| X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome GS Salomons, SJM van Dooren, NM Verhoeven, KM Cecil, WS Ball, ... The American Journal of Human Genetics 68 (6), 1497-1500, 2001 | 444 | 2001 |
| Effectiveness of amitriptyline in the prophylactic management of childhood headaches AD Hershey, SW Powers, AL Bentti, TJ DeGrauw Headache: The Journal of Head and Face Pain 40 (7), 539-549, 2000 | 268 | 2000 |
| Neuropsychological status at seizure onset in children: risk factors for early cognitive deficits PS Fastenau, CS Johnson, SM Perkins, AW Byars, TJ DeGrauw, ... Neurology 73 (7), 526-534, 2009 | 265 | 2009 |
| High prevalence of SLC6A8 deficiency in X-linked mental retardation EH Rosenberg, LS Almeida, T Kleefstra, RS deGrauw, HG Yntema, ... The American Journal of Human Genetics 75 (1), 97-105, 2004 | 245 | 2004 |
| HPLC Analysis of Reduced and Oxidized Coenzyme Q10 in Human Plasma PH Tang, MV Miles, A DeGrauw, A Hershey, A Pesce Clinical chemistry 47 (2), 256-265, 2001 | 234 | 2001 |
| Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect? KM Cecil, GS Salomons, WS Ball Jr, B Wong, G Chuck, NM Verhoeven, ... Annals of neurology 49 (3), 401-404, 2001 | 207 | 2001 |
| X‐linked creatine transporter defect: an overview GS Salomons, SJM Van Dooren, NM Verhoeven, D Marsden, C Schwartz, ... Journal of inherited metabolic disease 26 (2-3), 309-318, 2003 | 206 | 2003 |
| Leukaemia in patients treated with growth hormone S Watanabe, Y Tsunematsu, J Fujimoto, A Komiyama, ... The lancet 331 (8595), 1159-1160, 1988 | 197 | 1988 |
| Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations NI Wolf, A Vanderver, RML Van Spaendonk, R Schiffmann, B Brais, ... Neurology 83 (21), 1898-1905, 2014 | 194 | 2014 |
| Seizure frequency and characteristics in children with Down syndrome H Goldberg-Stern, RH Strawsburg, B Patterson, F Hickey, M Bare, ... Brain and Development 23 (6), 375-378, 2001 | 163 | 2001 |
| Age-related changes in plasma coenzyme Q10 concentrations and redox state in apparently healthy children and adults MV Miles, PS Horn, PH Tang, JA Morrison, L Miles, T DeGrauw, AJ Pesce Clinica chimica acta 347 (1-2), 139-144, 2004 | 129 | 2004 |
| Behavior problems in children at time of first recognized seizure and changes over the following 3 years JK Austin, SM Perkins, CS Johnson, PS Fastenau, AW Byars, TJ Degrauw, ... Epilepsy & behavior 21 (4), 373-381, 2011 | 125 | 2011 |
| Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia S Kure, K Kato, A Dinopoulos, C Gail, TJ DeGrauw, J Christodoulou, ... Human mutation 27 (4), 343-352, 2006 | 119 | 2006 |
| Characterization of chronic daily headaches in children in a multidisciplinary headache center AD Hershey, SW Powers, AL Bentti, S LeCates, TJ DeGrauw Neurology 56 (8), 1032-1037, 2001 | 118 | 2001 |
| Fetal growth retardation in rats from different levels of hypoxia TJ de Grauw, RE Myers, WJ Scott Neonatology 49 (2), 85-89, 1986 | 117 | 1986 |
| Creatine transporter (CrT; Slc6a8) knockout mice as a model of human CrT deficiency MR Skelton, TL Schaefer, DL Graham, TJ Degrauw, JF Clark, MT Williams, ... PloS one 6 (1), e16187, 2011 | 116 | 2011 |
| Bioequivalence of coenzyme Q10 from over-the-counter supplements MV Miles, P Horn, L Miles, P Tang, P Steele, T DeGrauw Nutrition research 22 (8), 919-929, 2002 | 114 | 2002 |
| The clinical syndrome of creatine transporter deficiency TJ deGrauw, KM Cecil, AW Byars, GS Salomons, WS Ball, C Jakobs Guanidino Compounds in Biology and Medicine, 45-48, 2003 | 113 | 2003 |
| Congenital creatine transporter deficiency TJ DeGrauw, GS Salomons, KM Cecil, G Chuck, A Newmeyer, ... Neuropediatrics 33 (05), 232-238, 2002 | 113 | 2002 |
| Fine motor function and oral-motor imitation skills in preschool-age children with speech-sound disorders AJ Newmeyer, S Grether, C Grasha, J White, R Akers, C Aylward, ... Clinical pediatrics 46 (7), 604-611, 2007 | 112 | 2007 |
