Anne Schänzer

Justus-Liebig-Universität Gießen — Germany

Medicine · Health Sciences

29h-index3.2kcitations167works2.22yr avg
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Research Topics

Inflammatory Myopathies and Dermatomyositis(27), Muscle Physiology and Disorders(22), Cardiomyopathy and Myosin Studies(20), Lysosomal Storage Disorders Research(17), Glycogen Storage Diseases and Myoclonus(16)

Publications167 total

Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanisms
Skeletal Muscle·2026Open Access
Author response to the letter to the editor regarding “Headaches and lymphocytic pleocytosis after COVID-19 require the exclusion of encephalitis”
Neurological Research and Practice·2026Open Access
Myopathy With Exercise‐Induced Intolerance due to Novel Biallelic Variants in <i>OBSCN</i> —A Clinical, Morphological and Molecular Analysis
Neuropathology and Applied Neurobiology·2026Open Access
Post-infectious autoimmune disorder involving the CNS and PNS following SARS-CoV-2 infection – a clinical-morphological case report
Neurological Research and Practice·2025· 3 citedOpen Access
Myopathology and Immune Profile of Granulomatous Myositis in Sarcoid Myopathy
Neuropathology and Applied Neurobiology·2025Open Access
23PMyopathology and immune profile of granulomatous myositis in sarcoid myopathy
Neuromuscular Disorders·2025
557PA muscular dystrophy associated with bi-allelic LEMD2 variants: expanding the genotype of nuclear envelopathies
Neuromuscular Disorders·2025
Lessons learned from a muscle study in nail-patella syndrome
Orphanet Journal of Rare Diseases·2025· 1 citedOpen Access
Deciphering <i>DST</i> -associated disorders: biallelic variants affecting DST-b cause a congenital myopathy
Brain·2025Open Access
Alpha‐Synuclein as a Potential Biomarker for Inclusion Body Myositis in Blood and Muscle
Neuropathology and Applied Neurobiology·2025· 1 citedOpen Access
Mitochondrial damage is associated with an early immune response in inclusion body myositis
Brain·2025· 13 cited
Differentielle immunologische Eigenschaften skelettaler Muskelgruppen in idiopathischen inflammatorischen Myopathien
Nervenheilkunde·2025
Muskelpathologie bei Late Onset Pompe Disease (LOPD) – Störung von Muskelzytoskelett und Autophagie-assoziierten Proteinen
Nervenheilkunde·2025
In vitro modeling of filaminopathies
Nervenheilkunde·2025
MALSU1 als Kandidatengen in einer Familie mit mitochondrialer Kardiomyopathie
Nervenheilkunde·2025
CIDP bei einem10-jährigen Mädchen mit Nachweis von Anti-Caspr-1-Antikörpern- und gutem Ansprechen auf Rituximab
Nervenheilkunde·2025
Molekulare Unterschiede der Skelettmuskulatur bei Patienten mit Morbus Pompe mit infantilem im Vergleich zum late-onset Phänotyp
Nervenheilkunde·2025
Biallelische Varianten in einem DST-b-spezifischen Exon verursachen eine schwere angeborene Myopathie mit Arthrogryposis, muskulärer Hypotonie und dilatativer Kardiomyopathie
Nervenheilkunde·2025
COVID-19-assoziierte axonale Neuritis und Enzephalitis
Nervenheilkunde·2025
Dominant rhabdomyolysis linked to a recurrent <i>ATP2A2</i> variant reducing SERCA2 function in muscle
Brain·2025· 1 citedOpen Access
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Frequent Co-authors

Andreas Hahn(18), Till Acker(11), Werner Stenzel(7), Corinna Preuße(6), Karl H. Plate(5), Bernd A. Neubauer(5), Andreas Roos(5), Boyan K. Garvalov(4), Hannah Schlierbach(4), Andreas Hentschel(4), Udo Schneider(4), Volker Seifert(3), Martin Zenker(3), Dietmar Schranz(3), Heidrun H. Krämer(3), Andreas Hahn(3), Stefan Rupp(3), Christian Jux(3), Akinori Uruha(3), Carsten Dittmayer(3)