Autism genome-wide copy number variation reveals ubiquitin and neuronal genes JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ... Nature 459 (7246), 569-573, 2009 | 1647 | 2009 |
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1644 | 2007 |
Pax6 3′ deletion results in aniridia, autism and mental retardation LK Davis, KJ Meyer, DS Rudd, AL Librant, EA Epping, VC Sheffield, ... Human genetics 123 (4), 371-378, 2008 | 147 | 2008 |
Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction LP Sowers, L Loo, Y Wu, E Campbell, JD Ulrich, S Wu, L Paemka, ... Molecular psychiatry 18 (10), 1077-1089, 2013 | 110 | 2013 |
Ketamine/Xylazine-Induced Corneal Damage in Mice D Koehn, KJ Meyer, NA Syed, MG Anderson PloS one 10 (7), e0132804, 2015 | 56 | 2015 |
Copy number variations and primary open-angle glaucoma LK Davis, KJ Meyer, EI Schindler, JS Beck, DS Rudd, AJ Grundstad, ... Investigative Ophthalmology & Visual Science 52 (10), 7122-7133, 2011 | 47 | 2011 |
Novel copy number variants in children with autism and additional developmental anomalies LK Davis, KJ Meyer, DS Rudd, AL Librant, EA Epping, VC Sheffield, ... Journal of neurodevelopmental disorders 1 (4), 292-301, 2009 | 47 | 2009 |
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism KJ Meyer, MS Axelsen, VC Sheffield, SR Patil, TH Wassink Psychiatric Genetics 22 (3), 137, 2012 | 43 | 2012 |
Genome-wide analysis of copy number variants in age-related macular degeneration KJ Meyer, LK Davis, EI Schindler, JS Beck, DS Rudd, AJ Grundstad, ... Human genetics 129 (1), 91-100, 2011 | 41 | 2011 |
Conservation genetics of a peripherally isolated population of the wood turtle (Glyptemys insculpta) in Iowa TA Spradling, JW Tamplin, SS Dow, KJ Meyer Conservation Genetics 11 (5), 1667-1677, 2010 | 33 | 2010 |
Identification of chronic brain protein changes and protein targets of serum auto-antibodies after blast-mediated traumatic brain injury MM Harper, D Rudd, KJ Meyer, AG Kanthasamy, V Anantharam, ... Heliyon 6 (2), e03374, 2020 | 27 | 2020 |
Determining the source of fecal contamination in recreational waters. KJ Meyer, CM Appletoft, AK Schwemm, JC Uzoigwe, EJ Brown Journal of environmental health 68 (1), 2005 | 26 | 2005 |
Genetic modifiers as relevant biological variables of eye disorders KJ Meyer, MG Anderson Human molecular genetics 26 (R1), R58-R67, 2017 | 25 | 2017 |
RetFM-J, an ImageJ-based module for automated counting and quantifying features of nuclei in retinal whole-mounts A Hedberg-Buenz, MA Christopher, CJ Lewis, KJ Meyer, DS Rudd, ... Experimental Eye Research 146, 386-392, 2016 | 24 | 2016 |
Effect of ocular hypertension on the pattern of retinal ganglion cell subtype loss in a mouse model of early-onset glaucoma S Daniel, KJ Meyer, AF Clark, MG Anderson, CM McDowell Experimental eye research 185, 107703, 2019 | 22 | 2019 |
Genetic evidence for differential regulation of corneal epithelial and stromal thickness DR Koehn, KJ Meyer, MG Anderson Investigative ophthalmology & visual science 56 (9), 5599-5607, 2015 | 17 | 2015 |
Update on animal models of exfoliation syndrome MG Anderson, KJ Meyer, A Hedberg-Buenz, JH Fingert Journal of glaucoma 27 (Suppl 1), S78, 2018 | 14 | 2018 |
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly RJ Hazlewood, BR Roos, F Solivan‐Timpe, RA Honkanen, LM Jampol, ... Human mutation 36 (3), 369-378, 2015 | 13 | 2015 |
Endothelial BBSome is essential for vascular, metabolic, and retinal functions J Jiang, JJ Reho, S Bhattarai, I Cherascu, A Hedberg-Buenz, KJ Meyer, ... Molecular metabolism 53, 101308, 2021 | 11 | 2021 |
Exome-based investigation of the genetic basis of human pigmentary glaucoma C van der Heide, W Goar, KJ Meyer, WLM Alward, EA Boese, NC Sears, ... BMC genomics 22 (1), 1-12, 2021 | 10 | 2021 |