| Standardizing global gene expression analysis between laboratories and across platforms Toxicogenomics Research Consortium Weis BK weis@ niehs. nih. gov 1 b Nature methods 2 (5), 351-356, 2005 | 602 | 2005 |
| Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of α-synuclein G Wang, JM van der Walt, G Mayhew, YJ Li, S Züchner, WK Scott, ... The American Journal of Human Genetics 82 (2), 283-289, 2008 | 571 | 2008 |
| Age at onset in two common neurodegenerative diseases is genetically controlled YJ Li, WK Scott, DJ Hedges, F Zhang, PC Gaskell, MA Nance, RL Watts, ... The American Journal of Human Genetics 70 (4), 985-993, 2002 | 384 | 2002 |
| Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease GW Beecham, ER Martin, YJ Li, MA Slifer, JR Gilbert, JL Haines, ... The American Journal of Human Genetics 84 (1), 35-43, 2009 | 325 | 2009 |
| Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease YJ Li, SA Oliveira, P Xu, ER Martin, JE Stenger, CR Scherzer, MA Hauser, ... Human molecular genetics 12 (24), 3259-3267, 2003 | 305 | 2003 |
| A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25 PG Hysi, TL Young, DA Mackey, T Andrew, A Fernández-Medarde, ... Nature genetics 42 (10), 902-905, 2010 | 283 | 2010 |
| Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p SA Riazuddin, NA Zaghloul, A Al-Saif, L Davey, BH Diplas, DN Meadows, ... The American Journal of Human Genetics 86 (1), 45-53, 2010 | 205 | 2010 |
| Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism MA Hauser, YJ Li, H Xu, MA Noureddine, YS Shao, SR Gullans, ... Archives of neurology 62 (6), 917-921, 2005 | 191 | 2005 |
| Synovial fluid biomarkers associated with osteoarthritis severity reflect macrophage and neutrophil related inflammation CA Haraden, JL Huebner, MF Hsueh, YJ Li, VB Kraus Arthritis research & therapy 21, 1-9, 2019 | 175 | 2019 |
| Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders L Zhu, X Wang, XL Li, A Towers, X Cao, P Wang, R Bowman, H Yang, ... Human molecular genetics 23 (6), 1563-1578, 2014 | 171 | 2014 |
| Apolipoprotein E controls the risk and age at onset of Parkinson disease YJ Li, MA Hauser, WK Scott, ER Martin, MW Booze, XJ Qin, JW Walter, ... Neurology 62 (11), 2005-2009, 2004 | 171 | 2004 |
| Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease JM Van Der Walt, MA Noureddine, R Kittappa, MA Hauser, WK Scott, ... The American Journal of Human Genetics 74 (6), 1121-1127, 2004 | 170 | 2004 |
| Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness Y Lu, DP Dimasi, PG Hysi, AW Hewitt, KP Burdon, TY Toh, JB Ruddle, ... PLoS genetics 6 (5), e1000947, 2010 | 168 | 2010 |
| Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese YJ Li, L Goh, CC Khor, Q Fan, M Yu, S Han, X Sim, RTH Ong, TY Wong, ... Ophthalmology 118 (2), 368-375, 2011 | 163 | 2011 |
| Genome-wide association identifies ATOH7 as a major gene determining human optic disc size S Macgregor, AW Hewitt, PG Hysi, JB Ruddle, SE Medland, AK Henders, ... Human molecular genetics 19 (13), 2716-2724, 2010 | 161 | 2010 |
| Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays AE Dellinger, SM Saw, LK Goh, M Seielstad, TL Young, YJ Li Nucleic acids research 38 (9), e105-e105, 2010 | 153 | 2010 |
| Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage MA Hauser, YJ Li, S Takeuchi, R Walters, M Noureddine, M Maready, ... Human molecular genetics 12 (6), 671-677, 2003 | 139 | 2003 |
| Mutations in SCO2 are associated with autosomal-dominant high-grade myopia KN Tran-Viet, C Powell, VA Barathi, T Klemm, S Maurer-Stroh, ... The American Journal of Human Genetics 92 (5), 820-826, 2013 | 138 | 2013 |
| Platelet counts, acute kidney injury, and mortality after coronary artery bypass grafting surgery MD Kertai, S Zhou, JA Karhausen, M Cooter, E Jooste, YJ Li, WD White, ... Anesthesiology 124 (2), 339, 2016 | 137 | 2016 |
| Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy NA Afshari, RP Igo Jr, NJ Morris, D Stambolian, S Sharma, VL Pulagam, ... Nature communications 8 (1), 14898, 2017 | 134 | 2017 |
Eden MartinProfessor of Human Genetics, University of MiamiΗ διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα med.miami.edu
