Ronald Wanders

Author PubWeight™ 9.92^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I.	Cell Metab	2010	2.21
2	Biochemical aspects of X-linked adrenoleukodystrophy.	Brain Pathol	2010	1.34
3	MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency.	J Pediatr	2003	1.33
4	Peroxisomal alterations in Alzheimer's disease.	Acta Neuropathol	2011	1.06
5	Valproic acid induces antioxidant effects in X-linked adrenoleukodystrophy.	Hum Mol Genet	2010	1.03
6	Peroxisomal disorders.	Handb Clin Neurol	2013	0.95
7	Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene Mutations.	JIMD Rep	2012	0.91
8	Complex lipids.	J Inherit Metab Dis	2015	0.80
9	D-bifunctional protein deficiency associated with drug resistant infantile spasms.	Brain Dev	2006	0.76
10	Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit".	Clin Neurol Neurosurg	2013	0.75
11	[Sjogren-Larsson syndrome: two cases with delayed diagnosis].	Ann Med Interne (Paris)	2002	0.75
12	Rapid prenatal diagnosis of fetal Zellweger syndrome by biochemical tests, complementation studies, and molecular analyses.	Prenat Diagn	2013	0.75
13	[A novel mutation in PEX 26 gene in Zellweger syndrome: a case report].	Tunis Med	2011	0.75