Margaret Yoon

Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline

I. Iossifov, G. Lyon, Han Fang, 2015, bioRxiv.

Genome Wide Variant Analysis of Simplex Autism Families with an Integrative Clinical-Bioinformatics Pipeline

I. Iossifov, G. Lyon, Han Fang, 2015, bioRxiv.

Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.

J. Rosenfeld, R. Pfundt, M. Shaw, 2018, American journal of human genetics.

Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine

Han Fang, David Mittelman, Gholson J. Lyon, 2017, BMC Medical Genomics.

Whole genome analysis of an extended pedigree with Prader–Willi Syndrome, hereditary hemochromatosis, and dysautonomia-like symptoms

G. Highnam, D. Mittelman, G. Lyon, 2015, bioRxiv.