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SC Currier et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Initial sequence of the chimpanzee genome and comparison with the human genome
TS Mikkelsen et al.
NATURE (2005)
Why do human diversity levels vary at a megabase scale?
I Hellmann et al.
GENOME RESEARCH (2005)
Hydrocephalus after intraventricular hemorrhage in preterm and low-birth weight infants: analysis of associated risk factors for ventriculoperitoneal shunting
S Kazan et al.
SURGICAL NEUROLOGY (2005)
Occult hydrocephalus in children with cerebral palsy
AL Albright et al.
NEUROSURGERY (2005)
Plant telomere biology
TD McKnight et al.
PLANT CELL (2004)
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus
VL Sheen et al.
BRAIN & DEVELOPMENT (2004)
POMGnT1 gene alterations in a family with neurological abnormalities
VS Vervoort et al.
ANNALS OF NEUROLOGY (2004)
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
DY Nishimura et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Development of hydrocephalus in mice lacking SOCS7
DL Krebs et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Graded phenotypic response to partial and complete deficiency of a brain-specific transcript variant of the winged helix transcription factor RFX4
PJ Blackshear et al.
DEVELOPMENT (2003)
Msx1 is required for dorsal diencephalon patterning
A Bach et al.
DEVELOPMENT (2003)
Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene
BE Davy et al.
HUMAN MOLECULAR GENETICS (2003)
Mutations in NR4A2 associated with familial Parkinson disease
WD Le et al.
NATURE GENETICS (2003)
EGF converts transit-amplifying neurogenic precursors in the adult brain into multipotent stem cells
F Doetsch et al.
NEURON (2002)
Diagnostic criteria for idiopathic intracranial hypertension
DI Friedman et al.
NEUROLOGY (2002)
Posthaemorrhagic ventricular dilatation in the premature infant: natural history and predictors of outcome
BP Murphy et al.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION (2002)
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
I Ibañez-Tallon et al.
HUMAN MOLECULAR GENETICS (2002)
A critical role for sonic hedgehog signaling in the early expansion of the developing brain
J Britto et al.
NATURE NEUROSCIENCE (2002)
The transcription factor Pax6 is required for development of the diencephalic dorsal midline secretory radial glia that form the subcommissural organ
G Estivill-Torrús et al.
MECHANISMS OF DEVELOPMENT (2001)
Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail
Z Kibar et al.
NATURE GENETICS (2001)
Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
PD Taulman et al.
MOLECULAR BIOLOGY OF THE CELL (2001)