List of works - NiCole A Finch

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

scientific article

Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study

scientific article published on 05 September 2013

Erratum to: Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

scientific article published on 23 May 2016

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

scientific article

Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

scientific article published on 08 October 2019

In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers

scientific article published on 15 May 2017

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

scientific article published on 25 December 2011

Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

scientific article published on 26 April 2016

Novel GRN mutation presenting as an aphasic dementia and evolving into corticobasal syndrome

scientific article published on 11 December 2017

Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72.

scientific article

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

scientific article published on 21 January 2009

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

scientific article

Progranulin protein levels are differently regulated in plasma and CSF.

scientific article

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

scholarly article by Monica Y Sanchez-Contreras published in July 2018

TYROBP genetic variants in early-onset Alzheimer's disease

scientific article published on 8 August 2016

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease

scientific article published on 6 May 2015

List of works by NiCole A Finch

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study

Erratum to: Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

Novel GRN mutation presenting as an aphasic dementia and evolving into corticobasal syndrome

Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72.

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Progranulin protein levels are differently regulated in plasma and CSF.

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

TYROBP genetic variants in early-onset Alzheimer's disease

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease