Leonard Jason

Professor

DePaul University

United States

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Professor Leonard Jason is a faculty member at DePaul University in the United States. His research primarily focuses on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and its related implications, including study design biases, sleep reversal, and population sampling methods. Additionally, he has explored the intersection of community-level factors with recovery home dynamics and the assessment of long COVID through psychometric evaluations.

Articles (27)

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2025

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2023

Collaborators (2)

Matthias Kohl

Professor for Mathematics in Biology and Medicine

GERMANY

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Francisco Westermeier

Senior Lecturer

FH Joanneum GmbH

AUSTRIA

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Leonard Jason

Research Interests

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About

Articles (27)

The impact of leading questions on ME/CFS research: bias and stigma in study design

The Implications and Predictability of Sleep Reversal for People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Machine Learning Approach

Improving myalgic encephalomyelitis population sampling: Applying an online respondent-driven method to address biases in G93.3 register data

Predisposing and Precipitating Factors in Epstein–Barr Virus-Caused Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

The Oxford House Stability Questionnaire: An Effort to Classify Recovery Homes

Psychometric evaluation of the DePaul Symptom Questionnaire-Short Form (DSQ-SF) among adults with Long COVID, ME/CFS, and healthy controls: A machine learning approach

Positive Associations between Women’s Employment at the Community-Level and Opportunities and Interpersonal Sharing within Recovery Homes

Perceptions of virtual versus in‐person recovery meetings: A cross‐sectional survey of Oxford House residents

Conceptual and Methodological Barriers to Understanding Long COVID

The influence of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) family history on patients with ME/CFS

Can a consensus occur on a research case definition for ME/CFS?

Effects of strength of relationship ties in recovery homes: A conundrum

Understanding Experiences of Youth with Long COVID: A Qualitative Approach

The Head-Up Tilt Table Test as a Measure of Autonomic Functioning among Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Ranking the community psychology research output of institutions and authors: A new system of evaluating the field

Methodologic and Policy Efforts to Improve a National Long COVID Study

Development of an ME/CFS Online Screener

Pediatric Post-Acute Sequelae of SARS-CoV-2 infection

Lived experiences of Oxford House residents prescribed medication‐assisted treatment

Risk factors for suicidal ideation in a chronic illness

Die Übersicht zur aktuellen Evidenz ignoriert die aktuelle Evidenz

Benefits of Continuing Linkages to Recovery Homes Following Departure

Comparing Frequency and Severity Ratings for ME/CFS versus Controls

Understanding length of stay in recovery homes

Do diagnostic criteria for ME matter to patient experience with services and interventions? Key results from an online RDS survey targeting fatigue patients in Norway

Predictors of impaired functioning among long COVID patients

Complex Contexts Within Oxford Houses: Psychiatrically Comorbid Social Networks

Collaborators (2)

Matthias Kohl

Francisco Westermeier

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