Kevin Carpenter - Concepedia

Author

Kevin Carpenter

Also Known As

Benn, Carpenter, Kevin, Joachim Campe, K Carpenter, K H Carpenter, K. Carpenter, K. H. Carpenter, K.H. Carpenter, Kent Carpenter, Kevin Carpenter

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Children's Hospital at Westmead The University of Sydney Sydney Children's Hospital Sheffield Children's Hospital UNSW Sydney

About

Kevin Carpenter is an author at Children's Hospital at Westmead specializing in medicine, pediatrics, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	25	1.3K
2	Health Sciences	3	3	241
3	Public Health	3	3	157
4	Engineering	2	2	38
5	Natural Sciences	2	2	145

Kevin Carpenter

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry Bridget Wilcken, Veronica Wiley, Judith Hammond, New England Journal of Medicine	2003	675
Overexpression of Carnitine Palmitoyltransferase-1 in Skeletal Muscle Is Sufficient to Enhance Fatty Acid Oxidation and Improve High-Fat Diet–Induced Insulin Resistance Clinton R. Bruce, Andrew J. Hoy, Nigel Turner, Diabetes	2008	359
Activating HSP72 in Rodent Skeletal Muscle Increases Mitochondrial Number and Oxidative Capacity and Decreases Insulin Resistance Darren C. Henstridge, Clinton R. Bruce, Brian G. Drew, Diabetes Insulin SignalingRat ModelOxidative StressObesityMetabolic Syndrome	2014	195
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud, Brain Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMendelian DisorderNeurological DisorderGenetic Disorder	2013	179
Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years Bridget Wilcken, Marion Haas, Pamela Joy, PEDIATRICS	2009	164
Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia Veronica Wiley, Kevin Carpenter, Bridget Wilcken Acta Paediatrica NutritionNeonatologyDiagnosisConsecutive NewbornsEarly Diagnosis	1999	131
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B Gladys Ho, Atsushi Yonezawa, Satohiro Masuda, Human Mutation Riboflavin TransportRiboflavin TransporterDevelopmental BiologyBiochemistryVitamin B2	2010	120
AAV2/8-mediated Correction of OTC Deficiency Is Robust in Adult but Not Neonatal Spfash Mice Sharon C. Cunningham, Afroditi Spinoulas, Kevin Carpenter, Molecular Therapy	2009	115
Medium-chain acyl-CoA dehydrogenase deficiency: Genotype–biochemical phenotype correlations Leigh B. Waddell, Veronica Wiley, Kevin Carpenter, Molecular Genetics and Metabolism Genotype–biochemical Phenotype CorrelationsBiochemistryGenetic DisorderGeneticsMolecular Genetics	2005	92
Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies Kevin Carpenter, Veronica Wiley, Keow Giak Sim, Archives of Disease in Childhood Fetal & Neonatal	2001	87

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