Raymond Louie

11PUBLICATIONS
48CO-AUTHORS
Genetic immunologyGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesNeurogenetics
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Publications (11)

|Dec 17, 2025
Phenotypic Variability and Paternal Inheritance of a CHD8 Variant Causing Intellectual Developmental Disorder With Autism and Macrocephaly Confirmed by Epigenetic and Structural Analyses.

Yutaka Furuta, Kimberly M Ezell, Rizwan Hamid

|Oct 27, 2022
X-Linked intellectual disability update 2022.

Charles E Schwartz, Raymond J Louie, Annick Toutain

|Aug 04, 2022
Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome.

Jessica A Cooley Coleman, Timothy Fee, Renee Bend

|Jan 18, 2022
Near complete deletion of KMT2D in a college student.

Catherine Gooch, Jaclyn Paige Souder, Matthew L Tedder

|May 29, 2021
Syndromic neurodevelopmental disorder associated with de novo variants in DDX23.

William Burns, Lynne M Bird, Delphine Heron

|May 04, 2021
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.

Ilaria Parenti, Daphné Lehalle, Caroline Nava

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Frequent Collaborators

2 joint publications

Roger E Stevenson

1 joint publications

Hannah E Warren

1 joint publications

Neena L Champaigne

1 joint publications

Elliot S Stolerman