Cory Smid, MGCS, CGC

Position title: Genetic Counselor

Profile

Cory Smid is a genetic counselor in the Medical Genetics clinic. He provides support, care coordination and genetic counseling for individuals and families with, or suspected of having inherited diseases.

Clinics

Medical Genetics Clinic

Professional Certifications and Education

MGCS Master of Genetic Counselor Studies, University of Wisconsin-Madison
BS, Genetics, University of Wisconsin-Madison
American Board of Genetic Counseling

Selected Publications

Legare JM, Smid CJ, Modaff P, Pauli RM. (2021). Achondroplasia is associated with increased occurrence of apparent life-threatening events. Acta Paediatrica, 110(6):1842-1846. doi: 10.1111/apa.15760.
Legare JM, Pauli RM, Hecht JT, Bober MB, Smid CJ, Modaff P, Little ME, Rodriguez-Buritica DF, Serna ME, Alade AY, Liu C, Hoover-Fong JE, Hashmi SS.(2021). CLARITY: Co-occurrences in achondroplasia-craniosynostosis, seizures, and decreased risk of diabetes mellitus. American Journal of Medical Genetics. Part A, 185(4):1168-1174. doi: 10.1002/ajmg.a.62096.
Smid CJ, Legare JM, Modaff P, Pauli RM. (2021). Craniocervical junction issues after infancy in achondroplasia. American Journal of Medical Genetics. Part A, 185(1):182-189. doi: 10.1002/ajmg.a.61941.
Smid CJ, Legare JM, Modaff P, Pauli RM. (2020). Apparently benign craniocervical signs in achondroplasia: “neurologic leftovers” identified through a retrospective dataset. Orphanet Journal of Rare Diseases, 15(1):301. doi: 10.1186/s13023-020-01584-5.
Smid CJ, Modaff P, Alade A, Legare JM, Pauli RM. (2018). Acanthosis nigricans in achondroplasia. American Journal of Medical Genetics Part A. 31:e40506. doi: 10.1002/ajmg.a.40506.