| Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ... Genome research 18 (9), 1433-1445, 2008 | 902 | 2008 |
| Tiny RNAs associated with transcription start sites in animals RJ Taft, EA Glazov, N Cloonan, C Simons, S Stephen, GJ Faulkner, ... Nature genetics 41 (5), 572-578, 2009 | 434 | 2009 |
| The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line Nature genetics 41 (5), 553-562, 2009 | 418 | 2009 |
| Effect of 5'UTR introns on gene expression in Arabidopsis thaliana BYW Chung, C Simons, AE Firth, CM Brown, RP Hellens BMC genomics 7, 1-13, 2006 | 257 | 2006 |
| Expression of distinct RNAs from 3′ untranslated regions TR Mercer, D Wilhelm, ME Dinger, G Solda, DJ Korbie, EA Glazov, ... Nucleic acids research 39 (6), 2393-2403, 2011 | 241 | 2011 |
| A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum C Simons, NI Wolf, N McNeil, L Caldovic, JM Devaney, A Takanohashi, ... The American Journal of Human Genetics 92 (5), 767-773, 2013 | 205 | 2013 |
| Nuclear-localized tiny RNAs are associated with transcription initiation and splice sites in metazoans RJ Taft, C Simons, S Nahkuri, H Oey, DJ Korbie, TR Mercer, J Holst, ... Nature structural & molecular biology 17 (8), 1030-1034, 2010 | 200 | 2010 |
| A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies S Parikh, G Bernard, RJ Leventer, MS van der Knaap, J van Hove, ... Molecular genetics and metabolism 114 (4), 501-515, 2015 | 197 | 2015 |
| Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity RJ Taft, A Vanderver, RJ Leventer, SA Damiani, C Simons, SM Grimmond, ... The American Journal of Human Genetics 92 (5), 774-780, 2013 | 192 | 2013 |
| Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms TA Forbes, SE Howden, K Lawlor, B Phipson, J Maksimovic, L Hale, ... The American Journal of Human Genetics 102 (5), 816-831, 2018 | 176 | 2018 |
| Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III I Thiffault, NI Wolf, D Forget, K Guerrero, LT Tran, K Choquet, ... Nature communications 6 (1), 7623, 2015 | 160 | 2015 |
| Whole exome sequencing in patients with white matter abnormalities A Vanderver, C Simons, G Helman, J Crawford, NI Wolf, G Bernard, ... Annals of neurology 79 (6), 1031-1037, 2016 | 146 | 2016 |
| Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy C Simons, LD Rash, J Crawford, L Ma, B Cristofori-Armstrong, D Miller, ... Nature genetics 47 (1), 73-77, 2015 | 145 | 2015 |
| Transposon-free regions in mammalian genomes C Simons, M Pheasant, IV Makunin, JS Mattick Genome research 16 (2), 164-172, 2006 | 143 | 2006 |
| Evolution, biogenesis and function of promoter-associated RNAs RJ Taft, CD Kaplan, C Simons, JS Mattick Cell cycle 8 (15), 2332-2338, 2009 | 136 | 2009 |
| Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect C Simons, LB Griffin, G Helman, G Golas, A Pizzino, M Bloom, ... The American Journal of Human Genetics 96 (4), 675-681, 2015 | 124 | 2015 |
| Bi-allelic CSF1R mutations cause skeletal dysplasia of dysosteosclerosis-pyle disease spectrum and degenerative encephalopathy with brain malformation L Guo, DR Bertola, A Takanohashi, A Saito, Y Segawa, T Yokota, ... The American Journal of Human Genetics 104 (5), 925-935, 2019 | 107 | 2019 |
| Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype–phenotype correlation EM Hamilton, E Polder, A Vanderver, S Naidu, R Schiffmann, K Fisher, ... Brain 137 (7), 1921-1930, 2014 | 104 | 2014 |
| Mural lymphatic endothelial cells regulate meningeal angiogenesis in the zebrafish NI Bower, K Koltowska, C Pichol-Thievend, I Virshup, S Paterson, ... Nature neuroscience 20 (6), 774-783, 2017 | 92 | 2017 |
| Whole exome sequencing in family trios reveals de novo mutations in PURA as a cause of severe neurodevelopmental delay and learning disability D Hunt, RJ Leventer, C Simons, R Taft, KJ Swoboda, M Gawne-Cain, ... Journal of medical genetics 51 (12), 806-813, 2014 | 91 | 2014 |
Ryan TaftVice President Scientific Research, Illumina Inc.Verified email at illumina.com
