Medical Genetics

About Us

The Division of Medical Genetics at NewYork-Presbyterian/Weill Cornell Medical Center specializes in providing evaluation, diagnosis, and care for children, adolescents, and adults with suspected or known genetic conditions.

We use the latest genetic technology to deliver expert clinical evaluation, risk assessment, and genetic counseling. Our team works closely with other Weill Cornell Medicine specialties to provide comprehensive care for our patients across the lifespan.

Click here to learn what you can expect during your visit, how to request an appointment and answers to frequently asked questions about genetic counseling.

Services & Programs

General Genetics Clinic

Our clinic is designed to assist you and your family in navigating the world of genetics medicine. We provide information and support to help you make informed decisions about your health and the health of your family. We see patients of all ages with suspected or known genetic conditions, discuss the potential use of genetic testing, and provide genetic counseling regarding a confirmed diagnosis. We are also able to see patients both in-person and virtually depending on the reason for the visit.

Genome Clinic

For children from 6 months through 13 years of age who have a diagnosis of autism, developmental delay, or intellectual disability, we can conduct online screening to determine if genetic testing using whole genome sequencing is an appropriate starting point. This can significantly reduce the wait times for children with neurodevelopmental disorders. Learn more.

Weill Cornell Brain and Spine Craniofacial Program

Within the WCM Craniofacial Clinic, we collaborate with colleagues from ENT and other specialty departments to provide a multidisciplinary approach for children and young adults with abnormalities of the head and neck - especially those with craniosynostosis, cleft lip and cleft palate. Learn more.

Weill Cornell Medicine X and Y Chromosome Variations Program/Klinefelter Syndrome Care Center

The Weill Cornell Medicine (WCM) Klinefelter Syndrome Care Center offers multidisciplinary care for children and adults with Klinefelter syndrome and other X and Y chromosome variations. Directed by Dr. Lilian Cohen of Medical Genetics, our program brings together a broad team of experts to offer our patients comprehensive evaluation and subspecialty care. Our goal is to provide the best care based on advances in health information and evidence-based treatment.

Prenatal Genetic Counseling and Fetal Care Center Program

Our expert team of physicians and genetic counselors at the Prenatal Genetic Counseling Program work closely with each patient and their obstetrician to address their genetic concerns about the health of the pregnancy. Learn more about Prenatal Genetic Counseling and about the Fetal Care Center.