K. Pierce

发表

Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults

Laurie M. Baker, E. Akbudak, D. Tate, 2014, AGE.

Neuronal fiber bundle lengths in healthy adult carriers of the ApoE4 allele: A quantitative tractography DTI study

Lauren E. Salminen, E. Akbudak, T. Conturo, 2013, Brain Imaging and Behavior.

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

J. Fullerton, P. Mitchell, P. Schofield, 2018, bioRxiv.

An examination of multiple classes of rare variants in extended families with bipolar disorder

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2018, Translational Psychiatry.

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2018, bioRxiv.

A Nonsense Mutation in the α1 Subunit of the Inhibitory Glycine Receptor Associated with Bovine Myoclonus

P. Schofield, R. Morris, C. Handford, 2001, Molecular and Cellular Neuroscience.

Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognition

Laurie M. Baker, Lauren E. Salminen, E. Akbudak, 2016, Behavioural Brain Research.

Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphism

Laurie M. Baker, Lauren E. Salminen, T. Conturo, 2015, Journal of Neural Transmission.

A Single P-loop Glutamate Point Mutation to either Lysine or Arginine Switches the Cation–Anion Selectivity of the CNGA2 Channel

T. Lewis, A. Moorhouse, K. Pierce, 2006, The Journal of general physiology.

Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder

Melissa J. Green, Janice M. Fullerton, J. Nurnberger, 2022, Translational Psychiatry.

Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults

Laurie M. Baker, Lauren E. Salminen, E. Akbudak, 2014, AGE.

Startle disease mutations reduce the agonist sensitivity of the human inhibitory glycine receptor.

P. Schofield, J. Lynch, C. French, 1994, The Journal of biological chemistry.

A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2021, Journal of psychiatry & neuroscience : JPN.

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

D. Geschwind, P. Mazzoni, P. Svenningsson, 2013, neurogenetics.

In vivo somatic delivery of plasmid DNA and retrograde transport to obtain cell‐specific gene expression in the central nervous system

R. Morris, T. Lewis, A. Pisano, 2004, Journal of neurochemistry.

Identification of intracellular and extracellular domains mediating signal transduction in the inhibitory glycine receptor chloride channel

P. Schofield, J. Lynch, K. Pierce, 1997, The EMBO journal.

Mutation of an arginine residue in the human glycine receptor transforms β-alanine and taurine from agonists into competitive antagonists

P. Schofield, J. Lynch, C. French, 1995, Neuron.

Role of Charged Residues in Coupling Ligand Binding and Channel Activation in the Extracellular Domain of the Glycine Receptor*

P. Schofield, N. Absalom, T. Lewis, 2003, Journal of Biological Chemistry.

Molecular cloning and expression of an adenosine A2b receptor from human brain.

J. Shine, T. Furlong, K. Pierce, 1992, Biochemical and biophysical research communications.

BDNF Genotype Interacts with Motor Function to Influence Rehabilitation Responsiveness Poststroke

Angelica G. Thompson-Butel, P. Schofield, P. McNulty, 2016, Front. Neurol..

Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder

Melissa J. Green, Janice M. Fullerton, J. Fullerton, 2021, Psychiatry Research: Neuroimaging.

Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging

Lauren E. Salminen, D. Tate, T. Conturo, 2017, Behavioural Brain Research.

Bovine myoclonus: Model of human hyperekplexia (Startle disease)

P. Schofield, P. Windsor, K. Pierce, 2002 .

The Surface Accessibility of the Glycine Receptor M2–M3 Loop Is Increased in the Channel Open State

P. Schofield, J. Lynch, J. Haddrill, 2001, The Journal of Neuroscience.

Preliminary Evidence of the Short Allele of the Serotonin Transporter Gene Predicting Poor Response to Cognitive Behavior Therapy in Posttraumatic Stress Disorder

K. Felmingham, P. Schofield, C. Dobson-Stone, 2010, Biological Psychiatry.

Zinc Potentiation of the Glycine Receptor Chloride Channel Is Mediated by Allosteric Pathways

P. Schofield, J. Lynch, K. Pierce, 1998, Journal of neurochemistry.

Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults

Laurie M. Baker, Lauren E. Salminen, P. Schofield, 2014, The International journal of neuroscience.

Cation-selective Mutations in the M2 Domain of the Inhibitory Glycine Receptor Channel Reveal Determinants of Ion-Charge Selectivity

P. Schofield, A. Keramidas, A. Moorhouse, 2002, The Journal of general physiology.

Molecular characterization of a human brain adenosine A2 receptor.

T J Furlong, K D Pierce, L A Selbie, 1992, Brain research. Molecular brain research.

Association between serotonin transporter promoter polymorphisms and psychological distress in a diabetic population

P. Schofield, C. Dobson-Stone, P. Mitchell, 2012, Psychiatry Research.

Bovine myoclonus: Model of human hyperekplexia (Startle disease)

P. Schofield, P. Windsor, K. Pierce, 2002 .