Publications by authors named "Alex D Shaw"

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A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
Claudio Toma, Alex D Shaw, Anna Heath, Kerrie D Pierce, Philip B Mitchell

J Psychiatry Neurosci· March 2021

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De Novo Gene Variants and Familial Bipolar Disorder.
Claudio Toma, Alex D Shaw, Bronwyn J Overs, Philip B Mitchell, Peter R Schofield

JAMA Netw Open· May 2020

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CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Carol Dobson-Stone, Marianne Hallupp, Hamideh Shahheydari, Audrey M G Ragagnin, Zac Chatterton, Alex D Shaw, Christopher E Shaw

Brain· March 2020

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Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
Bàrbara Torrico, Alex D. Shaw, Roberto Mosca, Norma Vivó-Luque, Amaia Hervás

J Psychiatry Neurosci· September 2019

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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
Claudio Toma, Kerrie D Pierce, Alex D Shaw, Anna Heath, Philip B Mitchell

PLoS Genet· December 2018

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An examination of multiple classes of rare variants in extended families with bipolar disorder.
Claudio Toma, Alex D Shaw, Richard J N Allcock, Anna Heath, Kerrie D Pierce

Transl Psychiatry· March 2018

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Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.
Janice M Fullerton, Paul Klauser, Rhoshel K Lenroot, Alex D Shaw, Bronwyn Overs

Transl Psychiatry· January 2018

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Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014.
Monica Aas, Gabriëlla A M Blokland, Samuel J R A Chawner, Shing-Wan Choi, Jose Estrada, Alex D Shaw

Psychiatr Genet· February 2016

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Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Carol Dobson-Stone, Alex D Shaw, Marianne Hallupp, Lauren Bartley, Heather McCann

Brain· October 2015

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Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder.
Alex D Shaw, Yash Tiwari, Warren Kaplan, Anna Heath, Philip B Mitchell

PLoS One· November 2014

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