Jessica E. Hoogendijk

University Medical Center Utrecht — Netherlands

Medicine · Health Sciences

34h-index5.8kcitations152works1.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Inflammatory Myopathies and Dermatomyositis(44), Hereditary Neurological Disorders(38), Genetic Neurodegenerative Diseases(21), Peripheral Neuropathies and Disorders(18), Neurogenetic and Muscular Disorders Research(17)

Publications151 total

Toxic Myopathies
Elsevier eBooks·2025
Neuromuscular Disease
Cambridge University Press eBooks·2024· 2 cited
SMDT1 variants impair EMRE-mediated mitochondrial calcium uptake in patients with muscle involvement
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2023· 7 citedOpen Access
Pathogenic variants in three families with distal muscle involvement
Neuromuscular Disorders·2022· 1 citedOpen Access
Rhabdomyolysis after COVID-19 Comirnaty Vaccination: A Case Report
Case Reports in Neurology·2022· 7 citedOpen Access
<i>SMDT1</i> variants impair EMRE-mediated mitochondrial calcium uptake in patients with muscle involvement
2022· 2 citedOpen Access
Fecal microbiome alterations in treatment-naive de novo Parkinson’s disease
npj Parkinson s Disease·2022· 28 citedOpen Access
Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease – Case series and review
Neuromuscular Disorders·2022· 8 citedOpen Access
Assessment of disability in idiopathic inflammatory myopathy: a call for linearity
Lara D. Veeken·2021· 1 citedOpen Access
Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study
Lara D. Veeken·2020· 45 citedOpen Access
Study protocol of the DUtch PARkinson Cohort (DUPARC): a prospective, observational study of de novo Parkinson’s disease patients for the identification and validation of biomarkers for Parkinson’s disease subtypes, progression and pathophysiology
BMC Neurology·2020· 30 citedOpen Access
Biomarker profiles of endothelial activation and dysfunction in rare systemic autoimmune diseases: implications for cardiovascular risk
Lara D. Veeken·2020· 31 citedOpen Access
P.182Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: the clinical and molecular spectrum of 244 patients
Neuromuscular Disorders·2019
Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Clinical Genetics·2019· 60 citedOpen Access
Galectin‐9 and CXCL10 as Biomarkers for Disease Activity in Juvenile Dermatomyositis: A Longitudinal Cohort Study and Multicohort Validation
Arthritis & Rheumatology·2019· 87 citedOpen Access
Effective cauda equina decompression in two siblings with Charcot–Marie–Tooth disease type 1B
Neuromuscular Disorders·2016
Myositis with endomysial cell invasion indicates inclusion body myositis even if other criteria are not fulfilled
Neuromuscular Disorders·2015· 25 cited
G.P.67
Neuromuscular Disorders·2014
Combining MRI and muscle biopsy improves diagnostic accuracy in subacute‐onset idiopathic inflammatory myopathy
Muscle & Nerve·2014· 125 citedOpen Access
Long-term follow-up of 62 patients with myositis
Journal of Neurology·2014· 74 cited
page 1 of 8Next →

Frequent Co-authors

Marjolein Visser(16), Pieter A. Bolhuis(15), Marianne de Visser(11), Linda J. Valentijn(8), Frank Baas(8), John H. J. Wokke(7), Gerard W. Hensels(7), M. F. G. van der Meulen(6), Ina Zorn(5), I. M. Bronner(5), Anneke J. van der Kooi(5), B.W. Ongerboer de Visser(5), Ernest Choy(4), Umesh A. Badrising(4), Baziel G.M. van Engelen(4), F.G.I. Jennekens(4), Axel R. Wintzen(4), Emiel A. M. Janssen(4), J. van de Vlekkert(4), Esther Brusse(4)