| Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome T Hearn, GL Renforth, C Spalluto, NA Hanley, K Piper, S Brickwood, ... Nature genetics 31 (1), 79-83, 2002 | 353 | 2002 |
| Development of the human pancreas from foregut to endocrine commitment RE Jennings, AA Berry, R Kirkwood-Wilson, NA Roberts, T Hearn, ... Diabetes 62 (10), 3514-3522, 2013 | 346 | 2013 |
| Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes T Hearn, C Spalluto, VJ Phillips, GL Renforth, N Copin, NA Hanley, ... Diabetes 54 (5), 1581-1587, 2005 | 261 | 2005 |
| Spectrum of ALMS1 variants and evaluation of genotype‐phenotype correlations in Alström syndrome JD Marshall, EG Hinman, GB Collin, S Beck, R Cerqueira, P Maffei, ... Human mutation 28 (11), 1114-1123, 2007 | 178 | 2007 |
| Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif–containing proteins C10orf90 and KIAA1731 VJ Knorz, C Spalluto, M Lessard, TL Purvis, FF Adigun, GB Collin, ... Molecular biology of the cell 21 (21), 3617-3629, 2010 | 125 | 2010 |
| Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to … MS Jackson, M Rocchi, G Thompson, T Hearn, M Crosier, J Guy, D Kirk, ... Human Molecular Genetics 8 (2), 205-215, 1999 | 116 | 1999 |
| ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits T Hearn Journal of Molecular Medicine 97 (1), 1-17, 2019 | 101 | 2019 |
| Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3 S Brickwood, DT Bonthron, LI Al-Gazali, K Piper, T Hearn, DI Wilson, ... Journal of medical genetics 40 (9), 685-689, 2003 | 98 | 2003 |
| Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q J Guy, C Spalluto, A McMurray, T Hearn, M Crosier, L Viggiano, V Miolla, ... Human molecular genetics 9 (13), 2029-2042, 2000 | 76 | 2000 |
| Narrowing the critical region within 11q24–qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis HM Phillips, GL Renforth, C Spalluto, T Hearn, ARJ Curtis, L Craven, ... Genomics 79 (4), 475-478, 2002 | 66 | 2002 |
| Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition C Spalluto, DI Wilson, T Hearn European journal of cell biology 91 (9), 675-686, 2012 | 64 | 2012 |
| Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p J Guy, T Hearn, M Crosier, J Mudge, L Viggiano, D Koczan, HJ Thiesen, ... Genome research 13 (2), 159-172, 2003 | 61 | 2003 |
| Current trends in oxysterol research WJ Griffiths, J Abdel-Khalik, T Hearn, E Yutuc, AH Morgan, Y Wang Biochemical Society Transactions 44 (2), 652-658, 2016 | 56 | 2016 |
| Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1 C Spalluto, DI Wilson, T Hearn FEBS open bio 3, 334-340, 2013 | 55 | 2013 |
| Cholesterolomics: an update WJ Griffiths, J Abdel-Khalik, E Yutuc, AH Morgan, I Gilmore, T Hearn, ... Analytical biochemistry 524, 56-67, 2017 | 53 | 2017 |
| Metabolism of non-enzymatically derived oxysterols: clues from sterol metabolic disorders WJ Griffiths, E Yutuc, J Abdel-Khalik, PJ Crick, T Hearn, A Dickson, ... Free Radical Biology and Medicine 144, 124-133, 2019 | 45 | 2019 |
| Elevated oxysterol levels in human and mouse livers reflect nonalcoholic steatohepatitis [S] T Raselli, T Hearn, A Wyss, K Atrott, A Peter, I Frey-Wagner, MR Spalinger, ... Journal of lipid research 60 (7), 1270-1283, 2019 | 42 | 2019 |
| Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1 TL Purvis, T Hearn, C Spalluto, VJ Knorz, KP Hanley, T Sanchez-Elsner, ... Gene 460 (1-2), 20-29, 2010 | 40 | 2010 |
| Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms M Crosier, L Viggiano, J Guy, D Misceo, R Stones, W Wei, T Hearn, ... Genome research 12 (1), 67-80, 2002 | 32 | 2002 |
| In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets KP Hanley, T Hearn, A Berry, MJ Carvell, AM Patch, LJ Williams, ... The Journal of endocrinology 207 (2), 151, 2010 | 30 | 2010 |
