| The human mitochondrial transcriptome TR Mercer, S Neph, ME Dinger, J Crawford, MA Smith, AMJ Shearwood, ... Cell 146 (4), 645-658, 2011 | 844 | 2011 |
| The Melanoma‐Upregulated Long Noncoding RNA SPRY4-IT1 Modulates Apoptosis and Invasion D Khaitan, ME Dinger, J Mazar, J Crawford, MA Smith, JS Mattick, ... Cancer research 71 (11), 3852-3862, 2011 | 567 | 2011 |
| Targeted RNA sequencing reveals the deep complexity of the human transcriptome TR Mercer, DJ Gerhardt, ME Dinger, J Crawford, C Trapnell, JA Jeddeloh, ... Nature biotechnology 30 (1), 99-104, 2012 | 553 | 2012 |
| SNORD-host RNA Zfas1 is a regulator of mammary development and a potential marker for breast cancer ME Askarian-Amiri, J Crawford, JD French, CE Smart, MA Smith, MB Clark, ... Rna 17 (5), 878-891, 2011 | 377 | 2011 |
| Genome-wide discovery of human splicing branchpoints TR Mercer, MB Clark, SB Andersen, ME Brunck, W Haerty, J Crawford, ... Genome research 25 (2), 290-303, 2015 | 242 | 2015 |
| Host cell invasion by apicomplexan parasites: insights from the co-structure of AMA1 with a RON2 peptide ML Tonkin, M Roques, MH Lamarque, M Pugnière, D Douguet, ... Science 333 (6041), 463-467, 2011 | 230 | 2011 |
| Cloning, characterization, and chromosomal location of a novel human K+-Cl− cotransporter K Hiki, RJ D'Andrea, J Furze, J Crawford, E Woollatt, GR Sutherland, ... Journal of Biological Chemistry 274 (15), 10661-10667, 1999 | 209 | 1999 |
| 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 |
| 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 |
| Targeted sequencing for gene discovery and quantification using RNA CaptureSeq TR Mercer, MB Clark, J Crawford, ME Brunck, DJ Gerhardt, RJ Taft, ... Nature protocols 9 (5), 989-1009, 2014 | 190 | 2014 |
| 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 | 177 | 2018 |
| Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencing MB Clark, TR Mercer, G Bussotti, T Leonardi, KR Haynes, J Crawford, ... Nature methods 12 (4), 339-342, 2015 | 175 | 2015 |
| The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene K Bhalla, HA Phillips, J Crawford, OLD McKenzie, JC Mulley, H Eyre, ... Journal of human genetics 49 (6), 308-311, 2004 | 170 | 2004 |
| 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 | 149 | 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 | 147 | 2016 |
| Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions AM Cleton-Jansen, DF Callen, R Seshadri, S Goldup, B McCallum, ... Cancer Research 61 (3), 1171-1177, 2001 | 140 | 2001 |
| Universal alternative splicing of noncoding exons IW Deveson, ME Brunck, J Blackburn, E Tseng, T Hon, TA Clark, MB Clark, ... Cell systems 6 (2), 245-255. e5, 2018 | 127 | 2018 |
| GPR56, a novel secretin-like human G-protein-coupled receptor gene M Liu, RMC Parker, K Darby, HJ Eyre, NG Copeland, J Crawford, ... Genomics 55 (3), 296-305, 1999 | 126 | 1999 |
| 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 | 125 | 2015 |
| Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16 JA Cavanaugh, DF Callen, SR Wilson, PM Stanford, ME Sraml, M Gorska, ... Annals of human genetics 62 (4), 291-298, 1998 | 124 | 1998 |
