Stephanie Galloway, MS

Genetic Counseling
Accepting New Patients
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Overview

Stephanie Galloway is a board certified genetic counselor who specializes in reproductive genetics. She received her bachelors from Presbyterian College and her Master of Science from the University of South Carolina School of Medicine. Since joining Columbia in 2017, she serves women and families throughout their family planning journey. She specializes in REI, embryo genetic testing counseling, preconception genetic risk, and prenatal genetics.

Areas of Expertise / Conditions Treated

  • Family History Analysis
  • Genetic Counseling
  • Genetic Disorders
  • Genetic Screening
  • Pre-Pregnancy Genetics
  • Pregnancy Losses
  • Prenatal Diagnosis
  • Women's Genetics

Academic Appointments

  • Lecturer in Genetic Counseling (in Obstetrics and Gynecology) at the Columbia University Medical Center

Languages

  • English

Gender

  • Female

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Insurance Accepted

Cigna

  • EPO
  • Great West (National)
  • HMO
  • Medicare Managed Care
  • POS
  • PPO

Emblem/HIP

  • POS

Empire Blue Cross/Blue Shield

  • Medicare Managed Care

MagnaCare (National)

  • MagnaCare

Quality Health Management

  • Quality Health Management

UnitedHealthcare

  • Compass (Exchange)
  • Empire Plan
  • HMO
  • Oxford Freedom
  • Oxford HMO
  • Oxford Liberty
  • POS
  • PPO

World Trade Center Health Plan

  • World Trade Center Health Plan

*Please contact the provider’s office directly to verify that your particular insurance is accepted.

Research

Selected Publications

1. Freud LR, Galloway S, Crowley TB, et al. Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age. Am J Obstet Gyneol 2023 Sep 16:S0002-9378(23)006611-7. doi: 10.1016/j.ajog.2023.09.005. PMID 37717890.

2. Kernie CG, Wynn J, Rosenbaum A, de Voest J, Galloway S, Giordano J, Stover S, Westerfield L, Gilmore K, Wapner RJ, Van den Veyver IB, Vora NL, Clifton RG, Caughey AB, Chung WK. Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. Prenat Diagn. 2022 Jun;42(7):947-954. doi:10.1002/pd.6513. Epub 2022 May 4. PMID: 35476893.

3. Pereira EM; Columbia University Clinical Genetics Professionals (Galloway S), Chung WK. COVID-19's Impact on Genetics at One Medical Center in New York. Genet Med. 2020 Sep;22(9):1467-1469.