| Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse MT Dattani, JP Martinez-Barbera, PQ Thomas, JM Brickman, R Gupta, ... Nature genetics 19 (2), 125-133, 1998 | 814 | 1998 |
| Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo P Thomas, R Beddington Current Biology 6 (11), 1487-1496, 1996 | 568 | 1996 |
| Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors PQ Thomas, A Brown, RS Beddington Development 125 (1), 85-94, 1998 | 548 | 1998 |
| The homeobox gene Hex is required in definitive endodermal tissues for normal forebrain, liver and thyroid formation JPM Barbera, M Clements, P Thomas, T Rodriguez, D Meloy, D Kioussis, ... Development 127 (11), 2433-2445, 2000 | 472 | 2000 |
| Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence S Benko, JA Fantes, J Amiel, DJ Kleinjan, S Thomas, J Ramsay, ... Nature genetics 41 (3), 359-364, 2009 | 366 | 2009 |
| X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment LM Dibbens, PS Tarpey, K Hynes, MA Bayly, IE Scheffer, R Smith, ... Nature genetics 40 (6), 776-781, 2008 | 357 | 2008 |
| GDNF is a chemoattractant for enteric neural cells HM Young, CJ Hearn, PG Farlie, AJ Canty, PQ Thomas, DF Newgreen Developmental biology 229 (2), 503-516, 2001 | 322 | 2001 |
| Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia PQ Thomas, MT Dattani, JM Brickman, D McNay, G Warne, M Zacharin, ... Human molecular genetics 10 (1), 39-45, 2001 | 319 | 2001 |
| Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency F Laumonnier, N Ronce, BCJ Hamel, P Thomas, J Lespinasse, ... The American Journal of Human Genetics 71 (6), 1450-1455, 2002 | 293 | 2002 |
| SOX3 is required during the formation of the hypothalamo-pituitary axis K Rizzoti, S Brunelli, D Carmignac, PQ Thomas, IC Robinson, ... Nature genetics 36 (3), 247-255, 2004 | 286 | 2004 |
| Mutations in DEPDC5 cause familial focal epilepsy with variable foci LM Dibbens, B De Vries, S Donatello, SE Heron, BL Hodgson, ... Nature genetics 45 (5), 546, 2013 | 258 | 2013 |
| PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome SE Heron, BE Grinton, S Kivity, Z Afawi, SM Zuberi, JN Hughes, ... The American Journal of Human Genetics 90 (1), 152-160, 2012 | 246 | 2012 |
| Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation PS Tarpey, FL Raymond, LS Nguyen, J Rodriguez, A Hackett, ... Nature genetics 39 (9), 1127-1133, 2007 | 231 | 2007 |
| Identification of SOX3 as an XX male sex reversal gene in mice and humans E Sutton, J Hughes, S White, R Sekido, J Tan, V Arboleda, N Rogers, ... The Journal of clinical investigation 121 (1), 328-341, 2011 | 227 | 2011 |
| Mutations in PHF6 are associated with Börjeson–Forssman–Lehmann syndrome KM Lower, G Turner, BA Kerr, KD Mathews, MA Shaw, ÁK Gedeon, ... Nature genetics 32 (4), 661-665, 2002 | 195 | 2002 |
| Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression LT Raetzman, SA Ross, S Cook, SL Dunwoodie, SA Camper, PQ Thomas Developmental biology 265 (2), 329-340, 2004 | 150 | 2004 |
| Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion G Agarwal, V Bhatia, S Cook, PQ Thomas The Journal of Clinical Endocrinology & Metabolism 85 (12), 4556-4561, 2000 | 133 | 2000 |
| Sequence, genomic organization, and expression of the novel homeobox gene Hesx1 PQ Thomas, BV Johnson, J Rathjen, PD Rathjen Journal of Biological Chemistry 270 (8), 3869-3875, 1995 | 127 | 1995 |
| Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3 NM Solomon, SA Ross, T Morgan, JL Belsky, FA Hol, PS Karnes, ... Journal of medical genetics 41 (9), 669-678, 2004 | 124 | 2004 |
| Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation KP Burdon, JD McKay, MM Sale, IM Russell-Eggitt, DA Mackey, MG Wirth, ... The American Journal of Human Genetics 73 (5), 1120-1130, 2003 | 114 | 2003 |
