Emilie M. Wigdor

Oxford, ENG OX39DU, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Journal: medRxiv : the preprint server for health sciences

Published: May 18, 2026

Genome-scale functional mapping of the mammalian whole brain with in vivo Perturb-seq.

Genome-scale functional mapping of the mammalian whole brain with in vivo Perturb-seq.

Journal: bioRxiv : the preprint server for biology

Published: April 27, 2026

Molecular dynamics of Brodmann Area 22 in development and autism.

Molecular dynamics of Brodmann Area 22 in development and autism.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

Disruption of Cell-Type-Specific Molecular Programs of Medium Spiny Neurons in Autism.

Disruption of Cell-Type-Specific Molecular Programs of Medium Spiny Neurons in Autism.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Genome-wide association studies of infant and toddler temperament in European and multi-ancestry populations.

Genome-wide association studies of infant and toddler temperament in European and multi-ancestry populations.

Journal: Nature human behaviour

Published: July 03, 2025

Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry.

Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry.

Journal: Nature human behaviour

Published: September 23, 2024

Examining the role of common variants in rare neurodevelopmental conditions.

Examining the role of common variants in rare neurodevelopmental conditions.

Journal: Nature

Published: February 12, 2024

AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.

AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.

Journal: bioRxiv : the preprint server for biology

Published: November 14, 2023

Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

Journal: Nature genetics

Published: July 24, 2023

Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders.

Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders.

Journal: Scientific reports

Published: April 19, 2023

Analysis of genetic dominance in the UK Biobank.

Analysis of genetic dominance in the UK Biobank.

Journal: Science (New York, N.Y.)

Published: March 30, 2023

Showing 1-12 of 19

Last Updated: 09/26/2026