| Analysis of numerical methods for computer simulation of kinetic processes: development of KINSIM—a flexible, portable system BA Barshop, RF Wrenn, C Frieden Analytical biochemistry 130 (1), 134-145, 1983 | 910 | 1983 |
| Metabolomics reveals signature of mitochondrial dysfunction in diabetic kidney disease K Sharma, B Karl, AV Mathew, JA Gangoiti, CL Wassel, R Saito, M Pu, ... Journal of the American Society of Nephrology 24 (11), 1901-1912, 2013 | 550 | 2013 |
| Multiple organic anion transporters contribute to net renal excretion of uric acid SA Eraly, V Vallon, T Rieg, JA Gangoiti, WR Wikoff, G Siuzdak, ... Physiological genomics 33 (2), 180-192, 2008 | 270 | 2008 |
| Decreased renal organic anion secretion and plasma accumulation of endogenous organic anions in OAT1 knock-out mice SA Eraly, V Vallon, DA Vaughn, JA Gangoiti, K Richter, M Nagle, ... Journal of Biological Chemistry 281 (8), 5072-5083, 2006 | 263 | 2006 |
| Atlas of metabolic diseases second edition WL Nyhan, BA Barshop, PT Ozand CRC Press, 2005 | 261 | 2005 |
| Mitochondrial DNA polymerase γ deficiency and mtDNA depletion in a child with Alpers' syndrome RK Naviaux, WL Nyhan, BA Barshop, J Poulton, D Markusic, ... Annals of Neurology: Official Journal of the American Neurological …, 1999 | 242 | 1999 |
| Agalsidase alfa and kidney dysfunction in Fabry disease M West, K Nicholls, A Mehta, JTR Clarke, R Steiner, M Beck, BA Barshop, ... Journal of the American Society of Nephrology 20 (5), 1132-1139, 2009 | 224 | 2009 |
| Promises and pitfalls of untargeted metabolomics I Gertsman, BA Barshop Journal of inherited metabolic disease 41, 355-366, 2018 | 216 | 2018 |
| Metabolomics identifies perturbations in human disorders of propionate metabolism WR Wikoff, JA Gangoiti, BA Barshop, G SIuzDAK Clinical chemistry 53 (12), 2169-2176, 2007 | 201 | 2007 |
| Autism associated with the mitochondrial DNA G8363A transfer RNALys mutation WD Graf, J Marin-Garcia, HG Gao, S Pizzo, RK Naviaux, D Markusic, ... Journal of child neurology 15 (6), 357-361, 2000 | 190 | 2000 |
| An international classification of inherited metabolic disorders (ICIMD) CR Ferreira, S Rahman, M Keller, J Zschocke, ICIMD Advisory Group, ... Journal of inherited metabolic disease 44 (1), 164-177, 2021 | 170 | 2021 |
| Nonketotic hyperglycinemia WL Nyhan, GF Hoffmann, AI Al-Aqeel, BA Barshop Atlas of Inherited Metabolic Diseases, 192-200, 2020 | 146 | 2020 |
| A mutation in adenylosuccinate lyase associated with mental retardation and autistic features RL Stone, J Aimi, BA Barshop, J Jaeken, G Van den Berghe, H Zalkin, ... Nature genetics 1 (1), 59-63, 1992 | 141 | 1992 |
| Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring S Stockler-Ipsiroglu, C Van Karnebeek, N Longo, GC Korenke, ... Molecular Genetics and Metabolism 111 (1), 16-25, 2014 | 138 | 2014 |
| Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancy JA Wolff, B Barshop, WL Nyhan, J Leslie, JE Seegmiller, H Gruber, ... Pediatric research 26 (2), 140-144, 1989 | 130 | 1989 |
| Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria JL Sloan, JJ Johnston, I Manoli, RJ Chandler, C Krause, ... Nature genetics 43 (9), 883-886, 2011 | 119 | 2011 |
| Effect of DTNB light chain on the interaction of vertebrate skeletal myosin with actin SS Margossian, S Lowey, B Barshop Nature 258 (5531), 163-166, 1975 | 114 | 1975 |
| Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype–phenotype correlation in 38 classical citrullinemia patients HZ Gao, K Kobayashi, A Tabata, H Tsuge, M Iijima, T Yasuda, ... Human mutation 22 (1), 24-34, 2003 | 110 | 2003 |
| Abnormalities of the brain in nonketotic hyperglycinemia: MR manifestations. GA Press, BA Barshop, RH Haas, WL Nyhan, RF Glass, JR Hesselink American journal of neuroradiology 10 (2), 315-321, 1989 | 99 | 1989 |
| A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency GL Arnold, DD Koeberl, D Matern, B Barshop, N Braverman, B Burton, ... Molecular genetics and metabolism 93 (4), 363-370, 2008 | 91 | 2008 |
