Medical Insights & Engagement
Scientific strategy that strengthens communication and drives informed action.
Medical Affairs Strategy
- Scientific platform and lexicon development
- Cross-functional insight integration
- Launch planning and lifecycle strategy
- Strategic advisory board design and execution
Publication Planning
- Peer-reviewed manuscripts (original research, clinical studies)
- Review articles (narrative, systematic)
- Scientific abstracts & posters
- Congress presentation slides and speaker notes
- Gap analysis and literature landscape reviews
Marketing Communications
- Thought leadership white papers
- Case studies and impact summaries
- Branded and unbranded press releases
- Social media content strategy (scientific tone of voice)
Education & Training
- Scientific slide decks and speaker kits
- Training manuals for field teams and investigators
- eLearning modules and microlearning content
- Workshop content and facilitation guides
Scientific Communications Planning
- Integrated scientific communication plans (iSCPs)
- global-to-local messaging alignment
- KPI tracking for communication impact
- Coordination of cross-functional messaging
KOL Development & Engagement
- Stakeholder mapping and engagement strategy
- Scientific exchange frameworks and SOPs
- KOL insight capture and analysis
- Advisory board facilitation
Scientific Strategy & Advisory
- Scientific positioning for AI-enabled/novel tech
- Value communication strategy with HEOR/RWE integration
- Benefit-risk communication and narrative development
- Innovation workshops and internal alignment
Congress & Conference Strategy
- Abstract and poster submission planning
- Presentation and speaker support
- Congress booth medical engagement planning
- Real-time insight capture at global congresses
Regulatory Scientific Content
- Clinical trial report (CSR) authoring and medical writing
- Scientific content for regulatory submissions (510(k), PMA, IDE, De Novo, Post-Market Surveillance)
- Labeling content development and review
- Regulatory meeting prep and background information
Select Examples of Publications (Peer-Reviewed, Educational, Whitepapers)
• Levy, Y., Rempel, D., Nguyen, M., Yassine, A., Burns, M., Salgia, P., Lim, B., Butler, S., Berkeley, A., Bayram, E.
*The Fusion of Wide Field Optical Coherence Tomography & AI: Advancing Breast Cancer Surgical Margin Visualization.*
_Life_, 2023; 13(12): 2340.
🔗 [Read article](https://www.mdpi.com/2075-1729/13/12/2340)
• Hufnagel, R.B., Zimmerman (Butler), S.L., Krueger, L.A., et al.
A novel frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.
American Journal of Medical Genetics Part A, 2016; 170(2): 487–491.
🔗 [Read article](https://doi.org/10.1002/art.39565)
• Liu, K., Kurien, B.T., Zimmerman (Butler), S.L., et al.
X chromosome dose and sex bias in autoimmune diseases: increased 47,XXX in SLE and Sjögren’s syndrome.
Arthritis & Rheumatology, 2016; 68(5): 1290–1300.
🔗 [Read article](https://doi.org/10.1177/0883073815575435)
• Hrabik, S.A., Standridge, S.M., Zimmerman (Butler), S.L., et al.
The clinical utility of a SNP microarray in patients with epilepsy at a tertiary medical center.
Journal of Child Neurology, 2015; 30(13): 1770–1777.
🔗 [Read article](https://doi.org/10.1177/0883073815575435)
• Rosenfeld, J.A., Zimmerman (Butler), S.L., et al.
Duplication of NSD1 causes growth retardation and microcephaly.
Molecular Syndromology, 2013; 3(6): 247–254.
🔗 [Read article](https://doi.org/10.1159/000346619)
• Sund, K., Zimmerman (Butler), S.L., et al.
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease.
Genetics in Medicine, 2013; 15(1): 70–80.
🔗 [Read article](https://doi.org/10.1038/gim.2012.115)
• George-Abraham, J.K., Zimmerman (Butler), S.L., et al.
Tetrasomy 15q25.2→qter identified by SNP microarray in a patient with multiple anomalies.
American Journal of Medical Genetics, 2012; 158A(8): 1971–1976.
🔗 [Read article](https://doi.org/10.1002/ajmg.a.35424)
• Myers, K., Zimmerman (Butler), S.L., et al.
The clinical phenotype of children with Fanconi anemia caused by biallelic BRCA2 mutations.
Pediatric Blood Cancer, 2012; 58(3): 462–465.
🔗 [Read article](https://doi.org/10.1002/pbc.23180)
• Sellars, E.A., Zimmerman (Butler), S.L., et al.
Ventricular noncompaction and absent thumbs in a newborn with tetrasomy 5q35.
American Journal of Medical Genetics, 2011; 155A(6): 1409–1413.
🔗 [Read article](https://doi.org/10.1002/ajmg.a.34040)
• Suzuki, T., Zimmerman (Butler), S.L., et al.
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.
The Journal of Experimental Medicine, 2008; 205(12): 2703–2710.
🔗 [Read article](https://doi.org/10.1084/jem.20081383)
• Zimmerman (Butler), S.L. and Krane, C.M.
Molecular-genetic and functional analysis of aquaporins in vitro and in vivo.
Doctoral Dissertation, University of Dayton, 2007.
• Zimmerman (Butler), S.L., Frisbie, J., Goldstein, D., et al.
Expression of aquaporins and glyceroporins during cold acclimation in Hyla chrysoscelis.
American Journal of Physiology, 2006; 292: R544–R555.
🔗 [Read article](https://doi.org/10.1152/ajpregu.00389.2005)
Select Whitepapers & Educational Publications
• Next-generation sequencing (NGS): Revolutionizing patient care in your oncology practice.
• Next-generation sequencing in pathology: Enabling personalized medicine.
• Next-generation sequencing.