Jessica L. Turnier

Jessica L. Turnier

Pediatric Rheumatology | Pediatrics

1540 E Hospital Dr
Floor 8 Reception B
Ann Arbor, MI 48109

Last Updated: 09/26/2026

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Found 22 publications

Nailfold capillary phenotypes distinguish juvenile myositis subtypes and associate with disease activity.

Nailfold capillary phenotypes distinguish juvenile myositis subtypes and associate with disease activity.

Journal: Clinical and translational medicine

Published: April 02, 2026

Dermatomyositis is characterized by JAK1-mediated monocyte-driven vasculopathy and inflammation.

Dermatomyositis is characterized by JAK1-mediated monocyte-driven vasculopathy and inflammation.

Journal: Science translational medicine

Published: December 24, 2025

Neutrophil lymphocyte ratio as a marker of skin disease activity in older children with juvenile dermatomyositis.

Neutrophil lymphocyte ratio as a marker of skin disease activity in older children with juvenile dermatomyositis.

Journal: Pediatric rheumatology online journal

Published: September 26, 2025

Unmasking inflammation in juvenile dermatomyositis: myokine profiles of patients and bioengineered human muscle.

Unmasking inflammation in juvenile dermatomyositis: myokine profiles of patients and bioengineered human muscle.

Journal: Frontiers in immunology

Published: August 28, 2025

Cross-disease comparison of dermatomyositis and lupus skin identifies inflammatory monocytes and JAK-1 signaling as drivers of vasculopathy in dermatomyositis.

Cross-disease comparison of dermatomyositis and lupus skin identifies inflammatory monocytes and JAK-1 signaling as drivers of vasculopathy in dermatomyositis.

Journal: bioRxiv : the preprint server for biology

Published: August 12, 2025

Insights from the 2024 pediatric rheumatology basic/translational years in review.

Insights from the 2024 pediatric rheumatology basic/translational years in review.

Journal: Pediatric rheumatology online journal

Published: March 21, 2025

Tape strip expression profiling of juvenile dermatomyositis skin reveals mitochondrial dysfunction contributing to disease endotype.

Tape strip expression profiling of juvenile dermatomyositis skin reveals mitochondrial dysfunction contributing to disease endotype.

Journal: JCI insight

Published: March 13, 2025

Epidermal ZBP1 stabilizes mitochondrial Z-DNA to drive UV-induced IFN signaling in autoimmune photosensitivity.

Epidermal ZBP1 stabilizes mitochondrial Z-DNA to drive UV-induced IFN signaling in autoimmune photosensitivity.

Journal: Science immunology

Published: March 07, 2025

Discovery of tissue-specific proteomic signatures in juvenile dermatomyositis highlights pathways reflecting persistent disease activity, clinical heterogeneity, and myositis-specific autoantibody subtype.

Discovery of tissue-specific proteomic signatures in juvenile dermatomyositis highlights pathways reflecting persistent disease activity, clinical heterogeneity, and myositis-specific autoantibody subtype.

Journal: Annals of the rheumatic diseases

Published: March 03, 2025

Expert Perspective: Diagnostic Approach to Differentiating Juvenile Dermatomyositis From Muscular Dystrophy.

Expert Perspective: Diagnostic Approach to Differentiating Juvenile Dermatomyositis From Muscular Dystrophy.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: April 10, 2024

Epidermal ZBP1 stabilizes mitochondrial Z-DNA to drive UV-induced IFN signaling in autoimmune photosensitivity.

Epidermal ZBP1 stabilizes mitochondrial Z-DNA to drive UV-induced IFN signaling in autoimmune photosensitivity.

Journal: bioRxiv : the preprint server for biology

Published: February 08, 2024

Non-criteria antiphospholipid antibodies and calprotectin as potential biomarkers in pediatric antiphospholipid syndrome.

Non-criteria antiphospholipid antibodies and calprotectin as potential biomarkers in pediatric antiphospholipid syndrome.

Journal: Clinical immunology (Orlando, Fla.)

Published: December 18, 2023

Showing 1-12 of 22

Last Updated: 09/26/2026