| Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ... Nature genetics 45 (3), 314-318, 2013 | 532 | 2013 |
| Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration CL Simpson, R Lemmens, K Miskiewicz, WJ Broom, VK Hansen, ... Human molecular genetics 18 (3), 472-481, 2009 | 348 | 2009 |
| Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error MS Tedja, R Wojciechowski, PG Hysi, N Eriksson, NA Furlotte, ... Nature genetics 50 (6), 834-848, 2018 | 300 | 2018 |
| 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 | 257 | 2014 |
| Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis JE Landers, J Melki, V Meininger, JD Glass, LH Van Den Berg, ... Proceedings of the National Academy of Sciences 106 (22), 9004-9009, 2009 | 227 | 2009 |
| Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ... The American Journal of Human Genetics 93 (2), 264-277, 2013 | 187 | 2013 |
| Using high-throughput SNP technologies to study cancer LJ Engle, CL Simpson, JE Landers Oncogene 25 (11), 1594-1601, 2006 | 165 | 2006 |
| Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height MB Lanktree, Y Guo, M Murtaza, JT Glessner, SD Bailey, ... The American Journal of Human Genetics 88 (1), 6-18, 2011 | 164 | 2011 |
| Genome-wide Association Study Identifies African-Specific Susceptibility Loci in African Americans with Inflammatory Bowel Disease SR Brant, DT Okou, CL Simpson, DJ Cutler, T Haritunians, JP Bradfield, ... Gastroenterology, 2016 | 144 | 2016 |
| Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error Q Fan, VJM Verhoeven, R Wojciechowski, VA Barathi, PG Hysi, ... Nature communications 7 (1), 11008, 2016 | 141 | 2016 |
| Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium Q Fan, X Guo, JWL Tideman, KM Williams, S Yazar, SM Hosseini, ... Scientific reports 6 (1), 25853, 2016 | 120 | 2016 |
| Amyotrophic lateral sclerosis as a complex genetic disease CL Simpson, A Al-Chalabi Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1762 (11-12 …, 2006 | 118 | 2006 |
| Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium VJM Verhoeven, PG Hysi, SM Saw, V Vitart, A Mirshahi, JA Guggenheim, ... Human genetics 131, 1467-1480, 2012 | 105 | 2012 |
| Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans C Huang, T Haritunians, DT Okou, DJ Cutler, ME Zwick, KD Taylor, ... Gastroenterology 149 (6), 1575-1586, 2015 | 86 | 2015 |
| Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with … D Stambolian, R Wojciechowski, K Oexle, M Pirastu, X Li, LJ Raffel, ... Human molecular genetics 22 (13), 2754-2764, 2013 | 78 | 2013 |
| Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study G Cuellar-Partida, KM Williams, S Yazar, JA Guggenheim, AW Hewitt, ... International journal of epidemiology 46 (6), 1882-1890, 2017 | 73 | 2017 |
| A recurrent mutation in PARK2 is associated with familial lung cancer D Xiong, Y Wang, E Kupert, C Simpson, SM Pinney, CR Gaba, D Mandal, ... The American Journal of Human Genetics 96 (2), 301-308, 2015 | 71 | 2015 |
| Fetal—Not Maternal—APOL1 Genotype Associated with Risk for Preeclampsia in Those with African Ancestry KJ Reidy, RC Hjorten, CL Simpson, AZ Rosenberg, SD Rosenblum, ... The American Journal of Human Genetics 103 (3), 367-376, 2018 | 64 | 2018 |
| Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci CL Simpson, R Wojciechowski, K Oexle, F Murgia, L Portas, X Li, ... PloS one 9 (9), e107110, 2014 | 64 | 2014 |
| Determination of the Allelic Frequency in Smith‐Lemli‐Opitz Syndrome by Analysis of Massively Parallel Sequencing Data Sets JL Cross, J Iben, C Simpson, A Thurm, S Swedo, E Tierney, ... Clinical genetics, 2014 | 62 | 2014 |
Joan E. Bailey-WilsonBranch Chief, National Human Genome Research Institute, National Institutes of HealthVerified email at mail.nih.gov
