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Janet Pope, MD, MPH, FRCPC

Dr. Janet Pope is a Professor of Medicine in the Division of Rheumatology at the University of Western Ontario (UWO), Schulich School of Medicine, London, Ontario, Canada.  She is the Division Head in Rheumatology at St. Joseph's Health Centre, London. Her research includes studies in scleroderma, SLE and RA, including outcome measurements, clinical trials and disease manifestations. She has published over 450 peer-reviewed articles, 15 chapters, 500 abstracts and several Cochrane meta-analysis reviews. Mentoring of research students and trainees numbers more than 125. She has received the Distinguished Investigator Award from the Canadian Rheumatology Association, Rheumatologist of the Year from the Ontario Rheumatology Association, Department of Medicine Research Achievement Award, and the Dean’s Award of Excellence in Research. She has been inducted into the Canadian Academy of Health Sciences.

 

Articles By Janet Pope, MD, MPH, FRCPC

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Do You Have to be Overweight for GLP-1s to Work?

Are there any data that GLP-1 RA drugs can be effective if a person has a normal BMI? 

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Tips for safe use of allopurinol

These are tips and hopefully the patients are abstaining from moderate alcohol and are not tipsy! Here are 5 tips that may not be totally obvious.

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How many CAR-T’s do we need to test drive?

CAR-T at #EULAR2026 raised as many questions as it answered. Here's what we know, what we're still asking, and why the answers matter.

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lupus SLE

How to treat SLE in 2026 and beyond!

There are so many SLE trials, and over the last year, many new ideas have been suggested.

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‘Strong’ treatment predictions in inflammatory myositis

Presented at EULAR 2026 London, Brepocitinib dual TYK2/JAK1 inhibitor with successful Phase 3 VALOR trial demonstrating significant improvement in skin and muscle symptoms in dermatomyositis (DM).

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What should head-to-head studies in inflammatory arthritis teach us?

The multimillion dollar question for inflammatory arthritis prescriptions is: which drug should I use next?

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IgG4: Rare, but new treatments on the horizon

IgG4 is a rare autoimmune disease with excessive IgG4 immunoglobulins that can affect multiple organs yielding plasma cell deposition (inflammation) and fibrosis.

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Big data

Rheumatoid arthritis and the ‘big bang’ at the ACR!

Is there ‘bang for the buck’ using big data to help predict who will develop RA in at-risk populations and similarly to predict response to csDMARDs, TNFi and JAKi in RA?

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magnifying glass with IPAF

What is IPAF?

Idiopathic Interstitial Pneumonia with Autoimmune Features - or IPAF - describes patients with interstitial pneumonia with autoimmune features, but they don’t meet a diagnosis of a CTD.

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How to assess ILD in your patients?

Have a high index of suspicion in your patients with connective tissue disease (especially systemic sclerosis, inflammatory myositis), and rheumatoid arthritis.

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