Boris Rolinski
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, HIV/AIDS drug development and treatment, HIV Research and Treatment, ATP Synthase and ATPases Research
Most-Cited Works
- → Megalin Knockout Mice as an Animal Model of Low Molecular Weight Proteinuria(1999)440 cited
- → Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency(2010)249 cited
- → Mitochondrial and Cytosolic Branched-chain Amino Acid Transaminases from Yeast, Homologs of the myc Oncogene-regulated Eca39 Protein(1996)171 cited
- → Bilirubin Measurement for Neonates: Comparison of 9 Frequently Used Methods(2006)127 cited
- → Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway(2011)120 cited
- → Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy(2010)118 cited
- → Spectrum of combined respiratory chain defects(2015)116 cited
- → Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency(2015)97 cited
- → Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings(2012)93 cited
- → Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9(2011)91 cited