H. Grayton

发表

Copy number variations in neurodevelopmental disorders

D. Rujescu, D. Collier, H. Grayton, 2012, Progress in Neurobiology.

Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice

T. Werge, P. Celada, J. Nielsen, 2017, Journal of psychiatry & neuroscience : JPN.

Prenatal exposure to maternal obesity leads to hyperactivity in offspring

P. Taylor, L. Poston, A. Samuelsson, 2012, Molecular Psychiatry.

Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders

D. Collier, M. Missler, H. Grayton, 2013, PloS one.

Ohnologs are overrepresented in pathogenic copy number mutations

E. Vassos, D. Collier, A. McLysaght, 2013, Proceedings of the National Academy of Sciences.

Clinical and radiological characterization of novel FIG4‐related combined system disease with neuropathy

I. Simonic, Soo-Mi Park, R. Horvath, 2020, Clinical genetics.

Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors

D. Collier, M. Missler, I. Dudanova, 2015, Front. Synaptic Neurosci..

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders

D. Collier, S. Curran, C. Ogilvie, 2013, Journal of molecular psychiatry.

NRXN 1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN 1 to neurodevelopmental disorders

D. Collier, S. Curran, C. Ogilvie, 2013 .