| A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice Y Yang, L Wang, P Bell, D McMenamin, Z He, J White, H Yu, C Xu, ... Nature biotechnology 34 (3), 334-338, 2016 | 619 | 2016 |
| Adeno-associated virus antibody profiles in newborns, children, and adolescents R Calcedo, H Morizono, L Wang, R McCarter, J He, D Jones, ML Batshaw, ... Clinical and Vaccine Immunology 18 (9), 1586-1588, 2011 | 329 | 2011 |
| GFAP mutations, age at onset, and clinical subtypes in Alexander disease M Prust, J Wang, H Morizono, A Messing, M Brenner, E Gordon, T Hartka, ... Neurology 77 (13), 1287-1294, 2011 | 244 | 2011 |
| Baseline human gut microbiota profile in healthy people and standard reporting template CH King, H Desai, AC Sylvetsky, J LoTempio, S Ayanyan, J Carrie, ... PloS one 14 (9), e0206484, 2019 | 189 | 2019 |
| Clinical characterization and prediction of clinical severity of SARS-CoV-2 infection among US adults using data from the US National COVID Cohort Collaborative TD Bennett, RA Moffitt, JG Hajagos, B Amor, A Anand, MM Bissell, ... JAMA network open 4 (7), e2116901-e2116901, 2021 | 184 | 2021 |
| Mutations and Polymorphisms in the Human Ornithine Transcarbamylase (otc) S Yamaguchi, LL Brailey, H Morizono, AE Bale, M Tuchman Human Mutation 27 (7), S1-S15, 2006 | 184* | 2006 |
| Systematic evaluation of AAV vectors for liver directed gene transfer in murine models L Wang, H Wang, P Bell, RJ McCarter, J He, R Calcedo, ... Molecular Therapy 18 (1), 118-125, 2010 | 151 | 2010 |
| The pleiotropic effects of natural AAV infections on liver-directed gene transfer in macaques L Wang, R Calcedo, H Wang, P Bell, R Grant, LH Vandenberghe, ... Molecular Therapy 18 (1), 126-134, 2010 | 149 | 2010 |
| Genotype–phenotype correlations in ornithine transcarbamylase deficiency: a mutation update L Caldovic, I Abdikarim, S Narain, M Tuchman, H Morizono Journal of Genetics and Genomics 42 (5), 181-194, 2015 | 143 | 2015 |
| Mutations and polymorphisms in the human ornithine transcarbamylase gene M Tuchman, N Jaleel, H Morizono, L Sheehy, MG Lynch Human mutation 19 (2), 93-107, 2002 | 142 | 2002 |
| The biochemical and molecular spectrum of ornithine transcarbamylase deficiency M Tuchman, H Morizono, BS Rajagopal, RJ Plante, NM Allewell Journal of inherited metabolic disease 21 (1), 40-58, 1998 | 118 | 1998 |
| Ornithine transcarbamylase deficiency U Lichter-Konecki, L Caldovic, H Morizono, K Simpson, A Mew, ... | 103 | 2022 |
| Long-term correction of ammonia metabolism and prolonged survival in ornithine transcarbamylase-deficient mice following liver-directed treatment with adeno-associated viral … D Moscioni, H Morizono, RJ McCarter, A Stern, J Cabrera-Luque, ... Molecular Therapy 14 (1), 25-33, 2006 | 97 | 2006 |
| Cloning and expression of the human N-acetylglutamate synthase gene L Caldovic, H Morizono, MG Panglao, R Gallegos, X Yu, D Shi, ... Biochemical and biophysical research communications 299 (4), 581-586, 2002 | 97 | 2002 |
| 1.85-Å Resolution Crystal Structure of Human Ornithine Transcarbamoylase Complexed withN-Phosphonacetyl-l-ornithine: CATALYTIC MECHANISM AND CORRELATION WITH INHERITED DEFICIENCY D Shi, H Morizono, Y Ha, M Aoyagi, M Tuchman, NM Allewell Journal of Biological Chemistry 273 (51), 34247-34254, 1998 | 93 | 1998 |
| N-acetylglutamate synthase: structure, function and defects L Caldovic, NA Mew, D Shi, H Morizono, M Yudkoff, M Tuchman Molecular genetics and metabolism 100, S13-S19, 2010 | 76 | 2010 |
| Genetic and clinical heterogeneity in eIF2B-related disorder J Maletkovic, R Schiffmann, JR Gorospe, ES Gordon, M Mintz, ... Journal of child neurology 23 (2), 205-215, 2008 | 75 | 2008 |
| Mammalian N-acetylglutamate synthase H Morizono, L Caldovic, D Shi, M Tuchman Molecular genetics and metabolism 81, 4-11, 2004 | 72 | 2004 |
| Human ornithine transcarbamylase: crystallographic insights into substrate recognition and conformational changes D SHI, H MORIZONO, X YU, L TONG, NM ALLEWELL, M TUCHMAN Biochemical journal 354 (3), 501-509, 2001 | 72 | 2001 |
| Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia L Caldovic, H Morizono, MG Panglao, SF Cheng, S Packman, M Tuchman Human genetics 112, 364-368, 2003 | 69 | 2003 |
Ljubica CaldovicAssociate Professor of Genomics and Precision Medicine, Children's National Medical CenterVerified email at childrensnational.org
