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
1337 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
805 2013 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
Nature genetics 42 (2), 123-127, 2010
697 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
581 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
482 2011 WNT16 Influences Bone Mineral Density, Cortical Bone Thickness, Bone Strength, and Osteoporotic Fracture RiskHF Zheng, JH Tobias, E Duncan, DM Evans, J Eriksson, L Paternoster, ...
PLoS genetics 8 (7), e1002745, 2012
320 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
316 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
294 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
267 2014 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
253 2017 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
251 2013 Collision Properties of Ultracold PJ Leo, CJ Williams, PS Julienne
Physical review letters 85 (13), 2721, 2000
247 2000 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
241 2008 Precision Feshbach spectroscopy of ultracold C Chin, V Vuletić, AJ Kerman, S Chu, E Tiesinga, PJ Leo, CJ Williams
Physical Review A—Atomic, Molecular, and Optical Physics 70 (3), 032701, 2004
241 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
176 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
174 2006 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
141 2015 Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study PJ Leo, MM Madeleine, S Wang, SM Schwartz, F Newell, ...
PLoS genetics 13 (8), e1006866, 2017
140 2017 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
139 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
138 2013 