer Genet. 2021 11; 258-259:110-119. Aref-Eshghi E, Lin F, Li MM, Zhong Y. PMID: 34710798.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    16. KMT2A-MAML2 rearrangement emerged and regressed during neuroblastoma therapy without leukemia after 12.8-year follow-up. Pediatr Blood Cancer. 2022 01; 69(1):e29344. Felix CA, Slater DJ, Davenport JW, Yu X, Gregory BD, Li MM, Rappaport EF, Cheung NV. PMID: 34550633; PMCID: PMC9616630.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    17. Mammary-type Myofibroblastoma with Leiomyomatous Differentiation: A Rare Variant with Potential Pitfalls. Int J Surg Pathol. 2022 Apr; 30(2):200-206. Strait AM, Bridge JA, Iafrate AJ, Li MM, Xu F, Tsongalis GJ, Linos K. PMID: 34338561.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia-related malignancies. Cold Spring Harb Mol Case Stud. 2021 04; 7(2). Lalonde E, Rentas S, Wertheim G, Cao K, Surrey LF, Lin F, Zhao X, Obstfeld A, Aplenc R, Luo M, Li MM. PMID: 33832921; PMCID: PMC8040732.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    19. BRAF fusions in pediatric histiocytic neoplasms define distinct therapeutic responsiveness to RAF paradox breakers. Pediatr Blood Cancer. 2021 06; 68(6):e28933. Jain P, Surrey LF, Straka J, Russo P, Womer R, Li MM, Storm PB, Waanders AJ, Hogarty MD, Resnick AC, Picarsic J. PMID: 33565241.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    20. NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome. JCO Precis Oncol. 2021; 1. Zhao X, Kotch C, Fox E, Surrey LF, Wertheim GB, Baloch ZW, Lin F, Pillai V, Luo M, Kreiger PA, Pogoriler JE, Linn RL, Russo PA, Santi M, Resnick AC, Storm PB, Hunger SP, Bauer AJ, Li MM. PMID: 34036219; PMCID: PMC8140782.
      View in: PubMed   Mentions: 9     Fields:    
    21. Genomic characterization of a PPP1CB-ALK fusion with fusion gene amplification in a congenital glioblastoma. Cancer Genet. 2021 04; 252-253:37-42. Zhong Y, Lin F, Xu F, Schubert J, Wu J, Wainwright L, Zhao X, Cao K, Fan Z, Chen J, Lang SS, Kennedy BC, Viaene AN, Santi M, Resnick AC, Storm PB, Li MM. PMID: 33341678.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    22. The spectrum of rare central nervous system (CNS) tumors with EWSR1-non-ETS fusions: experience from three pediatric institutions with review of the literature. Brain Pathol. 2021 01; 31(1):70-83. Lopez-Nunez O, Cafferata B, Santi M, Ranganathan S, Pearce TM, Kulich SM, Bailey KM, Broniscer A, Rossi S, Zin A, Nasrallah MP, Li MM, Zhong Y, Miele E, Alaggio R, Surrey LF. PMID: 32997853; PMCID: PMC8018079.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    23. Application of Next Generation Sequencing in Laboratory Medicine. Ann Lab Med. 2021 01; 41(1):25-43. Zhong Y, Xu F, Wu J, Schubert J, Li MM. PMID: 32829577; PMCID: PMC7443516.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    24. A germline PALB2 pathogenic variant identified in a pediatric high-grade glioma. Cold Spring Harb Mol Case Stud. 2020 08; 6(4). Zhong Y, Schubert J, Wu J, Xu F, Lin F, Cao K, Zelley K, Luo M, Foster JB, Cole KA, MacFarland SP, Resnick AC, Storm PB, Li MM. PMID: 32554798; PMCID: PMC7476410.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    25. A Novel KMT2A-ARHGEF12 Fusion Gene Identified in a High-Grade B-cell Lymphoma. Cancer Genet. 2020 08; 246-247:41-43. Jung HS, Lin F, Wolpaw A, Reilly AF, Margolskee E, Luo M, Wertheim GB, Li MM. PMID: 32805689.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    26. Congenital tumors of the central nervous system: an institutional review of 64 cases with emphasis on tumors with unique histologic and molecular characteristics. Brain Pathol. 2021 01; 31(1):45-60. Viaene AN, Pu C, Perry A, Li MM, Luo M, Santi M. PMID: 32681571; PMCID: PMC8018134.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    27. A Rare TP53 Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers. Cancer Res. 2020 09 01; 80(17):3732-3744. Powers J, Pinto EM, Barnoud T, Leung JC, Martynyuk T, Kossenkov AV, Philips AH, Desai H, Hausler R, Kelly G, Le AN, Li MM, MacFarland SP, Pyle LC, Zelley K, Nathanson KL, Domchek SM, Slavin TP, Weitzel JN, Stopfer JE, Garber JE, Joseph V, Offit K, Dolinsky JS, Gutierrez S, McGoldrick K, Couch FJ, Levin B, Edelman MC, Levy CF, Spunt SL, Kriwacki RW, Zambetti GP, Ribeiro RC, Murphy ME, Maxwell KN. PMID: 32675277; PMCID: PMC7484045.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    28. Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer Genet. 2020 07; 245:42-48. Rentas S, Pillai V, Wertheim GB, Akgumus GT, Nichols KE, Deardorff MA, Conlin LK, Li MM, Olson TS, Luo M. PMID: 32619790.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    29. Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2020 07; 22(7):1142-1148. Li MM, Chao E, Esplin ED, Miller DT, Nathanson KL, Plon SE, Scheuner MT, Stewart DR, ACMG Professional Practice and Guidelines Committee. PMID: 32321997.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    30. Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas. Cancer Cell. 2020 04 13; 37(4):569-583.e5. Ryall S, Zapotocky M, Fukuoka K, Nobre L, Guerreiro Stucklin A, Bennett J, Siddaway R, Li C, Pajovic S, Arnoldo A, Kowalski PE, Johnson M, Sheth J, Lassaletta A, Tatevossian RG, Orisme W, Qaddoumi I, Surrey LF, Li MM, Waanders AJ, Gilheeney S, Rosenblum M, Bale T, Tsang DS, Laperriere N, Kulkarni A, Ibrahim GM, Drake J, Dirks P, Taylor MD, Rutka JT, Laughlin S, Shroff M, Shago M, Hazrati LN, D'Arcy C, Ramaswamy V, Bartels U, Huang A, Bouffet E, Karajannis MA, Santi M, Ellison DW, Tabori U, Hawkins C. PMID: 32289278; PMCID: PMC7169997.
      View in: PubMed   Mentions: 67     Fields:    Translation:Humans
    31. Copy number assessment in the genomic analysis of CNS neoplasia: An evidence-based review from the cancer genomics consortium (CGC) working group on primary CNS tumors. Cancer Genet. 2020 05; 243:19-47. Neill SG, Hauenstein J, Li MM, Liu YJ, Luo M, Saxe DF, Ligon AH. PMID: 32203924.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. Pediatric Somatic Tumor Sequencing Identifies Underlying Cancer Predisposition. JCO Precis Oncol. 2019; 3. MacFarland SP, Zelley K, Surrey LF, Gallo D, Luo M, Raman P, Wertheim G, Hunger SP, Li MM, Brodeur GM. PMID: 32783018; PMCID: PMC7416724.
      View in: PubMed   Mentions: 3     Fields:    
    33. Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways. J Neuropathol Exp Neurol. 2019 12 01; 78(12):1100-1111. Surrey LF, Jain P, Zhang B, Straka J, Zhao X, Harding BN, Resnick AC, Storm PB, Buccoliero AM, Genitori L, Li MM, Waanders AJ, Santi M. PMID: 31617914.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    34. Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants. Genome Med. 2019 08 23; 11(1):53. He MM, Li Q, Yan M, Cao H, Hu Y, He KY, Cao K, Li MM, Wang K. PMID: 31443733; PMCID: PMC6708137.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    35. Adaptation of an asthma management program to a small clinic. Am J Manag Care. 2017 Jul 01; 23(7):e231-e237. Kwong KY, Redjal N, Scott L, Li M, Thobani S, Yang B. PMID: 28850792.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    36. 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 08; 53(6):629-34. Scott L, Li M, Thobani S, Nichols B, Morphew T, Kwong KY. PMID: 27221537.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    37. Factors affecting ability to achieve asthma control in adult patients with moderate to severe persistent asthma. J Asthma. 2016 08; 53(6):644-9. Scott L, Li M, Thobani S, Nichols B, Morphew T, Kwong KY. PMID: 27058241.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    38. Momentary Assessment of Psychosocial Stressors, Context, and Asthma Symptoms in Hispanic Adolescents. Behav Modif. 2016 Jan; 40(1-2):257-80. Dunton G, Dzubur E, Li M, Huh J, Intille S, McConnell R. PMID: 26438664; PMCID: PMC5731826.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    39. 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. Dzubur E, Li M, Kawabata K, Sun Y, McConnell R, Intille S, Dunton GF. PMID: 25661657; PMCID: PMC4387069.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    40. A school-based case identification process for identifying inner city children with asthma: the Breathmobile program. Chest. 2004 Mar; 125(3):924-34. Jones CA, Morphew T, Clement LT, Kimia T, Dyer M, Li M, Hanley-Lopez J, Breathmobile program. PMID: 15006951.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansPHPublic Health