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Genetics of dementia

The Lancet (British edition), 2014-03, Vol.383 (9919), p.828-840

2014

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Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease

PloS one, 2016-06, Vol.11 (6), p.e0157924-e0157924

2016

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C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients

PloS one, 2013-02, Vol.8 (2), p.e56899

2013

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GSK3B polymorphisms alter transcription and splicing in Parkinson's disease

Annals of neurology, 2005-12, Vol.58 (6), p.829-839

2005

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A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome

PloS one, 2012-10, Vol.7 (10), p.e47457

2012

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Renin-Angiotensin System Genetic Polymorphisms and Brain White Matter Lesions in Older Australians

American journal of hypertension, 2014-09, Vol.27 (9), p.1191-1198

2014

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TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.3110-3122

2015

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Srp20 regulates TrkB pre-mRNA splicing to generate TrkB-Shc transcripts with implications for Alzheimer's disease

Journal of neurochemistry, 2012-10, Vol.123 (1), p.159-171

2012

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Heritability in frontotemporal dementia: more missing pieces?

Journal of neurology, 2014-11, Vol.261 (11), p.2170-2177

2014

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Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis

Acta neuropathologica, 2013-04, Vol.125 (4), p.523-533

2013

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Mutations in progranulin explain atypical phenotypes with variants in MAPT

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3124-3126

2006

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Genetics of microstructure of the corpus callosum in older adults

PloS one, 2014-12, Vol.9 (12), p.e113181-e113181

2014

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C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts

Neurology, 2012-09, Vol.79 (10), p.995-1001

2012

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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

Nature (London), 1993-06, Vol.363 (6428), p.458-460

1993

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GSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individuals

PloS one, 2013-08, Vol.8 (8), p.e71750-e71750

2013

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DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro

Movement disorders, 2014-11, Vol.29 (13), p.1606-1614

2014

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Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Nature (London), 1998-06, Vol.393 (6686), p.702-705

1998

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Clinical and genetic predictors of paclitaxel neurotoxicity based on patient- versus clinician-reported incidence and severity of neurotoxicity in the ICON7 trial

Annals of oncology, 2017-11, Vol.28 (11), p.2733-2740

2017

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Genetic factors and epigenetic mechanisms of longevity: current perspectives

Epigenomics, 2015-12, Vol.7 (8), p.1339-1349

2015

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The Genetics of White Matter Lesions

CNS neuroscience & therapeutics, 2011-10, Vol.17 (5), p.525-540

2011

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Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele

Molecular psychiatry, 2006-04, Vol.11 (4), p.372-383

2006

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Elevated plasma ferritin in elderly individuals with high neocortical amyloid-β load

Molecular psychiatry, 2018-08, Vol.23 (8), p.1807-1812

2018

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Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: Expansion of the disease phenotype caused by tau gene mutations

Brain (London, England : 1878), 2000-05, Vol.123 (5), p.880-893

2000

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Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9

BMC neurology, 2008-08, Vol.8 (1), p.32-32, Article 32

2008

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Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory

Journal of Alzheimer's disease, 2018-01, Vol.62 (4), p.1777-1787

2018

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Genetics of dementia

Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease

C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients

GSK3B polymorphisms alter transcription and splicing in Parkinson's disease

A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome

Renin-Angiotensin System Genetic Polymorphisms and Brain White Matter Lesions in Older Australians

TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes

Srp20 regulates TrkB pre-mRNA splicing to generate TrkB-Shc transcripts with implications for Alzheimer's disease

Heritability in frontotemporal dementia: more missing pieces?

Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis

Mutations in progranulin explain atypical phenotypes with variants in MAPT

Genetics of microstructure of the corpus callosum in older adults

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

GSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individuals

DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Clinical and genetic predictors of paclitaxel neurotoxicity based on patient- versus clinician-reported incidence and severity of neurotoxicity in the ICON7 trial

Genetic factors and epigenetic mechanisms of longevity: current perspectives

The Genetics of White Matter Lesions

Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele

Elevated plasma ferritin in elderly individuals with high neocortical amyloid-β load

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: Expansion of the disease phenotype caused by tau gene mutations

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9

Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory

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