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Katherine Johnson

University of Chicago · US
Area of research
Rheumatology · Molecular Biology
Research interest
Research interests include Osteoarthritis Treatment and Mechanisms, Muscle Physiology and Disorders, Rheumatoid Arthritis Research and Therapies, and Pharmacological Effects of Medicinal Plants.
h-index
24
citations
2,267
works
89
NIH funding
primary concept
email

Recent publications

Mammalian Queuosine tRNA Modification Impacts Translation to Enhance Cell Proliferation and MHC-II Expression
Journal of Molecular Biology 2025cited by 4position: middledoi
A pairwise cytokine code explains the organism-wide response to sepsis
Nature Immunology 2024cited by 70position: middledoi
Diagnostic accuracy of elastography and magnetic resonance imaging in patients with NAFLD: A systematic review and meta-analysis
Journal of Hepatology 2021cited by 345position: middledoi
Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance
JHEP Reports 2021cited by 45position: firstdoi
Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis
Science Translational Medicine 2020cited by 444position: middledoi
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
Genetics in Medicine 2020cited by 108position: middledoi
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern
Acta Neuropathologica 2020cited by 39position: middledoi
Bi-allelic <i>TTC5</i> variants cause delayed developmental milestones and intellectual disability
Journal of Medical Genetics 2020cited by 9position: middledoi
SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain
Journal of Medical Genetics 2019cited by 40position: middledoi
Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness
Skeletal Muscle 2018cited by 53position: firstdoi
Limb girdle muscular dystrophy due to mutations in <i>POMT2</i>
Journal of Neurology Neurosurgery & Psychiatry 2017cited by 30position: middledoi
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms and GTPase binding in bipolar disorder
Molecular Psychiatry 2014cited by 126position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Volker Straub · ZHAW Zurich University of Applied Sciences2 papers (2017–2019)Nicolas Chevrier · Centre National de la Recherche Scientifique2 papers (2024–2025)Ana Töpf · Swansea University2 papers (2017–2019)Teresinha Evangelista · Newcastle University1 papers (2019–2019)Joel E. Kleinman · Johns Hopkins University1 papers (2014–2014)Michihiro Takahama · University of Chicago1 papers (2024–2024) · 1 papers (2017–2017)Monkol Lek · Yale University1 papers (2017–2017)Surya Pandey · Northwestern University1 papers (2024–2024)Peter J. Munson · National Heart Lung and Blood Institute1 papers (2014–2014)Jennifer McEvoy‐Venneri · Children’s Institute1 papers (2020–2020) · 1 papers (2019–2019)Willem De Ridder · University of Antwerp1 papers (2017–2017)Madison Plaster · University of Chicago1 papers (2024–2024)Ashleigh E. Schaffer · Oregon Health & Science University1 papers (2020–2020) · 1 papers (2017–2017)Liping Hou · Johnson & Johnson (United States)1 papers (2014–2014)Denis Cipurko · University of Chicago1 papers (2024–2024)Kristl G. Claeys · KU Leuven1 papers (2017–2017) · 1 papers (2019–2019)