![Emily K. Shabason, MD](/sites/default/files/styles/crop_and_center_300x375/public/providers-new-shabason-emily.jpg?itok=ttODoxzo)
Emily K. Shabason, MD
Areas of expertise: Autism spectrum disorder, Attention-Deficit/Hyperactivity Disorder (ADHD), Beckwith-Wiedemann syndrome, Behavioral and developmental support of children with developmental delays and disabilities, Neurofibromatosis, PTEN hamartoma tumor syndrome
About Emily K. Shabason
Titles
Developmental Pediatrician
Certifications
Developmental-Behavioral Pediatrics – American Board of Pediatrics
Education & training
Medical Degree
MD - University of Colorado School of Medicine, Aurora, CO
Residency
General Pediatrics - Children's Hospital of Philadelphia
Fellowship
Developmental and Behavioral Pediatrics - Children's Hospital of Philadelphia, PA
Publications
Publications
2019
Shabason EK, Brodsky C, Baran J, Isaac L, Minturn JE, Ginsberg JP, Hobbie W, Fisher M, Blum N, Hocking MC. Clinical diagnosis of attention-deficit/hyperactivity disorder in survivors of pediatric brain tumors. Journal of Neuro-Oncology 143(2):305-312 (June 2019).
2018
Hu T, Kruszka1 P, Martinez A, Ming J, Shabason EK, Raam MS, Shaikh TH, Pineda-Alvarez E, Muenke M. Cytogenetics and Holoprosencephaly: A Chromosomal Microarray Study of 222 Individuals with Holoprosencephaly. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 178(2):175-186 (June 2018).
2011
Kauvar EF, Hu P, Pineda-Alvarez DE, Solomon BD, Dutra A, Pak E, Blessing B, Rosenfeld JA, Schaffer LG, Shanske AL, Roessler E, Muenke M. Minimal evidence for a direct involvement of Twisted Gastrulation Homolog 1 (TWSG1) gene in human holoprosencephaly phenotypes. Molecular Genetics and Metabolism 102(4):470-480 (April 2011).
Keaton A, Solomon BD, Kauvar EF, El-Jaick KB, Gropman AL, Zafer Y, Meck JM, Bale SJ, Grange DK, Haddad BR, Gowans GC, Quintero-Rivera F, Martinez JA, Roessler E, Muenke M. Mutations in TGIF in human holoprosencephaly: Correlation between genotype and phenotype. Molecular Syndromology 1(5):211-222 (May 2011).
Gupta N, Oppenheim I, Kauvar EF, Tayebi N, Sidransky E. Type 2 Gaucher Disease: Phenotypic variation and genotypic heterogeneity. Blood Cells, Molecules & Diseases 46(1):75-84 (January 2011).
2010
Walter ND, Rice PL, Redente EF, Kauvar EF, Lemond L, Aly T, Wanebo K, Chan ED. Wound healing after trauma may predispose to lung cancer metastasis: Review of potential mechanisms. American Journal of Respiratory Cell and Molecular Biology 44(5):591-596 (December 2010).
Kauvar EF, Muenke M. Holoprosencephaly: Recommendations for diagnosis and management. Current Opinion in Pediatrics 22:687-695 (December 2010).
Kauvar EF, Solomon BD, Curry CJ, van Essen AJ, Janssen N, Dutra A, Roessler E, Muenke M. Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature. American Journal of Medical Genetics Part C (Seminars in Medical Genetics) 154C:158-169 (February 2010).