Daniele Merico

Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 80 publications

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects.

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects.

Journal: medRxiv : the preprint server for health sciences

Published: August 12, 2025

Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammation.

Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammation.

Journal: The Journal of allergy and clinical immunology

Published: September 27, 2024

Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing.

Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing.

Journal: NPJ genomic medicine

Published: July 29, 2024

Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency.

Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency.

Journal: The journal of allergy and clinical immunology. Global

Published: September 06, 2023

A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction.

A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction.

Journal: Frontiers in molecular biosciences

Published: July 12, 2023

Gene copy number variation and pediatric mental health/neurodevelopment in a general population.

Gene copy number variation and pediatric mental health/neurodevelopment in a general population.

Journal: Human molecular genetics

Published: March 09, 2023

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.

Journal: Nature genetics

Published: December 23, 2022

Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.

Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.

Journal: Blood

Published: September 08, 2022

Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric Disorders.

Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric Disorders.

Journal: JAMA psychiatry

Published: December 01, 2021

Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge.

Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge.

Journal: Molecular psychiatry

Published: December 01, 2021

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.

Journal: Nature communications

Published: November 01, 2021

Transcriptome-Wide Off-Target Effects of Steric-Blocking Oligonucleotides.

Transcriptome-Wide Off-Target Effects of Steric-Blocking Oligonucleotides.

Journal: Nucleic acid therapeutics

Published: August 13, 2021

Showing 1-12 of 80

Last Updated: 09/26/2026