Xueying Qiao MS, LCGC
Xueying Qiao is a board certified and licensed bilingual (English and Chinese) genetic counselor and a member of National Society of Genetic Counselors. His job is to perform genetic counseling for individuals and their family members who are at risk of developing a genetic disease. He also gives educational talks regarding genetic health for communities and organizations with various backgrounds.
Mr. Qiao received thorough, comprehensive training in genetic counseling. After graduated from the genetic counseling program at Sarah Lawrence College with a master’s degree in 2015, he received a one-year genetic counseling fellowship training in lysosomal disorders (metabolic diseases) at Cincinnati Children’s Hospital.
Mr. Qiao’s clinical experience covers a broad spectrum of specialties in genetic counseling. It includes pediatric, prenatal, and cancer genetic counseling at Cincinnati Children’s Hospital, Integrated Genetics/LabCorp diagnostic company, New York Presbyterian Hospital Queens and Discovery Genetics, serving patients with various ethnic, cultural and religious backgrounds.
Mr. Qiao gave presentations on topics about genetic health to general public, including the audience of Chinese Radio Network, the readers of World Journal and the members of about 30 various communities and organizations with different ethnic backgrounds such as Caucasian, African American, Hispanic, Jewish, Indian, Korean, Vietnam and Chinese.
Mr. Qiao had both teaching and research experience. After graduating from Fudan University in China in 1983, Mr. Qiao became a teacher at the university till 1987. He had worked as a microbiologist for over two decades at the Public Health Research Institute (USA) since 1987. His total scientific publications are about 30.
Mr. Qiao is a board certified genetic counselor at Discovery Genetics, LLC. He believes in independent genetic counseling. He also believes in patient-centered approach. His goals are to help more individuals have access to genetic counseling services, help patients find cause of genetic disease and help their doctors develop more effective medical management or prevention plans.