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

Steven M. Lipkin, MD, PhD

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

Locations and Appointments


New Patients

Gastroenterology and Hepatology at David H. Koch Center

1283 York Avenue
9th Floor
New York, NY 10065
US
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Insurances Accepted

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  • AETNA
  • Aetna - NYP
  • Emblem/Hip
  • Empire Blue Cross/Blue Shield
  • Empire Blue Cross/Blue Shield Healthplus
  • GHI
  • Health Insurance Plan of NY (HIP)
  • MVP Health Care
  • Oxford Health Plans
  • United Healthcare
  • VNSNY CHOICE

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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)
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Expertise

  • ATM Gene Mutation

  • BARD1 Gene mutation

  • BRCA1 Gene Mutation

  • BRCA2 Gene mutation

  • BRIP1 gene mutation

  • Cancer Genetics

  • CDH1 Gene Mutation

  • CHEK2 Gene Mutation

  • Familial Adenomatous Polyposis (FAP)

  • Family History of Cancer

  • Family History of Multiple Myeloma

  • Family History of Pancreatic Cancer

  • Gastrointestinal Cancer

  • Genetic Counseling

  • Genetic Screening

  • Genetic Testing

  • Grail Galleri Cancer Surveillance

  • Hereditary Breast Cancer

  • Hereditary Breast-Ovarian Cancer

  • Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome

  • Hereditary Ovarian Cancer

  • Inflammatory Bowel Disease

  • Inflammatory Bowel Diseases (IBD)

  • Intensive Cancer Surveillance

  • Juvenile Polyposis Syndrome

  • Lynch Syndrome

  • MYH-Associated Polyposis (MAP)

  • Neurofibromatosis Genetic Testing

  • PALB2 Gene Mutation

  • Personal History of Multiple Myeloma

  • Peutz-Jeghers Syndrome

  • PTEN Gene Mutation

  • RAD51C Gene Mutation

  • RAD51D Gene Mutation

  • Sessile Serrated Polypsis Syndrome

  • Whole Exome Sequencing

  • Whole Genome Sequencing

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Education

  • Fellowship: Duke University Medical Center, NC

  • Medical School: Duke University Medical Center, NC

  • Residency: Duke University Medical Center, NC

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Languages

  • English
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Titles & Positions

  • Attending Physician

  • Gladys and Roland Harriman Professor of Medicine

  • Professor of Genetic Medicine

  • Professor of Medicine

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Hospital Affiliations

  • NewYork-Presbyterian / Weill Cornell Medical Center

Education

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