| Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans DG MacArthur, JT Seto, JM Raftery, KG Quinlan, GA Huttley, JW Hook, ... Nature genetics 39 (10), 1261-1265, 2007 | 398 | 2007 |
| An Actn3 knockout mouse provides mechanistic insights into the association between α-actinin-3 deficiency and human athletic performance DG MacArthur, JT Seto, S Chan, KGR Quinlan, JM Raftery, N Turner, ... Human molecular genetics 17 (8), 1076-1086, 2008 | 365 | 2008 |
| Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding GE Martyn, B Wienert, L Yang, M Shah, LJ Norton, J Burdach, R Kurita, ... Nature genetics 50 (4), 498-503, 2018 | 287 | 2018 |
| Normative reference values for strength and flexibility of 1,000 children and adults MJ McKay, JN Baldwin, P Ferreira, M Simic, N Vanicek, J Burns, ... Neurology 88 (1), 36-43, 2017 | 276 | 2017 |
| Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy M Yuen, SA Sandaradura, JJ Dowling, AS Kostyukova, N Moroz, ... The Journal of clinical investigation 124 (11), 4693-4708, 2014 | 183 | 2014 |
| ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling JT Seto, KGR Quinlan, M Lek, XF Zheng, F Garton, DG MacArthur, ... The Journal of clinical investigation 123 (10), 4255-4263, 2013 | 170 | 2013 |
| Human KLF17 is a new member of the Sp/KLF family of transcription factors J Van Vliet, LA Crofts, KGR Quinlan, R Czolij, AC Perkins, M Crossley Genomics 87 (4), 474-482, 2006 | 150 | 2006 |
| Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling JT Seto, M Lek, KGR Quinlan, PJ Houweling, XF Zheng, F Garton, ... Human molecular genetics 20 (15), 2914-2927, 2011 | 139 | 2011 |
| Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin B Wienert, APW Funnell, LJ Norton, RCM Pearson, LE Wilkinson-White, ... Nature communications 6 (1), 7085, 2015 | 137 | 2015 |
| Wake-up sleepy gene: reactivating fetal globin for β-hemoglobinopathies B Wienert, GE Martyn, APW Funnell, KGR Quinlan, M Crossley Trends in Genetics 34 (12), 927-940, 2018 | 124 | 2018 |
| α-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle KGR Quinlan, JT Seto, N Turner, A Vandebrouck, M Floetenmeyer, ... Human molecular genetics 19 (7), 1335-1346, 2010 | 123 | 2010 |
| Reference values for developing responsive functional outcome measures across the lifespan MJ McKay, JN Baldwin, P Ferreira, M Simic, N Vanicek, J Burns, ... Neurology 88 (16), 1512-1519, 2017 | 113 | 2017 |
| Specific recognition of ZNF217 and other zinc finger proteins at a surface groove of C-terminal binding proteins KGR Quinlan, M Nardini, A Verger, P Francescato, P Yaswen, D Corda, ... Molecular and cellular biology, 2006 | 107 | 2006 |
| Mechanisms directing the nuclear localization of the CtBP family proteins A Verger, KGR Quinlan, LA Crofts, S Spanò, D Corda, EPW Kable, F Braet, ... Molecular and cellular biology 26 (13), 4882-4894, 2006 | 100 | 2006 |
| KLF1 drives the expression of fetal hemoglobin in British HPFH B Wienert, GE Martyn, R Kurita, Y Nakamura, KGR Quinlan, M Crossley Blood, The Journal of the American Society of Hematology 130 (6), 803-807, 2017 | 99 | 2017 |
| How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the ‘gene for speed’ FXZ Lee, PJ Houweling, KN North, KGR Quinlan Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1863 (4), 686-693, 2016 | 98 | 2016 |
| Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle KC Thomas, XF Zheng, F Garces Suarez, JM Raftery, KGR Quinlan, ... PloS one 9 (2), e88653, 2014 | 82 | 2014 |
| Amplification of zinc finger gene 217 (ZNF217) and cancer: when good fingers go bad KGR Quinlan, A Verger, P Yaswen, M Crossley Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 1775 (2), 333-340, 2007 | 82 | 2007 |
| Role of the C-terminal binding protein PXDLS motif binding cleft in protein interactions and transcriptional repression KGR Quinlan, A Verger, A Kwok, SHY Lee, J Perdomo, M Nardini, ... Molecular and cellular biology 26 (21), 8202-8213, 2006 | 75 | 2006 |
| Copper binding is the governing determinant of prion protein turnover CL Haigh, K Edwards, DR Brown Molecular and Cellular Neuroscience 30 (2), 186-196, 2005 | 71 | 2005 |
Merlin CrossleyUNSW SydneyE-mail megerősítve itt: unsw.edu.au