Reviews & Chapters

  • Trisomy X syndrome.

    Boedeker D, Morales Corado A, Hunkler K. 2026 Jul 5. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan. https://www.ncbi.nlm.nih.gov/books/NBK623725/

  • Angelman syndrome.

    Madaan M, Warner D, Morales Corado A. 2026 Jun 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan. PMID: 32809705. https://www.ncbi.nlm.nih.gov/books/NBK560870/

  • Urea cycle disorders.

    Bisht S, Morales A, Jaishankar GB. 2026 Apr 19. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan. https://www.ncbi.nlm.nih.gov/books/NBK482363/

  • Phenylketonuria (PKU).

    Daley SF, Morales A. 2026 Apr 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan. https://www.ncbi.nlm.nih.gov/books/NBK535378/

  • Kebilidi (eladocagene exuparvovec-tneq) for adults and children with aromatic L-amino acid decarboxylase (AADC) deficiency: a Therapeutics Bulletin of the American College of Medical Genetics and Genomics (ACMG).

    Porter J, Morales Corado A, Sen K, Elsea SH. Genet Med Open. 2026;8:103471.

  • Sepiapterin approved for children and adults with phenylketonuria (PKU): a Therapeutics Bulletin of the American College of Medical Genetics and Genomics (ACMG).

    Chang IJ, Miller DE, Morales Corado A, Neira J. Genet Med Open. 2026;6:104399.

  • Inborn errors of metabolism.

    Morales A, Asuka E, Shah M. 2026 Jan 31. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK459183/

  • Noonan syndrome.

    Sharma L, Winters R, Morales Corado A. 2025 Aug 2. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK532269/

  • Lenmeldy (atidarsagene autotemcel) for individuals with early metachromatic leukodystrophy (MLD): a Therapeutics Bulletin of the American College of Medical Genetics and Genomics (ACMG).

    Gangji RN, Ali QA, Dhamija R, Morales Corado A, Kharbanda S. Genet Med Open. 2025;3:103432. doi:10.1016/j.gimo.2025.103432

  • Jacobsen syndrome (11q terminal deletion syndrome).

    O’Brien MP, Morales Corado A. 2025 Mar 16. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Apr. https://www.statpearls.com/point-of-care/163566

  • Glycogen storage disease type II.

    Morales A, Siqueira Tavares De Melo MH, Anastasopoulou C. 2025 Jan 28. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan. PMID: 29262159. https://www.ncbi.nlm.nih.gov/books/NBK470558/

  • Casgevy (exagamglogene autotemcel) and Lyfgenia (lovotibeglogene autotemcel) for individuals 12 years and older with sickle cell disease (SCD) and recurrent vaso-occlusive crises (VOC): a Therapeutics Bulletin of the American College of Medical Genetics and Genomics (ACMG).

    Lesmana H, Kim SY, Morales Corado A, Poskanzer SA. Genet Med Open. 2024;9:101875. doi:10.1016/j.gimo.2024.101875

  • Trofinetide approved for children and adults with Rett syndrome (RTT): a Therapeutics Bulletin of the American College of Medical Genetics and Genomics (ACMG).

    Selvam P, Mares Beltrán CF, Sen K, Morales Corado A. Genet Med Open. 2024;2:101856. doi:10.1016/j.gimo.2024.101856

  • Hyperphenylalaninemia, BH4 deficient (HPABH4).

    Corado AM. 2023 Feb 12. In: Rezaei N (eds) Genetic Syndromes. Springer Cham. doi:10.1007/978-3-319-66816-1_1759-1

  • Carnitine-acylcarnitine translocase deficiency.

    Morales Corado JA, Lee CU, Enns GM. 2022 Jul 21. In: Adam MP, Everman DB, Mirzaa GM, et al., editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2022. PMID: 35862567. https://www.ncbi.nlm.nih.gov/books/NBK582032/