| MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes BL Cantarel, I Korf, SMC Robb, G Parra, E Ross, B Moore, C Holt, ... Genome research 18 (1), 188-196, 2008 | 2025 | 2008 |
| Genome annotation and curation using MAKER and MAKER‐P MS Campbell, C Holt, B Moore, M Yandell Current protocols in bioinformatics 48 (1), 4.11. 1-4.11. 39, 2014 | 711 | 2014 |
| Genome sequence of the necrotrophic plant pathogen Pythium ultimum reveals original pathogenicity mechanisms and effector repertoire CA Lévesque, H Brouwer, L Cano, JP Hamilton, C Holt, E Huitema, ... Genome biology 11, 1-22, 2010 | 443 | 2010 |
| Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency AF Rope, K Wang, R Evjenth, J Xing, JJ Johnston, JJ Swensen, ... The American Journal of Human Genetics 89 (1), 28-43, 2011 | 302 | 2011 |
| A probabilistic disease-gene finder for personal genomes M Yandell, C Huff, H Hu, M Singleton, B Moore, J Xing, LB Jorde, ... Genome research 21 (9), 1529-1542, 2011 | 269 | 2011 |
| Comparison of approaches for rational siRNA design leading to a new efficient and transparent method O Matveeva, Y Nechipurenko, L Rossi, B Moore, P Sætrom, AY Ogurtsov, ... Nucleic acids research 35 (8), e63, 2007 | 194 | 2007 |
| VAAST 2.0: Improved variant classification and disease‐gene identification using a conservation‐controlled amino acid substitution matrix H Hu, CD Huff, B Moore, S Flygare, MG Reese, M Yandell Genetic epidemiology 37 (6), 622-634, 2013 | 178 | 2013 |
| The maize mitochondrial genome: dynamic, yet functional C Fauron, M Casper, Y Gao, B Moore TRENDS in Genetics 11 (6), 228-235, 1995 | 171 | 1995 |
| Quantitative measures for the management and comparison of annotated genomes K Eilbeck, B Moore, C Holt, M Yandell BMC bioinformatics 10, 1-15, 2009 | 169 | 2009 |
| Quadruplet codons: implications for code expansion and the specification of translation step size B Moore, BC Persson, CC Nelson, RF Gesteland, JF Atkins Journal of molecular biology 298 (2), 195-209, 2000 | 151 | 2000 |
| An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ... Genome biology 15, 1-18, 2014 | 127 | 2014 |
| A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data H Hu, JC Roach, H Coon, SL Guthery, KV Voelkerding, RL Margraf, ... Nature biotechnology 32 (7), 663-669, 2014 | 118 | 2014 |
| Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases FM De La Vega, S Chowdhury, B Moore, E Frise, J McCarthy, ... Genome Medicine 13, 1-19, 2021 | 115 | 2021 |
| A standard variation file format for human genome sequences MG Reese, B Moore, C Batchelor, F Salas, F Cunningham, GT Marth, ... Genome biology 11, 1-9, 2010 | 108 | 2010 |
| A functional–1 ribosomal frameshift signal in the human paraneoplastic Ma3 gene NM Wills, B Moore, A Hammer, RF Gesteland, JF Atkins Journal of Biological Chemistry 281 (11), 7082-7088, 2006 | 101 | 2006 |
| Coordinated control of senescence by lncRNA and a novel T-box3 co-repressor complex P Kumar P, U Emechebe, R Smith, S Franklin, B Moore, M Yandell, ... Elife 3, e02805, 2014 | 93 | 2014 |
| Uteroplacental insufficiency increases visceral adiposity and visceral adipose PPARγ2 expression in male rat offspring prior to the onset of obesity LA Joss-Moore, Y Wang, MS Campbell, B Moore, X Yu, CW Callaway, ... Early Human Development 86 (3), 179-185, 2010 | 81 | 2010 |
| Novel venom peptides from the cone snail Conus pulicarius discovered through next-generation sequencing of its venom duct transcriptome AO Lluisma, BA Milash, B Moore, BM Olivera, PK Bandyopadhyay Marine Genomics 5, 43-51, 2012 | 80 | 2012 |
| Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications GJ Lyon, T Jiang, R Van Wijk, W Wang, PM Bodily, J Xing, L Tian, ... Discovery medicine 12 (62), 41, 2011 | 78 | 2011 |
| Identification of polycystic kidney disease 1 like 1 gene variants in children with biliary atresia splenic malformation syndrome JP Berauer, AI Mezina, DT Okou, A Sabo, DM Muzny, RA Gibbs, ... Hepatology 70 (3), 899-910, 2019 | 77 | 2019 |
Mark YandellProfessor of Human Genetics, University of UtahVerified email at genetics.utah.edu
