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CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Published in:
2020
By:
- Dobson-Stone, Carol;
- Hallupp, Marianne;
- Shahheydari, Hamideh;
- Ragagnin, Audrey M G;
- Chatterton, Zac;
- Carew-Jones, Francine;
- Shepherd, Claire E;
- Stefen, Holly;
- Paric, Esmeralda;
- Fath, Thomas;
- Thompson, Elizabeth M;
- Blumbergs, Peter;
- Short, Cathy L;
- Field, Colin D;
- Panegyres, Peter K;
- Hecker, Jane;
- Nicholson, Garth;
- Shaw, Alex D;
- Fullerton, Janice M;
- Luty, Agnes A
Publication type:
journal article
Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Published in:
2015
By:
- Dobson-Stone, Carol;
- Shaw, Alex D.;
- Hallupp, Marianne;
- Bartley, Lauren;
- McCann, Heather;
- Brooks, William S.;
- Loy, Clement T.;
- Schofield, Peter R.;
- Mather, Karen A.;
- Kochan, Nicole A.;
- Sachdev, Perminder S.;
- Halliday, Glenda M.;
- Piguet, Olivier;
- Hodges, John R.;
- Kwok, John B. J.;
- Bannwarth, Sylvie;
- Ait-El-Mkadem, Samira;
- Chaussenot, Annabelle;
- Genin, Emmanuelle C.;
- Lacas-Gervais, Sandra
Publication type:
commentary
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
Published in:
PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007535
By:
- Toma, Claudio;
- Pierce, Kerrie D.;
- Shaw, Alex D.;
- Heath, Anna;
- Mitchell, Philip B.;
- Schofield, Peter R.;
- Fullerton, Janice M.
Publication type:
Article
Characterisation of Genetic Variation in <i>ST8SIA2</i> and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder.
Published in:
PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092556
By:
- Shaw, Alex D.;
- Tiwari, Yash;
- Kaplan, Warren;
- Heath, Anna;
- Mitchell, Philip B.;
- Schofield, Peter R.;
- Fullerton, Janice M.
Publication type:
Article
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
Published in:
Journal of Psychiatry & Neuroscience, 2021, v. 46, n. 2, p. E247, doi. 10.1503/jpn.200083
By:
- Toma, Claudio;
- Shaw, Alex D.;
- Heath, Anna;
- Pierce, Kerrie D.;
- Mitchell, Philip B.;
- Schofield, Peter R.;
- Fullerton, Janice M.
Publication type:
Article
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
Published in:
Journal of Psychiatry & Neuroscience, 2019, v. 44, n. 5, p. 350, doi. 10.1503/jpn.180184
By:
- Torrico, Bàrbara;
- Shaw, Alex D.;
- Mosca, Roberto;
- Vivó-Luque, Norma;
- Hervás, Amaia;
- Fernàndez-Castillo, Noèlia;
- Aloy, Patrick;
- Bayés, Mònica;
- Fullerton, Janice M.;
- Cormand, Bru;
- Toma, Claudio
Publication type:
Article
An examination of multiple classes of rare variants in extended families with bipolar disorder.
Published in:
Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0113-y
By:
- Toma, Claudio;
- Shaw, Alex D.;
- Allcock, Richard J. N.;
- Heath, Anna;
- Pierce, Kerrie D.;
- Mitchell, Philip B.;
- Schofield, Peter R.;
- Fullerton, Janice M.
Publication type:
Article
Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.
Published in:
Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0052-z
By:
- Fullerton, Janice M.;
- Klauser, Paul;
- Lenroot, Rhoshel K.;
- Shaw, Alex D.;
- Overs, Bronwyn;
- Heath, Anna;
- Cairns, Murray J.;
- Atkins, Joshua;
- Scott, Rodney;
- The Australian Schizophrenia Research Bank;
- Schofield, Peter R.;
- Weickert, Cyndi Shannon;
- Pantelis, Christos;
- Fornito, Alex;
- Whitford, Thomas J.;
- Weickert, Thomas W.;
- Zalesky, Andrew
Publication type:
Article
De Novo Gene Variants and Familial Bipolar Disorder.
Published in:
JAMA Network Open, 2020, v. 3, n. 5, p. e203382, doi. 10.1001/jamanetworkopen.2020.3382
By:
- Toma, Claudio;
- Shaw, Alex D.;
- Overs, Bronwyn J.;
- Mitchell, Philip B.;
- Schofield, Peter R.;
- Cooper, Antony A.;
- Fullerton, Janice M.
Publication type:
Article

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