List of works - Kerry Miller

A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis

scientific article

A highly conserved Wnt-dependent TCF4 binding site within the proximal enhancer of the anti-myogenic Msx1 gene supports expression within Pax3-expressing limb bud muscle precursor cells

scientific journal article

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

scientific article

A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.

scientific article

An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice ⬇️

scientific article published on June 2, 2011

Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

scientific journal article

Diagnostic value of exome and whole genome sequencing in craniosynostosis

scientific article

Eeyore: a novel mouse model of hereditary deafness

scientific article

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

scientific article

Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease

scientific journal article

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

scientific article

Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

scientific article

Is there a functional link between gene interdigitation and multi-species conservation of synteny blocks?

scientific article published in November 2004

Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis

scientific article published on 29 June 2016

Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues.

scientific article

Postgenomic bioinformatic analysis of yeast artificial chromosome sequence.

scientific article

Prediction and characterisation of a highly conserved, remote and cAMP responsive enhancer that regulates Msx1 gene expression in cardiac neural crest and outflow tract.

scientific article published on 21 February 2008

YPEL1 overexpression in early avian craniofacial mesenchyme causes mandibular dysmorphogenesis by up-regulating apoptosis.

scientific article

bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1

scientific article

List of works by Kerry Miller

A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis

A highly conserved Wnt-dependent TCF4 binding site within the proximal enhancer of the anti-myogenic Msx1 gene supports expression within Pax3-expressing limb bud muscle precursor cells

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.

An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice ⬇️

Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

Diagnostic value of exome and whole genome sequencing in craniosynostosis

Eeyore: a novel mouse model of hereditary deafness

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

Is there a functional link between gene interdigitation and multi-species conservation of synteny blocks?

Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis

Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues.

Postgenomic bioinformatic analysis of yeast artificial chromosome sequence.

Prediction and characterisation of a highly conserved, remote and cAMP responsive enhancer that regulates Msx1 gene expression in cardiac neural crest and outflow tract.

YPEL1 overexpression in early avian craniofacial mesenchyme causes mandibular dysmorphogenesis by up-regulating apoptosis.

bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1