Ciencias de la Salud
Campo de conocimiento
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Klinikum der Universität München
Múnich, AlemaniaPublicaciones en colaboración con investigadoras/es de Klinikum der Universität München (66)
2024
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Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features
Brain, Vol. 147, Núm. 8, pp. 2867-2883
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Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis (Journal of Neurology, (2023), 270, 12, (5849-5865), 10.1007/s00415-023-11862-4)
Journal of Neurology
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Magnetic Resonance Imaging Measures to Track Atrophy Progression in Progressive Supranuclear Palsy in Clinical Trials
Movement Disorders
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Shared vulnerability and sex-dependent polygenic burden in psychotic disorders
European Neuropsychopharmacology, Vol. 86, pp. 49-54
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The magnitude and variability of neurocognitive performance in first-episode psychosis: a systematic review and meta-analysis of longitudinal studies
Translational Psychiatry, Vol. 14, Núm. 1
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Thyroid hormone receptor alpha modulates fibrogenesis in hepatic stellate cells
Liver International, Vol. 44, Núm. 1, pp. 125-138
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Type 1 Autoimmune Pancreatitis in Europe: Clinical Profile and Response to Treatment
Clinical Gastroenterology and Hepatology, Vol. 22, Núm. 5, pp. 994-1004.e10
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Umbrella Review: Atlas of the Meta-Analytical Evidence of Early-Onset Psychosis
Journal of the American Academy of Child and Adolescent Psychiatry, Vol. 63, Núm. 7, pp. 684-697
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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An umbrella review of candidate predictors of response, remission, recovery, and relapse across mental disorders
Molecular Psychiatry, Vol. 28, Núm. 9, pp. 3671-3687
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Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis
Journal of Neurology, Vol. 270, Núm. 12, pp. 5849-5865
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Common genetic variants contribute to heritability of age at onset of schizophrenia
Translational Psychiatry, Vol. 13, Núm. 1
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Comprehensive dissection of prevalence rates, sex differences, and blood level-dependencies of clozapine-associated adverse drug reactions
Psychiatry Research, Vol. 330
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Correction: Common genetic variants contribute to heritability of age at onset of schizophrenia (Translational Psychiatry, (2023), 13, 1, (201), 10.1038/s41398-023-02508-0)
Translational Psychiatry
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Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer” (eBioMedicine (2023) 92, (S2352396423001810), (10.1016/j.ebiom.2023.104616))
eBioMedicine
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Dissecting the genetic heterogeneity of gastric cancer
eBioMedicine, Vol. 92
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ESTRO ACROP consensus recommendation on the target volume definition for radiation therapy of macroscopic prostate cancer recurrences after radical prostatectomy
Clinical and Translational Radiation Oncology, Vol. 43
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Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)
Nature
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Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))
Nature communications
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Germline mutations in WNK2 could be associated with serrated polyposis syndrome
Journal of Medical Genetics, Vol. 60, Núm. 6, pp. 557-567