Xiaolan Fang

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Dna Methylation

Congenital Heart Disease

Top Venues

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

Cold Spring Harbor molecular case studies

This page only lists publications with an associated author ORCID identifier.

Publications

Jonathan K Merritt, Xiaolan Fang, Raymond C Caylor, Steven A Skinner, Michael J Friez, Alan K Percy, Jeffrey Lorenz Neul
Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome. Genes 15 (5) (2024)
Jonathan K Merritt, Xiaolan Fang, Raymond C Caylor, Steven A Skinner, Michael J Friez, Alan K Percy, Jeffrey Lorenz Neul
Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome. Genes 15 (5) (2024)
Jonathan K Merritt, Xiaolan Fang, Raymond C Caylor, Steven A Skinner, Michael J Friez, Alan K Percy, Jeffrey Lorenz Neul
Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome. Genes 15 (5) (2024)
Xiaolan Fang, Lauren M Baggett, Raymond C Caylor, Alan K Percy, Jeffrey Lorenz Neul, Jane B Lane, Daniel G Glaze, Timothy A Benke, Eric D Marsh, Kathleen J Motil, Judy O Barrish, Fran E Annese, Steven A Skinner
Parental age effects and Rett syndrome. American journal of medical genetics. Part A (2023)
Xiaolan Fang, Timothy Fee, Jessica Davis, Elliot S Stolerman, Raymond C Caylor
Clinical Case Report: Mosaic Genetic Variants in the ANK3 Gene are Associated with Neurodevelopmental Delays. Cold Spring Harbor molecular case studies (2023)
Xiaolan Fang, Kameryn M Butler, Fatima Abidi, Jennifer Gass, Arthur Beisang, Timothy Feyma, Robin C Ryther, Shannon Standridge, Peter Heydemann, Mary Jones, Richard Haas, David N Lieberman, Eric D Marsh, Tim A Benke, Steve Skinner, Jeffrey L Neul, Alan K Percy, Michael J Friez, Raymond C Caylor
Analysis of X-inactivation status in a Rett syndrome natural history study cohort. Molecular genetics & genomic medicine 10 (5) (2022)