Steven M. Lipkin, MD, PhD
Steven M. Lipkin, MD, PhD

Steven M. Lipkin, MD, PhD

Clinical Genetics and Genomics (MD)
Specialties
Clinical Genetics and Genomics (MD), Genetic Counseling, more

Locations and Appointments


New Patients

Gastroenterology and Hepatology at David H. Koch Center

1283 York Avenue
9th Floor
New York, NY 10065
US
Call to ScheduleNew and Existing Patients
Book an Appointment Online
Existing Patients
Login or sign-up to Connect Patient Portal to make an appointment
Existing Patients
Login to Connect Patient Portal make an appointment, view documentation or contact your doctor’s office.
NYP Connect App
The NYP Connect App allows you to access convenient services to help manage your health. Access the patient portal, communicate with your doctor, manage appointments, view test results, request prescription refills, pay a bill, and find a doctor.

insurance icon
Insurances Accepted

Please contact the doctor's office to verify that your insurance is accepted.

  • AETNA
  • Aetna - NYP
  • Anthem Blue Cross/Blue Shield
  • Anthem Blue Cross/Blue Shield Healthplus
  • CIGNA
  • Empire Blue Cross/Blue Shield
  • GHI
  • Health Insurance Plan of NY (HIP)
  • Oxford Health Plans
  • United Healthcare
  • UnitedHealthcare
  • VNSNY CHOICE

about icon
About Steven M. Lipkin, MD, PhD

GENETIC TESTING, WELLNESS WHOLE EXOME AND GENOME SEQUENCING, EXECUTIVE MEDICINE, ADULT GENETIC DISEASES INCLUDING LYNCH SYNDROME/HNPCC, FAMILIAL ADENOMATOUS POLYPOSIS, HEREDITARY BREAST AND PANCREATIC CANNCER, LI-FRAUMENI, JUVENILE POLYPOSIS, PEUTZ-JEGHERS SYNDROME AND OTHER DISORDERS


Dr. Lipkin is a board certified Medical Geneticist with a focus on genetic testing for adult and cancer genetic diseases, including the Lynch Syndrome, Familial Adenomatous Polyposis, and Hereditary Pancreatic Cancer among others. He is an authority on cancer and adult genetic syndromes, with a particular emphasis on hereditary Gastrointestinal cancer syndromes. He is the author of MAPP-MMR, a bioinformatic program that is used to interpret whether Lynch syndrome missense variants are deleterious mutations or benign polymorphisms. He practices at Weill Medical College of Cornell University and New York-Presbyterian Hospital. He trained in Internal Medicine at Duke University and Medical Genetics at the National Human Genome Research Institute.


Board Certifications

  • Clinical Genetics and Genomics (MD)
list icon

Expertise

  • ATM Gene Mutation

  • BARD1 Gene mutation

  • BRCA1 Gene Mutation

  • BRCA2 Gene mutation

  • Breast Cancer Genetic Susceptibility

  • BRIP1 gene mutation

  • Cancer Clinical Trials

  • Cancer Genetics

  • Cancer Screening

  • CDH1 Gene Mutation

  • CHEK2 Gene Mutation

  • Colon Cancer and Polyps

  • Colon Cancer Genetic Testing

  • Colon Cancer Screening

  • Ehlers-Danlos Syndrome

  • Endometrial Cancer Genetic Susceptibility

  • Familial Adenomatous Polyposis (FAP)

  • Family History of Cancer

  • Family History of Colorectal Cancer

  • Family History of Esophageal Cancer

  • Family History of Gastric Cancer

  • Family History of Multiple Myeloma

  • Family History of Pancreatic Cancer

  • FH: Bowel Obstruction

  • Gastrointestinal Cancer

  • Gastrointestinal Cancer Prevention

  • Genetic Counseling

  • Genetic Predisposition to Cancer

  • Genetic Predisposition to Ovarian Cancer

  • Genetic Screening

  • Genetic Susceptibility to Breast Cancer

  • Genetic Susceptibility to Cancer

  • Genetic Susceptibility to Endometrial Cancer

  • Genetic Susceptibility to Ovarian Cancer

  • Genetic Testing

  • Grail Galleri Cancer Surveillance

  • Hemochromatosis

  • Hereditary Breast Cancer

  • Hereditary Breast-Ovarian Cancer

  • Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome

  • Hereditary Ovarian Cancer

  • Inflammatory Bowel Disease

  • Inflammatory Bowel Disease (IBD)

  • Inflammatory Bowel Diseases (IBD)

  • Intensive Cancer Surveillance

  • Juvenile Polyposis Syndrome

  • Lynch Syndrome

  • Marfan Syndrome

  • Molecular Cancer Testing

  • MYH-Associated Polyposis (MAP)

  • Neurofibromatosis Genetic Testing

  • Ovarian Cancer, BRCA1 Positive

  • Ovarian Cancer, BRCA2 Positive

  • PALB2 Gene Mutation

  • Personal History of Multiple Myeloma

  • Peutz-Jeghers Syndrome

  • PRSS1 (Hereditary Pancreatitis)

  • PTEN Gene Mutation

  • RAD51C Gene Mutation

  • RAD51D Gene Mutation

  • Review of Cancer Care

  • Screening Computed Tomography For Coronary Artery Disease and Lung Cancer

  • Screening For Lung Cancer

  • Sessile Serrated Polypsis Syndrome

  • Surveillance For Colorectal Cancer

  • Thyroid Cancer

  • Whole Exome Sequencing

  • Whole Genome Sequencing

list icon

Education

  • Fellowship: Duke University Medical Center, NC

  • Medical School: Duke University Medical Center, NC

  • Residency: Duke University Medical Center, NC

list icon

Languages

  • English
list icon

Titles & Positions

  • Attending Physician

  • Gladys and Roland Harriman Professor of Medicine

  • Professor of Genetic Medicine

  • Professor of Medicine

list icon

Hospital Affiliations

  • NewYork-Presbyterian / Weill Cornell Medical Center

Education

  • Residency: Duke University Medical Center, NC
  • Medical School: Duke University Medical Center, NC
  • Fellowship: Duke University Medical Center, NC

Titles & Positions

  • Attending Physician
  • Gladys and Roland Harriman Professor of Medicine
  • Professor of Genetic Medicine
  • Professor of Medicine

Board Certifications

  • Clinical Genetics and Genomics (MD)

Languages Spoken

  • English