Human Genetics Application Guidelines

Guidelines for PIs to consider if submitting human genetics application to NIDA:

When preparing an application, researchers are strongly encouraged to present a rationale that carefully balances important substantive, methodological, and budgetary issues.  In particular, applicants are advised to address each of the following, when appropriate:

  • Substantive focus with clear hypothesis (e.g., specific heritable phenotypes, alternative phenotypes, endophenotypes)
  • Sample selection (e.g., particularly informative sub-samples and subgroups, understudied valuable populations) and generalizability (i.e., population to which findings can be applied)
  • Research design (e.g., genetically-informative, birth cohort, multi-generational, selection by prenatal exposure, case-control)
  • Statistical power (e.g., ability to detect effects within the proposed study or in combination with other studies) and population stratification
  • Number and timing of assessments when applicable (e.g., multiple waves ranging from pre- to post-drug exposure, or from disorder onset to remission)
  • Selection and quality of assessments (e.g., diagnostic and/or symptom-based scales, detailed measurement of salient individual and environmental factors)
  • Comorbidity (e.g., psychiatric, polysubstance, physical illness)
  • Flexibility for future use of the data (e.g., consent forms have potential for subsequent inquiry). 
  • Cost effectiveness
  • Biomaterial collected to isolate genetic information (e.g., blood, buccal cells, etc.)
  • Compatibility/overlap with extant studies in the NIDA Genetics Consortium: for a description of those studies see http://zork.wustl.edu/nida/study_descriptions/link.htm)

For studies requesting access to the NGC, the following additional points need to be addressed:

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Any questions or concerns regarding the genetics programs please contact Jonathan D. Pollock Ph.D. (301) 443-1887 or jp183r@nih.gov