Concepedia

Andrea Hardy

AH

Statistics

Publications

4

Citations

465

H-Index

4

Active since

2005

Affiliations

Mary Lyon Centre at MRC Harwell(Current)

Medical Research Council

Andrea Hardy is an author at Mary Lyon Centre at MRC Harwell specializing in life sciences, genetics, and developmental neuroscience.

Publications per year

2005–2014

4

Publications

4

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

Esther B. E. Becker, Peter L. Oliver, Maike D. Glitsch et al. · Proceedings of the National Academy of Sciences · 2009 · 227 citations · Full text

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Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features

Valter Tucci, Tjitske Kleefstra, Andrea Hardy et al. · Journal of Clinical Investigation · 2014 · 149 citations · Full text

, , +17

Stringent requirement of a proper level of canonical WNT signalling activity for head formation in mouse embryo

Nicolas Fossat, Vanessa Jones, Poh‐Lynn Khoo et al. · Development · 2011 · 56 citations

, , +17

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Debora Bogani, Catherine Willoughby, Jennifer R. Davies et al. · Proceedings of the National Academy of Sciences · 2005 · 33 citations · Full text

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