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Christine A. Peschken

Researcher at University of Manitoba

Publications -  144
Citations -  8860

Christine A. Peschken is an academic researcher from University of Manitoba. The author has contributed to research in topics: Population & Cohort. The author has an hindex of 38, co-authored 128 publications receiving 7040 citations. Previous affiliations of Christine A. Peschken include University of British Columbia & University of Toronto.

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Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus.

Michelle Petri, +51 more
TL;DR: The Systemic Lupus International Collaborating Clinics (SLICC) group revised and validated the American College of Rheumatology (ACR) systemic lupus erythematosus (SLE) classification criteria in order to improve clinical relevance, meet stringent methodology requirements, and incorporate new knowledge regarding the immunology of SLE.
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Factors associated with damage accrual in patients with systemic lupus erythematosus: results from the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort

Ian N. Bruce, +39 more
TL;DR: It is found that several potentially modifiable risk factors for damage accrual are identified and an integrated strategy to address these may improve long-term outcomes.
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The frequency and outcome of lupus nephritis: results from an international inception cohort study

John G. Hanly, +44 more
- 01 Feb 2016 - 
TL;DR: Despite current standard of care, nephritis was associated with ESRD and death, and renal insufficiency was linked to lower health-related quality of life.
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Cancer risk in systemic lupus: An updated international multi-centre cohort study

Sasha Bernatsky, +44 more
TL;DR: There is clearly an increased risk of NHL, and cancers of the vulva, lung, thyroid, and possibly liver in SLE relative to the general population, and it remains unclear to what extent the association with NHL is mediated by innate versus exogenous factors.
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Marked differences in fine specificity and isotype usage of the anti-citrullinated protein antibody in health and disease.

TL;DR: The fine specificity and isotype usage of the ACPA response are qualitatively different in health and disease, and Epitope spreading and expansion of the isotype repertoire might be necessary for development of RA, and this could be facilitated by the presence of RF antibodies.