Abell K, Tolusso L, Smith N, Hopkin R, Vawter-Lee M, Habli M, Riddle S, Calvo-Garcia MA, Guan Q, Bierbrauer K, Hwa V, & Saal HM. Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes Birth Defects Res. 2020. doi:10.1002/bdr2.1801 PMID:32935482 Shillington A, Lamy M, Vawter-Lee M, Erickson C, Saal H, Comoletti D, Abell K. Case Report: Is Catatonia a Clinical Feature of the Natural Progression of NLGN2-Related Neurodevelopmental Disorder? J Autism Dev Disord. 2020. PMID:32405903 Ahlee K, Abell K, Johnson J, Cizek S, Breech L, Ernst M, Hopkin R, Kennedy K, Stanek J, Strine A, Rutter M. . XY Gonadal Dysgenesis in a Phenotypic Female Identified by Direct-to-Consumer Genetic Testing Pediatrics. 2020.
Susan R. Rose, Ari J. Wassner, Kupper Wintergerst, Nana-Hawa Yayah Jones, Robert Hopkin, Janet Chuang, Jessica Smith, Katherine Abell, Stephen H. LaFranchi, Section on Endocrinology, Council on Genetics, Pediatric Endocrine Society, American Thyroid Association . Update on newborn screening and therapy for congenital hypothyroidism American Academy of Pediatics. 2019.
Abell K, May W, May PA, Kalberg W, Hoyme HE, Robinson LK, Manning M, Jones KL, Abdul-Rahman O. Fetal alcohol spectrum disorders and assessment of maxillary and mandibular arc measurements. Am J Med Genet A. 2016;170(7):1763-71. PMID:27253440 Abell K, Jackson J. Non-tender pre-auricular nodule and papules Journal of American Academy of Dermatology: Images in Dermatology. . 2015;37(1):e3-e4.
Kedar A, Nikitina Y, Henry OR, Abell KB, Vedanarayanan V, Griswold ME, Subramony C, Abell TL. Gastric dysmotility and low serum vitamin D levels in patients with gastroparesis. Horm Metab Res. 2013;45(1):47-53. PMCID:PMC5089061 PMID:22956309