Kathleen J. Millen

Reciprocal fusion transcripts of two novel Zn-finger genes in a female with absence of the corpus callosum, ocular colobomas and a balanced translocation between chromosomes 2p24 and 9q32.

Development and malformations of the cerebellum in mice.

Control of roof plate formation by Lmx1a in the developing spinal cord.

Control of roof plate development and signaling by Lmx1b in the caudal vertebrate CNS.

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.

Mechanisms of roof plate formation in the vertebrate CNS.

Roof plate-dependent patterning of the vertebrate dorsal central nervous system.

The roof plate regulates cerebellar cell-type specification and proliferation.

Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene.

Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.

Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool.

A developmental classification of malformations of the brainstem.

Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene.

Zic1 and Zic4 regulate zebrafish roof plate specification and hindbrain ventricle morphogenesis.

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.

Cerebellar development and disease.

Lmx1a is required for segregation of sensory epithelia and normal ear histogenesis and morphogenesis.

Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies.

Lmx1a maintains proper neurogenic, sensory, and non-sensory domains in the mammalian inner ear.

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.

Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth.

Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.

Looking at cerebellar malformations through text-mined interactomes of mice and humans.

A developmental and genetic classification for midbrain-hindbrain malformations.

Novel approaches to studying the genetic basis of cerebellar development.

Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem.

Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele.

Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis.

Wormless without wingless.