Kevin Flaherty

Dr. Kevin Flaherty

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
23 March 2013 in Acta Neuropathologica
Verified
Journal Article
Closed access
PDF file
JRJoan Richtsmeier
Joan Richtsmeier
KFKevin Flaherty
Kevin Flaherty

22 March 2016 in WIREs Developmental Biology
Verified
Journal Article
Closed access
PDF file
KFKevin Flaherty
Kevin Flaherty
NSNandini Singh
Nandini Singh
JRJoan Richtsmeier
Joan Richtsmeier

1 April 2018 in Development
Verified
Journal Article
Open access
PDF file
MMMarco Musy
Marco Musy
KFKevin Flaherty
Kevin Flaherty
JRJelena Raspopovic
Jelena Raspopovic
ARAlexandre Robert-Moreno
Alexandre Robert-Moreno
JRJoan Richtsmeier
Joan Richtsmeier
JSJames Sharpe
James Sharpe
To determine the developmental stage of embryonic mice, we apply a geometric morphometric approach to the changing shape of the mouse limb bud as it grows from embryonic day 10 to embryonic day 15 post-conception. As the ontogenetic sequence results in the de novo emergence of shape features not present in the early stages, we have created a standard ontogenetic trajectory for limb bud development – a quantitative characterization of shape change during limb morphogenesis. This trajectory of form as a function of time also gives us the reverse function: the ability to infer developmental stage from form, with a typical uncertainty of 2 h. We introduce eMOSS (embryonic mouse ontogenetic staging system) as a fast, reliable, convenient and freely available online tool for staging embryos from two-dimensional images of their limb buds, and illustrate its use in phenotyping early limb abnormalities.

15 December 2018 in Journal of Developmental Biology
Verified
Journal Article
Open access
PDF file
KFKevin Flaherty
Kevin Flaherty
JRJoan Richtsmeier
Joan Richtsmeier
The establishment of precise, high-resolution temporal sequences for morphogenetic events in laboratory mice remains a vexing issue in developmental biology. Mouse embryos collected at the same period of gestation, even those from the same litter, show wide variation in individual levels of progress along their developmental trajectory. Therefore, age at harvest does not provide sufficient information about developmental progress to serve as the basis for forming samples for the study of rapidly or near-simultaneously occurring events such as the sequence of ossification center formation. Here, we generate two measures of individual developmental progress (developmental age) for a large sample of mouse embryos using crown–rump lengths that measures size, and limbstaging ages produced by the embryonic Mouse Ontogenetic Staging System (eMOSS) that measure shape. Using these measures, we establish fine-grained sequences of ossification center appearance for mouse embryos. The two measures of developmental progress generate slightly different sequences of ossification center formation demonstrating that despite their tight correlation throughout the developmental period, size and shape are aspects of form that are at least partially dissociated in development.