Clinical Director, Division of Cancer Genetics and Prevention
Senior Physician, Dana-Farber Cancer Institute
Assistant Professor of Medicine, Harvard Medical School
Huma Q. Rana, MD, MPH is the Clinical Director
of the Division of Cancer Genetics and Prevention at Dana-Farber Cancer
Institute, and Assistant Professor of Medicine at Harvard Medical School. At
Dana-Farber and its affiliates and satellites, Dr. Rana oversees the medical
management and the clinical operations that provide care to individuals with
rare genetic susceptibilities to cancer.
In addition to her clinical work, Dr. Rana leads
multiple clinical research projects focused on developing cancer prevention and
screening for those with hereditary cancer risk, and novel approaches to
improving access to cancer genetics services.
Dr. Rana received her medical degree from the Rutgers
Robert Wood Johnson Medical School, completed her residencies in Internal
Medicine and Clinical Genetics at the Icahn School of Medicine at Mount Sinai,
and received her MPH from the Harvard T.H. Chan School of Public Health. She has been a member of the Dana-Farber
faculty since 2012.
Clinical Director, Division of Cancer Genetics and Prevention
Senior Physician, Dana-Farber Cancer Institute
Assistant Professor of Medicine, Harvard Medical School
Huma Q. Rana, MD, MPH is the Clinical Director
of the Division of Cancer Genetics and Prevention at Dana-Farber Cancer
Institute, and Assistant Professor of Medicine at Harvard Medical School. At
Dana-Farber and its affiliates and satellites, Dr. Rana oversees the medical
management and the clinical operations that provide care to individuals with
rare genetic susceptibilities to cancer.
In addition to her clinical work, Dr. Rana leads
multiple clinical research projects focused on developing cancer prevention and
screening for those with hereditary cancer risk, and novel approaches to
improving access to cancer genetics services.
Dr. Rana received her medical degree from the Rutgers
Robert Wood Johnson Medical School, completed her residencies in Internal
Medicine and Clinical Genetics at the Icahn School of Medicine at Mount Sinai,
and received her MPH from the Harvard T.H. Chan School of Public Health. She has been a member of the Dana-Farber
faculty since 2012.
Journal article
Concurrent pathogenic variants (PVs) in cancer predisposition genes have been reported in 0.1-2% of hereditary cancer (HC) patients. Determining concurrent PVs is crucial for the diagnosis, treatment, and risk assessment of unaffected family members. Next generation sequencing based diagnostic tests, which are widely used in HCs, enable the evaluation of multiple genes in parallel. We have screened the family members of a patient with bilateral breast cancer who was found to have concurrent PVs...
Journal article
CONCLUSIONS AND RELEVANCE: CHEK2 PVs, with few exceptions (p.I157T, p.S428F, and p.T476M), were associated with similar cancer phenotypes irrespective of variant type. CHEK2 PVs were not associated with colorectal cancer, but were associated with breast, kidney, and thyroid cancers. Compared with other CHEK2 PVs, the frequent p.I157T, p.S428F, and p.T476M alleles have an attenuated association with breast cancer and were not associated with nonbreast cancers. These data may inform the genetic...
