Joachim Weis

Universitätsklinikum Aachen — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

78h-index22.1kcitations660works3.12yr avg
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Research Topics

Muscle Physiology and Disorders(69), Nerve injury and regeneration(64), Hereditary Neurological Disorders(63), Genetic Neurodegenerative Diseases(47), Neurogenetic and Muscular Disorders Research(45)

Publications658 total

Automatic Extraction of Rules for Generating Synthetic Patient Data From Real-World Population Data Using Glioblastoma as an Example
arXiv (Cornell University)·2025Open Access
<i>REEP1</i> Accumulation Disrupts ER Integrity and Drives Spinal Motoneuron Degeneration in Distal Hereditary Motor Neuropathy
Advanced Science·2025Open Access
Charcot-Marie-Tooth–SORD: insights into pathology and pathophysiology from a human nerve biopsy series
Brain·2025
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
Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction
The Journal of General Physiology·2025
Iatrogenic cerebral amyloid angiopathy: two new cases and systematic review of case reports with neuropathological data
Neurological Research and Practice·2025Open Access
04PNovel mouse model for inclusion body myositis: transgenic upregulation of lymphotoxin together with impaired autophagy induces inflammation and protein accumulation in skeletal muscle
Neuromuscular Disorders·2025Open Access
Mutual reinforcement of lymphotoxin-driven myositis and impaired autophagy in murine muscle
Brain·2025Open Access
Deciphering <i>DST</i> -associated disorders: biallelic variants affecting DST-b cause a congenital myopathy
Brain·2025Open Access
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic Pain
Neuropediatrics·2025
Neue SCN11A-Variante p.Tyr66Ser: Klinisch-funktionelle Pathogenitätsdiskussion im Kontext von Small Fiber Dysfunktion
Nervenheilkunde·2025
Bioptische Befundkonstellationen bei Amyloid-Neuropathien
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
RNA Interference Targeting Small Heat Shock Protein B8 Failed to Improve Distal Hereditary Motor Neuropathy in the Mouse Model
The Journal of Gene Medicine·2025· 1 cited
Spatially resolved transcriptomics of benign and malignant peripheral nerve sheath tumors
Neuro-Oncology·2025· 5 citedOpen Access
Intraoperative Assessment of Nerve Traction Injury in Obstetric Brachial Plexus Palsy
Journal of Brachial Plexus and Peripheral Nerve Injury·2025Open Access
A Novel MYH14 Variant Presenting as a New Phenotype of MYH14-Associated Neuromuscular Disorders—Clinicohistologic Findings and Review of the Literature
Journal of Clinical Neuromuscular Disease·2024
Fatigue und Burn-out – Zwei Gesundheitsstörungen mit hoher medialer Präsenz
Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz·2024Open Access
Technique and Expected Benefit of Intraoperative Perfusion Imaging of Peripheral Nerves
Plastic & Reconstructive Surgery Global Open·2024· 1 citedOpen Access
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Frequent Co-authors

Peter De Jonghe(6), Jan Senderek(6), István Katona(5), Jonathan Baets(5), Claudia Stendel(5), Ingo Kurth(4), Ahmet Bozkurt(4), Gary A. Brook(4), Anand Goswami(4), Dirk Troost(4), Klaus Zerres(4), Carsten Bergmann(4), Tim M. Strom(4), Bernd Sellhaus(4), Ronald Deumens(3), Vincent Timmerman(3), Jochen H. Weishaupt(3), Albert C. Ludolph(3), Susanne Petri(3), Sabine Rudnik‐Schöneborn(3)