Articles with public access mandates - Matthew HuentelmanLearn more
Not available anywhere: 14
Review
Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study
EM Reiman, YT Quiroz, AS Fleisher, K Chen, C Velez-Pardo, ...
The Lancet Neurology 11 (12), 1048-1056, 2012
Mandates: US National Institutes of Health
Review
Necroptosis activation in Alzheimer's disease
A Caccamo, C Branca, IS Piras, E Ferreira, MJ Huentelman, WS Liang, ...
Nature neuroscience 20 (9), 1236-1246, 2017
Mandates: US National Institutes of Health
Review
DNA diagnostics of hereditary hearing loss: a targeted resequencing approach combined with a mutation classification system
M Sommen, I Schrauwen, G Vandeweyer, N Boeckx, JJ Corneveaux, ...
Human mutation 37 (8), 812-819, 2016
Mandates: Research Foundation (Flanders), Action on Hearing Loss, UK
Review
A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR‐based approach and next generation sequencing
I Schrauwen, M Sommen, JJ Corneveaux, RA Reiman, NJ Hackett, ...
American Journal of Medical Genetics Part A 161 (1), 145-152, 2013
Mandates: Research Foundation (Flanders), Action on Hearing Loss, UK
Review
Harsh parenting predicts novel HPA receptor gene methylation and NR3C1 methylation predicts cortisol daily slope in middle childhood
CR Lewis, RS Breitenstein, A Henderson, HA Sowards, IS Piras, ...
Cellular and Molecular Neurobiology 41 (4), 783-793, 2021
Mandates: US National Institutes of Health
Review
Pattern of gene expression in different stages of schizophrenia: Down-regulation of NPTX2 gene revealed by a meta-analysis of microarray datasets
M Manchia, IS Piras, MJ Huentelman, F Pinna, CC Zai, JL Kennedy, ...
European Neuropsychopharmacology 27 (10), 1054-1063, 2017
Mandates: Canadian Institutes of Health Research
Review
Association of AEBP1 and NRN1 RNA expression with Alzheimer’s disease and neurofibrillary tangle density in middle temporal gyrus
IS Piras, J Krate, E Delvaux, J Nolz, D Matthew, DF Mastroeni, ...
Brain Research 1719, 217-224, 2019
Mandates: US National Institutes of Health
Review
Integration of peripheral transcriptomics, genomics, and interactomics following trauma identifies causal genes for symptoms of post-traumatic stress and major depression
S Wuchty, AJ Myers, M Ramirez-Restrepo, M Huentelman, R Richolt, ...
Molecular psychiatry 26 (7), 3077-3092, 2021
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
A review and meta-analysis of gene expression profiles in suicide
IS Piras, MJ Huentelman, F Pinna, P Paribello, M Solmi, A Murru, ...
European Neuropsychopharmacology 56, 39-49, 2022
Mandates: Government of Spain
Review
Identification of a common variant affecting human episodic memory performance using a pooled genome-wide association approach: a case study of disease gene identification
TL Pawlowski, MJ Huentelman
Disease Gene Identification: Methods and Protocols, 261-269, 2011
Mandates: US National Institutes of Health
Review
Evaluating the association between genetically proxied ACE inhibition and dementias
M Nassan, I Daghlas, IS Piras, E Rogalski, LM Reus, Y Pijnenburg, ...
Alzheimer's & Dementia 19 (9), 3894-3901, 2023
Mandates: Netherlands Organisation for Health Research and Development
Review
RNA sequencing from laser capture microdissected brain tissue to study normal aging and Alzheimer’s disease
AL Siniard, JJ Corneveaux, M De Both, MK Chawla, CA Barnes, ...
Applied Neurogenomics, 111-120, 2015
Mandates: US National Institutes of Health
Review
The sinking platform test: a novel paradigm to measure persistence in animal models
G Floris, SC Godar, G Braccagni, IS Piras, A Ravens, MT Zanda, ...
Neuropsychopharmacology, 1-10, 2024
Mandates: US National Institutes of Health
Review
Transcriptomic insights into multiple system atrophy from a PLP-α-synuclein transgenic mouse model
L Nicholson, IS Piras, MD DeBoth, A Siniard, A Heras-Garvin, ...
Brain Research 1834, 148912, 2024
Mandates: Austrian Science Fund
Available somewhere: 208
Review
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Review
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
Mandates: US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
Review
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436-441, 2011
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Review
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Mandates: US National Institutes of Health, Swedish Research Council, Alzheimers's UK …
Review
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
Mandates: US Department of Defense, US National Institutes of Health, US Department of …
Review
Development of a definition of postacute sequelae of SARS-CoV-2 infection
T Thaweethai, SE Jolley, EW Karlson, EB Levitan, B Levy, GA McComsey, ...
Jama 329 (22), 1934-1946, 2023
Mandates: US National Institutes of Health
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