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Peter Bross | doi.page

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Peter Bross

Aarhus University(DK)Aarhus University Hospital(DK)

Publications by Year

Research Areas

Metabolism and Genetic Disorders, Heat shock proteins research, Mitochondrial Function and Pathology, Biochemical and Molecular Research, Endoplasmic Reticulum Stress and Disease

Most-Cited Works

→ Measuring Therapeutic Response in Chronic Graft-versus-Host Disease: National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: IV. Response Criteria Working Group Report(2006)564 cited
→ α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy(1999)394 cited
→ Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60(2002)368 cited
→ Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency(1999)300 cited
→ Protein Misfolding and Human Disease(2006)298 cited
→ Protein misfolding and degradation in genetic diseases(1999)241 cited

→ Clear relationship betweenETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency(2003)233 cited

→ Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency*(2001)232 cited

→ Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy(2008)210 cited

→ Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship(2001)198 cited