You are here

Office of the Director

The Office of the Director (OD) provides overall planning, direction, coordination, and evaluation of Lister Hill Center biomedical research and development initiatives and programs. The OD senior management team plays an active role in shaping the Lister Hill Center's research agenda and provides leadership in disseminating information to the scientific and health care communities and the lay public.

An important aspect of the Lister Hill Center's success has been the incorporation of an external Board of Scientific Counselors. The Board of Scientific Counselors, composed of experts in biomedical informatics, medical sciences, and information sciences, meets biannually to review the Center's research priorities.

Additionally, the OD supports and conducts meetings, workshops, and other similar activities essential to the effective coordination and exchange of biomedical information.


  • ""

    Multiple projects in this area continue to promote the development, enhancement, and adoption of clinical vocabulary standards. Inter-terminology mapping promotes the use of standard terminologies by creating maps to administrative terminologies, which allows re-use of encoded clinical data.

  • Infobuttons are context-aware links from one information system to another that anticipate users’ information needs, take them to appropriate resources, and assist with retrieval of relevant information.

  • LHNCBC cherry blossoms

    LHC-Forms is a web widget that renders input forms based on JSON form definitions.

  • Lindberg Q&A thumbnail

    Oral history is a method for documenting history in a vivid way by recording the voices of those who have experienced it. “Memory is the core of oral history, from which meaning can be extracted and preserved.”

  • Detail of baby toes.

    Newborn screening (NBS) in the United States is a complex public health program. The goals of NBS are to identify infants who appear healthy but have serious conditions, begin treatment before they suffer significant disability or death, and in doing so decrease the burden of disease on society.

  • LHNCBC, in cooperation with Regenstrief Institute, obtained and analyzed statistical data from many health care organizations to identify the most frequent subset that organizations could target for mapping. It obtained frequency distribution for three years of laboratory tests sources, including from Partners of Boston and the Indiana Network for Patient Care (an HIE), and United Healthcare, all of whom had mapped the test results to LOINC. The sample size of the combined sources was 490 million test results.