Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion L Montermini, A Richeter, K Morgan, CM Justice, D Julien, B Castellotti, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 303 | 1997 |
Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus CM Justice, NH Miller, B Marosy, J Zhang, AF Wilson Spine 28 (6), 589-594, 2003 | 266 | 2003 |
Identification of candidate regions for familial idiopathic scoliosis NH Miller, CM Justice, B Marosy, KF Doheny, E Pugh, J Zhang, ... Spine 30 (10), 1181-1187, 2005 | 201 | 2005 |
Idiopathic scoliosis: identification of candidate regions on chromosome 19p13 KJ Alden, B Marosy, N Nzegwu, CM Justice, AF Wilson, NH Miller Spine 31 (16), 1815-1819, 2006 | 147 | 2006 |
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9 CM Justice, G Yagnik, Y Kim, I Peter, EW Jabs, M Erazo, X Ye, ... Nature genetics 44 (12), 1360-1364, 2012 | 136 | 2012 |
Lack of association between the aggrecan gene and familial idiopathic scoliosis B Marosy, CM Justice, N Nzegwu, G Kumar, AF Wilson, NH Miller Spine 31 (13), 1420-1425, 2006 | 58 | 2006 |
Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13. 3, and 13q32 NH Miller, B Marosy, CM Justice, SM Novak, EY Tang, P Boyce, ... American Journal of Medical Genetics Part A 140 (10), 1059-1068, 2006 | 55 | 2006 |
Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31. 3–q34. 3 and 16p12. 3–q22. 2 NH Miller, CM Justice, B Marosy, K Swindle, Y Kim, MH Roy-Gagnon, ... Human heredity 74 (1), 36-44, 2012 | 49 | 2012 |
A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21 SA Boyadjiev, CM Justice, W Eyaid, VA McKusick, RS Lachman, ... Human genetics 113, 1-9, 2003 | 40 | 2003 |
Identification of susceptibility loci for scoliosis in FIS families with triple curves B Marosy, CM Justice, C Vu, A Zorn, N Nzegwu, AF Wilson, NH Miller American Journal of Medical Genetics Part A 152 (4), 846-855, 2010 | 38 | 2010 |
Phylogenetic analysis of the Friedreich ataxia GAA trinucleotide repeat CM Justice, Z Den, SV Nguyen, M Stoneking, PL Deininger, MA Batzer, ... Journal of Molecular Evolution 52, 232-238, 2001 | 38 | 2001 |
Comparison of year-of-exam-and age-matched estimates of heritability in the Framingham Heart Study data RA Mathias, MH Roy-Gagnon, CM Justice, GJ Papanicolaou, YT Fan, ... BMC genetics 4, 1-4, 2003 | 26 | 2003 |
Males with familial idiopathic scoliosis: a distinct phenotypic subgroup M Clough, CM Justice, B Marosy, NH Miller Spine 35 (2), 162-168, 2010 | 25 | 2010 |
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis CM Justice, A Cuellar, K Bala, JA Sabourin, ML Cunningham, K Crawford, ... Human genetics 139, 1077-1090, 2020 | 23 | 2020 |
CHD7 gene polymorphisms and familial idiopathic scoliosis MK Tilley, CM Justice, K Swindle, B Marosy, AF Wilson, NH Miller Spine 38 (22), E1432-E1436, 2013 | 21 | 2013 |
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis A Cuellar, K Bala, L Di Pietro, M Barba, G Yagnik, JL Liu, C Stevens, ... Bone 137, 115395, 2020 | 20 | 2020 |
A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non‐coding element CM Justice, J Kim, SD Kim, K Kim, G Yagnik, A Cuellar, B Carrington, ... American Journal of Medical Genetics Part A 173 (11), 2893-2897, 2017 | 17 | 2017 |
Sequencing of the TBX6 gene in families with familial idiopathic scoliosis EE Baschal, K Swindle, CM Justice, RM Baschal, A Perera, CI Wethey, ... Spine deformity 3 (4), 288-296, 2015 | 15 | 2015 |
Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis CM Justice, K Bishop, B Carrington, JC Mullikin, K Swindle, B Marosy, ... G3: Genes, Genomes, Genetics 6 (6), 1707-1712, 2016 | 13 | 2016 |
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data CL Simpson, CM Justice, M Krishnan, R Wojciechowski, H Sung, J Cai, ... BMC proceedings 5, 1-6, 2011 | 13 | 2011 |