Paul Q. Thomas

<i>Hex</i>: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors

Paul Q. Thomas, Angus M. Brown, R. S. P. Beddington · Development · 1998 · 530 citations

Life Sciences, Developmental Biology, Genetics +17

The homeobox gene <i>Hex</i> is required in definitive endodermal tissues for normal forebrain, liver and thyroid formation

Juan Pedro Martı́nez-Barberá, Melanie Clements, Paul Q. Thomas et al. · Development · 2000 · 474 citations

Life Sciences, Genetics, Embryogenesis +15

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Leanne M. Dibbens, Patrick Tarpey, Kim Hynes et al. · Nature Genetics · 2008 · 450 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens, Boukje de Vries, Simona Donatello et al. · Nature Genetics · 2013 · 364 citations · Full text

Life Sciences, Genetics, Neuroscience +14

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

Paul Q. Thomas · Human Molecular Genetics · 2001 · 319 citations

Medicine, Genetics, Molecular Genetics +12