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Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.Human Molecular Genetics|June 5, 2019
RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathwaysOlivia K Gardner, Lily Wang, Derek Van Booven, et al.American Journal of Human Genetics|February 8, 2011
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosaStephan Züchner, Julia Dallman, Rong Wen, et al.Molecular Autism|January 14, 2014
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disordersHolly N Cukier, Nicole D Dueker, Susan H Slifer, et al.Journal of Alzheimer'S Disease : JAD|June 30, 2020
Immune and Inflammatory Pathways Implicated by Whole Blood Transcriptomic Analysis in a Diverse Ancestry Alzheimer's Disease CohortAnthony J Griswold, Sathesh K Sivasankaran, Derek Van Booven, et al.Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.JAMA Neurology|July 25, 2017
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal TransportBrian W Kunkle, Badri N Vardarajan, Adam C Naj, et al.Human Molecular Genetics|April 6, 2022
Genetic architecture of RNA editing regulation in Alzheimer's disease across diverse ancestral populationsOlivia K Gardner, Derek Van Booven, Lily Wang, et al.Molecular Autism|April 5, 2012
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate lociDale J Hedges, Kara L Hamilton-Nelson, Stephanie J Sacharow, et al.Annals of Human Genetics|May 22, 2009
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Deqiong Ma, Daria Salyakina, James M Jaworski, et al.Pageof 5