I. Barber

发表

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Nick C Fox, Cory C. Funk, D. G. Clark, 2017, Nature Genetics.

Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease

D. Hernandez, A. Singleton, J. Hardy, 2018, Neurobiology of Aging.

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Erick R. Scott, Michelle K. Lupton, D. Hernandez, 2013, Nature.

INVESTIGATING THE ROLE OF CLU, PICALM, AND CR1 IN ALZHEIMER'S DISEASE

K. Morgan, K. Brown, C. Medway, 2014, Alzheimer's & Dementia.

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer ' s disease

D. G. Clark, M. Fornage, A. Hofman, 2022 .

Title : Polygenic risk score in post-mortem diagnosed sporadic early onset Alzheimer ’ s disease

D. Hernandez, A. Singleton, J. Hardy, 2018 .

A plasma protein classifier for predicting amyloid burden for preclinical Alzheimer’s disease

Kathryn Goozee, Dag Aarsland, Colin L. Masters, 2019, Science Advances.

Polygenic risk score in post-mortem diagnosed sporadic early onset Alzheimer’s disease

D. Hernandez, K. Morgan, J. Bras, 2017 .

Screening Exon 16 and 17 of the Amyloid Precursor Protein Gene in Sporadic Early-Onset Alzheimer’s Disease (sEOAD)

A. Singleton, K. Morgan, D. Mann, 2016 .

Investigating Splicing Variants Uncovered by Next-Generation Sequencing the Alzheimer’s Disease Candidate Genes, CLU, PICALM, CR1, ABCA7, BIN1, the MS4A Locus, CD2AP, EPHA1 and CD33

K. Morgan, P. Passmore, D. Mann, 2016 .

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

Sonja W. Scholz, John D. Eicher, D. Hernandez, 2018, The Lancet Neurology.

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

W. M. van der Flier, D. Hernandez, M. Nalls, 2014, Human molecular genetics.

Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

Michelle K. Lupton, W. M. van der Flier, D. Hernandez, 2016, Neurobiology of Aging.

Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease

K. Morgan, E. Hollox, K. Brookes, 2018, bioRxiv.

Heritability and genetic variance of dementia with Lewy bodies

Sonja W. Scholz, John D. Eicher, D. Hernandez, 2018, Neurobiology of Disease.

Evaluating pathogenic dementia variants in posterior cortical atrophy

Minerva M. Carrasquillo, Nilüfer Ertekin-Taner, Bradley F. Boeve, 2016, Neurobiology of Aging.

LRP10 in α-synucleinopathies

D. Hernandez, J. Morris, J. Trojanowski, 2018, The Lancet Neurology.

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

D. Hernandez, A. Singleton, J. Hardy, 2017, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset

D. Hernandez, A. Singleton, D. Neary, 2015 .

Methylation Profiling RIN3 and MEF2C Identifies Epigenetic Marks Associated with Sporadic Early Onset Alzheimer’s Disease

K. Morgan, J. Craigon, G. Seymour, 2017, Journal of Alzheimer's disease reports.

Investigating the genetic architecture of Dementia with Lewy bodies: a genome-wide association study

Sonja W. Scholz, D. Hernandez, A. Singleton, 2018 .

A comprehensive screening of copy number variability in dementia with Lewy bodies

Sonja W. Scholz, John D. Eicher, D. Hernandez, 2019, Neurobiology of Aging.

DEEP SEQUENCING ALZHEIMER'S DISEASE ASSOCIATED GENES, CLU, PICALM, CR1, ABCA7, BIN1, MS4A, CD2AP, EPHA1, AND CD33 IDENTIFIES POTENTIAL FUNCTIONAL SNPS

K. Morgan, K. Brown, C. Medway, 2014, Alzheimer's & Dementia.

Missense variant in TREML2 protects against Alzheimer's disease

Michelle K. Lupton, A. Singleton, J. Haines, 2014, Neurobiology of Aging.

Missense variant in TREML 2 protects against Alzheimer ’ s Disease

Timothy Edward John Behrens, Denise, Michelle K. Lupton, 2013 .

Identification of a possible proteomic biomarker in Parkinson’s disease: discovery and replication in blood, brain and cerebrospinal fluid

S. Lovestone, L. Winchester, Y. Ben-Shlomo, 2022, Brain communications.

Identification of a novel proteomic Biomarker in Parkinson's Disease: Discovery and Replication in Blood, brain and CSF

S. Lovestone, L. Winchester, Y. Ben-Shlomo, 2021, medRxiv.

Identification of a possible proteomic biomarker in Parkinson’s disease: discovery and replication in blood, brain and cerebrospinal fluid

S. Lovestone, L. Winchester, Y. Ben-Shlomo, 2022, Brain communications.

INVESTIGATING THE ROLE OF CLU, PICALM, AND CR1 IN ALZHEIMER'S DISEASE

K. Morgan, K. Brown, C. Medway, 2014, Alzheimer's & Dementia.

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Erick R. Scott, Michelle K. Lupton, D. Hernandez, 2013, Nature.

Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies

D. Hernandez, D. Stone, R. Petersen, 2017, Neurobiology of Aging.

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

D. Warden, C. Medway, H. Kölsch, 2017, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease

D. Neary, P. Passmore, J. Snowden, 2016, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's

C. Medway, H. Kölsch, A. Richardson, 2015 .