scispace - formally typeset
N

Natalie C. Butterfield

Researcher at Imperial College London

Publications -  34
Citations -  1857

Natalie C. Butterfield is an academic researcher from Imperial College London. The author has contributed to research in topics: Gene & Limb development. The author has an hindex of 14, co-authored 32 publications receiving 1195 citations. Previous affiliations of Natalie C. Butterfield include University of Queensland & Harvard University.

Papers
More filters
Journal ArticleDOI

An atlas of genetic influences on osteoporosis in humans and mice

John A. Morris, +66 more
- 01 Feb 2019 - 
TL;DR: This genetic atlas provides evidence linking associated SNPs to causal genes, offers new insight into osteoporosis pathophysiology, and highlights opportunities for drug development.
Journal ArticleDOI

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis

TL;DR: The results implicate GPC6 as a novel determinant of BMD, and also identify abnormal skeletal phenotypes in knockout mice associated with a further 100 prioritized genes.
Journal ArticleDOI

Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption

TL;DR: This article showed that osteomorphs are transcriptionally distinct from osteoclasts and macrophages and express a number of non-canonical osteoclast genes that are associated with structural and functional bone phenotypes when deleted in mice.
Journal ArticleDOI

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

TL;DR: It is shown that all ten MommeDs link to unique sites in the genome, that homozygosity for the mutations is associated with severe developmental abnormalities and that heterozygosity results in phenotypic abnormalities and reduced reproductive fitness in some cases.
Journal ArticleDOI

Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies

TL;DR: An N-ethyl-N-nitrosourea-derived mouse mutant with a hypomorphic missense mutation in the IFT144 gene is described, which phenocopies a number of the skeletal and craniofacial anomalies seen in patients with human skeletal ciliopathies.