Lisa Jerome
Clinical Research Specialist at MAPS PBC
Data updated
Research Footprint
Lisa Jerome appears in 20 tracked papers (2010–2023), most studied alongside MDMA and Placebo, across PTSD, Anxiety Disorders and Safety & Risk Management.
Most-cited paper: The safety and efficacy of ±3,4-methylenedioxymethamphetamine-assisted psychotherapy in subjects with chronic, treatment-resistant posttraumatic stress disorder: the first randomized controlled pilot study (667 citations).
Frequent co-authors: Berra Yazar-Klosinski, Rick Doblin and Michael Mithoefer.
Publication Landscape
How the 20 papers Blossom tracks for Lisa Jerome line up by year, topic, and journal. These are the psychedelic-relevant papers in Blossom's records as of July 2026, not a complete bibliography.
How has Lisa Jerome's publishing grown?
SourcedTracked papers by publication year. Click a year for the running total.
Don't read as total output: only the 20 of 20 tracked papers with a recorded publication date are counted, and these are the psychedelic-relevant papers Blossom tracks, not a complete bibliography. The current year is still filling in.
What does Lisa Jerome publish on?
SourcedTracked papers per topic. Orange marks the largest research focus.
Don't read shares as adding to 100%: a paper tagged with several topics counts once per topic. These are the psychedelic-relevant papers Blossom tracks, not a complete bibliography.
Where does Lisa Jerome publish?
SourcedTracked papers per journal. Orange marks the most-used journal.
Counts the journal recorded on each tracked paper; preprints and papers with no journal on file are not shown. These are the psychedelic-relevant papers Blossom tracks, not a complete bibliography.
Background & Research
Dr. Lisa Jerome is a psychologist and clinical researcher whose work has been foundational to the scientific documentation of MDMA's effects. At MAPS, she specializes in analyzing clinical data, assessing risks and benefits, and maintaining the intellectual archive of psychedelic trials. Her research supports the design of rigorous clinical protocols for psychedelic-assisted therapy.
Key Impact
Key figure in archival research and data analysis for MAPS-supported clinical trials of MDMA.
Collaboration Network
22 collaborators· click a node to visit their profile
Full network →Collaboration Network
See Lisa Jerome's full collaboration network, shared papers, and research connections.
Compounds
Topics
Top Collaborators
Top Collaborators
Unlock clinical summaries, full texts, and related trial mapping.
Affiliations
Institutions, companies, and organisations Lisa Jerome is associated with.
MAPS
nonprofitMAPS, the Multidisciplinary Association for Psychedelic Studies, is a U.S.-based 501(c)(3) nonprofit research and educational organization founded in 1986. It works nationally and with a broader global audience to develop medical, legal, and cultural contexts for the careful use of psychedelics and marijuana. Its core activities include research, education, advocacy, and convening the field through large public events. In psychedelic medicine and policy, MAPS positions itself as an advocate for legal access, drug policy reform, harm reduction, and health equity. Its Policy & Advocacy work includes legislative advocacy, community organizing, and impact litigation, and it has also launched work on access for system-impacted people and broader health equity in the legal psychedelic ecosystem. Current documented initiatives include the Psychedelic Science conference series, the Health Equity Program, The Zendo Project, and Ask MAPS, which handles public inquiries about therapy, research, and policy reform.
View stakeholder →Resilient Pharmaceuticals
Public Benefit CorpResilient Pharmaceuticals (formerly Lykos Therapeutics, formerly MAPS PBC) is a US-based public benefit corporation developing MDMA-assisted therapy for PTSD. It was founded in 2014 by MAPS as a commercial spinout to carry MAPS MDMA research through late-stage trials and regulatory approval. After two Phase 3 trials and an NDA filing, FDA issued a Complete Response Letter in August 2024 and requested an additional Phase 3 trial before approval. The company subsequently restructured and rebranded, while the public Lykos web presence continues to describe the organisation as pursuing FDA approval for MDMA-assisted therapy. As of the June 2026 review, no public company announcement of a new pivotal trial start or NDA resubmission date was found. VA/DoD-backed MDMA/PTSD research is proceeding in the broader field, but it should not be treated as direct support for Resilient/Lykos NDA resubmission unless linked by company or FDA evidence.
View stakeholder →