Citation Impact
Citing Papers
Human genetic disorders of sphingolipid biosynthesis
2014
Genetics of Neurodegeneration with Brain Iron Accumulation
2011
Fatty acid 2-Hydroxylation in mammalian sphingolipid biology
2009
Changes in Lipidome Composition during Brain Development in Humans, Chimpanzees, and Macaque Monkeys
2017 StandoutNobel
Neurodegeneration with brain iron accumulation — Clinical syndromes and neuroimaging
2011
Sphingolipids and their metabolism in physiology and disease
2017 Standout
The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease
2015 Standout
Making Proteins in the Powerhouse
2014
The genetics and neuropathology of Parkinson’s disease
2012
Mitochondrial dysfunction induces RNA interference in C. elegans through a pathway homologous to the mammalian RIG-I antiviral response
2020 StandoutNobel
Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)
2013
Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy
2011
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA)
2010
Current Concepts and Controversies in Neurodegeneration with Brain Iron Accumulation
2012
The role of iron in brain ageing and neurodegenerative disorders
2014 Standout
The Crystal Structure of an Integral Membrane Fatty Acid α-Hydroxylase
2015
Role of Galactosylceramide and Sulfatide in Oligodendrocytes and CNS Myelin: Formation of a Glycosynapse
2014
A GENERAL REVIEW OF THE ADENOVIKUSES
1962
Epidemiology and etiology of severe infantile diarrhea
1968
OUTBREAK OF INFANTILE GASTROENTERITIS DUE TO TYPE 40 ADENOVIRUS
1983 Standout
Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet
2011 StandoutNobel
An Adenovirus Isolated from the Feces of Mice
1967
Mouse adenovirus: Growth of plaque-purified FL virus in cell lines and characterization of viral DNA
1977 StandoutNobel
Works of Katherine Dick being referenced
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)
2010
Defective Mitochondrial mRNA Maturation Is Associated with Spastic Ataxia
2010
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23
2008
Association between Diarrhoea and Adenovirus Type 7
1960