| Defining the role of common variation in the genomic and biological architecture of adult human height AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ... Nature genetics 46 (11), 1173-1186, 2014 | 2201 | 2014 |
| Biological interpretation of genome-wide association studies using predicted gene functions TH Pers, JM Karjalainen, Y Chan, HJ Westra, AR Wood, J Yang, JC Lui, ... Nature communications 6, 2015 | 902 | 2015 |
| Mechanisms limiting body growth in mammals JC Lui, J Baron Endocrine reviews 32 (3), 422-440, 2011 | 196 | 2011 |
| An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs JC Lui, GP Finkielstain, KM Barnes, J Baron American Journal of Physiology-Regulatory, Integrative and Comparative …, 2008 | 174 | 2008 |
| Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations O Nilsson, MH Guo, N Dunbar, J Popovic, D Flynn, C Jacobsen, JC Lui, ... The Journal of Clinical Endocrinology & Metabolism 99 (8), E1510-E1518, 2014 | 139 | 2014 |
| EZH1 and EZH2 promote skeletal growth by repressing inhibitors of chondrocyte proliferation and hypertrophy JC Lui, P Garrison, Q Nguyen, M Ad, C Keembiyehetty, W Chen, YH Jee, ... Nature Communications 7, 13685, 2016 | 111 | 2016 |
| Recent research on the growth plate: Recent insights into the regulation of the growth plate JC Lui, O Nilsson, J Baron Journal of molecular endocrinology 53 (1), T1-T9, 2014 | 105 | 2014 |
| Heat shock protein 70 inhibits the nuclear import of apoptosis-inducing factor to avoid DNA fragmentation in TF-1 cells during erythropoiesis JCK Lui, SK Kong FEBS letters 581 (1), 109-117, 2007 | 99 | 2007 |
| Growth plate senescence and catch-up growth JC Lui, O Nilsson, J Baron Karger Publishers 21, 23-29, 2011 | 94 | 2011 |
| An extensive genetic program occurring during postnatal growth in multiple tissues GP Finkielstain, P Forcinito, JCK Lui, KM Barnes, R Marino, S Makaroun, ... Endocrinology 150 (4), 1791-1800, 2009 | 94 | 2009 |
| Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein A Dauber, SH LaFranchi, Z Maliga, JC Lui, JE Moon, C McDeed, K Henke, ... The Journal of Clinical Endocrinology & Metabolism 97 (11), E2140-E2151, 2012 | 93 | 2012 |
| Copy number variants in patients with short stature. HA van Duyvenvoorde, JC Lui, SG Kant, W Oostdijk, AC Gijsbers, ... European journal of human genetics: EJHG 22 (5), 602-609, 2014 | 91 | 2014 |
| Synthesizing genome-wide association studies and expression microarray reveals novel genes that act in the human growth plate to modulate height JC Lui, O Nilsson, Y Chan, CD Palmer, AC Andrade, JN Hirschhorn, ... Human molecular genetics 21 (23), 5193-5201, 2012 | 84 | 2012 |
| Spatial and temporal regulation of gene expression in the mammalian growth plate JCK Lui, AC Andrade, P Forcinito, A Hegde, WP Chen, J Baron, O Nilsson Bone 46 (5), 1380-1390, 2010 | 83 | 2010 |
| Differential aging of growth plate cartilage underlies differences in bone length and thus helps determine skeletal proportions JC Lui, YH Jee, P Garrison, JR Iben, S Yue, M Ad, Q Nguyen, B Kikani, ... PLoS biology 16 (7), e2005263, 2018 | 75 | 2018 |
| Organization of the Indian hedgehog–parathyroid hormone-related protein system in the postnatal growth plate M Chau, P Forcinito, AC Andrade, A Hegde, S Ahn, JC Lui, J Baron, ... Journal of molecular endocrinology 47 (1), 99-107, 2011 | 71 | 2011 |
| Effects of glucocorticoids on the growth plate JC Lui, J Baron Karger Publishers 20, 187-193, 2011 | 69 | 2011 |
| Cordycepin induced eryptosis in mouse erythrocytes through a Ca 2+-dependent pathway without caspase-3 activation JCK Lui, JWY Wong, YK Suen, TT Kwok, KP Fung, SK Kong Archives of toxicology 81 (12), 859-865, 2007 | 69 | 2007 |
| Redefining the progeroid form of Ehlers–Danlos syndrome: Report of the fourth patient with B4GALT7 deficiency and review of the literature MH Guo, J Stoler, J Lui, O Nilsson, DW Bianchi, JN Hirschhorn, A Dauber American Journal of Medical Genetics Part A 161 (10), 2519-2527, 2013 | 64 | 2013 |
| Ezh2 mutations found in the Weaver overgrowth syndrome cause a partial loss of H3K27 histone methyltransferase activity JC Lui, KM Barnes, L Dong, S Yue, E Graber, R Rapaport, A Dauber, ... The Journal of Clinical Endocrinology & Metabolism, 2017 | 58 | 2017 |
Crystal CheungScientist, Vaccine Research Center, NIAIDVahvistettu sähköpostiosoite verkkotunnuksessa nih.gov
