| Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture K Estrada, U Styrkarsdottir, E Evangelou, YH Hsu, EL Duncan, EE Ntzani, ... Nature genetics 44 (5), 491-501, 2012 | 1289 | 2012 |
| Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci Groupe Française d'Etude Génétique des Spondylarthrites (GFEGS), ... Nature genetics 45 (7), 730-738, 2013 | 746 | 2013 |
| Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci Nature genetics 42 (2), 123-127, 2010 | 666 | 2010 |
| Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ... Nature 526 (7571), 112-117, 2015 | 535 | 2015 |
| Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 KP Burdon, S Macgregor, AW Hewitt, S Sharma, G Chidlow, RA Mills, ... Nature genetics 43 (6), 574-578, 2011 | 462 | 2011 |
| WNT16 Influences Bone Mineral Density, Cortical Bone Thickness, Bone Strength, and Osteoporotic Fracture Risk HF Zheng, JH Tobias, E Duncan, DM Evans, J Eriksson, L Paternoster, ... PLoS genetics 8 (7), e1002745, 2012 | 304 | 2012 |
| Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk EL Duncan, P Danoy, JP Kemp, PJ Leo, E McCloskey, GC Nicholson, ... PLoS genetics 7 (4), e1001372, 2011 | 303 | 2011 |
| Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1 A Cortes, SL Pulit, PJ Leo, JJ Pointon, PC Robinson, MH Weisman, ... Nature communications 6 (1), 7146, 2015 | 267 | 2015 |
| Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ... Nature genetics 46 (10), 1126-1130, 2014 | 252 | 2014 |
| Collision Properties of Ultracold Atoms PJ Leo, CJ Williams, PS Julienne Physical review letters 85 (13), 2721, 2000 | 245 | 2000 |
| Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ... The American Journal of Human Genetics 93 (5), 915-925, 2013 | 236 | 2013 |
| Mitochondrial translocation of α-synuclein is promoted by intracellular acidification NB Cole, D DiEuliis, P Leo, DC Mitchell, RL Nussbaum Experimental cell research 314 (10), 2076-2089, 2008 | 230 | 2008 |
| NAD deficiency, congenital malformations, and niacin supplementation H Shi, A Enriquez, M Rapadas, EMMA Martin, R Wang, J Moreau, CK Lim, ... New England Journal of Medicine 377 (6), 544-552, 2017 | 228 | 2017 |
| Precision Feshbach spectroscopy of ultracold C Chin, V Vuletić, AJ Kerman, S Chu, E Tiesinga, PJ Leo, CJ Williams Physical Review A 70 (3), 032701, 2004 | 227 | 2004 |
| Multistage genome-wide association meta-analyses identified two new loci for bone mineral density L Zhang, HJ Choi, K Estrada, PJ Leo, J Li, YF Pei, Y Zhang, Y Lin, H Shen, ... Human molecular genetics 23 (7), 1923-1933, 2014 | 167 | 2014 |
| Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons A Antonellis, SQ Lee-Lin, A Wasterlain, P Leo, M Quezado, LG Goldfarb, ... Journal of Neuroscience 26 (41), 10397-10406, 2006 | 165 | 2006 |
| Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB A Zankl, EL Duncan, PJ Leo, GR Clark, EA Glazov, MC Addor, T Herlin, ... The American Journal of Human Genetics 90 (3), 494-501, 2012 | 134 | 2012 |
| Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy M Schmidts, J Vodopiutz, S Christou-Savina, CR Cortés, ... The American Journal of Human Genetics 93 (5), 932-944, 2013 | 133 | 2013 |
| Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60 AM McInerney-Leo, M Schmidts, CR Cortés, PJ Leo, B Gener, ... The American Journal of Human Genetics 93 (3), 515-523, 2013 | 130 | 2013 |
| Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis PC Robinson, TAM Claushuis, A Cortes, TM Martin, DM Evans, P Leo, ... Arthritis & rheumatology 67 (1), 140-151, 2015 | 128 | 2015 |
