Peter Schneiderat - Concepedia

Concepedia

Author

Peter Schneiderat

Ludwig-Maximilians-Universität München

Also Known As

P Schneiderat, P. Schneiderat, Peter Schneiderat, Schneiderat, P., Schneiderat, Peter

31

Publications

1.2K

Citations

16

H-Index

47

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Friedrich Baur Stiftung Newcastle University University College London Medical Genetics Center

PS

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	674
2	Cell Biology	2	2	39
3	Health Sciences	1	1	317
4	Biochemistry	1	1	317
5	Biology	1	1	34

Peter Schneiderat

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17

Publications

1.2K

Citations

15

H-Index

	Year	Citations
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, Brain Metabolic DisorderCoenzyme Q10GeneticsMolecular BiologyPathology	2007	317
Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy Francesco Saverio Tedesco, M Gerli, Laura Perani, Science Translational Medicine	2012	285
Coenzyme Q10 deficiency and isolated myopathy Rita Horváth, Peter Schneiderat, Benedikt Schoser, Neurology Serum Creatine KinaseAutoimmune DiseaseCoq10 LevelsDisease MechanismGenetic Disorder	2006	117
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases Marina Mora, C. Angelini, Fabrizia Bignami, European Journal of Human Genetics	2014	81
miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors Naoe Harafuji, Peter Schneiderat, Maggie C. Walter, Orphanet Journal of Rare Diseases	2013	44
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2 Maggie C. Walter, Birgit Czermin, Solvig Müller-Ziermann, Journal of Neurology Late-onset PtosisPathologyCommon DiseasesDermatologyHeterozygous Insertion	2010	42
Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle Cells Cibely Cristine Fontes de Oliveira, Maarten M. Steinz, Peter Schneiderat, Scientific Reports	2017	36
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNAVal causing MNGIE-like gastrointestinal dysmotility and cachexia Rita Horváth, Andreas Bender, Angela Abicht, Journal of Neurology BiologyMngie-like Gastrointestinal DysmotilityMitochondrial BiogenesisMitochondrial FunctionGenetics	2009	34
A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A) Peter Reilich, Sabine Krause, Nicolai Schramm, Journal of Neurology Novel MutationRare DiseasesDevelopmental BiologyMendelian DisorderSkeletal Muscle	2011	30
Demyelinating disease of central and peripheral nervous systems associated with a A8344G mutation in tRNALys İlknur Erol, F. Alehan, Rita Horváth, Neuromuscular Disorders Neurodegenerative DiseasesPeripheral NervesA8344g MutationNeurological DisorderGenetic Disorder	2009	30

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