Concepedia

Peter Schneiderat

PS

17

Publications

1.2K

Citations

15

H-Index

2006

Active since

Affiliations

Ludwig-Maximilians-Universität München(Current)

Friedrich Baur Stiftung

Newcastle University

University College London

Medical Genetics Center

Peter Schneiderat is an author at Ludwig-Maximilians-Universität München specializing in medicine, pathology, and genetics.

Top concepts

MedicinePathologyGeneticsPhysiologyInherited Metabolic DiseaseImmunologyMetabolismCell BiologyCommon DiseasesMolecular Genetics

Publications per year

2006–2021

17

Publications

17

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

Klaus Gempel, Haluk Topaloğlu, Beril Talim et al. · Brain · 2007 · 317 citations · Full text

Metabolic Disorder, Coenzyme Q10, Genetics +21

Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy

Francesco Saverio Tedesco, M Gerli, Laura Perani et al. · Science Translational Medicine · 2012 · 285 citations

Coenzyme Q10 deficiency and isolated myopathy

Rita Horváth, Peter Schneiderat, Benedikt Schoser et al. · Neurology · 2006 · 117 citations

Serum Creatine Kinase, Autoimmune Disease, Coq10 Levels +8

The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases

Marina Mora, C. Angelini, Fabrizia Bignami et al. · European Journal of Human Genetics · 2014 · 81 citations · Full text

miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors

Naoe Harafuji, Peter Schneiderat, Maggie C. Walter et al. · Orphanet Journal of Rare Diseases · 2013 · 44 citations · Full text

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