List of works - Edoardo Marcora

A Tale of Two Genes: Microglial Apoe and Trem2.

scientific article

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

scientific article published on 19 June 2017

Comparison of phosphodiesterase 10A, dopamine receptors D1 and D2 and dopamine transporter ligand binding in the striatum of the R6/2 and BACHD mouse models of Huntington's disease.

scientific article

Context-dependent regulation of NeuroD activity and protein accumulation.

scientific article

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

scientific article published on 21 October 2019

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease

scientific article published on 01 August 2018

Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes

scientific article published on 12 March 2021

Molecular basis for the loss-of-function effects of the Alzheimer's disease-associated R47H variant of the immune receptor TREM2

scientific article published on 24 May 2018

Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases

scientific article published on 20 August 2021

N-(4-hydroxyphenyl)retinamide: a Potent Inducer of Apoptosis in Human Neuroblastoma Cells

scientific article published on 01 August 1994

NeuroD1 in the endocrine pancreas: localization and dual function as an activator and repressor.

scientific article

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture

scientific article published on 23 September 2020

Stimulation of NeuroD activity by huntingtin and huntingtin-associated proteins HAP1 and MLK2

scientific article

SynGAP regulates steady-state and activity-dependent phosphorylation of cofilin.

scientific article published in December 2008

The Huntington's disease mutation impairs Huntingtin's role in the transport of NF-κB from the synapse to the nucleus.

scientific article

The NeuroD1/BETA2 sequences essential for insulin gene transcription colocalize with those necessary for neurogenesis and p300/CREB binding protein binding

scientific article

The variant call format provides efficient and robust storage of GWAS summary statistics

scientific article published on 13 January 2021

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

List of works by Edoardo Marcora

A Tale of Two Genes: Microglial Apoe and Trem2.

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

Comparison of phosphodiesterase 10A, dopamine receptors D1 and D2 and dopamine transporter ligand binding in the striatum of the R6/2 and BACHD mouse models of Huntington's disease.

Context-dependent regulation of NeuroD activity and protein accumulation.

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease

Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes

Molecular basis for the loss-of-function effects of the Alzheimer's disease-associated R47H variant of the immune receptor TREM2

Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases

N-(4-hydroxyphenyl)retinamide: a Potent Inducer of Apoptosis in Human Neuroblastoma Cells

NeuroD1 in the endocrine pancreas: localization and dual function as an activator and repressor.

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture

Stimulation of NeuroD activity by huntingtin and huntingtin-associated proteins HAP1 and MLK2

SynGAP regulates steady-state and activity-dependent phosphorylation of cofilin.

The Huntington's disease mutation impairs Huntingtin's role in the transport of NF-κB from the synapse to the nucleus.

The NeuroD1/BETA2 sequences essential for insulin gene transcription colocalize with those necessary for neurogenesis and p300/CREB binding protein binding

The variant call format provides efficient and robust storage of GWAS summary statistics

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation