Irene E. Drmic

Functional impact of global rare copy number variation in autism spectrum disorders

Gary D Bader, Joseph T. Glessner, Stephen J. Guter, 2010, Nature.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.

S. Scherer, C. Lajonchere, D. Merico, 2013, American journal of human genetics.

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

B. Frey, J. R. MacDonald, John Wei, 2017, Nature Neuroscience.

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

D. Pinto, S. Scherer, D. Collier, 2012, American journal of human genetics.

Altered White Matter Organization in the TUBB3 E410K Syndrome.

Cynthia T. Laurentys, Irene E. Drmic, P. Grant, 2018, Cerebral cortex.

Regional EEG alpha power, coherence, and behavioral symptomatology in autism spectrum disorder

Michelle K. Jetha, Louis A. Schmidt, Karen J. Mathewson, 2012, Clinical Neurophysiology.

MYmind: a Concurrent Group-Based Mindfulness Intervention for Youth with Autism and Their Parents

Irene E. Drmic, D. Nicholas, J. Weiss, 2019, Mindfulness.

A large data resource of genomic copy number variation across neurodevelopmental disorders

J. R. MacDonald, John Wei, S. Scherer, 2019, npj Genomic Medicine.

Behavioral and cardiac responses to emotional stroop in adults with autism spectrum disorders: influence of medication

S. Bryson, Irene E. Drmic, S. Segalowitz, 2011, Autism research : official journal of the International Society for Autism Research.

Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage

S. Scherer, Irene E. Drmic, S. Walker, 2017, npj Genomic Medicine.