L. Smith

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Jeffrey D. Mandell, Michael F. Walker, Stephan J Sanders, 2017, Neuron.

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Christopher S. Poultney, Jeffrey D. Mandell, Michael F. Walker, 2015, Neuron.

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Ryan L. Collins, Ryan M. Layer, Jeffrey D. Mandell, 2018, Nature Genetics.

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2017, bioRxiv.

Single-cell genomics improves the discovery of risk variants and genes of cardiac traits

L. Smith, H. Eckart, I. Moskowitz, 2022, medRxiv.

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2018, Nature Genetics.